US20140209166A1 - Method for producing monocrystalline n-silicon solar cells, as well as a solar cell produced according to such a method - Google Patents
Method for producing monocrystalline n-silicon solar cells, as well as a solar cell produced according to such a method Download PDFInfo
- Publication number
- US20140209166A1 US20140209166A1 US14/244,476 US201414244476A US2014209166A1 US 20140209166 A1 US20140209166 A1 US 20140209166A1 US 201414244476 A US201414244476 A US 201414244476A US 2014209166 A1 US2014209166 A1 US 2014209166A1
- Authority
- US
- United States
- Prior art keywords
- solar cell
- layer
- aluminum
- emitter
- regions
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 53
- 229910052710 silicon Inorganic materials 0.000 title claims abstract description 27
- 239000010703 silicon Substances 0.000 title claims abstract description 27
- 238000004519 manufacturing process Methods 0.000 title abstract description 14
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 65
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 65
- 239000010410 layer Substances 0.000 claims description 110
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 23
- 238000009792 diffusion process Methods 0.000 claims description 23
- 229910052698 phosphorus Inorganic materials 0.000 claims description 23
- 239000011574 phosphorus Substances 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 21
- 238000005530 etching Methods 0.000 claims description 18
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 claims description 16
- 230000008569 process Effects 0.000 claims description 15
- 238000002161 passivation Methods 0.000 claims description 13
- 238000007669 thermal treatment Methods 0.000 claims description 13
- 239000011241 protective layer Substances 0.000 claims description 11
- 238000001312 dry etching Methods 0.000 claims description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 9
- 229910019213 POCl3 Inorganic materials 0.000 claims description 8
- 238000007641 inkjet printing Methods 0.000 claims description 8
- 229910000789 Aluminium-silicon alloy Inorganic materials 0.000 claims description 7
- 239000002019 doping agent Substances 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 230000008021 deposition Effects 0.000 claims description 5
- 238000009413 insulation Methods 0.000 claims description 5
- 238000007639 printing Methods 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 238000007650 screen-printing Methods 0.000 claims description 4
- 239000005368 silicate glass Substances 0.000 claims description 4
- 238000010981 drying operation Methods 0.000 claims 1
- 235000012431 wafers Nutrition 0.000 description 31
- 210000004027 cell Anatomy 0.000 description 22
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000004065 semiconductor Substances 0.000 description 8
- 210000002381 plasma Anatomy 0.000 description 7
- 239000007789 gas Substances 0.000 description 6
- 229910052814 silicon oxide Inorganic materials 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 238000000608 laser ablation Methods 0.000 description 5
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 230000005496 eutectics Effects 0.000 description 4
- 229910052731 fluorine Inorganic materials 0.000 description 4
- 239000011737 fluorine Substances 0.000 description 4
- 230000000873 masking effect Effects 0.000 description 4
- 229910052581 Si3N4 Inorganic materials 0.000 description 3
- 238000000137 annealing Methods 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 230000000149 penetrating effect Effects 0.000 description 3
- 230000006798 recombination Effects 0.000 description 3
- 238000005215 recombination Methods 0.000 description 3
- 230000002787 reinforcement Effects 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 3
- 238000003631 wet chemical etching Methods 0.000 description 3
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 238000005137 deposition process Methods 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- DOTMOQHOJINYBL-UHFFFAOYSA-N molecular nitrogen;molecular oxygen Chemical compound N#N.O=O DOTMOQHOJINYBL-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000005546 reactive sputtering Methods 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000004377 microelectronic Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 1
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/06—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers
- H01L31/068—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PN homojunction type, e.g. bulk silicon PN homojunction solar cells or thin film polycrystalline silicon PN homojunction solar cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/02—Details
- H01L31/0224—Electrodes
- H01L31/022408—Electrodes for devices characterised by at least one potential jump barrier or surface barrier
- H01L31/022425—Electrodes for devices characterised by at least one potential jump barrier or surface barrier for solar cells
- H01L31/022441—Electrode arrangements specially adapted for back-contact solar cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/06—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers
- H01L31/068—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PN homojunction type, e.g. bulk silicon PN homojunction solar cells or thin film polycrystalline silicon PN homojunction solar cells
- H01L31/0682—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PN homojunction type, e.g. bulk silicon PN homojunction solar cells or thin film polycrystalline silicon PN homojunction solar cells back-junction, i.e. rearside emitter, solar cells, e.g. interdigitated base-emitter regions back-junction cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/18—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
- H01L31/1804—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof comprising only elements of Group IV of the Periodic Table
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/547—Monocrystalline silicon PV cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Definitions
- the present invention relates to a method for producing monocrystalline n-silicon solar cells having a p + emitter on the rear side and spatially separate, heavily doped n ++ base regions near the surface on the rear side, as well as an interdigitated rear-side contact finger structure, which is in conductive contact with the p + emitter regions and the n ++ base regions, and it also relates to a solar cell produced according to such a method.
- the A300 cell is a so-called interdigitated back contact cell (IBC), which means that both the emitter and the BSF (back surface field) or base contact strips are situated on the rear side of the cell and are developed in the form of two meshing fork structures.
- IBC interdigitated back contact cell
- the required electrical separation of adjacently located n-doped and p-doped semiconductor regions on the same surface may be achieved in different ways. For example, there is the possibility of placing the two regions at different levels by removing the silicon oxide precipitated on the rear surface around the regions provided as base contacts using laser ablation (P. Engelhardt, N.-P. Harder, T. Neubert, H. Plagwitz, B. Fischer, R. Meyer and R. Brendel, “Laser Processing of 22% Efficient Back-Contacted Silicon Solar Cells,” 21st European Photovoltaic Solar Energy Conference, Dresden, 2006, p. 1).
- the emitter doping with phosphorus into the deeper-lying regions of the rear side, the front side and the connecting holes between front emitter and rear side emitter is implemented simultaneously, with the aid of a standard POCl 3 process.
- the metallic coating of both regions then takes place in a single aluminum vapor deposit step, the contact regions being electrically separated from each other by tearing the thin metal layer at the produced, virtually perpendicular step structure in the semiconductor surface.
- the local opening of the passivation layer which simultaneously is the insulation between the semiconductor regions and the superposed metallic current paths, is increasingly implemented with the aid of lasers.
- so-called laser ablation is employed for removing the insulation layer only locally.
- the so-called laser-fired contact method is employed, in which laser flashes move the vapor-deposited or sputtered aluminum layer through the insulating layer in order to contact the semiconductor regions lying underneath.
- wafer-protecting technologies known from the production of microelectronics chips, such as sputtering, vapor deposition, CVD, masked dry-etching of aluminum and of oxides using different halogen plasmas, as well as ink-jetting are to be made available for the production of solar cells.
- this objective is achieved by the features described herein, and with regard to the solar cell, it is achieved by a subject matter according to the feature combination as further described herein, the further embodiments representing at least useful specific developments and further improvements.
- An important aspect as to the exemplary embodiments and/or exemplary methods of the present invention is the production of a rear-side, locally diffused and passivated aluminum emitter and the possibility of carrying out simultaneous two-sided and local n + doping of n-silicon in the rear-side and front-side n-base regions near the surface.
- the diffusion steps for the emitters and the BSF or FSF region to be produced may be carried out in a common thermal treatment step for the diffusion of the selected emitter doping material of aluminum and the selected BSF/FSF dopant of phosphorus.
- the wafer may already be textured on one side before the aluminum-containing starting layer for the emitter doping is deposited and structured. However, it is also quite possible to carry out the texturing of the wafer only after the aluminum has been deposited and coated with an etch-resistant oxide on the rear side, so that the emitter, and thus the largest part of the rear side, remains untextured.
- the exemplary embodiments and/or exemplary methods of the present invention also shows the process sequence leading up to the finished rear-contacted solar cell, i.e., including the passivation of the front and back sides as well as the production of the contact structure, including the chemical or galvanic reinforcement.
- Essential for the exemplary embodiments and/or exemplary methods of the present invention is also the lateral separation of the emitter and base doping materials embodied in the finished solar cell, and thus the cell production technology, which is novel for solar cells.
- the basis of the method according to the present invention is the deposition of an aluminum or aluminum-containing thin layer on the rear side of the n-silicon wafer as well as the subsequent structuring of this thin layer, through which openings are obtained in the region of the future base contacts.
- the aluminum is then diffused into the n-silicon wafer in order to form a structured emitter layer.
- the aluminum or aluminum-containing layer is structured before being diffused into the wafer itself.
- the mentioned aluminum thin layer may be deposited on the wafer by a vapor-deposition or sputter process.
- the structuring of the deposited aluminum thin layer is performed in the form of strips, which may be by selective etching.
- dry-etching methods via a metal shadow mask may be employed, but the use of an organic mask is possible as well.
