CVD apparatus and method for forming CVD film
09831069 · 2017-11-28
Assignee
Inventors
Cpc classification
Y02E10/50
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
H01L31/02168
ELECTRICITY
H01L21/0217
ELECTRICITY
C23C16/45595
CHEMISTRY; METALLURGY
International classification
H01L31/18
ELECTRICITY
C23C16/455
CHEMISTRY; METALLURGY
Abstract
Heretofore, silicon nitride film formed by low pressure plasma CVD has been used for an antireflection film of a solar battery. But it is difficult to reduce the production cost of a solar battery, because, in a low pressure process, facility cost and process cost are expensive. As disclosed, a nitride film is formed by atmospheric pressure plasma CVD using dielectric barrier discharge generated by a plasma head where a plurality of plasma head unit parts is installed in parallel to generate plasma by applying electric field or magnetic field via a dielectric member. Stable glow discharge is formed even under atmospheric pressure by dielectric barrier discharge. And nitride film deposition under atmospheric pressure and low cost production of a solar battery is materialized by using dielectric barrier discharge and by reacting different plasmas generated from plasma supply openings laying side-by-side.
Claims
1. A plasma CVD apparatus, comprising: plural flow passage plates, the flow passage plates being stacked, each flow passage plate having a gas passage and a gas outlet side, each of the flow passage plates respectively also having a discharge electrode located at an end face of the gas outlet side, each discharge electrode composed of a ceramic member having a hollow portion; and an electrode wire located in each hollow portion and not making contact with the ceramic member, wherein a layer made of emitter material is formed on the surface of the electrode wire, and the emitter material has a smaller work function than the material of the electrode.
2. The plasma CVD apparatus according to claim 1, wherein the emitter material has a perovskite-type crystal structure.
3. The plasma CVD apparatus according to claim 1, wherein the emitter material is more than or equal to one chemical compound selected from the chemical compound group comprising TiSrO, MgO, TiO.
4. The plasma CVD apparatus according to claim 1, wherein the emitter layer is formed by a process wherein material of emitter layer is torn into pieces in a mortar, and resultant powder is solved in water, and the solution mixed with glue is coated on the surface of the electrode wire, and emitter layer is formed by sintering of coated wire.
5. The plasma CVD apparatus according to claim 1, wherein the emitter layer is formed by MOCVD.
6. A plasma CVD apparatus, comprising: plural stacked flow passage plates; plural discharge electrodes, each flow passage plate having a gas outlet side, each of the flow passage plates having a respective one of the plural discharge electrodes located at the gas outlet side, each discharge electrode composed of a ceramic member having a hollow portion; and an electrode wire located in each hollow portion and not making contact with the ceramic member, wherein a layer made of emitter material is formed on the surface of the electrode wire, and the emitter material has a smaller work function than the material of the electrode.
7. The plasma CVD apparatus according to claim 6, wherein the emitter material has a perovskite-type crystal structure.
8. The plasma CVD apparatus according to claim 6, wherein the emitter material is more than or equal to one chemical compound selected from the chemical compound group comprising TiSrO, MgO, TiO.
9. The plasma CVD apparatus according to claim 6, wherein the emitter layer is formed by a process wherein material of emitter layer is torn into pieces in a mortar, and resultant powder is solved in water, and the solution mixed with glue is coated on the surface of the electrode wire, and emitter layer is formed by sintering of coated wire.
