AU602109B2 - Improvements in plasma generators - Google Patents
Improvements in plasma generators Download PDFInfo
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- AU602109B2 AU602109B2 AU20679/88A AU2067988A AU602109B2 AU 602109 B2 AU602109 B2 AU 602109B2 AU 20679/88 A AU20679/88 A AU 20679/88A AU 2067988 A AU2067988 A AU 2067988A AU 602109 B2 AU602109 B2 AU 602109B2
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- plasma
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- electrons
- fragmenter
- plasma generator
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- 150000002500 ions Chemical class 0.000 claims description 44
- 239000002245 particle Substances 0.000 claims description 14
- 230000007935 neutral effect Effects 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 230000010355 oscillation Effects 0.000 claims description 8
- 238000012856 packing Methods 0.000 claims description 8
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 8
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 6
- 238000013467 fragmentation Methods 0.000 claims description 5
- 238000006062 fragmentation reaction Methods 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- 229910052715 tantalum Inorganic materials 0.000 claims description 5
- 239000000835 fiber Substances 0.000 claims description 4
- 230000003993 interaction Effects 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 229910052697 platinum Inorganic materials 0.000 claims description 4
- 230000005284 excitation Effects 0.000 claims description 3
- 238000005086 pumping Methods 0.000 claims description 2
- 239000003870 refractory metal Substances 0.000 claims 1
- 210000002381 plasma Anatomy 0.000 description 79
- 239000007789 gas Substances 0.000 description 43
- 239000000758 substrate Substances 0.000 description 25
- 125000004429 atom Chemical group 0.000 description 14
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 14
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 8
- 238000000576 coating method Methods 0.000 description 6
- 238000000151 deposition Methods 0.000 description 6
- 230000008021 deposition Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 229910052786 argon Inorganic materials 0.000 description 4
- 239000012159 carrier gas Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 3
- 229910003460 diamond Inorganic materials 0.000 description 3
- 239000010432 diamond Substances 0.000 description 3
- 239000010408 film Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 229910000077 silane Inorganic materials 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 235000015842 Hesperis Nutrition 0.000 description 1
- 235000012633 Iberis amara Nutrition 0.000 description 1
- 229910001423 beryllium ion Inorganic materials 0.000 description 1
- -1 carbon ions Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000005137 deposition process Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000000407 epitaxy Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 229910021385 hard carbon Inorganic materials 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000007733 ion plating Methods 0.000 description 1
- 238000010884 ion-beam technique Methods 0.000 description 1
- 229910052754 neon Inorganic materials 0.000 description 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
- 229910052756 noble gas Inorganic materials 0.000 description 1
- 230000005658 nuclear physics Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000005211 surface analysis Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000000427 thin-film deposition Methods 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/02—Details
- H01J37/04—Arrangements of electrodes and associated parts for generating or controlling the discharge, e.g. electron-optical arrangement or ion-optical arrangement
- H01J37/08—Ion sources; Ion guns
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05H—PLASMA TECHNIQUE; PRODUCTION OF ACCELERATED ELECTRICALLY-CHARGED PARTICLES OR OF NEUTRONS; PRODUCTION OR ACCELERATION OF NEUTRAL MOLECULAR OR ATOMIC BEAMS
- H05H1/00—Generating plasma; Handling plasma
- H05H1/24—Generating plasma
- H05H1/46—Generating plasma using applied electromagnetic fields, e.g. high frequency or microwave energy
- H05H1/461—Microwave discharges
Landscapes
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Plasma & Fusion (AREA)
- Electromagnetism (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Chemical Vapour Deposition (AREA)
Description
COMMONWEALTH OF AUSTRA 0 orm '0 Patents Act 1, 1969 V U COMPLETE SPECIFICATION
(ORIGINAL)
FOR OFFICE USE: Class Int. Class Application Number: Lodged: Complete Application No.