- Wet-chemical etching may of course be performed as well or selective etching using local printing of an etching paste.
- the structured emitter layer is covered by a dielectric protective layer across the entire surface. Furthermore, this protective layer is opened up in future base doping regions, which may again be realized by etching or with the aid of an etching mask.
- the silicon wafer is subjected to texturing, which takes place on the front side of the wafer and in the region of the openings in the dielectric protective layer.
- These openings may be formed via a strip-etching mask, the width of the produced openings being smaller than the width of the strip-shaped regions in the aluminum-free wafer.
- Material having high phosphorus content is deposited in the region of the openings in the dielectric protective layer in order to produce the heavily doped n ++ BSF base regions near the surface.
- This deposition may also be implemented by applying a paste using screen printing or stencil printing, by ink-jetting in local deposits or by similar methods.
- the applied paste is subjected to a drying step.
- the BSF doping material is then diffused in a thermal treatment step consisting of one step or multiple steps.
- the diffusing of the aluminum as emitter dopant and the diffusing of the BSF doping material may be performed in a common treatment step in an especially economic process.
- a flat phosphorus diffusion layer (FSF—front surface field) on the front side of the wafer in the region of the openings in the dielectric protective layer may be produced by an additional thermal treatment in a phosphorus-containing atmosphere, in particular a POCl 3 atmosphere, which has a layer resistance that is adjustable via the treatment temperature and the treatment time.
- a phosphorus-containing atmosphere in particular a POCl 3 atmosphere
- the wafer is covered by a passivation layer, e.g., a silicon oxide layer.
- the passivation layer is then locally removed in the emitter regions and the BSF regions on the rear side of the wafer.
- the entire rear side of the wafer is then covered by a conductive layer, especially an aluminum layer. This conductive layer is used to form the interdigitated contact-finger structure.
- a new type of solar cell is obtained as a result of the briefly outlined method, the n ++ base regions on the wafer's rear side having a lateral clearance from the p + -emitter regions, and at least the n ++ -base regions having a concentration of the emitter doping material that lies below the n-base concentration of the initial wafer.
- FIG. 1 shows in a first method step, an entire rear side 2 b of n-silicon wafer 1 , which is untextured in the illustrated example, is covered by an aluminum or aluminum-containing layer 3 , which forms the emitter dopant.
- FIG. 2 shows aluminum-containing layer 3 is brought into contact with a shadow mask 5 a.
- FIG. 3 shows a dry-etching step in plasma 7 a containing chlorine gas.
- FIG. 4 shows a further process step according to the present invention that pertains to the coating of the strip-shaped, structured, aluminum-containing layer 3 by a dielectric layer 8 .
- FIG. 5 shows, in a further method step, dielectric layer 8 is then removed by a masked etching step in the region of openings 6 b of an additional mask 5 b.
- FIG. 6 shows standard-type texturing is then implemented by dipping in a bath of KOH and isopropyl alcohol (IPA).
- IPA isopropyl alcohol
- FIG. 7 and FIG. 8 show a first thermal treatment step takes place at temperatures ranging from 900° C. to 1100° C. in a nitrogen-oxygen mixture, which causes the desired co-diffusion.
- FIG. 9 shows an optional second thermal treatment step at said usually lower temperatures, only this time using the POCl 3 atmosphere.
- FIG. 10 shows, in the following further course of the process, the residues of doping paste 10 b, produced phosphorus silicate glass PSG 14 b, dielectric masking layer 8 , and AlSi eutectic layer 3 b are etched off in suitable etch baths, so that emitter regions 11 , BSF region 12 , and front-side n + layer 14 are exposed.
- FIG. 11 shows both sides are coated by a dielectric in a further method step, e.g., by thermal oxidation of both sides of the wafer in a water vapor atmosphere, so that a silicon oxide layer results on front side 15 a and rear side 15 b.
- FIG. 12 shows that the annealing process realized in the manner described leads to excellent surface-passivation results.
- FIG. 13 shows passivation layer 15 b is locally removed on the rear side in all emitter and BSF regions, i.e., simultaneously by masked dry etching in a plasma 7 b containing fluorine gas, or without masking by laser ablation, for instance.
- FIG. 14 shows, in the following process step, the entire rear side is covered by an aluminum layer 20 , so that all contact surfaces 20 a and 20 b exposed in the preceding etching step are metalized, but otherwise are insulated from the semiconductor regions emitter 11 and BSF 12 by layer 15 b.
- FIG. 15 shows that by applying an acid-resistant layer 21 , which may be by structured inkjet-printing, aluminum layer 20 is then subdivided into emitter contact traces and BSF contact traces, and this application is performed so that narrow interspaces 22 a between planned contact regions 22 b are left free, in which the aluminum is removed by an acid 23 that etches aluminum selectively, that is to say, does not attack silicon oxide.
- an acid-resistant layer 21 which may be by structured inkjet-printing
- FIG. 16 shows, in a supplementary process step, an anti-reflection layer 24 , which may be of silicon nitride, is formed on the front side.
- FIG. 17 shows all contacts on the rear side may simultaneously and additionally be provided with a thick metallic conductive layer in a chemical or galvanic bath 25 or with the aid of a possibly light-based deposition process.
- FIG. 18 shows, after rinsing and drying the wafer, the back-contacted solar cell is functional.
- n-silicon wafer 1 which is untextured in the illustrated example, is covered by an aluminum or aluminum-containing layer 3 , which forms the emitter dopant.
- the front side of the wafer is denoted by reference numeral 2 a, and the rear side by reference numeral 2 b.
- aluminum-containing layer 3 is brought into contact with a shadow mask 5 a and structured by a dry-etching step in plasma 7 a containing chlorine gas (cf. FIGS. 2 and 3 ).
- an organic mask layer may be applied as well, e.g., by so-called ink-jetting, and the aluminum in the regions that have remained free then be etched in a wet-chemical manner.
- the two discussed technological variants produce longitudinal openings 4 in the form of strips in the region of breakthroughs 6 a of mask 5 a.
- the BSF doping material is diffused into strip-shaped openings 4 in aluminum layer 3 at a lateral distance to the aluminum edge.
- a further process step according to the exemplary embodiments and/or exemplary methods of the present invention then pertains to the coating of the strip-shaped, structured, aluminum-containing layer 3 by a dielectric layer 8 (cf. FIG. 4 ).
- Dielectric layer 8 may be made from an oxide, e.g., SiO 2 , TiO 2 , or Al 2 O 3 .
- layer 8 may be formed by reactive sputtering or by a CVD- or PECVD method.
- dielectric layer 8 is then removed by a masked etching step in the region of openings 6 b of an additional mask 5 b according to FIG. 5 .
- This may be a dry-etching step in a plasma 7 b containing fluorine gas, penetrating a metal foil mask, or by a dry-etching step in a plasma atmosphere containing fluorine gas, penetrating an organic mask layer, or a wet-chemical etching process, penetrating an organic mask layer.
- the strip-shaped openings 6 b in mask 5 b and the resulting strip-shaped regions 9 exposed in dielectric layer 8 are smaller than the strip-shaped openings 6 a in mask 5 a, and thus in aluminum-containing layer 3 .
- standard-type texturing is then implemented by dipping in a bath of KOH and isopropyl alcohol (IPA), for example. Since aluminum-containing layer 3 is protected by dielectric layer 8 , the texturing in the desired manner takes place only on front side 2 a of the wafer and in the exposed strip-shaped regions 9 b on the rear side of the wafer.
- IPA isopropyl alcohol
- openings 9 in cover layer 8 in the openings of emitter layer 4 are covered by a material having a large phosphorus component, which may be a paste, which is able to be deposited on the surface of wafer 1 in local deposits 10 by screen printing, stencil printing or ink-jetting, for example. If necessary, this paste is subjected to a drying step at temperatures of 150° C. to 200° C., for example.
- a material having a large phosphorus component which may be a paste, which is able to be deposited on the surface of wafer 1 in local deposits 10 by screen printing, stencil printing or ink-jetting, for example. If necessary, this paste is subjected to a drying step at temperatures of 150° C. to 200° C., for example.
- a one-step, or optionally a two-step, thermal treatment takes place with the possibility of a co-diffusion of the emitter dopant aluminum and the BSF doping material phosphorus from the dried, phosphorus-containing layer 10 b.
- a first thermal treatment step takes place at temperatures ranging from 900° C. to 1100° C. in a nitrogen-oxygen mixture, which causes the desired co-diffusion ( FIG. 8 ).
- a second treatment step optionally takes place at temperatures between 800° C. and 1000° C., i.e., in a phosphorus-containing gas 13 , which may be POCl 3 .
- the first high-temperature step causes an interdiffusion of silicon and aluminum and leads to a near-surface, mixed crystal layer 3 b having an eutectic AlSi structure and the p + -doping layer with Al profile 11 .