10. The plasma CVD apparatus according to claim 6, wherein the emitter layer is formed by MOCVD.
Description
BRIEF DESCRIPTION OF THE DRAWING
(1)
(2)
(3)
(4)
(5)
(6)
(7)
(8)
(9)
(10)
(11)
(12)
(13)
(14)
DESCRIPTION OF THE SYMBOLS
(15) 1, 2, 3: plasma head unit member
(16) 4, 11, 15: gas inlet
(17) 5, 12, 16: dielectric member
(18) 6, 13, 17: plasma generation passage
(19) 7, 14, 18: plasma supply opening
(20) 8, 9: electrode
(21) 10: shock absorbing member
(22) 21, 22, 23: plasma head unit member
(23) 24, 35: gas distribution passage
(24) 25, 33: dielectric member
(25) 26, 36: plasma generation passage
(26) 27, 37: plasma supply opening
(27) 28, 29: electrode
(28) 30: shock absorbing member
(29) 31: gas distribution passage region
(30) 32: plasma generation passage region
(31) 34: gas supply pipe
(32) 41, 47, 51: gas introduction opening
(33) 42, 48, 52: dielectric member
(34) 43, 49, 53: plasma generation passage
(35) 44, 50, 54: plasma supply opening
(36) 45, 46: electrode
(37) 61, 66, 71: gas introduction opening
(38) 62, 67, 72: dielectric member
(39) 63, 68, 73: plasma generation passage
(40) 65, 70, 75: plasma supply opening
(41) 64, 69, 74: induction coil
(42) 81, 88, 95: gas introduction opening
(43) 82, 89, 96: dielectric member
(44) 83, 90, 97: plasma generation passage
(45) 85, 91, 98: plasma supply opening
(46) 84, 92, 99: induction coil
(47) 86, 87, 93, 94: coil terminal
(48) 101, 102: source gas supply unit
(49) 103: power source
(50) 104: plasma head
(51) 105, 106: plasma
(52) 107: plasma reaction region
(53) 108: thin film
(54) 109: substrate
(55) 110: substrate conveyance unit
(56) 111: gas introduction opening
(57) 112: power source
(58) 113: container
(59) 114, 115: electrode
(60) 116, 117: solid dielectric body
(61) 118: plasma
(62) 119: plasma supply opening
(63) 120: thin film
(64) 121: substrate
(65) 201, 202: flow passage plate
(66) 203, 204: quartz member
(67) 205, 206: electrode wire
(68) 207, 208: gas flow direction
(69) 209: substrate
(70) 210: support member
(71) 211, 215: quartz member
(72) 212, 216: electrode wire
(73) 213, 217: electrode lead wire
(74) 214: opening
(75) 218: enclosing member
(76) 301, 306, 311, 321: flow passage plate
(77) 302, 307, 312, 322: discharge electrode
(78) 303, 308, 313, 323: plasma
(79) 304, 309, 314, 324: substrate
(80) 305, 310, 315, 325: dielectric substrate
(81) 326: electrode for applying bias voltage
(82) 327: power source for applying bias voltage
(83) 328: positive argon ion
(84) 331, 335, 339: flow passage plate
(85) 332, 336, 340: flow passage
(86) 333, 334, 337, 338, 341, 342: dielectric member
BEST MODE EMBODIMENTS FOR CARRYING OUT THE INVENTION
(87) Best mode embodiments for carrying out the present invention are described in detail as follows.
(88) (Glow Discharge by Dielectric-Barrier Discharge)
(89) Inventors of the present invention have earnestly studied plasma deposition for realization of silicon nitride CVD under atmospheric pressure. First they have employed plasma-blowing deposition for preventing plasma damage on a substrate, and have employed plasma formation by dielectric-barrier discharge for stable glow discharge. In order to prevent plasma reaction in a plasma generation chamber which was a problem of conventional method, a plasma head, which is a plasma generation member, is composed of a plurality of unit parts respectively having an independent plasma blow opening. For example, silicon plasma and nitrogen plasma are generated separately in each unit part in silicon nitride CVD process. Furthermore inventors have discovered that the parallel configuration wherein a unit part for silicon plasma generation is placed next to a unit part for nitrogen plasma generation is effective for improvement in uniformity of deposited film. Plasma supplied from a blow opening does not react in a plasma head, but it reacts in a space between a blow opening and a substrate to deposit silicon nitride film. Therefore highly effective silicon nitride deposition on a substrate becomes possible. And also, material gases are supplied independently to each unit parts of the plasma head, and electrodes are placed so that electrical energy can be controlled independently which is applied for plasma generation. By these arrangements, thin film deposition becomes possible using best conditions for each plasma generation.