Specification Lodged Published I' Prriority: Related art: Name of Applicant: TO BE COMPLETED BY APPLICANT THE COMMONWEALTH OF AUSTRALIA Address of Applicant: care of The Secretary, Department of Defence, Anzac Park West Building, Constitution Avenue, Canberra, Australian Capital Territory, Commonwealth of Australia.
Actual Inventor: ISTVAN KRISTOF VARGA Address for Service: COLLISON CO., Patent Attorneys, 117 King William Street, Adelaide, South Australia, 5000.
Complete Specification for the invention entitled: "IMPROVEMENTS IN PLASMA GENERATORS" The following statement is a full description of this invention, including the best method of performing it known to.w- us: A000345 PATENT, MAr";S DESIGNS SUD-Oi:ICE i 2 AU 3 SOUTH AUSTRALIA L7 2 This invention relates to techniques which may be used to expand and intensify plasma formed in a working chamber for deposition of ions and atoms onto substrates and for other purposes.
In the last two decades, but particularly in recent years, significant developments have taken place in the area of plasma generation.
0:2:0: These have been prompted by the usefulness of plasma in all aspects of semio conductor technology and by an ever increasing number of new applications.
s e Some of the areas where plasma, or its separated charged particles are used, are as ion sources, in ion rockets, in nuclear physics, in heavy-ion science, in 04- ion plating, in crystal growth also known as ion beam epitaxy, synthesis of compound materials also known as plasma polymerization, in reactive S, 15 sputtering, in ion sputtered activated reactive evaporation, in surface analysis in medical applications, in surface treatment in ion-assisted thin film deposition 0o° and in lasers and in many other applications.
S0 000 As an example of the art, reference may be had to the proceedings of the International Engineering Congress, ISIAT'83 and IPAT'83 Kyoto (1983) in which a plasma system is described which was used for plasma oxidation of 0o silicon surfaces as used in VLSI production, but the present invention has many o applications besides these.
Also reference may be had to the specification of United States Patent No.
3660715 in the name of Richard F. Post assigned to the United States Energy Commission which relates to plasma generator using a stack of pulsed washers to release ionize and heat the gas. This present invention relates to improvements in plasma generators as described in our earlier Patent Application No. PCT/AU86/00128.
The present invention generally consists of a plasma generator which allows both electrons and ions to oscillate in an applied field at low frequency excitation with electrons and ions moving in opposite directions, but with two sources of ions and electrons to provide increased and more efficient deposition rates.
3 The invention also proposes improvements in plasma generators, particularly in the fragmentation and ionization of gas molecules introduced into such generators for some of the purposes discussed above.
In our earlier Patent Application, we discussed introduction of gases for ionization in the plasma generation region of the plasma generator but this invention also includes the proposal to introduce alternative methods of gas fragmentation to 1 0 introduce fragmented gas particles into the plasma. In one form, therefore, the invention is said to reside in a plasma generator which allows both electrons and ions to oscillate in an applied field at low frequency excitation with electrons and ions moving in opposite directions, characterised by two sources of ions and electrons at opposite sides of a plasma chamber to provide an increased and 1 5 more efficient plasma, within the plasma chamber and an electrode in the plasma chamber which is polarised to extract or utilize electrically neutral or positive or negative charged particles generated in the plasma chamber.
Such a plasma generator may include a thermal fragmenter.
Alternatively, the invention may be said to reside in a plasma generator having a plasma chamber and two sources ions and electrons consisting of two plain cylindrical magnetrons at opposite ends of the plasma chamber, the chamber and the two magnetrons being pumped through by a high vacuum pumping system, the magnetrons each having means to produce electrons and including magnetic means to cause the electrons to rotate and spiral and ionize gas atoms or molecules introduced to the magnetrons to produce a plasma region in the chamber and means to establish an axial oscillation of electrons and ions in opposite directions, the chamber including an electrode adjacent to the plasma region which is polarised to extract or utilize electrically neutral or positive or negative charged particles generated in the plasma chamber.
J
4 iI4 Preferably, the means to produce oscillation of electrons and ions comprises magnetic mirror means, the outlet of each of the magnetrons adjacent to the chamber whereby to increase significantly ion, electron interaction to facilitate multiple ionization and additionally to enhance neutral particle ionization.
Alternatively, the means to produce oscillation of the ions and electrons in the chamber may include an alternating potential difference between each magnetron and the chamber, the alternating potential difference being out of phase by 1800 between the two magnetrons so that the ions from one magnetron and electrons from the other magnetron may be the same volume space within the chamber at the same time and vice versa.
Each of the magnetrons of this invention may have means to cause the electrons to rotate comprising a cylindrical anode and an axial magnet thereby forming a confined plasma.
The plasma generator of this form of the invention may further include a thermal fragmenter to assist in the fragmentation of gas molecules introduced into the chamber.
The thermal fragmenter may be placed into the chamber adjacent to, or extending into the plasma region formed within the chamber and the thermal fragmenter may be floated at the plasma potential.
In one preferred form, the thermal fragmenter may comprise a hollow heated filament of refractory material through which the gas to be ionized is passed with a vent hole in the filament in the region of the plasma region to allow the escape of fragmented molecules of the gas.
I 4a Such a filament may be made from a metal selected from tantalum, platinum, or other suitable material depending upon the type of gas which is to be fragmented and the proposed conditions in the chamber.
i Alternatively, the thermal fragmenter may comprise an oven which includes a high surface area packing over which the gases to be fragmented, are passed.
Such an oven may have electrical heating by means of an electrical I filament around the oven.
ii IS
.I
i i The packing may be a fibre mesh of a metal selected from tantalum or platinum or may be a carbon fibre packing whereby the nature of the packing is selected forthe type of gas to be fragmented.
Such a thermal fragmenter may be inserted into the plasma chamber in one wall of the plasma chamber and its junction with the wall of the chamber may be cooled and also the electrical elements extending into the thermal fragmenter may also be cooled.
By means of this present invention, considerable benefits can be obtained. The second magnetron can be identical in all respects to the first magnetron and they may each use the main magnet of the other as an opposite end of a magnetic mirror system which enables confinement of the plasma within the plasma chamber.
The temperature to which the thermal fragmenter may be raised will depend upon the type of gas to be fragmented and the materials of the fragmenter which may act as a catalyst for the fragmentation. For instance, in the coating of silicon onto a substrate, a gas which may be used is silane (SiHl 4 which requires a temperature of about 3000C or greater. Alternatively, if the gas to be fragmented is methane, so as to give a carbon deposition, a temperature of between 8500C S or greater is required.
2t For the process of the present invention, carrier gas is introduced into the magnation chamber to pass over the magnetron filament in the normal manner.
For instance, a carrier gas such as argon, neon, nitrogen or other noble gas may be used. Once the carrier gas has ionized it will ion irradiate the substrate in the plasma chamber to assist in keeping the surface of the substrate clean Iand assist in film formation by neutral or ionized molecules or atoms.
The plasma chamber of the present invention including a thermal fragmenter may be used for any particular purpose for which ionized energetic atoms or gas molecules are required to be deposited onto a substrate to form films of desired characteristics. An electric field between the thermal fragmenter and the substrate may be used to draw the ions onto the substrate.
One example of this is in the application of a hard durable diamond like carbon coating to a semi-conducting substrate. For this, the temperature of the thermal fragmenter is raised to about 85000 and methane gas is passed into the thermal fragmenter to project atoms of carbon and hydrogen into the plasma which are then ionized mainly by collisions with electrons in the plasma and then by suitable charging of the substrate the required carbon ions may be drawn onto the substrate surface to form the hard durable diamond like coating.
The thermal fragmenter of the various embodiments of the present invention, may be designed such that in affect, a jet of atoms of the fragmented gas is projected from it into the plasma where they are ionized before being drawn onto the substrate and, if necessary, by suitable movement of the thermal fragmenter or the substrate, various type and layers of coatings may be provided onto the substrate. There may, for instance, be several thermal fragmenters in a plasma chamber each adapted in turn to provide a particular coating onto the substrate with each fragmenter being moved into the required position as desired or the substrate being moved to be positioned adjacent to each fragmenter as desired.
Benefit may be obtained from the thermal fragmenter incorporated in the 4 present invention if the atoms of the thermally fragmented gas molecules are ionized as they leave the fragmenter. This can be achieved if instead of a D.C.
electrical power, an R.F. or combination of D.C. and R.F. power is used to heat a suitably structured fragmenter. The frequency and power input of the R.F.
component is adjusted to give optimum ionization of atoms as the atoms are emerging through the aperture or apertures from the hollowed filament of the fragmenter.
This then generally describes the present invention, but to assist with understanding of the invention, reference will now be made to the accompanying drawings which show preferred embodiments of the invention and in which the drawings are schematic diagrammatic views of plasma generators.
In the drawings:- 7 FIG. 1 is a plasma generator incorporating two magnetrons, FIG. 2 is one form of thermal fragmenter suitable for the present invention, FIG. 3 shows a second form of thermal fragmenter suitable for the present invention, and FIG. 4 shows a plasma chamber including a thermal fragmenter.
Now looking closely at the drawings and in particular FIG. 1, it will be seen that the main components of the plasma generator are a first magnetron 1, a second magnetron 2 and an evacuated plasma chamber 3. The magnetrons 1 and 2 are arranged on either side of the plasma chamber 3 and diametrically opposed to each other on a line which may be referred to as a magnetron axis.
Now looking particularly at the magnetron 1, the initial ionization takes place in the magnetron 1 which has an electron source 7 provided by a heated tungsten or tantalum or other filament placed at or near the magnetron axis. A cylindrical anode 8 and an axial magnet 11 form a magnetic field such that electrons emitted from the filament 7 are confined radially and prevented by the magnetic field from reaching the anode 8. The presence of the electric field and magnetic field causes the electrons emitted to rotate and spiral and as these become more energetic they ionise gas atoms of molecules introduced to the inlet 5 to form a confined plasma which may persist as long as suitable conditions are maintained. An opening 4 to the plasma chamber 3 extends to an evacuation apparatus (not shown).
According to this invention, the intensity of the plasma is increased by establishing an axial oscillation of electrons and ions. This may be achieved if consideration is given to the rate at which ions may respond to axial forces. Generally with respect to electrons in a plasma, ions are considered stationary or of low mobility due to the very much larger mass compared to electrons. However, it has been found that if a suitable low frequency potential is applied along the magnetron axis, both electrons and positive ions may be made to oscillate axially. Negative ions, which are the result of electron attachment, may also move in c-pposite directions to the movement of the positive ions so that
AJ
8 these are also subjected to collision with other particles. Ions achieve no nett movement if a high frequency potential is applied.
The nature of this mass transport is such that the particles with opposite charge polarity will move in opposite directions under the influence of the applied potential and this transportation mode will increase significantly the probability of ion-electron and ion-ion interaction, facilitating ionized molecule fracture and multiple ionization in addition to the enhancement of the neutral particle go ionization.
o, The frequency used may depend on the nature of the ions but with gas ions produced by admitting Hydrogen, Argon, Nitrogen, Methane or other similar gases or vapours to the magnetron, it has been found that a frequency of oscillation of 50 Hz is effective, but that frequency can be selected over a wide range. Beyond 1MHz, however, ions can be considered to be unaffected by the o t applied field.
o 44e Now still looking only at one magnetron to facilitate the energy transfer described above, the magnetron chamber 1 and vacuum 3 combination is used such that at a low frequency alternating voltage is applied between the magnetron 1 and the vacuum 3 as indicated by symbol 9. To contain the plasma and to enhance further process of ionization, a magnetic field in the form of a magnetic mirror is formed by the field of electromagnet 11 and electromagnet 12. The electromagnet 12 is, however, the electromagnet of a second magnetron 2 which in a similar manner to magnetron 1 has a filament 13 producing electrons which are confined by means of cylindrical anode 14 and electromagnet 12 and by which electrons are caused to spin and to ionize molecules of gas to produce a further plasma which may then, in a similar manner to the first magnetron, enter the main plasma chamber 3.
Once the plasma is formed, the electromagnets 11 and 12, as discussed above, act as a magnetic mirror and maintain the plasma within the chamber 3.
While the magnetic mirror has little or no effect on the ions, it strongly influences electrons under static conditions. However, when the axial potential variation is applied above a certain voltage value, electrons are removed in an axial 9 direction with sufficient energy to ionize additional gas particles. They will move alternatively between the magnetron 1 and the vacuum chamber 3 and the magnetron 2, as driven by the low frequency voltage gradient 9 and the corresponding voltage gradient on the other magnetron 2, shown by 16.
Similarly, the positive ions are made to move by the same potential variation in the opposite direction to that of the electrons or negative ions.
As was mentioned earlier, the result of interaction with the charged particles with each other or with neutral atom or molecules generates more ionized particles which will also be influenced by the low frequency axial potential.
The low frequency potentials 9 and 16 may be utilized 1800 out of phase so that electrons are available at all times and surface charging of a substrate 18 on an electrode 17 within the plasma chamber can be reduced or eliminated with an appropriate biased potential.
S The electrode 17 supporting the substrate 18 may be positioned so that ion deposition from the plasma may occur, provided a suitable biased potential is provided to electrode 17 under suitable conditions. The bias of the off-axis substrate 18 may also be amended or include the possibility of using pulsed voltage 20 of square or sinusoidal wave form or other form of suitable period and mark to space ratio to optimise the control over the surface charging affects.
As we have discussed earlier, the production of a plasma within the plasma chamber may be enhanced by introducing of the gas to be ionized directly into the plasma chamber 3 rather than into the ionizing gas inlets 5 and 6. If the gas to be ionized such as methane is not allowed to enter through the gas inlets and 6, then poisoning of the electrodes 7 and 13 will be reduced or not occur.
Hence, it is necessary to provide some form of device to introduce gas molecules or fragmented gas molecules into the for instance, argon, plasma.
This may be done by use of the thermal fragment as shown in FIGS. 2 and 3.
In the thermal fragmenter shown in FIG. 2, a flange 20 fitted into the wall 21 of the plasma chamber may support an oven 22. Inside the oven 22 is a fine tantalum wire wool or other suitable high surface area material 23 which is heated by means of electrical wires 24 which extend through the flange 20. The electrical wire 24 extend into a heating element 25 and the walls of the oven 22.
It will be realised, however, that other forms of heating for the oven may also be 00 0 0 0 0 A gas inlet 26 is provided into the oven so that gas to be fragmented may be introduced into the oven before being ejected out of the relatively narrow opening 28 into the plasma region shown by 29. The shape and positioning of the relatively narrow opening 28, opening into the plasma from the oven may be used to direct gas atoms into the plasma in such a way that they can be directed into the required patterns or arrangements onto the substrate 32.- The flange may include cooling coils 30 to cool the flange and a cooling jacket 31 to cool the gas inlet.
FIG. 3 shows an alternative form of thermal fragmenter in which gas is allowed into an inlet 40 to pass into arms 41 and 42, which extend through a flange 43 in the wall 44 of a plasma chamber to direct gas into a heating filament generally shown by 46. The arms 41 and 42 are cooled by means of cooling jackets 47 and are insulated from each other so that an electrical current may be passed in through the electrodes 48 and 49 so that the filament 46 acts as a heated filament. Hence, gas which is passed in through the opening 14, is heated as it passes into the filament and is thermally cracked before exiting through aperture 50 in the plasma region 51.
In this particular embodiment, the gas entering is methane and hence, disassociated atoms of carbon and hydrogen are ejected through the aperture and, by use of suitable potentials, may be deposited onto the substrate 52.
Once again, cooling coils 53 may be provided in the flange 43.
FIG. 4 shows an arrangement of plasma generator which has a first magnetron and a second magnetron 61 with a plasma chamber 62 between the two magnetrons and with a thermal fragmenter generally shown as 63 extending into the plasma chamber and also a substrate holding electrode 64 extending into the plasma chamber.
I,
L In this embodiment, the magnetrons 60 and 61 act in exactly the same manner as the magnetrons 1 and 2 as shown in FIG. 1, but the gas which enters through the inlet 65 for magnetron 60 and 66 for magnetron 61 is only the carrier gas such as argon and not the gas to be ionized such as methane or silane. The methane or silane is introduced through gas aperture 67 into thermal fragmenter 63 which is of the type as discussed in FIG. 2.
By this means, the filaments 68 and 69 of the magnetron 60 and 61 respectively have less tendency to become poisoned by the introduction of the gas to be ionized adjacent them and hence, more efficient plasma generation occurs.
As discussed earlier, there may be a number of thermal fragmenters 63 mounted, for instance, on a turntable within the plasma generator so that any one of the thermal fragmenters may be selected so that at various times during the deposition process, for instance, onto a substrate 70 on the electrode 64 different atoms of gas molecules may be deposited onto the substrate 70 by means of selection of different thermal fragmenters.
It will be seen that by this invention, there is provided an arrangement where, owing to the fact that two magnetrons are each producing plasmas of ions and electrons and, preferably, when operated 1800 out of phase, there will be ions and electrons available at the substrate surface if ion deposition is being carried out or on any other form of target or application which the plasma generator, of the present invention, may be applied and, as such, much more efficient use of the plasma is obtained.
In particular, with use of a substrate as discussed above, the present invention may increase deposition rates while maintaining quality of adhesion, hardness and thickness consistency on diamond like carbon films and, further, it can reduce the time taken to process a hard carbon coating by 50% or more.
Claims (14)
1. A plasma generator which allows both electrons and ions to oscillate in an applied field at low frequency excitation with electrons and ions moving in opposite directions, characterised by two sources of ions and electrons at opposite sides of a plasma chamber to provide an increased and more efficient plasma, within the plasma chamber and an electrode in the plasma chamber which is 1 0 polarised to extract or utilize electrically neutral or positive or negative charged particles generated in the plasma chamber.
2. A plasma generator as in claim 1 further including at least one thermal fragmenter.
3. A plasma generator having a plasma chamber and two sources ions and electrons consisting of two plain cylindrical magnetrons at opposite ends of the plasma chamber, the chamber and the two magnetrons being pumped through oy a high vacuum pumping system, the magnetrons each having means to produce electrons and including magnetic means to cause the electrons to rotate and spiral and ionize gas atoms or molecules introduced to the magnetrons to produce a plasma region in the chamber and means to establish an axial oscillation of electrons and ions in opposite directions, the chamber including an electrode :I adjacent to the plasma region which is polarised to extract or utilize electrically neutral or positive or negative charged particles generated in the plasma chamber.
4. A plasma generator as in claim 3 wherein the means to produce oscillation of electrons and ions comprises magnetic mirror means at the outlet of each of the magnetrons adjacent to the chamber whereby to increase significantly ion electron interaction to facilitate multiple ionization and additionally to enhance neutral particle ionization. 13 A plasma generator as in claim 3, wherein the means to produce oscillation of the ions and electrons in the chamber includes an alternating potential difference between each magnetron and the chamber, the alternating potential difference being out of phase by 1800 between the two magnetrons si that ions from one magnetron and electrons from the other magnetron may be in the same volume space within the chamber at the same time and vice versa.
6. A plasma generator as in any one of claims 3 to 5 wherein the means to cause the electrons to rotate in each of the magnetrons is a cylindrical anode and an axial magnet thereby forming a confined plasma.
7. A plasma generator as in any one of claims 3 to 6 further including a thermal fragmenter to assist in the fragmentation of gas molecules introduced into the chamber.
8. A plasma generator as in claim 7 wherein the thermal fragmenter is placed in the chamber adjacent or extending into the plasma region.
9. A plasma generator as in claim 8 wherein the thermal fragmenter extends into the plasma region and is floated at the plasma potential. A plasma generator as in any one of claims 7 to 9 wherein the thermal fragmenter is a hollow heated filament of refractory metal through which the gas to be ionized is passed with a vent hole in the filament in the region of the plasma region to allow the escape of the fragmented molecules of the gas.
11. A plasma generator as in claim 10 wherein the filament is made from a metal selected from tantalum, platinum or other suitable material depending upon the type of gas which is to be fragmented and the proposed conditions in the chamber. 14
12. A plasma generator as in any one of claims 7 to 9 wherein the thermal fragmenter comprises an oven, which includes a high surface area packing over which the gas to be fragmented is passed.
13. A plasma generator as in claim 12, wherein the oven has electrical heating by means of an electrical filament around the oven.
14. A plasma generator as in claim 11 or claim 12 wherein the packing is a fibre mesh of a metal selected from tantalum or platinum or is a carbon fibre packing whereby the nature of the packing is selected for the type of gas to be fragmented. Oo 15 15. A plasma generator as in any one of claims 7 to 14 wherein the I thermal fragmenter is inserted into the plasma chamber through one wall of the plasma chamber and its junction with the wall of the chamber j is cooled and electrical elements extending into thermal fragmenter are also cooled. "t o
16. A plasma generator substantially as hereinbefore described with i reference to and as illustrated by FIG. 1.
17. A plasma generator including a thermal fragmenter substantially as hereinbefore described with reference to and as illustrated by FIG. 2 to 4. Dated this 26th day of February 1990. THE COMMONWEALTH OF AUSTRALIA By its Patent Attorneys COLLISON CO
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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AU20679/88A AU602109B2 (en) | 1987-08-13 | 1988-08-12 | Improvements in plasma generators |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
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AUPI3733 | 1987-08-13 | ||
AUPI373387 | 1987-08-13 | ||
AUPI6336 | 1988-01-18 | ||
AUPI633688 | 1988-01-18 | ||
AU20679/88A AU602109B2 (en) | 1987-08-13 | 1988-08-12 | Improvements in plasma generators |
Publications (2)
Publication Number | Publication Date |
---|---|
AU2067988A AU2067988A (en) | 1989-02-16 |
AU602109B2 true AU602109B2 (en) | 1990-09-27 |
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Application Number | Title | Priority Date | Filing Date |
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AU20679/88A Ceased AU602109B2 (en) | 1987-08-13 | 1988-08-12 | Improvements in plasma generators |
Country Status (1)
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AU (1) | AU602109B2 (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3655508A (en) * | 1968-06-12 | 1972-04-11 | Itt | Electrostatic field apparatus for reducing leakage of plasma from magnetic type fusion reactors |
WO1986006922A1 (en) * | 1985-05-09 | 1986-11-20 | The Commonwealth Of Australia | Plasma generator |
-
1988
- 1988-08-12 AU AU20679/88A patent/AU602109B2/en not_active Ceased
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3655508A (en) * | 1968-06-12 | 1972-04-11 | Itt | Electrostatic field apparatus for reducing leakage of plasma from magnetic type fusion reactors |
WO1986006922A1 (en) * | 1985-05-09 | 1986-11-20 | The Commonwealth Of Australia | Plasma generator |
Also Published As
Publication number | Publication date |
---|---|
AU2067988A (en) | 1989-02-16 |
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