- the phosphorus from precursor deposit 10 b diffuses into BSF regions 9 b, into the silicon surface, and leads to a deep n ++ doping 12 .
- the diffusion profile of the phosphorus Due to the high temperatures of >1000° C. required for the aluminum diffusion, the diffusion profile of the phosphorus has a deeper characteristic than in P-diffusion processes around 900° C. that are otherwise the norm.
- the optional second thermal treatment step at said usually lower temperatures, only this time using the POCl 3 atmosphere according to FIG. 9 brings about not only the deep P-diffusion in the BSF regions of rear side 9 b, but additionally a flat P-diffusion on front side 2 a, which forms an FSF layer (front surface field) 14 having a layer resistance that is adjustable via the temperature and time, i.e., which may be high layer resistance.
- the first thermal treatment step may also be performed prior to the step of coating with the phosphorus-containing paste and independently of the subsequent second thermal treatment step.
- one advantage results from the fact that the process parameters of the second diffusion step at a lower temperature are able to be optimized, regardless of the process parameters of the first diffusion step at a higher temperature.
- the additional flat diffusion in the phosphorus-containing gas atmosphere which may be by using POCl 3 , may also be omitted if no front surface field layer 14 is desired as front-side passivation.
- this passivation could also be performed in an additional third diffusion process, in particular if the first phosphorus diffusion step has also been realized using POCl 3 .
- the residues of doping paste 10 b, produced phosphorus silicate glass PSG 14 b, dielectric masking layer 8 , and AlSi eutectic layer 3 b are etched off in suitable etch baths, so that emitter regions 11 , BSF region 12 , and front-side n + layer 14 are exposed, i.e., according to FIG. 10 .
- both sides are coated by a dielectric in a further method step, e.g., by thermal oxidation of both sides of the wafer in a water vapor atmosphere, so that a silicon oxide layer results on front side 15 a and rear side 15 b.
- both sides with a thin aluminum layer once a thermal oxide has formed on both wafer surfaces.
- the layer thickness may amount to a range between 10 nm and 100 nm.
- An aluminum layer 16 a subsequently results on the front side, and an aluminum layer 16 b on the rear side.
- the wafers, coated in this way, are then subjected to a thermal treatment at a range between 350° C. and 450° C.
- the annealing process realized in this manner leads to excellent surface-passivation results (cf. FIG. 12 ).
- the wafer is once again in a state as shown in FIG. 11 .
- passivation layer 15 b is locally removed on the rear side in all emitter and BSF regions, i.e., simultaneously by masked dry etching in a plasma 7 b containing fluorine gas, or without masking by laser ablation, for instance.
- the generally known LFC method may be used once the base metal coating has been deposited.
- Openings 18 a above emitter regions 11 , and openings 18 b above the BSF regions in mask 17 are smaller than openings 6 b in mask 5 b of the preceding etching step.
- this facilitates the adjustment of the shadow mask or mask layer 17 on the already existing structure; for another, the contact regions of the metallization to the semiconductor material are to be small, if possible, in order to restrict the surface recombination.
- the entire rear side is covered by an aluminum layer 20 , so that all contact surfaces 20 a and 20 b exposed in the preceding etching step are metalized, but otherwise are insulated from the semiconductor regions emitter 11 and BSF 12 by layer 15 b (cf. FIG. 14 ).
- an acid-resistant layer 21 which may be by structured inkjet-printing
- aluminum layer 20 is then subdivided into emitter contact traces and BSF contact traces.
- This application is performed in such a way that narrow interspaces 22 a between planned contact regions 22 b are left free, in which the aluminum is removed by an acid 23 that etches aluminum selectively, that is to say, does not attack silicon oxide (cf. FIG. 15 ).
- an organic paste is used which dries on the surface, or a hot-melt wax is used, which is injected while warm and then solidifies on the wafer while cooling.
- suitable ink which is subjected to a drying process.
- an anti-reflection layer 24 which may be of silicon nitride, is formed on the front side. With regard to thickness and refractive index, this anti-reflection layer is developed with a view toward optimum efficiency with respect to trapping energy from sunlight. Plasma-aided CVD or reactive sputtering, for instance, may be used to deposit this anti-reflection layer 24 .
- the plasma CVD method is used for this purpose because it takes place at temperatures above 400° C. yet below 500° C. and therefore causes annealing of aluminum contact layer 20 and thus a reduction in the contact resistance, without risking an AlSi liquefaction at the eutectic temperature of 577° C.
- all contacts on the rear side may simultaneously and additionally be provided with a thick metallic conductive layer in a chemical or galvanic bath 25 or with the aid of a possibly light-based deposition process.
- the individual layers may either consist of a single material of nickel, copper or silver, or of a plurality of individual layers of different metals, such as Ni+Cu+Sn or Ni+Ag or Ni+Au, for example.
- the back-contacted solar cell After rinsing and drying the wafer, the back-contacted solar cell is functional, as shown in FIG. 18 .
- An edge insulation is not required since the lateral clearance and the oxide cover ensure the separation of emitter regions 11 and BSF regions.
Landscapes
- Engineering & Computer Science (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Electromagnetism (AREA)
- Sustainable Development (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Physics & Mathematics (AREA)
- Sustainable Energy (AREA)
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Photovoltaic Devices (AREA)
- Electrodes Of Semiconductors (AREA)
Abstract
A method for producing monocrystalline n-silicon solar cells having a rear-side passivated p+ emitter and rear-side, spatially separate heavily doped n++-base regions near the surface, as well as an interdigitated rear-side contact finger structure, which is in conductive connection with the p+-emitter regions and the n++-base regions. An aluminum thin layer or an aluminum-containing thin layer is first deposited on the rear side of the n-silicon wafer, and the thin layer is subsequently structured so that openings are obtained in the region of the future base contacts. In a further process step, the aluminum is then diffused into the n-silicon wafer in order to form a structured emitter layer.
Description
- The present application is a divisional application of U.S. patent application Ser. No. 12/735,751, filed on Oct. 25, 2010, which is a national phase application of International Patent Application No. PCT/EP2009/051569, filed Feb. 11, 2009, and claims priority to German Patent Application No. 10 2008 009 268.1, filed Feb. 15, 2008 and to German Patent Application No. 10 2008 013 446.5, filed Mar. 10, 2008, all of which are hereby incorporated herein by reference in their entireties.
- The present invention relates to a method for producing monocrystalline n-silicon solar cells having a p+ emitter on the rear side and spatially separate, heavily doped n++ base regions near the surface on the rear side, as well as an interdigitated rear-side contact finger structure, which is in conductive contact with the p+ emitter regions and the n++ base regions, and it also relates to a solar cell produced according to such a method.
- Back contact solar cells on monocrystalline n-Si wafers have been developed by different solar cell manufacturers for a number of years, and some of these cells are already available on the market.
- For example, reference is made to the so-called A300 cell by SunPower (cf. W. D. Mulligan, D. H. Rose, M. J. Cudzinovic, D. M. DeCeuster, K. R. McIntosh, D. D. Smith, R. M. Swanson, “Manufacture of solar cells with 21% efficiency,” Proceedings of the 19th European Photovoltaic Solar Energy Conference, Paris, France (2004)). The A300 cell is a so-called interdigitated back contact cell (IBC), which means that both the emitter and the BSF (back surface field) or base contact strips are situated on the rear side of the cell and are developed in the form of two meshing fork structures.
- The required electrical separation of adjacently located n-doped and p-doped semiconductor regions on the same surface may be achieved in different ways. For example, there is the possibility of placing the two regions at different levels by removing the silicon oxide precipitated on the rear surface around the regions provided as base contacts using laser ablation (P. Engelhardt, N.-P. Harder, T. Neubert, H. Plagwitz, B. Fischer, R. Meyer and R. Brendel, “Laser Processing of 22% Efficient Back-Contacted Silicon Solar Cells,” 21st European Photovoltaic Solar Energy Conference, Dresden, 2006, p. 1).
- Once the surface damage caused by the laser process, and approx. 20 μm of the silicon have been removed by wet-chemical etching, the emitter doping with phosphorus into the deeper-lying regions of the rear side, the front side and the connecting holes between front emitter and rear side emitter is implemented simultaneously, with the aid of a standard POCl3 process.
- The metallic coating of both regions then takes place in a single aluminum vapor deposit step, the contact regions being electrically separated from each other by tearing the thin metal layer at the produced, virtually perpendicular step structure in the semiconductor surface.
- Technologies for the production of passivated emitters and of local spot contacts to the two semiconductor regions of base and emitter are likewise known and acknowledged in the literature (cf. R. A. Sinton, Y. Kwark, R. M. Swanson, “Recombination Mechanisms in Silicon Solar Cells,” 14th Project Integration Meeting, Photovoltaic Concentrator Technology Project, June 1986, p. 117-125).