(90) And also, in conventional method, there is a problem that it is difficult to generate continuously stable plasma when plasma is generated under atmospheric pressure. Inventors of the present invention have taken notice of the structure of an electrode and the structure of apart where a substrate is placed. And they have discovered that stable plasma generation, the enhancement of nitride film deposition rate, and the improvement of reproducibility in film thickness and film quality become possible by the arrangement wherein an electrode is enclosed in a quartz member, and the electrode is separated from the quartz member by empty space, and a substrate is placed on a quartz supporting member, and plasma is supplied from a plasma head to the substrate.
(91) In addition, “atmospheric pressure” in this specification specifically means pressure between 8×10.sup.4 and 12×10.sup.4 Pa, while it depends on the atmospheric pressure and the altitude of the place where the CVD apparatus is placed. When the pressure of CVD process is within this range, it is possible to reduce facility cost because expensive equipment for compression and decompression is not needed.
(92) (Specific Example of an Electrode Structure)
(93)
(94) And also, electrodes can be placed under the supporting member 210 for controlling bias voltage applied to the plasma. In this case, electrodes placed above the substrate 209, such as electrodes 205, 206, are called as upper electrodes, and electrodes placed under the substrate 209 (under the supporting member 210) are called as lower electrodes.
(95) As shown in
(96) It is found that plasma is not generated when nitrogen or ammonia gas which is process gas for nitride film deposition is introduced from the beginning of the process, but plasma can be generated when Ar gas is introduced. Therefore, it is found that plasma which is necessary for nitride film deposition can be stably generated by process steps characterized in that plasma is generated by introducing Ar gas first, and then the number of electrons is increased, and then the flow rate of nitrogen or ammonia gas is gradually increased.
(97) In the embodiment as shown in
(98) The material of an insulating member of the electrode which corresponds to the above-mentioned members 203, 204 is preferably ceramics in both cases where a hollow portion is prepared or not around the electrode. Furthermore the material is preferably quartz or translucent alumina. And the material of the flow passage plate is preferably heat-resistant metal or ceramics.
(99) The structure of an electrode used in the conventional CVD apparatus is the structure where carbon members are exposed, so there is a leakage problem of impurities included in carbon material. Meanwhile, there is no leakage problem of impurities in the structure of the electrode according to the present invention wherein an electrode wire is covered by a quartz tube.
(100) The material of an electrode wire is preferably W. It is more preferably W which contains Th or ThO. The content of Th is preferably less than or equal to 4% by weight. This arrangement reduces the work function of the electrode wire, and facilitates the emission of thermal electrons so that plasma can be easily generated.
(101) It is preferable that an electrode wire is entirely heated by appropriate external current supply to the wire. When the temperature of the wire is low, nitride or silicon film can be deposited on the surface of the electrode. Then it is not preferable because the flow passage may be reduced in thickness or clogged up. To the contrary, it is possible to prevent the growth of deposited material on the surface of the electrode by heating it. And also, it is possible to control the work function of metal such as Th or PTO which is added to electrode material such as W by controlling the temperature of the electrode. By these arrangements, electron density emitted from metal can be controlled so that CVD process can be controlled more precisely.
(102) And radioactive material is preferably coated on the surface of electrode material. For example, strontium is preferably coated. Plasma can be easily excited by coating radioactive material.
(103) And also, material with smaller work function than the material of the electrode is preferably used as emitter material, and a layer of the emitter material is preferably formed on the surface of the electrode wire. Material with perovskite-type crystal structure is preferably used as the emitter material. And more than or equal to one chemical compound selected from the chemical compound group comprising TiSrO, MgO, TiO is preferably used as the material. Any of these arrangements reduces the work function of the electrode wire, and facilitates the emission of thermal electrons so that plasma can be easily generated.