- The local opening of the passivation layer, which simultaneously is the insulation between the semiconductor regions and the superposed metallic current paths, is increasingly implemented with the aid of lasers. On the one hand, so-called laser ablation is employed for removing the insulation layer only locally. On the other hand, the so-called laser-fired contact method (LFC) is employed, in which laser flashes move the vapor-deposited or sputtered aluminum layer through the insulating layer in order to contact the semiconductor regions lying underneath.
- From DE 696 31 815 T2, it is known to use an AlSi eutecticum as conductor base for the p-emitter structure, which is produced on the surface once the aluminum has diffused into the silicon through a previously inwardly diffused n+ layer of the rear side. The solution there also uses screen printing of aluminum paste through oxide windows above the n-base regions. The disadvantage of this solution is that the aluminum doping and the contacting of the aluminum emitter must be implemented in one step, i.e., across a large surface, so that the surface of the emitter and the surface of the metal contacting are identical. Thus, no passivation of the emitter with local contacts is possible. This results in a large surface recombination rate and thus relatively low efficiency.
- Both the laser ablation and the LFC method for the production of local contacts have the disadvantage that these methods are of sequential nature. In other words, the holes for each wafer must be produced individually, one after the other.
- In view of the above, it therefore is an object of the exemplary embodiments and/or exemplary methods of the present invention to provide a further developed method for producing monocrystalline n-silicon solar cells having rear-side, passivated p+ emitters and spatially separate, heavily doped n++ base regions near the surface, as well as an interdigitated rear-side contact finger structure, which allows high productivity and avoids the disadvantages of the related art.
- Furthermore, it should be possible to combine technological steps, particularly steps that cost considerable time in the production process, in order to ensure a further improvement in productivity.
- Furthermore, the use of wafer-protecting technologies known from the production of microelectronics chips, such as sputtering, vapor deposition, CVD, masked dry-etching of aluminum and of oxides using different halogen plasmas, as well as ink-jetting are to be made available for the production of solar cells.
- According to the exemplary embodiments and/or exemplary methods of the present invention, for the method this objective is achieved by the features described herein, and with regard to the solar cell, it is achieved by a subject matter according to the feature combination as further described herein, the further embodiments representing at least useful specific developments and further improvements.
- An important aspect as to the exemplary embodiments and/or exemplary methods of the present invention is the production of a rear-side, locally diffused and passivated aluminum emitter and the possibility of carrying out simultaneous two-sided and local n+ doping of n-silicon in the rear-side and front-side n-base regions near the surface. According to the exemplary embodiments and/or exemplary methods of the present invention, the diffusion steps for the emitters and the BSF or FSF region to be produced may be carried out in a common thermal treatment step for the diffusion of the selected emitter doping material of aluminum and the selected BSF/FSF dopant of phosphorus.
- The wafer may already be textured on one side before the aluminum-containing starting layer for the emitter doping is deposited and structured. However, it is also quite possible to carry out the texturing of the wafer only after the aluminum has been deposited and coated with an etch-resistant oxide on the rear side, so that the emitter, and thus the largest part of the rear side, remains untextured.
- As for the rest, the exemplary embodiments and/or exemplary methods of the present invention also shows the process sequence leading up to the finished rear-contacted solar cell, i.e., including the passivation of the front and back sides as well as the production of the contact structure, including the chemical or galvanic reinforcement.
- Essential for the exemplary embodiments and/or exemplary methods of the present invention is also the lateral separation of the emitter and base doping materials embodied in the finished solar cell, and thus the cell production technology, which is novel for solar cells.
- The basis of the method according to the present invention is the deposition of an aluminum or aluminum-containing thin layer on the rear side of the n-silicon wafer as well as the subsequent structuring of this thin layer, through which openings are obtained in the region of the future base contacts. In a further process step, the aluminum is then diffused into the n-silicon wafer in order to form a structured emitter layer. Thus, the aluminum or aluminum-containing layer is structured before being diffused into the wafer itself.
- The mentioned aluminum thin layer may be deposited on the wafer by a vapor-deposition or sputter process.
- The structuring of the deposited aluminum thin layer is performed in the form of strips, which may be by selective etching. Toward this end, dry-etching methods via a metal shadow mask may be employed, but the use of an organic mask is possible as well. Wet-chemical etching may of course be performed as well or selective etching using local printing of an etching paste.
- In a further method step, the structured emitter layer is covered by a dielectric protective layer across the entire surface. Furthermore, this protective layer is opened up in future base doping regions, which may again be realized by etching or with the aid of an etching mask.
- Then, the silicon wafer is subjected to texturing, which takes place on the front side of the wafer and in the region of the openings in the dielectric protective layer.
- These openings may be formed via a strip-etching mask, the width of the produced openings being smaller than the width of the strip-shaped regions in the aluminum-free wafer.
- Material having high phosphorus content is deposited in the region of the openings in the dielectric protective layer in order to produce the heavily doped n++ BSF base regions near the surface.
- This deposition may also be implemented by applying a paste using screen printing or stencil printing, by ink-jetting in local deposits or by similar methods.
- If necessary, the applied paste is subjected to a drying step.
- The BSF doping material is then diffused in a thermal treatment step consisting of one step or multiple steps.
- The diffusing of the aluminum as emitter dopant and the diffusing of the BSF doping material may be performed in a common treatment step in an especially economic process.
- A flat phosphorus diffusion layer (FSF—front surface field) on the front side of the wafer in the region of the openings in the dielectric protective layer may be produced by an additional thermal treatment in a phosphorus-containing atmosphere, in particular a POCl3 atmosphere, which has a layer resistance that is adjustable via the treatment temperature and the treatment time.
- With the aid of an etch bath, residual doping material, produced phosphorus silicate glass, residue from the insulation layer as well as produced AlSi eutecticum layers are removed, so that the emitter regions, the BSF region, and the possibly existing front-side n+-FSF structure are exposed.
- Subsequently, the wafer is covered by a passivation layer, e.g., a silicon oxide layer. The passivation layer is then locally removed in the emitter regions and the BSF regions on the rear side of the wafer. The entire rear side of the wafer is then covered by a conductive layer, especially an aluminum layer. This conductive layer is used to form the interdigitated contact-finger structure.
- A new type of solar cell is obtained as a result of the briefly outlined method, the n++ base regions on the wafer's rear side having a lateral clearance from the p+-emitter regions, and at least the n++-base regions having a concentration of the emitter doping material that lies below the n-base concentration of the initial wafer.
- The exemplary embodiments and/or exemplary methods of the present invention will be explained in greater detail in the following text with the aid of an exemplary embodiment, using schematic illustrations of the individual process steps.
-
FIG. 1 shows in a first method step, an entirerear side 2 b of n-silicon wafer 1, which is untextured in the illustrated example, is covered by an aluminum or aluminum-containinglayer 3, which forms the emitter dopant. -
FIG. 2 shows aluminum-containinglayer 3 is brought into contact with ashadow mask 5 a. -
FIG. 3 shows a dry-etching step inplasma 7 a containing chlorine gas. -
FIG. 4 shows a further process step according to the present invention that pertains to the coating of the strip-shaped, structured, aluminum-containinglayer 3 by adielectric layer 8. -
FIG. 5 shows, in a further method step,dielectric layer 8 is then removed by a masked etching step in the region ofopenings 6 b of anadditional mask 5 b. -
FIG. 6 shows standard-type texturing is then implemented by dipping in a bath of KOH and isopropyl alcohol (IPA). -
FIG. 7 andFIG. 8 show a first thermal treatment step takes place at temperatures ranging from 900° C. to 1100° C. in a nitrogen-oxygen mixture, which causes the desired co-diffusion. -
FIG. 9 shows an optional second thermal treatment step at said usually lower temperatures, only this time using the POCl3 atmosphere. -
FIG. 10 shows, in the following further course of the process, the residues ofdoping paste 10 b, produced phosphorussilicate glass PSG 14 b,dielectric masking layer 8, and AlSieutectic layer 3 b are etched off in suitable etch baths, so thatemitter regions 11,BSF region 12, and front-side n+ layer 14 are exposed. -
FIG. 11 shows both sides are coated by a dielectric in a further method step, e.g., by thermal oxidation of both sides of the wafer in a water vapor atmosphere, so that a silicon oxide layer results onfront side 15 a andrear side 15 b. -
FIG. 12 shows that the annealing process realized in the manner described leads to excellent surface-passivation results. -
FIG. 13 shows passivation layer 15 b is locally removed on the rear side in all emitter and BSF regions, i.e., simultaneously by masked dry etching in aplasma 7 b containing fluorine gas, or without masking by laser ablation, for instance. -
FIG. 14 shows, in the following process step, the entire rear side is covered by analuminum layer 20, so that all contact surfaces 20 a and 20 b exposed in the preceding etching step are metalized, but otherwise are insulated from thesemiconductor regions emitter 11 andBSF 12 bylayer 15 b. -
FIG. 15 shows that by applying an acid-resistant layer 21, which may be by structured inkjet-printing,aluminum layer 20 is then subdivided into emitter contact traces and BSF contact traces, and this application is performed so thatnarrow interspaces 22 a betweenplanned contact regions 22 b are left free, in which the aluminum is removed by an acid 23 that etches aluminum selectively, that is to say, does not attack silicon oxide. -
FIG. 16 shows, in a supplementary process step, ananti-reflection layer 24, which may be of silicon nitride, is formed on the front side. -
FIG. 17 shows all contacts on the rear side may simultaneously and additionally be provided with a thick metallic conductive layer in a chemical orgalvanic bath 25 or with the aid of a possibly light-based deposition process. -
FIG. 18 shows, after rinsing and drying the wafer, the back-contacted solar cell is functional. - In a first method step according to
FIG. 1 , entirerear side 2 b of n-silicon wafer 1, which is untextured in the illustrated example, is covered by an aluminum or aluminum-containinglayer 3, which forms the emitter dopant. The front side of the wafer is denoted byreference numeral 2 a, and the rear side byreference numeral 2 b. - In a further step, aluminum-containing
layer 3 is brought into contact with ashadow mask 5 a and structured by a dry-etching step inplasma 7 a containing chlorine gas (cf.FIGS. 2 and 3 ). - As an alternative, an organic mask layer may be applied as well, e.g., by so-called ink-jetting, and the aluminum in the regions that have remained free then be etched in a wet-chemical manner.
- The two discussed technological variants produce
longitudinal openings 4 in the form of strips in the region ofbreakthroughs 6 a ofmask 5 a. - At a later point, the BSF doping material is diffused into strip-shaped
openings 4 inaluminum layer 3 at a lateral distance to the aluminum edge. - A further process step according to the exemplary embodiments and/or exemplary methods of the present invention then pertains to the coating of the strip-shaped, structured, aluminum-containing
layer 3 by a dielectric layer 8 (cf.FIG. 4 ).Dielectric layer 8 may be made from an oxide, e.g., SiO2, TiO2, or Al2O3. - It is also possible to form a silicon nitride layer, which likewise is impermeable to phosphorus diffusion. The deposition of
layer 8 may be performed by reactive sputtering or by a CVD- or PECVD method. - In a further method step,
dielectric layer 8 is then removed by a masked etching step in the region ofopenings 6 b of anadditional mask 5 b according toFIG. 5 . - This may be a dry-etching step in a
plasma 7 b containing fluorine gas, penetrating a metal foil mask, or by a dry-etching step in a plasma atmosphere containing fluorine gas, penetrating an organic mask layer, or a wet-chemical etching process, penetrating an organic mask layer. - According to the exemplary embodiments and/or exemplary methods of the present invention, the strip-shaped
openings 6 b inmask 5 b and the resulting strip-shapedregions 9 exposed indielectric layer 8 are smaller than the strip-shapedopenings 6 a inmask 5 a, and thus in aluminum-containinglayer 3. - This prevents the occurrence of a short-circuit between the emitter regions and the BSF regions during the phosphorus doping in the next process step.
- According to the illustration in
FIG. 6 , standard-type texturing is then implemented by dipping in a bath of KOH and isopropyl alcohol (IPA), for example. Since aluminum-containinglayer 3 is protected bydielectric layer 8, the texturing in the desired manner takes place only onfront side 2 a of the wafer and in the exposed strip-shapedregions 9 b on the rear side of the wafer. - Subsequently,
openings 9 incover layer 8 in the openings ofemitter layer 4 are covered by a material having a large phosphorus component, which may be a paste, which is able to be deposited on the surface ofwafer 1 inlocal deposits 10 by screen printing, stencil printing or ink-jetting, for example. If necessary, this paste is subjected to a drying step at temperatures of 150° C. to 200° C., for example. - According to the illustrations in
FIGS. 8 and 9 , a one-step, or optionally a two-step, thermal treatment takes place with the possibility of a co-diffusion of the emitter dopant aluminum and the BSF doping material phosphorus from the dried, phosphorus-containinglayer 10 b. - A first thermal treatment step takes place at temperatures ranging from 900° C. to 1100° C. in a nitrogen-oxygen mixture, which causes the desired co-diffusion (
FIG. 8 ). A second treatment step optionally takes place at temperatures between 800° C. and 1000° C., i.e., in a phosphorus-containinggas 13, which may be POCl3. - The first high-temperature step causes an interdiffusion of silicon and aluminum and leads to a near-surface,
mixed crystal layer 3 b having an eutectic AlSi structure and the p+-doping layer withAl profile 11. - At the same time, the phosphorus from
precursor deposit 10 b diffuses intoBSF regions 9 b, into the silicon surface, and leads to a deep n++ doping 12. - Due to the high temperatures of >1000° C. required for the aluminum diffusion, the diffusion profile of the phosphorus has a deeper characteristic than in P-diffusion processes around 900° C. that are otherwise the norm.
- The optional second thermal treatment step at said usually lower temperatures, only this time using the POCl3 atmosphere according to
FIG. 9 , brings about not only the deep P-diffusion in the BSF regions ofrear side 9 b, but additionally a flat P-diffusion onfront side 2 a, which forms an FSF layer (front surface field) 14 having a layer resistance that is adjustable via the temperature and time, i.e., which may be high layer resistance. - Of course, the first thermal treatment step may also be performed prior to the step of coating with the phosphorus-containing paste and independently of the subsequent second thermal treatment step. In this case one advantage results from the fact that the process parameters of the second diffusion step at a lower temperature are able to be optimized, regardless of the process parameters of the first diffusion step at a higher temperature.
- In the same way, the additional flat diffusion in the phosphorus-containing gas atmosphere, which may be by using POCl3, may also be omitted if no front
surface field layer 14 is desired as front-side passivation. On the other hand, this passivation could also be performed in an additional third diffusion process, in particular if the first phosphorus diffusion step has also been realized using POCl3. - In the following further course of the process, the residues of
doping paste 10 b, produced phosphorussilicate glass PSG 14 b,dielectric masking layer 8, and AlSieutectic layer 3 b are etched off in suitable etch baths, so thatemitter regions 11,BSF region 12, and front-side n+ layer 14 are exposed, i.e., according toFIG. 10 . - As illustrated in
FIG. 11 , both sides are coated by a dielectric in a further method step, e.g., by thermal oxidation of both sides of the wafer in a water vapor atmosphere, so that a silicon oxide layer results onfront side 15 a andrear side 15 b. - Optionally, it is possible to coat both sides with a thin aluminum layer once a thermal oxide has formed on both wafer surfaces. The layer thickness may amount to a range between 10 nm and 100 nm. An
aluminum layer 16 a subsequently results on the front side, and analuminum layer 16 b on the rear side. The wafers, coated in this way, are then subjected to a thermal treatment at a range between 350° C. and 450° C. The annealing process realized in this manner leads to excellent surface-passivation results (cf.FIG. 12 ). - When the aluminum layer has been etched off, the wafer is once again in a state as shown in
FIG. 11 . - Furthermore, as shown in
FIG. 13 ,passivation layer 15 b is locally removed on the rear side in all emitter and BSF regions, i.e., simultaneously by masked dry etching in aplasma 7 b containing fluorine gas, or without masking by laser ablation, for instance. In the same way, the generally known LFC method may be used once the base metal coating has been deposited. -
Openings 18 aabove emitter regions 11, andopenings 18 b above the BSF regions inmask 17 are smaller thanopenings 6 b inmask 5 b of the preceding etching step. - For one, this facilitates the adjustment of the shadow mask or
mask layer 17 on the already existing structure; for another, the contact regions of the metallization to the semiconductor material are to be small, if possible, in order to restrict the surface recombination. - In the following process step, the entire rear side is covered by an
aluminum layer 20, so that all contact surfaces 20 a and 20 b exposed in the preceding etching step are metalized, but otherwise are insulated from thesemiconductor regions emitter 11 andBSF 12 bylayer 15 b (cf.FIG. 14 ). - By applying an acid-
resistant layer 21, which may be by structured inkjet-printing,aluminum layer 20 is then subdivided into emitter contact traces and BSF contact traces. This application is performed in such a way that narrow interspaces 22 a betweenplanned contact regions 22 b are left free, in which the aluminum is removed by an acid 23 that etches aluminum selectively, that is to say, does not attack silicon oxide (cf.FIG. 15 ). During the inkjet printing, either an organic paste is used which dries on the surface, or a hot-melt wax is used, which is injected while warm and then solidifies on the wafer while cooling. Another possibility is the use of suitable ink, which is subjected to a drying process. - In a supplementary process step, as shown in
FIG. 16 , ananti-reflection layer 24, which may be of silicon nitride, is formed on the front side. With regard to thickness and refractive index, this anti-reflection layer is developed with a view toward optimum efficiency with respect to trapping energy from sunlight. Plasma-aided CVD or reactive sputtering, for instance, may be used to deposit thisanti-reflection layer 24. - It is preferred if the plasma CVD method is used for this purpose because it takes place at temperatures above 400° C. yet below 500° C. and therefore causes annealing of
aluminum contact layer 20 and thus a reduction in the contact resistance, without risking an AlSi liquefaction at the eutectic temperature of 577° C. - According to
FIG. 17 , all contacts on the rear side may simultaneously and additionally be provided with a thick metallic conductive layer in a chemical orgalvanic bath 25 or with the aid of a possibly light-based deposition process. This results in the production of emittercircuit trace reinforcements 26 a or BSFcircuit trace reinforcements 26 b. The individual layers may either consist of a single material of nickel, copper or silver, or of a plurality of individual layers of different metals, such as Ni+Cu+Sn or Ni+Ag or Ni+Au, for example. - After rinsing and drying the wafer, the back-contacted solar cell is functional, as shown in
FIG. 18 . An edge insulation is not required since the lateral clearance and the oxide cover ensure the separation ofemitter regions 11 and BSF regions.