(104) The emitter layer is formed by a process wherein material of emitter layer is torn into pieces in a mortar, and resultant powder is solved in water, and the solution mixed with glue is coated on the surface of the electrode wire, and emitter layer is formed by sintering of coated wire. Or it can be formed by MOCVD. When the electrode wire is formed with coil-like shape, space formed in the electrode can be sufficiently filled by emitter material. And the emitter layer can be formed more densely, and its composition ratio can be improved.
(105) And also, a quartz electrode placed in a quartz member is preferably used not only for an electrode for high frequency radiation but also used for a heater. The temperature control of a body on which deposition film is formed can be controlled, for example, by heating, by using the quartz electrode as a heater.
(106) (Method for Fabricating an Electrode)
(107)
(108) Noble gas such as Ar or Ne is preferably used for filler gas when a hollow portion is depressurized. It is more preferable that clean gas such as Ar with impurity concentration less than or equal to 10 ppb is introduced as purge gas into the hollow portion before the filler gas is introduced.
(109) (The First Specific Example of a Unit Part of a Plasma Head)
(110)
(111) And also it is not necessary that a hole is prepared for a gas passage in dielectric member as shown in
(112) Material of dielectric members is preferably plastic, glass, carbon dioxide, metal oxide such as aluminum oxide. Especially, quartz glass is preferably used. Dielectric material with relative permittivity greater than or equal to 2 is preferably used. Dielectric material with relative permittivity greater than or equal to 10 is more preferably used. The thickness of dielectric material is preferably in the range from 0.01 mm to 4 mm. If it is too thick, excessively high voltage is necessary for plasma generation. If it is too thin, arc discharge tends to take place.
(113) Material of electrode is preferably metal such as copper, aluminum, stainless-steel or metal alloy. The distance between electrodes, which depends on the thickness of dielectric member and applied voltage, is preferably in the range from 0.1 mm to 50 mm.
(114) (The Structure of a Plasma Head)
(115) (The First Specific Example of a Plasma Head)
(116)
(117) (The Second Specific Example of a Plasma Head)
(118)
(119) (The Structure of a CVD Apparatus)
(120)
(121) In addition, a lower electrode which is not shown in the diagram is placed under the substrate 109, and it can apply bias voltage from under the substrate.
(122) Plasma supply openings can be placed downward as shown in
(123) Because plasma discharge is dielectric barrier discharge, plasma becomes stable glow discharge, and it becomes non-equilibrium plasma where the temperature of electrons is high and that of radicals and ions is low.
(124) When silicon nitride is deposited, for example, silane gas and ammonia gas are used as material gas. Silane gas and ammonia gas are supplied alternately to adjacent plasma head unit parts, and silicon plasma 105 and nitrogen plasma 106 are generated in each plasma generation passage. Silicon plasma and nitrogen plasma reach downward until several mm to several cm from plasma supply opening, then plasma reaction region 107 is formed.
(125) When silicon nitride is deposited, other silicon source gas or nitrogen source gas can be used. As silicon source gas, silane, disilane, or mixed gas made of these gases attenuated by inert gas can be used. As nitrogen source gas, ammonia, nitrogen, or mixed gas made of these gases attenuated by inert gas can be used.
(126) Silicon nitride film can be deposited by independently supplying silicon source gas and nitrogen source gas through flow passage plates laying side-by-side among a plurality of flow passage plates. During this process, it is possible to flow curtain-enclosed gas made of inert gas such as nitrogen through flow passage plates surrounding the plates for source gases. The flow rate of silicon source gas and nitrogen source gas can be independently controlled, which enables precise control of process conditions.
(127) Alternatively, silicon nitride film can be deposited by supplying a mixed gas made of silicon source gas and nitrogen source gas through identical flow passage plates. The configuration of an apparatus can be simplified.