Claims (28)
1. A monocrystalline n-silicon solar cell, comprising:
a deposited thin layer, formed of one of aluminum and an aluminum-containing material, on a rear-side of an n-silicon wafer, wherein the thin layer is structured so that openings in the region of future base doping are obtained; and
a structured emitter layer, which is formed by diffusing aluminum into the n-silicon wafer in a further process;
wherein the monocrystalline n-silicon solar cell includes:
a p+ emitter on the rear-side of the n-silicon wafer;
heavily doped n++-base regions near the surface on the rear-side of the n-silicon wafer and spatially separate from the p+ emitter; and
an interdigitated rear-side contact finger structure, which is in conductive connection with the p+-emitter regions and the n++-base regions.
2. The solar cell of claim 1 , wherein the n++ base regions on the rear side of the wafer have a lateral clearance from the p+-emitter, and wherein at least the n++-base regions have a concentration of the emitter doping material that is below the n-base concentration of the n-silicon wafer.
3. The solar cell of claim 1 , wherein:
the n++-base regions are formed of base doping deposited in the openings, and the rear-side p+ emitter includes p+ emitter regions in which the openings that include the base doping are formed; and
the diffused aluminum is aluminum of the thin layer.
4. The solar cell of claim 3 , wherein the diffusion of the aluminum as emitter dopant and a diffusion of the doping material for the n++-base regions occurs in a common treatment operation.
5. The solar cell of claim 4 , wherein an insulaing layer is deposited over the the thin layer, and the doping material for the n++-base regions is deposited into the openings subsequent to the deposition of the insulating layer.
6. The solar cell of claim 4 , wherein the thin layer is deposited by one of a vapor deposit process and a sputter process.
7. The solar cell of claim 4 , wherein the structure of the deposited thin layer is in the form of strips by selective etching.
8. The solar cell of claim 7 , wherein the selective etching includes dry-etching with a metal shadow mask.
9. The solar cell of claim 7 , wherein the selective etching includes dry-etching with an organic mask.
10. The solar cell of claim 7 , wherein the selective etching is performed in a wet-chemical manner using an organic ink mask.
11. The solar cell of claim 7 , wherein the selective etching is performed by local printing of an etching paste.
12. The solar cell of claim 4 , wherein residue of the existing thin layer is removed once the aluminum diffusion has been completed.
13. The solar cell of claim 4 , wherein the structured emitter layer is covered by a dielectric protective layer across the full surface, and wherein the dielectric protective layer is opened up in the regions of the future base contacts.
14. The solar cell of claim 13 , wherein the openings are formed in regions of the future base doping, with the aid of an etching mask.
15. The solar cell of claim 14 , wherein the openings are formed via a strip-mask, and wherein the width of the produced openings are smaller than the width of the aluminum-free, strip-shaped regions in the wafer.
16. The solar cell of claim 13 , wherein the silicon wafer is subjected to texturation.
17. The solar cell of claim 1 , wherein:
the diffused aluminum is aluminum of the thin layer;
the structured emitter layer is covered by a dielectric protective layer across the full surface;
the dielectric protective layer is opened up in the regions of the future base contacts; and
the silicon wafer is subjected to texturation that takes place on the front side of the wafer and in the region of the openings in the dielectric protective layer.
18. The solar cell of claim 17 , wherein material having a high phosphorus content is deposited in the region of the openings in the dielectric protective layer to produce the heavily doped n++-base regions as back surface field (BSF) regions located near the surface.
19. The solar cell of claim 18 , wherein the deposition is implemented by applying a paste using one of screen printing, stencil printing, and ink-jetting in local deposits.
20. The solar cell of claim 19 , wherein the deposited paste is subjected to a drying operation.
21. The solar cell of claim 18 , wherein the doping material for the n++-base regions is diffused in a thermal treatment operation.
22. The solar cell of claim 21 , wherein a further thermal treatment in a phosphorus-containing atmosphere, which includes POCl3, occurs to produce a flat phosphorus diffusion layer (FSF—front surface field) on the front side of the wafer featuring a layer resistance that is adjustable by the treatment temperature and the treatment time.
23. The solar cell of claim 1 , wherein:
the diffused aluminum is aluminum of the thin layer; and
the p+ emitter and the n++-base regions are exposed by removal of the following via an etch bath: a residual doping material, a produced phosphorus silicate glass, residues of an insulation layer, and a produced AlSi eutecticum layer material.
24. The solar cell of claim 23 , wherein the wafer is covered by at least one passivation layer.
25. The solar cell of claim 24 , wherein the rear side of the wafer is locally freed of the passivation layer in the p+-emitter and n++-base regions to form local contact points.
26. The solar cell of claim 25 , wherein the entire rear side of the wafer is covered by a conductive layer, which includes an aluminum layer.
27. The solar cell of claim 26 , wherein the conductive layer is structured to form the interdigitated contact fingers.
28. The solar cell of claim 23 , wherein the diffusion of the aluminum as emitter dopant and diffusion of the doping material for the n++-base regions occurs in a common treatment operation.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14/244,476 US20140209166A1 (en) | 2008-02-15 | 2014-04-03 | Method for producing monocrystalline n-silicon solar cells, as well as a solar cell produced according to such a method |
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102008009268.1 | 2008-02-15 | ||
DE102008009268 | 2008-02-15 | ||
DE102008013446.5 | 2008-03-10 | ||
DE102008013446A DE102008013446A1 (en) | 2008-02-15 | 2008-03-10 | Process for producing monocrystalline n-silicon solar cells and solar cell, produced by such a process |
PCT/EP2009/051569 WO2009101107A1 (en) | 2008-02-15 | 2009-02-11 | Method for the production of monocrystalline n-silicon solar cells, and solar cell produced according to such a method |
US73575110A | 2010-10-25 | 2010-10-25 | |
US14/244,476 US20140209166A1 (en) | 2008-02-15 | 2014-04-03 | Method for producing monocrystalline n-silicon solar cells, as well as a solar cell produced according to such a method |
Related Parent Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2009/051569 Division WO2009101107A1 (en) | 2008-02-15 | 2009-02-11 | Method for the production of monocrystalline n-silicon solar cells, and solar cell produced according to such a method |
US12/735,751 Division US8728922B2 (en) | 2008-02-15 | 2009-02-11 | Method for producing monocrystalline N-silicon solar cells, as well as a solar cell produced according to such a method |
Publications (1)
Publication Number | Publication Date |
---|---|
US20140209166A1 true US20140209166A1 (en) | 2014-07-31 |
Family
ID=40896795
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/735,751 Expired - Fee Related US8728922B2 (en) | 2008-02-15 | 2009-02-11 | Method for producing monocrystalline N-silicon solar cells, as well as a solar cell produced according to such a method |
US14/244,476 Abandoned US20140209166A1 (en) | 2008-02-15 | 2014-04-03 | Method for producing monocrystalline n-silicon solar cells, as well as a solar cell produced according to such a method |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/735,751 Expired - Fee Related US8728922B2 (en) | 2008-02-15 | 2009-02-11 | Method for producing monocrystalline N-silicon solar cells, as well as a solar cell produced according to such a method |
Country Status (7)
Country | Link |
---|---|
US (2) | US8728922B2 (en) |
EP (1) | EP2250675B1 (en) |
JP (1) | JP2011512661A (en) |
KR (1) | KR20100136462A (en) |
CN (1) | CN102017165A (en) |
DE (1) | DE102008013446A1 (en) |
WO (1) | WO2009101107A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017007972A1 (en) * | 2015-07-07 | 2017-01-12 | Crystal Solar, Inc. | High efficiency single crystal silicon solar cell with epitaxially deposited silicon layers with deep junction(s) |
US10134940B2 (en) | 2010-07-30 | 2018-11-20 | Panasonic Intellectual Property Management Co., Ltd. | Method of manufacturing solar cell |
US10224453B2 (en) | 2014-11-04 | 2019-03-05 | Lg Electronics Inc. | Solar cell and method for manufacturing the same |
WO2019195806A3 (en) * | 2018-04-06 | 2020-11-05 | Sunpower Corporation | Local patterning and metallization of semiconductor structures using a laser beam |
Families Citing this family (41)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102009008786A1 (en) * | 2008-10-31 | 2010-06-10 | Bosch Solar Energy Ag | Process for producing a solar cell and solar cell |
DE102009015764A1 (en) * | 2008-10-31 | 2010-06-17 | Bosch Solar Energy Ag | Process for producing monocrystalline n-silicon back contact solar cells |
TWI455385B (en) * | 2009-08-20 | 2014-10-01 | Univ Nat Taiwan | Organic solar cell and method forming the same |
CN102074599B (en) | 2009-09-07 | 2014-10-29 | Lg电子株式会社 | Solar cell and method for manufacturing the same |
US8525018B2 (en) | 2009-09-07 | 2013-09-03 | Lg Electronics Inc. | Solar cell |
US8962380B2 (en) | 2009-12-09 | 2015-02-24 | Solexel, Inc. | High-efficiency photovoltaic back-contact solar cell structures and manufacturing methods using thin planar semiconductor absorbers |
NL2004065C2 (en) * | 2010-01-06 | 2011-07-07 | Stichting Energie | Solar panel module and method for manufacturing such a solar panel module. |
KR101027829B1 (en) * | 2010-01-18 | 2011-04-07 | 현대중공업 주식회사 | Method for fabricating back contact solar cell |
FR2956242A1 (en) * | 2010-02-05 | 2011-08-12 | Commissariat Energie Atomique | Substrate i.e. P-type silicon substrate, realizing method for forming photovoltaic cell, involves realizing diffusion heat treatment to form first and second volumes doped respectively from sources of dopants |
DE102010027940A1 (en) * | 2010-04-20 | 2011-10-20 | Robert Bosch Gmbh | Process for producing a solar cell and solar cell produced by this process |
US8524524B2 (en) * | 2010-04-22 | 2013-09-03 | General Electric Company | Methods for forming back contact electrodes for cadmium telluride photovoltaic cells |
DE102010028189B4 (en) | 2010-04-26 | 2018-09-27 | Solarworld Industries Gmbh | solar cell |
DE102010028187A1 (en) * | 2010-04-26 | 2011-10-27 | Robert Bosch Gmbh | A method of making a metal wrap-through solar cell and a metal wrap-through solar cell made by this method |
KR20140015247A (en) | 2010-08-05 | 2014-02-06 | 솔렉셀, 인크. | Backplane reinforcement and interconnects for solar cells |
CN102148283A (en) * | 2010-09-28 | 2011-08-10 | 常州天合光能有限公司 | Method for preparing N-type solar battery by one-step diffusion |
KR101145472B1 (en) * | 2010-11-29 | 2012-05-15 | 현대중공업 주식회사 | Method for fabricating solar cell |
US8889981B2 (en) | 2011-10-18 | 2014-11-18 | Samsung Sdi Co., Ltd. | Photoelectric device |
KR20130050721A (en) | 2011-11-08 | 2013-05-16 | 삼성에스디아이 주식회사 | Solar cell |
KR101902887B1 (en) * | 2011-12-23 | 2018-10-01 | 엘지전자 주식회사 | Method for manufacturing the same |
US11038080B2 (en) * | 2012-01-19 | 2021-06-15 | Utica Leaseco, Llc | Thin-film semiconductor optoelectronic device with textured front and/or back surface prepared from etching |
KR101948206B1 (en) * | 2012-03-02 | 2019-02-14 | 인텔렉츄얼 키스톤 테크놀로지 엘엘씨 | thin film type solar cell and the fabrication method thereof |
US8828784B2 (en) * | 2012-04-23 | 2014-09-09 | Solexel, Inc. | Resistance component extraction for back contact back junction solar cells |
AU2013272248A1 (en) * | 2012-04-24 | 2014-11-13 | Solexel, Inc. | Manufacturing methods and structures for large-area thin-film solar cells and other semiconductor devices |
CN103107237B (en) * | 2012-12-06 | 2016-03-23 | 杭州赛昂电力有限公司 | Monocrystaline silicon solar cell and preparation method thereof |
US8912071B2 (en) | 2012-12-06 | 2014-12-16 | International Business Machines Corporation | Selective emitter photovoltaic device |
US20140158192A1 (en) * | 2012-12-06 | 2014-06-12 | Michael Cudzinovic | Seed layer for solar cell conductive contact |
US20140166093A1 (en) * | 2012-12-18 | 2014-06-19 | Paul Loscutoff | Solar cell emitter region fabrication using n-type doped silicon nano-particles |
US8642378B1 (en) | 2012-12-18 | 2014-02-04 | International Business Machines Corporation | Field-effect inter-digitated back contact photovoltaic device |
US8785233B2 (en) * | 2012-12-19 | 2014-07-22 | Sunpower Corporation | Solar cell emitter region fabrication using silicon nano-particles |
US9525082B2 (en) * | 2013-09-27 | 2016-12-20 | Sunpower Corporation | Solar cell contact structures formed from metal paste |
US9437756B2 (en) * | 2013-09-27 | 2016-09-06 | Sunpower Corporation | Metallization of solar cells using metal foils |
TWI509826B (en) * | 2013-10-09 | 2015-11-21 | Neo Solar Power Corp | Back-contact solar cell and manufacturing method thereof |
CN104576312A (en) * | 2013-10-29 | 2015-04-29 | 中芯国际集成电路制造(上海)有限公司 | Method for preventing crystal defect from being produced on surface of phosphor-doped silicon oxide film |
TWI496299B (en) * | 2013-10-30 | 2015-08-11 | Inventec Solar Energy Corp | Electrode structure and solar cell using the same |
US20150270421A1 (en) * | 2014-03-20 | 2015-09-24 | Varian Semiconductor Equipment Associates, Inc. | Advanced Back Contact Solar Cells |
CN103943726B (en) * | 2014-04-22 | 2016-03-23 | 英利集团有限公司 | The preparation method of N-type solar cell and the preparation method of height knot thereof |
KR101661807B1 (en) * | 2014-07-28 | 2016-09-30 | 엘지전자 주식회사 | Solar cell and the manufacturing mathod thereof |
CN105244392A (en) * | 2015-11-09 | 2016-01-13 | 常州天合光能有限公司 | Photovoltaic cell applied to automobile roof for improving shadow shading reliability, and manufacturing method thereof |
KR102610637B1 (en) * | 2016-12-13 | 2023-12-05 | 신에쓰 가가꾸 고교 가부시끼가이샤 | High-efficiency back electrode type solar cell, solar cell module, and solar power generation system |
CN110718604A (en) * | 2018-06-26 | 2020-01-21 | 上海硅洋新能源科技有限公司 | Back surface field of P-type crystalline silicon solar cell and back passivation layer preparation method |