(128) As another example of deposited film, silicon film can be deposited by not supplying nitrogen source gas but supplying silicon source gas.
(129) During the excitation of plasma for deposition process, it is preferable to cool down an electrode by introducing a mixed gas comprising or including noble gas (for example, Ar and N.sub.2) nearby the electrode in the flow passage plate. When an electrode is not cooled down, and the temperature of the electrode itself rises by plasma excitation, a film which is not a dielectric member in use or extraneous material is attached on the surface of the electrode, and the function of the electrode is disabled. To prevent this problem, it is preferable to circulate cooling gas in a temperature of about 20 deg C.
(130) And also, a movable dielectric member is preferably fit in a space in gas passage or flow passage plate through which process gas or carrier gas flows. Quartz is preferably used as a dielectric member. By this arrangement, it is possible to control the cross-sectional area of flow passage so that the controllability of the process can be improved.
(131) (Plasma Generation Parameters)
(132) Process conditions to generate plasma are appropriately determined according to the purpose to utilize plasma. When capacitance coupling plasma is generated, plasma is generated by applying constant electric field, high frequency electric field, pulsed electric field, micro-wave electric field between a pair of electrodes. When electric field is applied other than constant electric field, the used frequency can be 13.56 MHz which is used in a general plasma apparatus, or it can be higher than or lower than 13.56 MHz. In Patent Document 6, a technology to prevent plasma damage on the deposited film by using high frequency plasma of 100 MHz in a plasma apparatus is disclosed. By controlling the frequency of electric field, characteristics such as deposition rate, the quality of deposited film can be optimized.
(133) Pulsed electric field is preferably used for plasma generation. Its field intensity is preferably in the range from 10 to 1000 kV/cm. Its frequency is preferably higher than or equal to 0.5 kHz.
(134) (Inductive Coupling Plasma Apparatus)
(135) (The Second Specific Example of a Unit Part of a Plasma Head)
(136) Technical idea concerning plasma head according to the present invention is not limited to be applied for a plasma head for capacitance coupling plasma, but for example, it can be applied for a plasma head for inductive coupling plasma.
(137)
(138) (The Third Specific Example of a Plasma Head)
(139)
(140) (Method for Producing a Plasma Head)
(141) (Bonding Method)
(142) To fabricate dielectric members making up a plasma head according to the present invention, it is necessary to process a hollow portion with a complicated shape such as a plasma generation passage and a gas distribution passage. Such a dielectric member with a hollow portion can be fabricated by bonding dielectric members with a hollow portion or by bonding a dielectric member with a hollow portion and a flat dielectric member after forming a hollow portion on the surface of a plurality of dielectric members.
(143) A plasma head unit part is formed by stacking an electrode or an inductive coil on the dielectric member with a hollow portion formed by this way. Furthermore, a plasma head is formed by stacking a plurality of plasma head unit parts via a shock absorbing member made of material such as Teflon™.
(144) (Injection Molding Method)
(145) A plasma head unit part can be fabricated by an injection molding method. A hydraulic core and an electrode or an inductive coil are placed in a mold, and material of a dielectric member is injected in the mold, then a fabricated part is unmolded and the hydraulic core is removed with the electrode or the inductive coil left behind. Furthermore, a plasma head is formed by stacking a plurality of plasma head unit parts via a shock absorbing member made of material such as Teflon™.
(146) (Points of Difference with Similar Technologies)
(147) In Patent Document 4, a process to reform the property or sterilize on the surface of an object by blowing out plasma to the object is disclosed, the plasma generated by dielectric discharge from a plasma head formed by bundling a plurality of dielectric thin tubes. A plurality of plasma supply openings is equipped in the technology disclosed in Patent Document 4, but gas inlets and electrodes to generate plasma of each thin tube do not function independently. And there is no description to suggest a technology where gas inlets and electrodes are independently equipped in each thin tube. Therefore it is not easy to invent a technology according to the present invention wherein a plurality of different plasmas is generated in a plurality of plasma generation units, and plasma reaction is carried out in a space between a plasma head and a substrate by referring to this document.
(148) In Patent Document 5, a process to form an organic thin film including metal such as silicon oxide by a reaction of gas including metal such as TEOS and oxygen is disclosed. But the technology described in Patent Document 5 is a technology wherein a thin film is formed by mixing and reacting reaction gas which is in plasma state and metal-including gas which is not in plasma state. Therefore this technology is different from the technology of the present invention wherein a plasma head is composed of a plurality of unit parts installed in parallel, and different plasmas are generated in each unit part, and film deposition is carried out by the reaction between the different plasmas. The technology according to the present invention is a technology wherein a plurality of plasma supply openings to generate different plasmas can be very closely and densely placed by stacking alternately a plurality of dielectric members and electrodes. Therefore it is not easy to invent a technology according to the present invention by referring to this document.
INDUSTRIAL APPLICABILITY
(149) As above mentioned, by using a CVD apparatus and a method for forming CVD film according to the present invention, low cost production of a high quality nitride film can be materialized for the purpose of, for example, forming antireflection film of a solar battery, which makes a huge contribution to the field of electronics.
PREFERRED EMBODIMENTS
(150) Several embodiments of a method for forming CVD film according to the present invention are described in detail as follows, but the present invention is not limited to these embodiments.
Preferred Embodiment 1
(151) (The First Test on Electrodes)
(152) Minimum supply voltage necessary to spontaneously generate plasma was measured by setting different several conditions for the ambient of a hollow portion and gas which flows in the flow passage plate in order to investigate optimum conditions for plasma generation for an electrode (upper electrode) with a hollow portion according to the present invention. For comparison, the voltage was measured for an electrode without a hollow portion. And also, a flow passage plate was formed using ceramic members, and a gas flow passage was formed on the lateral side of the flow passage plate.
(153) TABLE-US-00001 TABLE 1 Minimum RF power (W) necessary for spontaneously generating plasma Gas (carrier gas) which flows in a flow passage plate Ar 70% Ambient in a hollow portion Ar 100% Ar 85% N.sub.2 15% N.sub.2 30% Ar gas enclosed at 50 Torr 500 900 2000 (W) Ar gas enclosed at 250 Torr 700 1100 1800 Ar gas enclosed at 500 Torr 800 1600 2000 Ne gas enclosed at 50 Torr 400 1000 2200 Ne gas enclosed at 250 Torr 600 1100 1700 Ne gas enclosed at 500 Torr 900 1500 2100 Atmospheric pressure 600 1500 1300 Vacuum 500 1500 2100 Without a hollow portion 600 1000 2100
(154) In addition, members as follows were used for the components of a discharge electrode.
(155) An electrode wire: a linear electrode wire made of Ni, one terminal was connected to a metal foil made of Mo, emitter material was not used
(156) Ceramic member: quartz
(157) It was found that an optimum CVD condition was when RF power necessary for spontaneously generating plasma was less than or equal to 700 W because spark discharge was not generated and plasma state was stable. And it was found that Ar gas not including N.sub.2 was preferable for carrier gas flowing in a flow passage plate to maintain stable plasma. And it was found that vacuum or Ar gas enclosed at less than or equal to 250 Torr was preferable as an ambient of a hollow portion. And according to the other experiment using other gases as enclosed gas, excellent result was obtained when noble gas such as Ne was used as carrier gas and enclosed gas in the hollow portion, the result being similar to the result when Ar was used.
Preferred Embodiment 2
(158) (The Second Test on Electrodes)
(159) Next, minimum RF power necessary for spontaneous plasma generation was measured using an electrode formed according to the present invention by changing the material of members and the condition of gas which flows in a flow passage plate. Discharge electrodes were equipped with hollow portions filled with noble gas at a pressure of 250 Torr. The flow passage plate was made of heat resisting metal and flow passages were formed along the side of the plate.
(160) TABLE-US-00002 TABLE 2 Minimum RF power (W) necessary for spontaneously generating plasma Gas (carrier gas) Ambient which flows in a flow passage plate in a hollow portion Ar 100% Ar 85% N.sub.2 15% Ar 70% N.sub.2 30% Condition 1 700 1000 1700 (W) Condition 2 800 1100 1800 Condition 3 600 900 1600 Condition 4 800 1000 1800 Condition 5 1000 1300 2100 Condition 6 700 1000 1700 Condition 7 700 1100 1600 Condition 8 600 1000 1600
Condition 1: a linear electrode wire made of Ni alloy, one terminal was connected to a metal foil made of Mo, emitter material was not used, ceramic member was made of quartz, Ni—W alloy was used as Ni alloy.
Condition 2: a linear electrode wire made of Ni, one terminal was connected to a metal foil made of Mo alloy, emitter material was not used, ceramic member was made of quartz, Mo—W alloy was used as Mo alloy.
Condition 3: a linear electrode wire made of W including 1 weight % of Th, one terminal was connected to a metal foil made of Mo, emitter material was not used, ceramic member was made of quartz.
Condition 4: a linear electrode wire made of W including 4 weight % of Th, one terminal was connected to a metal foil made of Mo, emitter material was not used, ceramic member was made of quartz.
Condition 5: a linear electrode wire made of W including 10 weight % of Th, one terminal was connected to a metal foil made of Mo, emitter material was not used, ceramic member was made of quartz.
Condition 6: a linear electrode wire made of W including 4 weight % of ThO, one terminal was connected to a metal foil made of Mo, emitter material was not used, ceramic member was made of quartz.
Condition 7: a linear electrode wire made of Ni, one terminal was connected to a metal foil made of Mo, emitter material was not used, ceramic member was made of translucent alumina.
Condition 8: a coiled electrode wire made of Ni, one terminal was connected to a metal foil made of Mo, emitter material was not used, ceramic member was made of quartz.
Preferred Embodiment 3
(161) (The Third Test on Electrodes)
(162) Next, minimum RF power necessary for spontaneous plasma generation was measured using an electrode formed according to the present invention by changing a layer made of emitter material formed on the surface of an electrode wire and the condition of gas which flows in a flow passage plate. Discharge electrodes were equipped with hollow portions filled with noble gas at a pressure of 250 Torr.
(163) TABLE-US-00003 TABLE 3 Minimum RF power (W) necessary for spontaneously generating plasma Gas (carrier gas) Atmosphere which flows in a flow passage plate in a hollow portion Ar 100% Ar 85% N.sub.2 15% Ar 70% N.sub.2 30% Condition 9 800 1100 1800 (W) Condition 10 600 900 1500 Condition 11 700 1000 1400 Condition 12 700 900 1600 Condition 13 600 900 1600 Condition 14 700 1000 1500 Condition 15 700 900 1400
Condition 9: a linear electrode wire made of Ni, one terminal was connected to a metal foil made of Mo, emitter material was not used, ceramic member was made of quartz, Ni—W alloy was used as Ni alloy.
Condition 10: a linear electrode wire made of Ni, one terminal was connected to a metal foil made of Mo, emitter material was made of TiSrO having perovskite type crystal structure formed by glue coating and firing, ceramic member was made of quartz.
Condition 11: a linear electrode wire made of Ni, one terminal was connected to a metal foil made of Mo, emitter material was made of MgO having perovskite type crystal structure formed by glue coating and firing, ceramic member was made of quartz.
Condition 12: a linear electrode wire made of Ni, one terminal was connected to a metal foil made of Mo, emitter material was made of TiO having perovskite type crystal structure formed by glue coating and firing, ceramic member was made of quartz.
Condition 13: a linear electrode wire made of Ni, one terminal was connected to a metal foil made of Mo, emitter material was made of TiSrO having perovskite type crystal structure formed by MOCVD, ceramic member was made of quartz.
Condition 14: a linear electrode wire made of Ni, one terminal was connected to a metal foil made of Mo, emitter material was made of MgO having perovskite type crystal structure formed by MOCVD, ceramic member was made of quartz.
Condition 15: a linear electrode wire made of Ni, one terminal was connected to a metal foil made of Mo, emitter material was made of TiO having perovskite type crystal structure formed by MOCVD, ceramic member was made of quartz.
Preferred Embodiment 4
(164) (The First Evaluation of Nitride Film)
(165) When atmospheric pressure plasma is generated by supplying power from RF or LF power source via electrodes prepared for dielectric-barrier discharge, it is possible to soften the collision energy of electrons or charged reactive molecules which collide the surface of a substrate so as to control substrate damage and enhance desired reaction by, for example, applying bias voltage to the lower electrode in addition to simply applying appropriate effective voltage between the upper electrode and the lower electrode. The film quality of silicon nitride film was evaluated which was deposited by applying bias voltage so that plasma was generated not only between an electrode and a substrate but also between an electrode and other electrode.
(166)
(167) Film quality was evaluated. In the case of
(168) TABLE-US-00004 TABLE 4 The deposition rate of silicon nitride film and its film quality evaluation (relative value) Conventional Film depsited thermal according to the present invention CVD film FIG. 9(a) FIG. 9(b) FIG. 9(c) Upper electrode (+) 200 (V) 200 200 voltage Upper electrode (−) 0 0 NA voltage Lower electrode (−) 0 float 0 voltage Deposition rate 10 20~40 15~35 10~30 Etching rate 10 10~30 40~60 40~60
Discharge electrode was made of the following members. Plasma excitation frequency was 13.56 MHz.
Electrode wires were placed in the hollow portion. The ambient of the hollow portion is vacuum state.
Electrode wire: a linear electrode wire made of Ni, one terminal was connected to a metal foil made of Mo, emitter material was not used, ceramic member was made of quartz.
(169) The technology according to the present invention was compared with nitride film deposition by conventional thermal CVD. In all the case of bias voltage application as shown in
Preferred Embodiment 5
(170) (The Second Evaluation of Nitride Film
(171) The experiment of deposition and evaluation similar to the embodiment 4 was done by changing plasma excitation frequency.
(172) TABLE-US-00005 TABLE 5 Plasma excitation frequency: 10 MHz The deposition rate of silicon nitride film and its film quality evaluation (relative value) Film deposited according to the present invention FIG. 9(a) FIG. 9(b) FIG. 9(c) Upper electrode (+) voltage 200 (V) 200 200 Upper electrode (−) voltage 0 0 NA Lower electrode (−) voltage 0 float 0 Deposition rate 15~45 20~30 10~25 Etching rate 15~35 45~55 35~65
Preferred Embodiment 6
(173) In order to relax the damage of a substrate due to the collision of positive ions such as Ar ions, the effect of a method was evaluated, the method wherein a positive bias voltage was applied to the substrate.
(174) TABLE-US-00006 TABLE 6 Plasma excitation frequency: 20 MHz The deposition rate of silicon nitride film and its film quality evaluation (relative value) Film deposited according to the present invention FIG. 9(a) FIG. 9(b) FIG. 9(c) Upper electrode (+) voltage 200 V 200 200 Upper electrode (−) voltage 0 0 NA Lower electrode (−) voltage 0 float 0 Deposition rate 20~45 15~30 15~35 Etching rate 20~35 40~50 45~65
Preferred Embodiment 7
(175) In order to investigate a cooling effect by a discharge electrode, an electrode temperature was measured after Ar gas plasma was generated for one hour under RF power of 2000 W applied at 13.56 MHz. The electrode temperature was 150° C. when cooling down was not done. On the other hand, when cooling down was done using Ar gas or nitrogen gas, the temperature was 50° C. and 60° C. respectively, which showed that adequate cooling effect was obtained.