CN117810310B (en) * | 2024-02-29 | 2024-06-07 | 浙江晶科能源有限公司 | Solar cell preparation method, solar cell and photovoltaic module |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5641362A (en) * | 1995-11-22 | 1997-06-24 | Ebara Solar, Inc. | Structure and fabrication process for an aluminum alloy junction self-aligned back contact silicon solar cell |
US6262359B1 (en) * | 1999-03-17 | 2001-07-17 | Ebara Solar, Inc. | Aluminum alloy back junction solar cell and a process for fabrication thereof |
US20010008145A1 (en) * | 2000-01-19 | 2001-07-19 | Agency Of Industrial Science & Technology, Ministry Of International Trade & Industry | Photovoltaic device |
US20050126627A1 (en) * | 2003-11-19 | 2005-06-16 | Sharp Kabushiki Kaisha | Solar cell and method for producing the same |
US20080072953A1 (en) * | 2006-09-27 | 2008-03-27 | Thinsilicon Corp. | Back contact device for photovoltaic cells and method of manufacturing a back contact device |
Family Cites Families (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4478879A (en) * | 1983-02-10 | 1984-10-23 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Screen printed interdigitated back contact solar cell |
JPH03285360A (en) * | 1990-03-31 | 1991-12-16 | Mitsubishi Materials Corp | Solar cell |
DE59303176D1 (en) * | 1992-04-28 | 1996-08-14 | Siemens Solar Gmbh | Semiconductor body with well adhering metallization |
US5609775A (en) * | 1995-03-17 | 1997-03-11 | Chartered Semiconductor Manufacturing Pte Ltd. | Dry etch process for titanium-tungsten films |
JP3368145B2 (en) * | 1996-06-20 | 2003-01-20 | シャープ株式会社 | Method of manufacturing solar cell |
US6552414B1 (en) * | 1996-12-24 | 2003-04-22 | Imec Vzw | Semiconductor device with selectively diffused regions |
US6180869B1 (en) | 1997-05-06 | 2001-01-30 | Ebara Solar, Inc. | Method and apparatus for self-doping negative and positive electrodes for silicon solar cells and other devices |
JP2000138386A (en) | 1998-11-04 | 2000-05-16 | Shin Etsu Chem Co Ltd | Manufacturing method of solar cell and solar cell manufactured by the method |
DE10021440A1 (en) | 2000-05-03 | 2001-11-15 | Univ Konstanz | Process for producing a solar cell and solar cell produced by this process |
US6586270B2 (en) * | 2000-06-01 | 2003-07-01 | Canon Kabushiki Kaisha | Process for producing a photovoltaic element |
US6656532B2 (en) * | 2001-05-17 | 2003-12-02 | Honeywell International Inc. | Layered hard mask and dielectric materials and methods therefor |
US6853076B2 (en) * | 2001-09-21 | 2005-02-08 | Intel Corporation | Copper-containing C4 ball-limiting metallurgy stack for enhanced reliability of packaged structures and method of making same |
US6593224B1 (en) * | 2002-03-05 | 2003-07-15 | Bridge Semiconductor Corporation | Method of manufacturing a multilayer interconnect substrate |
US7388147B2 (en) * | 2003-04-10 | 2008-06-17 | Sunpower Corporation | Metal contact structure for solar cell and method of manufacture |
FR2854497B1 (en) * | 2003-04-29 | 2005-09-02 | Commissariat Energie Atomique | METHOD FOR MAKING A SEMICONDUCTOR DEVICE WITH SELF-ALIGNED METALLISATIONS |
US6998288B1 (en) * | 2003-10-03 | 2006-02-14 | Sunpower Corporation | Use of doped silicon dioxide in the fabrication of solar cells |
US20050172996A1 (en) | 2004-02-05 | 2005-08-11 | Advent Solar, Inc. | Contact fabrication of emitter wrap-through back contact silicon solar cells |
EP1763086A1 (en) * | 2005-09-09 | 2007-03-14 | Interuniversitair Micro-Elektronica Centrum | Photovoltaic cell with thick silicon oxide and silicon nitride passivation and fabrication method |
US20070137692A1 (en) * | 2005-12-16 | 2007-06-21 | Bp Corporation North America Inc. | Back-Contact Photovoltaic Cells |
JP2007281044A (en) * | 2006-04-04 | 2007-10-25 | Canon Inc | Solar battery |
US7807556B2 (en) * | 2006-12-05 | 2010-10-05 | General Electric Company | Method for doping impurities |
-
2008
- 2008-03-10 DE DE102008013446A patent/DE102008013446A1/en not_active Withdrawn
-
2009
- 2009-02-11 CN CN2009801134617A patent/CN102017165A/en active Pending
- 2009-02-11 JP JP2010546320A patent/JP2011512661A/en active Pending
- 2009-02-11 KR KR1020107020690A patent/KR20100136462A/en not_active Application Discontinuation
- 2009-02-11 WO PCT/EP2009/051569 patent/WO2009101107A1/en active Application Filing
- 2009-02-11 EP EP09711197.5A patent/EP2250675B1/en not_active Not-in-force
- 2009-02-11 US US12/735,751 patent/US8728922B2/en not_active Expired - Fee Related
-
2014
- 2014-04-03 US US14/244,476 patent/US20140209166A1/en not_active Abandoned
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5641362A (en) * | 1995-11-22 | 1997-06-24 | Ebara Solar, Inc. | Structure and fabrication process for an aluminum alloy junction self-aligned back contact silicon solar cell |
US6262359B1 (en) * | 1999-03-17 | 2001-07-17 | Ebara Solar, Inc. | Aluminum alloy back junction solar cell and a process for fabrication thereof |
US20010008145A1 (en) * | 2000-01-19 | 2001-07-19 | Agency Of Industrial Science & Technology, Ministry Of International Trade & Industry | Photovoltaic device |
US20050126627A1 (en) * | 2003-11-19 | 2005-06-16 | Sharp Kabushiki Kaisha | Solar cell and method for producing the same |
US20080072953A1 (en) * | 2006-09-27 | 2008-03-27 | Thinsilicon Corp. | Back contact device for photovoltaic cells and method of manufacturing a back contact device |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10134940B2 (en) | 2010-07-30 | 2018-11-20 | Panasonic Intellectual Property Management Co., Ltd. | Method of manufacturing solar cell |
US10224453B2 (en) | 2014-11-04 | 2019-03-05 | Lg Electronics Inc. | Solar cell and method for manufacturing the same |
US10714654B2 (en) | 2014-11-04 | 2020-07-14 | Lg Electronics Inc. | Solar cell and method for manufacturing the same |
US10749069B2 (en) | 2014-11-04 | 2020-08-18 | Lg Electronics Inc. | Solar cell and method for manufacturing the same |
WO2017007972A1 (en) * | 2015-07-07 | 2017-01-12 | Crystal Solar, Inc. | High efficiency single crystal silicon solar cell with epitaxially deposited silicon layers with deep junction(s) |
WO2019195806A3 (en) * | 2018-04-06 | 2020-11-05 | Sunpower Corporation | Local patterning and metallization of semiconductor structures using a laser beam |
US11362234B2 (en) | 2018-04-06 | 2022-06-14 | Sunpower Corporation | Local patterning and metallization of semiconductor structures using a laser beam |
Also Published As
Publication number | Publication date |
---|---|
EP2250675A1 (en) | 2010-11-17 |
CN102017165A (en) | 2011-04-13 |
JP2011512661A (en) | 2011-04-21 |
US8728922B2 (en) | 2014-05-20 |
KR20100136462A (en) | 2010-12-28 |
DE102008013446A1 (en) | 2009-08-27 |
EP2250675B1 (en) | 2016-04-27 |
WO2009101107A1 (en) | 2009-08-20 |
US20110041902A1 (en) | 2011-02-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US8728922B2 (en) | Method for producing monocrystalline N-silicon solar cells, as well as a solar cell produced according to such a method | |
US9373731B2 (en) | Dielectric structures in solar cells | |
EP2171762B1 (en) | Method for producing a silicon solar cell with a back-etched emitter as well as a corresponding solar cell | |
JP5277485B2 (en) | Manufacturing method of solar cell | |
NL2004310C2 (en) | Method of fabrication of a back-contacted photovoltaic cell, and back-contacted photovoltaic cell made by such a method. | |
US7144751B2 (en) | Back-contact solar cells and methods for fabrication | |
US8722453B2 (en) | Photovoltaic device and method for manufacturing the same | |
US20110253211A1 (en) | Solar cell and method for manufacturing same | |
US20080290368A1 (en) | Photovoltaic cell with shallow emitter | |
EP2071632B1 (en) | Thin-film solar cell and process for its manufacture | |
EP2460178B1 (en) | Surface treatment of silicon | |
JP2008529265A (en) | Semiconductor device having heterojunction and interfinger structure | |
KR20110123663A (en) | Method and structure of photovoltaic grid stacks by solution-based process | |
WO2008141415A1 (en) | Photovoltaic cell with shallow emitter | |
CA2731158A1 (en) | Crystalline silicon pv cell with selective emitter produced with low temperature precision etch back and passivation process | |
KR101597532B1 (en) | The Manufacturing Method of Back Contact Solar Cells | |
CN113380922A (en) | Preparation method and selective emitter solar cell | |
EP3493272B1 (en) | Solar cell element and method for manufacturing solar cell element | |
WO2012031608A1 (en) | Method for the fabrication of a rear side contacted solar cell | |
WO2013143350A1 (en) | Solar cell, module and method for manufacturing solar cell electrode | |
WO2013000025A1 (en) | Metallisation method | |
CN117691000B (en) | Preparation method of solar cell, solar cell and photovoltaic module | |
JP2008159997A (en) | Manufacturing method for solar cell element, and conductive paste | |
WO2009150741A1 (en) | Photovoltaic device manufacturing method | |
TW201316541A (en) | Method of fabricating plate-through solar cell |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |