TWI767918B - Plasma etching method, plasma etching apparatus, and substrate stage - Google Patents
Plasma etching method, plasma etching apparatus, and substrate stage Download PDFInfo
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- 238000001020 plasma etching Methods 0.000 title claims abstract description 167
- 239000000758 substrate Substances 0.000 title claims abstract description 136
- 238000000034 method Methods 0.000 title claims abstract description 111
- 238000012545 processing Methods 0.000 claims abstract description 106
- 238000005108 dry cleaning Methods 0.000 claims abstract description 79
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 33
- 239000007789 gas Substances 0.000 claims description 325
- 239000010408 film Substances 0.000 claims description 139
- 239000000460 chlorine Substances 0.000 claims description 58
- 230000007246 mechanism Effects 0.000 claims description 47
- 239000011737 fluorine Substances 0.000 claims description 46
- 229910052731 fluorine Inorganic materials 0.000 claims description 46
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 45
- 239000000463 material Substances 0.000 claims description 44
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 38
- 229910052801 chlorine Inorganic materials 0.000 claims description 38
- 239000007921 spray Substances 0.000 claims description 35
- 238000012805 post-processing Methods 0.000 claims description 30
- 229910052751 metal Inorganic materials 0.000 claims description 29
- 239000002184 metal Substances 0.000 claims description 29
- 238000001179 sorption measurement Methods 0.000 claims description 27
- 150000003377 silicon compounds Chemical class 0.000 claims description 17
- 230000007797 corrosion Effects 0.000 claims description 13
- 238000005260 corrosion Methods 0.000 claims description 13
- 229910052782 aluminium Inorganic materials 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 11
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 claims description 11
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 10
- 230000005764 inhibitory process Effects 0.000 claims description 10
- 229910052750 molybdenum Inorganic materials 0.000 claims description 10
- 238000005507 spraying Methods 0.000 claims description 10
- 229910052721 tungsten Inorganic materials 0.000 claims description 10
- 239000000919 ceramic Substances 0.000 claims description 9
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 9
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 7
- 239000010409 thin film Substances 0.000 claims description 6
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 5
- 239000011733 molybdenum Substances 0.000 claims description 5
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 5
- 239000010937 tungsten Substances 0.000 claims description 5
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 4
- 239000000047 product Substances 0.000 claims description 4
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims description 4
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 3
- 239000001301 oxygen Substances 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- 239000010703 silicon Substances 0.000 claims 1
- 238000012423 maintenance Methods 0.000 abstract description 7
- 238000005530 etching Methods 0.000 description 46
- 239000010410 layer Substances 0.000 description 38
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- 229910004298 SiO 2 Inorganic materials 0.000 description 7
- 230000005684 electric field Effects 0.000 description 7
- 238000009616 inductively coupled plasma Methods 0.000 description 7
- 229910017077 AlFx Inorganic materials 0.000 description 6
- 229910018503 SF6 Inorganic materials 0.000 description 5
- 238000009832 plasma treatment Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
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- 239000000243 solution Substances 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
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- 229910052717 sulfur Inorganic materials 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 240000006829 Ficus sundaica Species 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
- 238000000137 annealing Methods 0.000 description 1
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- 230000008021 deposition Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000001312 dry etching Methods 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
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- 239000010453 quartz Substances 0.000 description 1
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- 238000003860 storage Methods 0.000 description 1
- 229960000909 sulfur hexafluoride Drugs 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
- -1 that is Substances 0.000 description 1
- 238000007751 thermal spraying Methods 0.000 description 1
- 230000007723 transport mechanism Effects 0.000 description 1
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 1
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- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/302—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to change their surface-physical characteristics or shape, e.g. etching, polishing, cutting
- H01L21/306—Chemical or electrical treatment, e.g. electrolytic etching
- H01L21/3065—Plasma etching; Reactive-ion etching
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3205—Deposition of non-insulating-, e.g. conductive- or resistive-, layers on insulating layers; After-treatment of these layers
- H01L21/321—After treatment
- H01L21/3213—Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer
- H01L21/32133—Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only
- H01L21/32135—Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only by vapour etching only
- H01L21/32136—Physical or chemical etching of the layers, e.g. to produce a patterned layer from a pre-deposited extensive layer by chemical means only by vapour etching only using plasmas
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- 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
- H01J37/32—Gas-filled discharge tubes
- H01J37/32431—Constructional details of the reactor
- H01J37/32798—Further details of plasma apparatus not provided for in groups H01J37/3244 - H01J37/32788; special provisions for cleaning or maintenance of the apparatus
- H01J37/32853—Hygiene
- H01J37/32862—In situ cleaning of vessels and/or internal parts
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- H01L21/67005—Apparatus not specifically provided for elsewhere
- H01L21/67011—Apparatus for manufacture or treatment
- H01L21/67017—Apparatus for fluid treatment
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Abstract
提供可以導入乾洗淨,且可以延長處理容器之維修週期的電漿蝕刻方法。 Provide a plasma etching method that can be introduced into dry cleaning and can prolong the maintenance period of the processing vessel.
一種藉由電漿蝕刻裝置對被形成基板之特定膜進行電漿蝕刻之電漿蝕刻方法,具有:在電漿蝕刻裝置的電漿蝕刻處理中,選定處理氣體,以使被生成之反應生成物成為能夠乾洗淨的工程;在電漿蝕刻裝置中,對特定膜,使用事先被選定之處理氣體而進行電漿蝕刻處理的工程;於將進行電漿蝕刻處理之工程進行一次或兩次以上之特定次數之後,藉由乾洗淨氣體之電漿,將電漿蝕刻裝置之腔室內予以乾洗淨的工程。 A plasma etching method for plasma etching a specific film of a substrate to be formed by a plasma etching device, comprising: in the plasma etching process of the plasma etching device, a process gas is selected so that a reaction product is generated A process capable of dry cleaning; in a plasma etching apparatus, a process of performing plasma etching treatment on a specific film using a pre-selected process gas; a process of performing plasma etching treatment once or twice or more After a certain number of times, the process of dry cleaning the chamber of the plasma etching device by the plasma of the dry cleaning gas.
Description
本發明係關於電漿蝕刻方法、電漿蝕刻裝置及使用於此之基板載置台。 The present invention relates to a plasma etching method, a plasma etching apparatus, and a substrate stage used therefor.
被使用於FPD(Flat Panel Display)之薄膜電晶體(TFT:Thin Film Transistor)係藉由在玻璃基板等之基板上,一面圖案製作閘極電極或閘極絕緣膜、半導體層等,一面依序予以疊層而形成。 Thin Film Transistor (TFT: Thin Film Transistor) used in FPD (Flat Panel Display) is patterned on one side of a glass substrate, such as a gate electrode, a gate insulating film, a semiconductor layer, etc., and one side is sequentially formed by lamination.
在形成TFT的時候,存在例如蝕刻被連接於半導體層之源極電極或汲極電極之工程,或蝕刻閘極電極之工程。源極電極或汲極電極,有使用Ti/Al/Ti之疊層膜等之含Al金屬膜之情形,作為此情況之蝕刻氣體使用含氯氣體,例如Cl2氣體(例如,專利文獻1)。再者,作為藉由含氯氣體之腐蝕對策,有以含氯氣體對蝕刻後之腔室內供給O2氣體,或是O2氣體及CF4氣體等之氟系氣體而進行腐蝕抑制處理之情況。 When forming a TFT, there is, for example, a process of etching a source electrode or a drain electrode connected to a semiconductor layer, or a process of etching a gate electrode. A source electrode or a drain electrode may use an Al-containing metal film such as a laminated film of Ti/Al/Ti, and a chlorine-containing gas such as Cl 2 gas is used as the etching gas in this case (for example, Patent Document 1) . In addition, as a countermeasure against corrosion by chlorine-containing gas, there are cases where chlorine-containing gas is used to supply O 2 gas to the chamber after etching, or fluorine-based gas such as O 2 gas and CF 4 gas to perform corrosion inhibition treatment. .
再者,作為閘極電極,有使用含Mo膜之情形,作為此情況之蝕刻氣體,使用例如SF6氣體和O2氣體之混合氣體(例如,專利文獻2)。 Furthermore, as the gate electrode, there is a case where a film containing Mo is used, and as the etching gas in this case, a mixed gas of SF 6 gas and O 2 gas is used (for example, Patent Document 2).
然而,在對複數基板重複進行蝕刻處理之情況,因反應生成物附著於腔室內而成為堆積物(附著物),此剝落而成為微粒對製品造成壞影響,故以特定周期開放腔室,進行以酒精擦拭堆積物,或以特殊藥液洗淨等之腔室洗淨(濕洗淨)。 However, when the etching process is repeated on a plurality of substrates, the reaction product adheres to the chamber and becomes a deposit (deposit), which peels off and becomes particles, which adversely affects the product. Use alcohol to wipe deposits, or use special chemical solution to clean the chamber (wet cleaning).
另外,如上述般以Cl2氣體等之含氯氣體蝕刻含Al金屬膜之後,對腔室內供給O2氣體及氟氣體之情況,及以SF6氣體和O2氣體之混合氣體蝕刻含Mo膜之情況,因多量生成成為微粒之原因的蒸氣壓之低反應生成物,其附著於腔室內而成為堆積物(附著物),故腔室洗淨之周期,即是維修週期變短。 In addition, after etching the Al-containing metal film with chlorine-containing gas such as Cl 2 gas as described above, the case where O 2 gas and fluorine gas are supplied into the chamber, and the case where the Mo-containing film is etched with a mixed gas of SF 6 gas and O 2 gas In this case, since a large amount of reaction products with low vapor pressure, which are the cause of particles, are generated, they adhere to the chamber and become deposits (deposits), so the cycle of cleaning the chamber, that is, the maintenance cycle is shortened.
於是,為了增長電漿蝕刻裝置之維修循環,藉由供給洗淨用之氣體,不開放腔室而除去附著於腔室內之反應生成物之腔室洗淨(乾洗淨)被探討著。 Therefore, in order to increase the maintenance cycle of the plasma etching apparatus, chamber cleaning (dry cleaning) for removing reaction products adhering to the chamber without opening the chamber by supplying a cleaning gas has been studied.
〔專利文獻1〕日本特開2015-173159號公報 [Patent Document 1] Japanese Patent Application Laid-Open No. 2015-173159
〔專利文獻2〕日本特開2016-48286號公報 [Patent Document 2] Japanese Patent Application Laid-Open No. 2016-48286
但是,證明了藉由上述般之電漿蝕刻而被生成之蒸氣壓的低反應生成物,在乾蝕刻中無法有效地除 去。 However, it has been proved that the low vapor pressure reaction product generated by the plasma etching as described above cannot be effectively removed by dry etching. go.
再者,不在基板載置台載置基板而進行乾洗淨之情況,藉由乾洗淨氣體之電漿,有對靜電夾具造成損傷,壽命變短之虞。因此,雖然考慮載置素玻璃而進行乾洗淨,但是在此情況,生產性下降。 Furthermore, when dry cleaning is performed without placing the substrate on the substrate mounting table, the electrostatic jig may be damaged by the plasma of the dry cleaning gas, and the lifetime may be shortened. Therefore, although it is considered that the plain glass is placed and dry cleaning is performed, in this case, the productivity is lowered.
因此,本發明係以提供可以導入乾洗淨,並可以延長處理容器之維修週期之電漿蝕刻方法,及即使進行乾洗淨亦可以確保靜電夾具之壽命的電漿蝕刻裝置及使用於此之基板載置台為課題。 Therefore, the present invention aims to provide a plasma etching method capable of introducing dry cleaning and prolonging the maintenance period of the processing container, and a plasma etching apparatus capable of ensuring the life of the electrostatic jig even if dry cleaning is performed, and use thereof. The substrate stage is a problem.
為了解決上述課題,本發明之第1觀點係提供一種電漿蝕刻方法,其係藉由電漿蝕刻裝置對被形成基板之特定膜進行電漿蝕刻之電漿蝕刻方法,其特徵在於具有:在上述電漿蝕刻裝置的電漿蝕刻處理中,選定處理氣體,以使被生成之反應生成物成為能夠乾洗淨的工程;在上述電漿蝕刻裝置中,對上述特定膜,使用事先被選定之處理氣體而進行電漿蝕刻處理的工程;於將進行上述電漿蝕刻處理之工程進行一次或兩次以上之特定次數之後,藉由乾洗淨氣體之電漿,將上述電漿蝕刻裝置之腔室內予以乾洗淨的工程。 In order to solve the above-mentioned problems, a first aspect of the present invention is to provide a plasma etching method for plasma etching a specific film to be formed on a substrate by a plasma etching apparatus, characterized by comprising: In the plasma etching process of the above-mentioned plasma etching apparatus, a process gas is selected so that the produced reaction product can be dry-cleaned; in the above-mentioned plasma etching apparatus, the above-mentioned specific film is used. The process of processing gas to carry out plasma etching treatment; after the process of carrying out the above-mentioned plasma etching process is carried out one or more times for a specific number of times, the cavity of the above-mentioned plasma etching device is cleaned by the plasma of the dry cleaning gas. Indoor dry cleaning works.
在上述第1觀點之電漿蝕刻方法中,作為上述乾洗淨之時的上述乾洗淨氣體,可以使用與於上述電漿蝕刻之時所使用之上述處理氣體相同之氣體。 In the plasma etching method according to the first aspect, as the dry cleaning gas in the dry cleaning, the same gas as the processing gas used in the plasma etching can be used.
上述第1觀點之電漿蝕刻方法,可以適用於上述特定膜為含Al金屬膜,上述處理氣體為含氯氣體,上述反應生成物係AlClx,進一步具有在上述電漿蝕刻裝置進行上述電漿蝕刻之後,將處理後之基板搬運至個別被設置之後處理裝置,使用O2氣體,或是O2氣體及含氟氣體,進行腐蝕抑制用之後處理的工程,上述乾洗淨之工程可以適用於將進行上述電漿蝕刻處理之工程及進行上述後處理之工程進行一次或兩次以上之特定次數之後的情況。再者,作為上述處理氣體之上述含氯氣體,可以使用Cl2氣體。 The plasma etching method of the above-mentioned first aspect can be applied to the above-mentioned specific film being an Al-containing metal film, the above-mentioned processing gas being a chlorine-containing gas, the above-mentioned reaction product being AlClx, and further comprising performing the above-mentioned plasma etching in the above-mentioned plasma etching apparatus. After that, the processed substrate is transported to a post-processing device installed separately, and the post-processing process for corrosion inhibition is performed using O 2 gas, or O 2 gas and fluorine-containing gas. The above dry cleaning process can be applied to the The situation after the above-mentioned plasma etching process and the above-mentioned post-treatment process are performed once or twice for a specific number of times. In addition, Cl2 gas can be used as the said chlorine - containing gas of the said process gas.
作為上述含Al金屬膜,可以使用用以形成薄膜電晶體之源極電極及汲極電極之Ti/Al/Ti膜。 As the above-mentioned Al-containing metal film, a Ti/Al/Ti film for forming a source electrode and a drain electrode of a thin film transistor can be used.
上述第1觀點之電漿蝕刻方法可以適用於上述特定膜為Mo系材料膜,上述處理氣體為含氟氣體,上述反應生成物為MoFx的情況。再者,作為上述處理氣體之上述含氟氣體,可以使用SF6氣體。 The plasma etching method according to the first aspect can be applied to the case where the specific film is a Mo-based material film, the processing gas is a fluorine-containing gas, and the reaction product is MoFx. In addition, as the said fluorine-containing gas of the said process gas, SF6 gas can be used.
作為上述Mo系材料膜,可以使用用以形成薄膜電晶體之閘極電極或遮光膜的Mo膜或MoW膜。 As the Mo-based material film, a Mo film or a MoW film for forming a gate electrode or a light-shielding film of a thin film transistor can be used.
本發明之第2觀點係提供一種電漿蝕刻裝置,其係對被形成在基板之特定膜施予電漿蝕刻處理之電漿蝕刻裝置,其特徵在於具有:收容基板之處理容器、在上述處理容器內載置基板之基板載置台、對上述處理容器內供給蝕刻氣體及乾洗淨氣體之氣體供給機構、對上述處理容器內進行排氣之排氣機構,和在上述處理容器內生成上述蝕刻氣體及上述乾洗淨氣體之電漿的電漿生成機構,上述 基板載置台具有基材、被設置在上述基材上,且具有由陶瓷熔射膜所構成之介電體層及被設置在上述介電體層之內部的吸附電極之靜電夾具,上述乾洗淨氣體為含氯氣體,上述靜電夾具之上述介電體層係熔射氧化鋁和氧化釔和矽化合物之混合物而被形成的混合熔射膜。 A second aspect of the present invention is to provide a plasma etching apparatus for subjecting a specific film formed on a substrate to a plasma etching process, comprising: a process container for accommodating the substrate; A substrate stage for placing a substrate in a container, a gas supply mechanism for supplying etching gas and dry cleaning gas into the processing container, an exhaust mechanism for evacuating the inside of the processing container, and generating the etching in the processing container A plasma generation mechanism for the plasma of the gas and the above-mentioned dry cleaning gas, the above-mentioned The substrate stage has a base material, is disposed on the base material, has a dielectric layer made of a ceramic spray film, and an electrostatic jig having an adsorption electrode disposed inside the dielectric layer, the dry cleaning gas For chlorine-containing gas, the above-mentioned dielectric layer of the above-mentioned electrostatic jig is a mixed spray film formed by spraying a mixture of aluminum oxide, yttrium oxide and silicon compound.
在上述第2觀點之電漿蝕刻裝置中,構成上述靜電夾具之上述介電體層的混合熔射膜係以使用氧化矽或氮化矽以作為矽化合物為佳。作為上述靜電夾具之上述吸附電極,可以使用由鎢或鉬所構成者。作為上述乾洗淨氣體,可以使用Cl2氣體。 In the plasma etching apparatus according to the second aspect, it is preferable that the hybrid spray film of the dielectric layer constituting the electrostatic chuck is made of silicon oxide or silicon nitride as a silicon compound. As the said adsorption electrode of the said electrostatic clip, what consists of tungsten or molybdenum can be used. As the above-mentioned dry cleaning gas, Cl 2 gas can be used.
本發明之第3觀點係提供一種電漿蝕刻裝置,其係對被形成在基板之特定膜施予電漿蝕刻處理之電漿蝕刻裝置,其特徵在於具有:收容基板之處理容器、在上述處理容器內載置基板之基板載置台、對上述處理容器內供給蝕刻氣體及乾洗淨氣體之氣體供給機構、對上述處理容器內進行排氣之排氣機構,和在上述處理容器內生成上述蝕刻氣體及上述乾洗淨氣體之電漿的電漿生成機構,上述基板載置台具有基材、被設置在上述基材上,且具有由陶瓷熔射膜所構成之介電體層及被設置在上述介電體層之內部的吸附電極之靜電夾具,上述乾洗淨氣體為含氟氣體,上述吸附電極係由鋁所構成。 A third aspect of the present invention is to provide a plasma etching apparatus for subjecting a specific film formed on a substrate to a plasma etching process, comprising: a process container for accommodating the substrate; A substrate stage for placing a substrate in a container, a gas supply mechanism for supplying etching gas and dry cleaning gas into the processing container, an exhaust mechanism for evacuating the inside of the processing container, and generating the etching in the processing container The plasma generation mechanism of the plasma of the gas and the dry cleaning gas, wherein the substrate mounting table has a base material, is provided on the base material, has a dielectric layer made of a ceramic spray film, and is provided on the above-mentioned base material. In the electrostatic jig of the adsorption electrode inside the dielectric layer, the dry cleaning gas is a fluorine-containing gas, and the adsorption electrode is made of aluminum.
在上述第3觀點之電漿蝕刻裝置中,上述靜電夾具之上述介電體層可以設為熔射氧化鋁和氧化釔和矽化合物之混合物而形成的混合熔射膜,或是由氧化釔所構成 者。作為上述乾洗淨氣體,可以使用SF6氣體。 In the plasma etching apparatus according to the third aspect, the dielectric layer of the electrostatic jig may be a mixed spray film formed by spraying a mixture of aluminum oxide, yttrium oxide and silicon compound, or may be formed of yttrium oxide By. As the above-mentioned dry cleaning gas, SF 6 gas can be used.
在上述第2及第3觀點之電漿蝕刻裝置中,作為上述蝕刻氣體,可以使用與上述乾洗淨氣體相同的氣體。 In the plasma etching apparatus of the above-mentioned second and third viewpoints, the same gas as the above-mentioned dry cleaning gas can be used as the above-mentioned etching gas.
本發明之第4觀點係提供一種基板載置台,其係於對被形成在基板之特定膜,在處理容器內藉由蝕刻氣體進行電漿蝕刻,並且藉由乾洗淨氣體之電漿,將上述處理容器內予以乾洗淨之電漿蝕刻裝置中,在上述處理容器內載置基板,該基板載置台之特徵在於具有:基材、被設置在上述基材上,且具有由陶瓷熔射膜所構成之介電體層及被設置在上述介電體層之內部之吸附電極的靜電夾具,上述乾洗淨氣體為含氯氣體,上述靜電夾具之上述介電體層係熔射氧化鋁和氧化釔和矽化合物之混合物而形成的混合熔射膜。 A fourth aspect of the present invention is to provide a substrate stage in which a specific film formed on a substrate is subjected to plasma etching with an etching gas in a processing container, and the plasma of a dry cleaning gas is used to etch a specific film. In the plasma etching apparatus for dry cleaning in the above-mentioned processing container, a substrate is placed in the above-mentioned processing container, and the substrate mounting table is characterized by having a base material, being provided on the base material, and having a surface formed by ceramic spraying. A dielectric layer composed of a film and an electrostatic jig with an adsorption electrode disposed inside the dielectric layer, the dry cleaning gas is a chlorine-containing gas, and the dielectric layer of the electrostatic jig is a fusion-sprayed aluminum oxide and yttrium oxide. Hybrid spray film formed with a mixture of silicon compounds.
本發明之第5觀點係提供一種基板載置台,其係於對被形成在基板之特定膜,在處理容器內藉由蝕刻氣體進行電漿蝕刻,並且藉由乾洗淨氣體之電漿,將上述處理容器內予以乾洗淨之電漿蝕刻裝置中,在上述處理容器內載置基板,該基板載置台之特徵在於具有:基材、被設置在上述基材上,且具有由陶瓷熔射膜所構成之介電體層及被設置在上述介電體層之內部之吸附電極的靜電夾具,上述乾洗淨氣體為含氟氣體,上述靜電夾具之上述吸附電極係由鋁所構成。 A fifth aspect of the present invention is to provide a substrate stage in which a specific film formed on a substrate is subjected to plasma etching with an etching gas in a processing container, and the plasma of a dry cleaning gas is used to etch a specific film. In the plasma etching apparatus for dry cleaning in the above-mentioned processing container, a substrate is placed in the above-mentioned processing container, and the substrate mounting table is characterized by having a base material, being provided on the base material, and having a surface formed by ceramic spraying. The electrostatic jig including the dielectric layer and the adsorption electrode provided inside the dielectric layer, the dry cleaning gas is a fluorine-containing gas, and the adsorption electrode of the electrostatic jig is made of aluminum.
若藉由本發明時,在電漿蝕刻裝置之電漿蝕刻處理中,選定處理氣體,以使被生成之反應生成物成為能夠乾洗淨,於電漿蝕刻處理之後,可以延長處理容器之維修週期。 According to the present invention, in the plasma etching process of the plasma etching apparatus, the process gas is selected so that the generated reaction product can be dry cleaned, and the maintenance period of the process container can be extended after the plasma etching process. .
因可以將靜電夾具設為對含氯電漿或含氟電漿耐性高之構成,故即使進行乾洗淨亦可以確保靜電夾具之壽命。 Since the electrostatic jig can be constructed with high resistance to chlorine-containing plasma or fluorine-containing plasma, the life of the electrostatic jig can be ensured even if dry cleaning is performed.
1:玻璃基板 1: glass substrate
2:遮光層 2: shading layer
4:多晶矽膜 4: Polysilicon film
5:閘極絕緣膜 5: Gate insulating film
6:閘極電極 6: Gate electrode
7:層間絕緣膜 7: Interlayer insulating film
8a:源極電極 8a: source electrode
8b:汲極電極 8b: drain electrode
10:真空搬運室 10: Vacuum transfer room
20:裝載鎖定室 20: Load lock chamber
30、90:電漿蝕刻裝置 30, 90: Plasma etching device
40:後處理裝置 40: Aftertreatment device
50:載體 50: carrier
60:搬運機構 60: Handling mechanism
70:真空搬運機構 70: Vacuum transfer mechanism
80:控制部 80: Control Department
100、200:處理系統 100, 200: Processing system
101:處理容器 101: Handling Containers
102:介電體壁 102: Dielectric Wall
104:腔室 104: Chamber
111:噴淋框體 111: Spray frame
113:高頻天線 113: high frequency antenna
115:高頻電源 115: High frequency power supply
120、120’、220:處理氣體供給機構 120, 120', 220: Process gas supply mechanism
130:基板載置台 130: Substrate stage
132、232:靜電夾具 132, 232: electrostatic clamp
145、245:介電體層 145, 245: Dielectric layer
146、246:吸附電極 146, 246: adsorption electrode
160:排氣機構 160: Exhaust mechanism
S:基板 S: substrate
圖1為表示適用與本發明之實施型態有關之電漿處理方法之基板之構成的剖面圖。 FIG. 1 is a cross-sectional view showing the structure of a substrate to which a plasma processing method according to an embodiment of the present invention is applied.
圖2為表示用以實施第1實施型態之處理方法之處理系統的概略俯視圖。 FIG. 2 is a schematic plan view showing a processing system for implementing the processing method of the first embodiment.
圖3為表示被搭載於圖2之處理系統之電漿蝕刻裝置之剖面圖。 FIG. 3 is a cross-sectional view showing a plasma etching apparatus mounted in the processing system of FIG. 2 .
圖4為表示被搭載於圖2之處理系統之後處理裝置之概略圖。 FIG. 4 is a schematic diagram showing a processing apparatus after being installed in the processing system of FIG. 2 .
圖5為與第1實施型態有關之電漿處理方法的流程圖。 FIG. 5 is a flowchart of a plasma processing method related to the first embodiment.
圖6為表示使用Cl2氣體作為處理氣體而對含Al金屬膜進行蝕刻之情況,在腔室內生成的反應生成物之概略圖。 6 is a schematic view showing a reaction product generated in a chamber when the Al-containing metal film is etched using Cl 2 gas as a processing gas.
圖7為使用Cl2氣體作為處理氣體而對含Al金屬膜進行蝕刻之後,使用O2氣體,或是O2氣體及CF4氣體而進行後 處理之情況,在腔室內生成的反應生成物之概略圖。 FIG. 7 shows the reaction products generated in the chamber when the Al-containing metal film is etched using Cl 2 gas as the processing gas, and then post-processing is performed using O 2 gas, or O 2 gas and CF 4 gas. Sketch map.
圖8為表示用以實施第2實施型態之處理方法之處理系統的概略俯視圖。 FIG. 8 is a schematic plan view showing a processing system for implementing the processing method of the second embodiment.
圖9為表示被搭載於圖8之處理系統之電漿蝕刻裝置之剖面圖。 FIG. 9 is a cross-sectional view showing a plasma etching apparatus mounted in the processing system of FIG. 8 .
圖10為與第2實施型態有關之電漿處理方法的流程圖。 FIG. 10 is a flowchart of a plasma processing method related to the second embodiment.
圖11為表示使用SF6氣體作為處理氣體而對Mo系材料膜進行蝕刻之情況,在腔室內生成的反應生成物之概略圖。 11 is a schematic view showing a reaction product generated in a chamber when the Mo-based material film is etched using SF 6 gas as a processing gas.
圖12為表示使用SF6氣體及O2氣體作為處理氣體而對Mo系材料膜進行蝕刻之情況,在腔室內生成的反應生成物之概略圖。 12 is a schematic view showing a reaction product generated in a chamber when the Mo-based material film is etched using SF 6 gas and O 2 gas as processing gases.
以下,參照附件圖面針對本發明之實施型態予以說明。 Hereinafter, embodiments of the present invention will be described with reference to the attached drawings.
圖1為表示適用與本發明之實施型態有關之電漿處理方法之基板之構成的剖面圖。 FIG. 1 is a cross-sectional view showing the structure of a substrate to which a plasma processing method according to an embodiment of the present invention is applied.
該基板S具有在玻璃基板上形成頂閘極型TFT的構造。具體而言,如圖1所示般,在玻璃基板1上形成由Mo
系材料(Mo、MoW)所構成之遮光層2,在其上方隔著絕緣膜3而形成半導體層亦即由多晶矽所構成之多晶矽膜(p-Si膜)4,在其上方隔著閘極絕緣膜5而形成由Mo系材料(Mo、MoW)所構成之閘極電極6,在其上方形成層間絕緣膜7。在層間絕緣膜7,形成接觸孔,在層間絕緣膜7之上方形成經由接觸孔而被連接於p-Si膜4之源極電極8a及汲極電極8b。源極電極8a及汲極電極8b由例如依鈦膜、鋁膜、鈦膜之順序疊層而形成之Ti/Al/Ti構造的含Al金屬膜所構成。在源極電極8a及汲極電極8b上,形成由例如SiN膜所構成之保護膜(無圖示),在保護膜之上方形成被連接於源極電極8a及汲極電極8b之透明電極(無圖示)。
This substrate S has a structure in which a top-gate TFT is formed on a glass substrate. Specifically, as shown in FIG. 1 , on the
首先,針對第1實施型態予以說明。 First, the first embodiment will be described.
在第1實施型態中,舉例說明形成圖1所示之基板S之源極電極8a及汲極電極8b之時的含Al金屬膜之蝕刻處理。另外,於用以形成源極電極8a及汲極電極8b之含Al金屬膜之蝕刻時,在其上方形成具有特定圖案之抗蝕劑膜(無圖示),將此予以遮罩而進行電漿蝕刻。
In the first embodiment, the etching process of the Al-containing metal film at the time of forming the
首先,針對用於第1實施型態之處理系統及電漿蝕刻 裝置等之裝置構成予以說明。 First, for the processing system and plasma etching used in the first embodiment The device configuration of the device and the like will be described.
圖2為表示用以實施第1實施型態之處理方法的處理系統的概略俯視圖,圖3為表示被搭載於圖2之處理系統之電漿蝕刻裝置的剖面圖,圖4為表示被搭載於圖2之處理系統之後處理裝置的概略圖。 2 is a schematic plan view showing a processing system for carrying out the processing method of the first embodiment, FIG. 3 is a cross-sectional view showing a plasma etching apparatus mounted in the processing system of FIG. 2 , and FIG. 4 is a The schematic diagram of the processing apparatus after the processing system of FIG. 2 is shown.
如圖2所示般,處理系統100係多腔室型之處理系統,具有真空搬運室10、裝載鎖定室20、兩個電漿蝕刻裝置30和後處理裝置40。電漿蝕刻裝置30及後處理裝置40係在特定減壓氛圍下進行處理。真空搬運室10之俯視形狀構成矩形狀,裝載鎖定室20、兩個電漿蝕刻裝置30、後處理裝置40經由閘閥G被連接於真空搬運室10之各壁部。在裝載鎖定室20之外側,配置收容矩形狀之基板S之載體50。
As shown in FIG. 2 , the
在該些兩個載體50之間,設置有搬運機構60,該搬運機構60具有被設置成上下兩段之拾取器61(僅圖示1個),及能夠與該些一體性地進出退避及旋轉的底座62。
Between the two
真空搬運室10能夠保持在特定之減壓氛圍,其中如圖2所示般,設置有真空搬運機構70。而且,藉由該真空搬運機構70,在裝載鎖定室20、兩個電漿蝕刻裝置30及後處理裝置40之間搬運基板S。真空搬運機構70係在能夠旋動及上下移動之基座71上,以能夠前後移動之方式設置有兩個基板搬運臂72(僅圖示一個)。
The
裝載鎖定室20係用以在處於大氣氛圍之載體
50和處於減壓氛圍之真空搬運室10之間進行基板S之收授者,成為可以在短時間切換真空氛圍和大氣氛圍。裝載鎖定室20係基板收容部被設置成上下2段,在各基板收容部內,成為基板S藉由定位器(無圖示)被位置對準。
The
電漿蝕刻裝置30係用以蝕刻基板S之含Al金屬膜者,如圖3所示般,例如具有內壁面被陽極氧化處理之由鋁所構成之角筒形狀之氣密的本體容器101。該本體容器101被組裝成可分解,且被接地。本體容器101係藉由介電體壁102被區劃成上下,上側成為區劃天線室之天線容器103,下側成為區劃處理室之腔室(處理容器)104。介電體壁102構成腔室104之頂壁,由Al2O3等之陶瓷、石英等所構成。
The
在本體容器101中之天線容器103之側壁103a和腔室104之側壁104a之間,設置有突出於內側之支撐架105,在該支撐架105上載置介電體壁102。
Between the
在介電體壁102之下側部分,嵌入有處理氣體供給用之噴淋框體111。噴淋框體111係被設置成十字狀,成為從下方支撐介電體壁102之樑構造。噴淋框體111成為藉由複數根之吊桿(無圖示),成為被吊在本體容器101之頂棚的狀態。
A
該噴淋框體111係由導電性材料,例如其內面或外面被陽極氧化處理之鋁所構成。在該噴淋框體111形成有水平延伸之氣體流路112,在該氣體流路112,連貫有朝下方延伸之複數氣體吐出孔112a。
The
另外,在介電體壁102之上面中央,以連通於該氣體流路112之方式設置有氣體供給管121。氣體供給管121係從本體容器101之頂棚貫通至其外側,分歧至分歧管121a、121b。分歧管121a連接有供給含氯氣體,例如Cl2氣體之含氯氣體供給源122。再者,分歧管121b連接有供給當作沖洗氣體或稀釋氣體使用之Ar氣體、N2氣體等之惰性氣體的惰性氣體供給源123。含氯氣體當作蝕刻氣體及乾洗淨氣體被使用。在分歧管121a、121b設置有質量流量控制器等之流量控制器或閥系統。
In addition, a
氣體供給管121、分歧管121a、121b、含氯氣體供給源122、惰性氣體供給源123以及流量控制器及閥系統構成處理氣體供給機構120。
The
在電漿蝕刻裝置30中,從處理氣體供給機構120被供給之含氯氣體,被供給至噴淋框體111內,從其下面之氣體吐出孔112a朝腔室104內吐出,進行基板S之含Al金屬膜之蝕刻或腔室104之乾洗淨。作為含氯氣體,以氯(Cl2)氣體為佳,但是亦可以使用三氯化硼(BCl3)氣體、四氯化碳(CCl4)氣體等。
In the
在天線容器103內配設有高頻(RF)天線113。高頻天線113係將由銅或鋁等之良導電性之金屬所構成之天線113a配置成環狀或旋渦狀等之以往所使用之任意形狀而被構成。即使為具有複數天線部之多重天線亦可。該高頻天線113係藉由由絕緣構件所構成之間隔物117而與介電體壁102間隔開。
A high frequency (RF)
在天線113a之端子118連接有朝天線容器103之上方延伸的供電構件116。在供電構件116之上端,連接有供電線119,在供電線119連接有匹配器114及高頻電源115。而且,藉由從高頻電源115對高頻天線113供給頻率例如13.56MHz之高頻電力,在腔室104內形成感應電場,藉由該感應電場,從噴淋框體111所供給之處理氣體被電漿化,生成感應耦合電漿。
A
在腔室104內之底壁,隔著構成框緣狀之由絕緣性所構成之間隔物134,設置有載置基板G之基板載置台130。基板載置台130具有被設置在上述之間隔物134上之基材131、被設置在基材131上之靜電夾具132,和覆蓋基材131及靜電夾具132之側壁的側壁絕緣構件133。基材131及靜電夾具132構成與基板S之形狀對應的矩形狀,基板載置台130之全體形成四角板狀或柱狀。間隔物134及側壁絕緣構件133係由氧化鋁等之絕緣性陶瓷所構成。
On the bottom wall in the
靜電夾具132具有被形成在基材131之表面的由陶瓷熔射膜所構成之介電體層145,和被設置在介電體層145之內部的吸附電極146。吸附電極146可以取得板狀、膜狀、格子狀、網狀等之各種型態。在吸附電極146經由供電線147連接有直流電源148,在吸附電極146被施加直流電壓。對吸附電極146之供電成為以開關(無圖示)而被接通斷開。藉由對吸附電極146施加直流電壓,產生庫倫力或強生拉貝克力等之靜電吸附力,基板S被吸附。
The
靜電夾具132之介電體層145以混合熔射膜所構成。混合熔射膜係熔射氧化鋁(Al2O3)和氧化釔(Y2O3)和矽化合物之混合物而形成者。因Y2O3材質上電漿耐性高,再者,Al2O3相對於含氯氣體其化學性耐性高,並且矽化合物具有成為玻璃質掩埋Y2O3及Al2O3之晶界而予以緻密化的作用,故混合熔射膜相對於Cl2氣體等之含氯氣體之電漿具有高的耐性。作為混合熔射膜,以使用氧化矽(SiO2)以作為矽化合物的Al2O3、Y2O3、SiO2膜為佳。
The
再者,亦可以適合使用採用氮化矽(Si3N4)以作為矽化合物的Al2O3、Y2O3、SiO2、Si3N4膜。靜電夾具132之吸附電極146係自以往所使用之鎢(W)或鉬(Mo)所構成。該些相對於含氯氣體之電漿的耐性高。
Furthermore, Al 2 O 3 , Y 2 O 3 , SiO 2 , and Si 3 N 4 films using silicon nitride (Si 3 N 4 ) as the silicon compound can also be suitably used. The
在基材131,經由供電線151連接有偏壓施加用之高頻電源153。再者,在供電線151之基材131和高頻電源153之間設置有匹配器152。高頻電源153係用以將離子拉入至基材131上之基板S者,使用50kHz~10MHz之範圍的頻率,例如3.2MHz。
A high-
另外,在基板載置台130之基材131內,設置有用以控制基板S之溫度的調溫機構及溫度感測器(任一者皆無圖示)。再者,在基板載置台130載置基板S之狀態,設置有對基板S和基板載置台130之間用以熱傳遞之導熱氣體,例如供給He氣體之導熱氣體供給機構(無圖示)。而且,在基板載置台130,以能夠對靜電夾具132之
上面突陷之方式,設置有用以進行基板S之收授的複數之升降銷(無圖示),基板S之收授係對從靜電夾具132之上面突出至上方之狀態的升降銷進行。
Moreover, in the
在腔室之側壁104a,設置有用以對腔室104搬入搬出基板S之搬入搬出口155,搬入搬出口155成為藉由閘閥G能夠開關。藉由開啟閘閥G,基板S能夠依據被設置在真空搬運室10內之真空搬運機構70而經由搬入搬出口155進行搬入搬出。
The
在腔室104之底壁之緣部或角部形成有複數之排氣口159(僅兩個圖示),在各排氣口159設置有排氣部160。排氣部160具有被連接於排氣口159之排氣配管161,和藉由調整排氣配管161之開口度,控制腔室104內之壓力的自動壓力控制閥(APC)162,和用以經排氣配管161使腔室104內予以排氣之真空泵163。而且,藉由真空泵163使腔室104內排氣,在電漿蝕刻處理中,調整自動壓力控制閥(APC)162之開口度而將腔室104內設定、維持在特定之真空氛圍。
A plurality of exhaust ports 159 (only two are shown) are formed at the edge or corner of the bottom wall of the
後處理裝置40係在蝕刻基板S之含Al金屬膜之後,用以進行用以抑制腐蝕之後處理者。後處理裝置40如圖4所示般,具有供給與電漿蝕刻裝置30不同之氣體的處理氣體供給機構120’以取代處理氣體供給機構120。在圖4中雖然省略除此以外之構成,但是被構成與電漿蝕刻裝置30相同。另外,在以下之說明中,對與電漿蝕刻裝置30相同之構件賦予相同符號予以說明。
The
後處理裝置40之處理氣體供給機構120’具有氣體供給管121’、在本體容器101之上方外側,從氣體供給管121’分歧之分歧管121a’、121b’、121c’,和被連接於分歧管121a’之供給O2氣體之O2氣體供給源124,和被連接於分歧管121b’之供給含氟氣體之含氟氣體供給源125,和被連接於分歧管121c’之供給作為沖洗氣體或稀釋氣體之Ar氣體、N2氣體等之惰性氣體的惰性氣體供給源126。氣體供給管121’與電漿蝕刻裝置30之氣體供給管121相同,被連接於噴淋框體111之氣體流路112(參照圖3)。在分歧管121a’、121b’、121c’設置有質量流量控制器等之流量控制器或閥系統。
The processing gas supply mechanism 120' of the
在後處理裝置40中,從處理氣體供給機構120’被供給之O2氣體,或是O2氣體和含氟氣體經由噴淋框體111而被吐出至腔室104內,進行基板S之蝕刻後之含Al金屬膜之腐蝕抑制處理。作為含氟氣體,雖可以適合使用四氟化碳(CF4),但是亦可以使用六氟化硫(SF6)等。
In the
另外,在後處理裝置40中,因靜電夾具132之介電體層145不被要求含氯氣體之對電漿的耐性,故可以與以往相同以由Al2O3或Y2O3所構成之熔射膜構成介電體層145。再者,後處理裝置40由於僅進行腐蝕抑制處理,故即使不設置靜電夾具132亦可。
In addition, in the
處理系統100進一步具有控制部80。控制部80係由具備CPU及記憶部之電腦所構成,處理系統100之各構成部(真空搬運室10、裝載鎖定室20、電漿蝕刻裝置
30、後處理裝置40、搬運機構60、真空搬運機構70之各構成部)被控制成根據被記憶於記憶部之處理配方(程式)而進行特定處理。處理配方被儲存於硬碟、光碟、半導體記憶體等之記憶媒體。
The
接著,針對與藉由以上之處理系統100之第1實施型態有關之電漿處理方法,參照圖5之流程圖而予以說明。
Next, the plasma processing method related to the first embodiment of the
在此,藉由處理系統100,進行用以形成被形成在基板S之源極電極8a及汲極電極8b之含Al金屬膜亦即Ti/Al/Ti膜之電漿蝕刻處理。
Here, by the
最初,在電漿蝕刻裝置30之電漿蝕刻處理中,選定處理氣體,以使被生成之反應生成物成為能夠乾洗淨者(步驟1)。
Initially, in the plasma etching process of the
具體而言,在本實施型態中,作為處理氣體,選定含氯氣體,例如Cl2氣體。在使用含氯氣體而電漿蝕刻Ti/Al/Ti膜之情況,如圖6所示般,主要生成AlClx以作為反應生成物,雖然該些之一部分附著於腔室壁而成為堆積物(附著物),但是AlClx蒸氣壓高,能夠以乾洗淨除去。 Specifically, in this embodiment, a chlorine-containing gas such as Cl 2 gas is selected as the processing gas. In the case of plasma etching the Ti/Al/Ti film using a chlorine-containing gas, as shown in FIG. 6 , AlClx is mainly formed as a reaction product, although a part of these adheres to the chamber wall and becomes a deposit (adhered to material), but AlClx has a high vapor pressure and can be removed by dry cleaning.
另外,如以往般,以Cl2氣體蝕刻Ti/Al/Ti膜之後,在相同的腔室內進行腐蝕抑制之後處理之情況,如圖7所示般,當供給作為後處理氣體之O2氣體進行電漿處理之時,附著之AlClx和O2氣體反應而在腔室內生成蒸氣壓 低之AlOx,再者,為了進一步提高腐蝕抑制效果,當除了O2氣體外,又供給含氟氣體,例如CF4氣體時,在腔室內除了AlOx外,仍然也生成蒸氣壓低之AlFx。該些AlOx及AlFx因蒸氣壓低,故不揮發,附著於腔室壁而容易成為堆積物(附著物)。而且,當此剝落時,成為微粒之原因,對製品造成壞影響。再者,該些因穩定性高,故在乾洗淨中難以除去。 In addition, as in the past, after etching the Ti/Al/Ti film with Cl 2 gas, and performing post - treatment for corrosion inhibition in the same chamber, as shown in FIG. During the plasma treatment, the adhered AlClx reacts with the O 2 gas to generate AlOx with a low vapor pressure in the chamber. Furthermore, in order to further improve the corrosion inhibition effect, in addition to the O 2 gas, a fluorine-containing gas such as CF 4 is supplied. In the case of gas, in addition to AlOx, AlFx with a low vapor pressure is also generated in the chamber. Since these AlOx and AlFx have a low vapor pressure, they do not volatilize, and they adhere to the chamber wall and tend to become deposits (deposits). Furthermore, when this peeling off, it becomes a cause of fine particles and has a bad influence on the product. Furthermore, since these are highly stable, they are difficult to remove by dry cleaning.
於是,在本實施型態中,在腔室內,生成能夠乾洗淨之AlClx以作為反應生成物,以不會生成成為微粒之原因,且在乾洗淨中難以除去的AlOx及AlFx之方式,將在電漿蝕刻裝置30中之基板S之處理氣體,僅設為蝕刻氣體亦即含氯氣體(Cl2氣體)。
Therefore, in the present embodiment, in the chamber, AlClx that can be dry cleaned is generated as a reaction product, so that AlOx and AlFx, which are the cause of fine particles and are difficult to be removed by dry cleaning, are not generated. The processing gas of the substrate S in the
如此一來於選定電漿蝕刻之時之處理氣體之後,對被形成在基板S之含Al金屬膜亦即Ti/Al/Ti膜,藉由電漿蝕刻裝置30,使用事先被選定之處理氣體亦即含氯氣體,例如Cl2氣體施予電漿蝕刻處理(步驟2)。
In this way, after the process gas at the time of plasma etching is selected, the process gas selected in advance is used by the
以下,針對步驟2之電漿蝕刻處理,具體性予以說明。
Hereinafter, the specificity of the plasma etching process in
從載體50藉由搬運機構60,取出基板S,搬運至裝載鎖定室20,真空搬運室10內之真空搬運機構70從裝載鎖定室20接取基板S而搬運至電漿蝕刻裝置30。
The substrate S is taken out from the
在電漿蝕刻裝置30中,首先,藉由真空泵163將腔室104內調整成適合於真空搬運室10之壓力,開放閘閥G將基板S從搬入搬出口155藉由真空搬運機構70搬入至
腔室104內,使基板S載置於基板載置台130上。於使真空搬運機構70從腔室104退避之後,關閉閘閥G。
In the
在該狀態,藉由自動壓力控制閥(APC)162,將腔室104內之壓力調整成特定真空度,同時從處理氣體供給機構120經由噴淋框體111,將作為處理氣體之蝕刻氣體亦即含氯氣體,例如Cl2氣體供給至腔室104內。除了含氯氣體之外,即使供給Ar氣體等之惰性氣體以作為稀釋氣體亦可。
In this state, the pressure in the
此時,基板S藉由靜電夾具132被吸附,藉由調溫機構(無圖示)被調溫。
At this time, the substrate S is adsorbed by the
接著,從高頻電源115對高頻天線113施加例如13.56MHz之高頻,藉此經介電體壁102在腔室104內形成均勻之感應電場。藉由如此所形成之感應電場,生成含氯氣體之電漿。藉由如此被生成之高密度之感應耦合電漿,蝕刻基板S之含Al金屬膜亦即Ti/Al/Ti膜。
Next, a high frequency such as 13.56 MHz is applied to the
此時,在電漿蝕刻裝置30中,如上述般生成AlClx以作為反應生成物,其一部分附著於腔室104內之壁部等。另外,幾乎不生成AlOx及AlFx。
At this time, in the
接著,對電漿蝕刻後之基板S之含Al金屬膜亦即Ti/Al/Ti膜,藉由後處理裝置40,使用O2氣體,或是O2氣體及含氟氣體,例如CF4氣體,進行腐蝕抑制用之後處理(步驟3)。
Next, for the Al-containing metal film of the substrate S after plasma etching, that is, the Ti/Al/Ti film, the
以下,針對步驟3之後處理,具體性予以說明。
Hereinafter, the specificity of the processing after
藉由真空搬運機構70,從電漿蝕刻裝置30取出蝕刻處理後之基板S,搬運至後處理裝置40。
The substrate S after the etching process is taken out from the
在後處理裝置40中,與電漿蝕刻裝置30相同,將基板S搬入至腔室104內,使載置於基板載置台130上,將腔室104內之壓力調整成特定真空度之同時,從處理氣體供給機構120’經由噴淋框體111,朝腔室104內供給O2氣體,或是O2氣體和含氟氣體,例如CF4氣體以作為後處理氣體。除了該些外,即使供給Ar等之惰性氣體以作為稀釋氣體亦可。
In the
而且,與電漿蝕刻裝置30相同,藉由感應電場,生成後處理氣體亦即O2氣體,或O2氣體和含氟氣體的電漿,藉由如此被生成之感應耦合電漿,進行被蝕刻之含Al金屬膜亦即Ti/Al/Ti膜之腐蝕抑制處理。
Also, as in the
此時,在後處理裝置40中,因不進行蝕刻處理,故反應生成物之產生量少。
At this time, in the
藉由真空搬運機構70,從後處理裝置40之腔室104取出在後處理裝置40進行後處理之後的基板S,搬運至裝載鎖定室20,藉由搬運機構60返回至載體50。
The substrate S after post-processing by the
將上述般之電漿蝕刻處理(步驟2)及後處理(步驟3)進行一次或兩次以上之特定次數之後,進行電漿蝕刻裝置30之腔室104內之乾洗淨處理(步驟4)。
After performing the above-mentioned plasma etching process (step 2) and post-processing (step 3) for a specific number of times or more, the dry cleaning process in the
乾洗淨係在基板載置台130上不載置基板S之狀態,對腔室104內,與電漿蝕刻之時的蝕刻氣體相同,供給含氯氣體例如Cl2氣體,以作為乾洗淨氣體,藉由與
電漿蝕刻之時相同之感應耦合電漿而進行。
The dry cleaning is a state in which the substrate S is not placed on the substrate mounting table 130 , and the
藉由該乾洗淨,可以除去附著於電漿蝕刻裝置30之腔室104的AlClx。即是,電漿蝕刻裝置30中,因不進行以往般之O2氣體,或是O2氣體和含氟氣體所致腐蝕抑制處理,故以反應生成物而言,不生成藉由乾洗淨難以除去之AlOx及AlFx,成為能夠乾洗淨。
By this dry cleaning, AlClx adhering to the
再者,於乾洗淨之時,因在基板載置台130上不載置基板S,而在靜電夾具132不存在基板S,故乾洗淨氣體亦即含氯氣體之電漿直接作用於靜電夾具132。
Furthermore, during the dry cleaning, since the substrate S is not placed on the substrate mounting table 130 and the substrate S does not exist on the
以往,因電漿蝕刻裝置不進行乾洗淨,故不會在未將基板S載置於靜電夾具之狀態下,進行電漿處理,靜電夾具之介電體層以Y2O3或Al2O3之熔射膜就足夠。但是,證實在乾洗淨之時,若含氯氣體之電漿直接作用,在介電體層為Y2O3或Al2O3之熔射膜中,會造成損傷,有壽命變短之虞。為了解決該問題,雖然考慮於乾洗淨之時,在基板載置台130上載置虛設基板亦即素玻璃之狀態下進行乾洗淨,但是在此情況下,產生對電漿蝕刻裝置30搬入/搬出素玻璃之工程,生產性下降。 Conventionally, since the plasma etching apparatus does not perform dry cleaning, plasma processing is not performed without placing the substrate S on the electrostatic jig, and the dielectric layer of the electrostatic jig is made of Y 2 O 3 or Al 2 O 3 of the spray film is sufficient. However, it has been confirmed that if the plasma containing chlorine gas acts directly during dry cleaning, damage will be caused to the spray film whose dielectric layer is Y 2 O 3 or Al 2 O 3 , and there is a possibility of shortening its life. . In order to solve this problem, in consideration of dry cleaning, dry cleaning is performed in a state where the dummy substrate, ie, plain glass, is mounted on the substrate mounting table 130 . In the process of moving out plain glass, productivity decreased.
於是,在本實施型態中,作為靜電夾具132之介電體層145,使用熔射Al2O3和Y2O3和矽化合物之混合物而形成的混合熔射膜。因Y2O3材質上電漿耐性高,再者,Al2O3相對於含氯氣體其化學性耐性高,並且矽化合物具有成為玻璃質掩埋Y2O3及Al2O3之晶界而予以緻密化的作用,故混合熔射膜相對於Cl2氣體等之含氯氣體之電漿具
有高的耐性,於乾洗淨之時,不載置素玻璃,可以保持期待之壽命。
Therefore, in this embodiment, as the
如上述般,作為混合熔射膜,以Al2O3、Y2O3、SiO2膜為佳。再者,也可以適合使用Al2O3、Y2O3、SiO2、Si3N4膜。靜電夾具132之吸附電極146藉由使用自以往所使用之鎢(W)或鉬(Mo),顯示對含氯氣體之電漿高的耐性。
As described above, as the mixed spray film, Al 2 O 3 , Y 2 O 3 and SiO 2 films are preferable. In addition, Al 2 O 3 , Y 2 O 3 , SiO 2 , and Si 3 N 4 films can also be suitably used. The
實際上,針對Al2O3和混合熔射膜(Al2O3、Y2O3、SiO2),比較相對於含氯氣體亦即Cl2氣體之電漿的切削量。其結果,確認出將混合熔射膜之切削量當作1而予以規格化之切削量,在Al2O3成為9,混合熔射膜相對於含氯氣體之電漿具有高的耐性。 In fact, for Al 2 O 3 and mixed spray films (Al 2 O 3 , Y 2 O 3 , SiO 2 ), the cutting amount with respect to the plasma of chlorine-containing gas, that is, Cl 2 gas was compared. As a result, it was confirmed that the cutting amount normalized by taking the cutting amount of the mixed spray film as 1 was 9 in Al 2 O 3 , and it was confirmed that the mixed spray film had high resistance to plasma containing chlorine gas.
如此一來,在進行電漿蝕刻處理(步驟2)及後處理(步驟3)特定次數之後,當重覆進行乾洗淨(步驟4)之循環時,附著於電漿蝕刻裝置30之腔室104內之堆積物(附著物)開始產生剝離。因此,於重複如此循環特定次數之後,開放腔室104而進行腔室洗淨(步驟5)。腔室洗淨係藉由以酒精擦拭堆積物,或以特殊藥液洗淨等來進行。
In this way, after performing the plasma etching process (step 2) and post-processing (step 3) for a certain number of times, when the cycle of dry cleaning (step 4) is repeated, it adheres to the chamber of the
如上述般在本實施型態中,在電漿蝕刻裝置30的蝕刻處理中,以被生成之反應生成物成為能夠乾洗淨者之方式,將處理基板S之處理氣體,僅設為蝕刻氣體亦即含氯氣體例如Cl2氣體,在個別設置的後處理裝置40進行以往在蝕刻後在相同的腔室內進行的腐蝕抑制用之O2氣
體,或是O2氣體和含氟氣體所致的電漿處理。因此,於電漿蝕刻處理之時,不產生蒸氣壓低之AlOx及AlFx,在腔室產生之堆積物(附著物)僅成為蒸氣壓高的AlClx。因此,比起以往,腔室內之堆積物(附著物)本身減少,同時腔室內之堆積物(附著物)能夠藉由乾洗淨除去,可以明顯地增長開放腔室而進行的腔室洗淨之週期,即是維修週期。
As described above, in the present embodiment, in the etching process of the
再者,因在電漿蝕刻裝置30中之靜電夾具132之介電體層145,相對於乾洗淨之時的含氯電漿具有耐性,故即使進行乾洗淨亦可以確保靜電夾具之壽命。
Furthermore, since the
接著,針對第2實施型態予以說明。 Next, the second embodiment will be described.
在本實施型態中,以例說明形成圖1所示之基板S之閘極電極6或遮光層2之時的Mo系材料膜之蝕刻處理。另外,於用以形成閘極電極6或遮光層2之Mo系材料膜之蝕刻時,在其上方形成具有特定圖案之抗蝕劑膜(無圖示),將此予以遮罩而進行電漿蝕刻。
In the present embodiment, the etching process of the Mo-based material film when the
首先,針對用於第2實施型態之處理系統及電漿蝕刻裝置等之裝置構成予以說明。 First, the apparatus structure used for the processing system and the plasma etching apparatus etc. of 2nd Embodiment is demonstrated.
圖8為表示用以實施本實施型態之處理方法之處理系 統的概略俯視圖,圖9為表示被搭載於圖8之處理系統的電漿蝕刻裝置的剖面圖。 FIG. 8 shows a processing system for implementing the processing method of this embodiment. FIG. 9 is a schematic plan view of the system, and FIG. 9 is a cross-sectional view showing a plasma etching apparatus mounted in the processing system of FIG. 8 .
如圖8所示般,處理系統200係被構成基本上與圖2之處理系統100相同之多腔室型之處理系統。本實施型態之處理系統200具有兩個電漿蝕刻裝置30,和設置有三個電漿蝕刻裝置90,以取代後處理裝置40,另外具有與圖2之處理系統100相同之構成。因其他構成與圖2相同,賦予相同符號省略說明。
As shown in FIG. 8 , the
電漿蝕刻裝置90係用以蝕刻基板S之Mo系材料膜者,如圖9所示般,設置處理氣體供給機構220以取代處理氣體供給機構120,設置有靜電夾具232以取代靜電夾具132之外,具有與圖3之電漿蝕刻裝置30相同之構成。因此,對與圖3相同者賦予相同符號而省略說明。
The
處理氣體供給機構220具有氣體供給管221、在本體容器101之上方外側從氣體供給管221分歧之分歧管221a、221b、被連接於分歧管221a之供給含氟氣體亦即SF6氣體之SF6氣體供給源222、被連接於分歧管221b之供給Ar氣體、N2氣體等之惰性氣體以作為沖洗氣體或稀釋氣體之惰性氣體供給源223。氣體供給管221與圖3之電漿蝕刻裝置30之氣體供給管121相同,被連接於噴淋框體111之氣體流路112。含氟氣體當作蝕刻氣體及乾洗淨氣體被使用。另外,除SF6氣體之外,亦可以使用CF4或NF3以作為含氟氣體。
The processing
靜電夾具232具有被形成在基材131之表面的
由陶瓷熔射膜所構成之介電體層245,和被設置在介電體層245之內部的吸附電極246。吸附電極246可以取得板狀、膜狀、格子狀、網狀等之各種型態。在吸附電極246經由供電線147連接有直流電源148,在吸附電極246被施加直流電壓。對吸附電極246之供電成為以開關(無圖示)而被接通斷開。藉由對吸附電極246施加直流電壓,產生庫倫力或強生拉貝克力等之靜電吸附力,基板S被吸附。
The
靜電夾具232之介電體層245係以熔射氧化鋁(Al2O3)和氧化釔(Y2O3)和矽化合物之混合物而形成的混合熔射膜,或Y2O3所構成。再者,靜電夾具232之吸附電極246係以鋁(Al)所構成。構成介電體層245之氧化鋁(Al2O3)和氧化釔(Y2O3)和矽化合物之混合物,及Y2O3,以及構成吸附電極246之Al相對於氟系氣體亦即SF6之電漿具有高的耐性。
The
接著,針對與藉由以上之處理系統200之第2實施型態有關之電漿處理方法,參照圖10之流程圖而予以說明。
Next, the plasma processing method related to the second embodiment of the
在此,藉由處理系統200,進行被形成在基板S之Mo系材料膜,例如Mo膜或MoW膜之電漿蝕刻處理。
Here, the plasma etching process of the Mo-based material film formed on the substrate S, for example, a Mo film or a MoW film, is performed by the
最初,在電漿蝕刻裝置90之蝕刻處理中,選定處理氣體,以使被生成之反應生成物成為能夠乾洗淨者(步驟11)。
Initially, in the etching process of the
具體而言,在本實施型態中,作為處理氣體,選定含氟氣體亦即SF6氣體。在使用SF6氣體而電漿蝕刻Mo膜或MoW膜般之Mo系材料膜之情況,如圖11所示般,主要生成MoFx以作為反應生成物,雖然該些之一部分附著於腔室壁而成為堆積物(附著物),但是MoFx蒸氣壓高,能夠以乾洗淨除去。 Specifically, in the present embodiment, SF 6 gas, which is a fluorine-containing gas, is selected as the processing gas. When using SF 6 gas to plasma-etch a Mo film or a Mo-based material film such as a MoW film, as shown in FIG. 11 , MoFx is mainly generated as a reaction product, although a part of these adheres to the chamber wall and It becomes a deposit (deposition), but MoFx has a high vapor pressure and can be removed by dry cleaning.
另外,如以往般,使用SF6氣體和O2氣體蝕刻Mo系材料膜之情況,如圖12所示般,作為反應生成物,除MoFx之外,也生成MoFxOy或MoOx。該些中,MoOx因蒸氣壓低,故不揮發,附著於腔室壁而容易成為堆積物(附著物)。而且,當堆積物亦即MoOx剝落時,成為微粒之原因,對製品造成壞影響。再者,MoOx因穩定性高,故在乾洗淨中難以除去。 In addition, when the Mo-based material film is etched using SF 6 gas and O 2 gas in the conventional manner, as shown in FIG. 12 , MoFxOy or MoOx is produced as a reaction product in addition to MoFx. Among these, MoOx does not volatilize due to its low vapor pressure, and adheres to the chamber wall to easily become a deposit (adhesion). Furthermore, when MoOx, which is a deposit, is peeled off, it becomes a cause of fine particles and adversely affects the product. Furthermore, since MoOx has high stability, it is difficult to remove it by dry cleaning.
於是,在本實施型態中,在腔室內,生成能夠乾洗淨之MoFx以作為反應生成物,以不會生成成為微粒之原因,且在乾洗淨中難以除去的MoOx之方式,將在電漿蝕刻裝置90中之基板S之處理氣體,僅設為含氟氣體亦即SF6氣體。
Therefore, in this embodiment, in the chamber, MoFx that can be dry-cleaned is generated as a reaction product, so that MoOx, which is a cause of particles and is difficult to be removed by dry-cleaning, is not generated in the chamber. The processing gas for the substrate S in the
如此一來於選定電漿蝕刻之時之處理氣體之後,對被形成在基板S之Mo材料膜,藉由電漿蝕刻裝置90,使用事先被選定之處理氣體亦即SF6氣體施予電漿蝕刻處理(步驟12)。
In this way, after the process gas at the time of plasma etching is selected, the Mo material film formed on the substrate S is subjected to plasma by the
以下,針對步驟12之電漿蝕刻處理,具體性予以說明。 Hereinafter, the specificity of the plasma etching process in step 12 will be described.
從載體50藉由搬運機構60,取出基板S,搬運至裝載鎖定室20,真空搬運室10內之真空搬運機構70從裝載鎖定室20接取基板S而搬運至電漿蝕刻裝置90。
The substrate S is taken out from the
在電漿蝕刻裝置90中,於將腔室104內調整成適合於真空搬運室10之壓力之後,開放閘閥G將基板S從搬入搬出口155藉由真空搬運機構70搬入至腔室104內,使基板S載置於基板載置台130上。於使真空搬運機構70從腔室104退避之後,關閉閘閥G。
In the
在該狀態,藉由自動壓力控制閥(APC)162,將腔室104內之壓力調整成特定真空度,同時從處理氣體供給機構220經由噴淋框體111,將作為處理氣體之含氟氣體亦即SF6氣體供給至腔室104內。除了SF6氣體之外,即使供給Ar氣體等之惰性氣體以作為稀釋氣體亦可。
In this state, the pressure in the
此時,基板S藉由靜電夾具232被吸附,藉由調溫機構(無圖示)被調溫。
At this time, the substrate S is attracted by the
接著,從高頻電源115對高頻天線113施加例如13.56MHz之高頻,藉此經介電體壁102在腔室104內形成均勻之感應電場。藉由如此所形成之感應電場,生成含氟氣體亦即SF6氣體之電漿。藉由如此被生成之高密度之感應耦合電漿,基板S之Mo系材料膜被蝕刻。
Next, a high frequency such as 13.56 MHz is applied to the
此時,在電漿蝕刻裝置90中,如上述般生成MoFx以作為反應生成物,附著於腔室104內之壁部等。另外,幾乎不生成MoOx。
At this time, in the
在以電漿蝕刻裝置90進行步驟12之電漿蝕刻
處理之後,藉由真空搬運機構70取出基板S,搬運至裝載鎖定室20,藉由搬運機構60返回至載體50。
The plasma etching in step 12 is performed by the
將上述般之步驟12的電漿蝕刻處理進行一次或兩次以上之特定次數之後,進行電漿蝕刻裝置90之腔室104內之乾洗淨處理(步驟13)。
After the above-mentioned plasma etching process in step 12 is performed once or twice for a specific number of times, the dry cleaning process in the
乾洗淨係在基板載置台130上不載置基板S之狀態,對腔室104內,與電漿蝕刻之時的蝕刻氣體相同,供給含氟氣體亦即SF6氣體,以作為乾洗淨氣體,藉由與電漿蝕刻之時相同之感應耦合電漿而進行。
The dry cleaning is a state in which the substrate S is not placed on the substrate mounting table 130 , and the
藉由該乾洗淨,可以除去附著於電漿蝕刻裝置90之腔室104的MoFx。即是,在電漿蝕刻裝置90中,因作為蝕刻氣體不含以往使用的O2氣體,故作為反應生成物,不生成藉由乾洗淨難除去之MoOx而成為能夠乾洗淨。
By this dry cleaning, MoFx adhering to the
再者,於乾洗淨之時,因在基板載置台130上不載置基板S,而在靜電夾具232不存在基板S,故乾洗淨氣體亦即SF6氣體之電漿直接作用於靜電夾具232。
Furthermore, during the dry cleaning, since the substrate S is not placed on the substrate mounting table 130 and the substrate S does not exist on the
以往,因電漿蝕刻裝置不進行乾洗淨,故不使靜電夾具載置基板S之狀態下,不進行電漿處理,作為靜電夾具,以使用Y2O3或Al2O3之熔射膜當作介電體層,作為吸附電極,以使用W或Mo就足夠。但是,即使於乾洗淨之時,含氟氣體亦即SF6氣體電漿直接作用於靜電夾具,介電體層亦即Y3O3或Al2O3之熔射膜亦具有耐性,但是證實了當熔射膜之封孔處理材藉由電漿被除去,電漿及 含氟氣體到達至吸附面時,有在吸附電極為W或Mo會造成損傷,靜電夾具之壽命變短之虞。為了解決該問題,雖然考慮於乾洗淨之時,在基板載置台130上載置虛設基板亦即素玻璃之狀態下進行乾洗淨,但是在此情況下,產生對電漿蝕刻裝置90搬入/搬出素玻璃之工程,生產性下降。 Conventionally, since the plasma etching apparatus does not perform dry cleaning, plasma treatment is not performed in the state where the electrostatic jig is not placed on the substrate S, and as the electrostatic jig, thermal spraying using Y 2 O 3 or Al 2 O 3 is used. It is sufficient to use W or Mo as the film as a dielectric layer and as an adsorption electrode. However, even during dry cleaning, the fluorine-containing gas, ie, SF 6 gas plasma, acts directly on the electrostatic jig, and the dielectric layer, ie, the spray film of Y 3 O 3 or Al 2 O 3 has resistance, but it was confirmed that When the sealing material of the spray film is removed by plasma and the plasma and fluorine-containing gas reach the adsorption surface, W or Mo in the adsorption electrode may cause damage and shorten the life of the electrostatic clamp. In order to solve this problem, it is considered that dry cleaning is performed in a state where the dummy substrate, that is, plain glass, is placed on the substrate mounting table 130 in the case of dry cleaning. In the process of moving out plain glass, productivity decreased.
於是,在本實施型態中,作為靜電夾具232之吸附電極246,使用Al。因Al較W或Mo對含氟氣體亦即SF6氣體之電漿的耐性高,故於乾洗淨之時,不載置素玻璃,可以保持期待之壽命。
Therefore, in the present embodiment, Al is used as the
再者,因熔射氧化鋁(Al2O3)和氧化釔(Y2O3)和矽化合物之混合物而形成的混合熔射膜,及Y2O3相對於含氟氣體亦即SF6氣體之電漿的耐性高,故除了使用Al作為吸附電極246之外,藉由使用混合熔射膜或Y2O3作為介電體層245,可以更提高對SF6氣體之電漿的耐性。
Furthermore, the mixed spray film formed by spraying a mixture of aluminum oxide (Al 2 O 3 ) and yttrium oxide (Y 2 O 3 ) and a silicon compound, and Y 2 O 3 relative to the fluorine-containing gas that is SF 6 Gas plasma resistance is high, so in addition to using Al as the
實際上,作為吸附電極之材料,針對W、Mo、Al,比較相對於含氟氣體亦即SF6氣體之電漿的切削量。其結果,確認出將Al之切削量以1而予以規格化之切削量,在W及Mo也成為10,Al相對於含氟氣體亦即SF6之電漿具有高的耐性。再者,作為介電體層之材料,針對Al2O3和Y2O3和混合熔射膜(Al2O3、Y2O3、SiO2),比較相對於含氟氣體亦即SF6氣體之電漿的切削量。其結果,確認出將混合熔射膜之切削量當作1而予以規格化的切削量,在Al2O3成為3,在Y2O3成為1,混合熔射膜及Y2O3相 對於含氟氣體亦即SF6之電漿具有高的耐性。 In fact, as the material of the adsorption electrode, W, Mo, and Al were compared with respect to the cutting amount of the plasma of the fluorine-containing gas, that is, the SF 6 gas. As a result, it was confirmed that the cutting amount normalized with the cutting amount of Al as 1 was 10 in W and Mo, and it was confirmed that Al has high resistance to the plasma of SF 6 , which is a fluorine-containing gas. Furthermore, as the material of the dielectric layer, for Al 2 O 3 and Y 2 O 3 and the mixed spray film (Al 2 O 3 , Y 2 O 3 , SiO 2 ), compared with the fluorine-containing gas, that is, SF 6 The cutting amount of gas plasma. As a result, it was confirmed that the cutting amount normalized by taking the cutting amount of the mixed spray film as 1 was 3 for Al 2 O 3 and 1 for Y 2 O 3 , and the mixed spray film and Y 2 O 3 were relatively High resistance to plasma containing fluorine gas, ie SF6 .
如此一來,在進行電漿蝕刻處理(步驟12)特定次數之後,當重覆進行乾洗淨(步驟13)之循環時,附著於電漿蝕刻裝置90之腔室104內之堆積物(附著物)開始產生剝離。因此,於重複如此循環特定次數之後,開放腔室104而進行腔室洗淨(步驟14)。腔室洗淨係藉由以酒精擦拭堆積物,或以特殊藥液洗淨等來進行。
In this way, when the cycle of dry cleaning (step 13 ) is repeated after the plasma etching process (step 12 ) is performed a certain number of times, the deposits (adhering to the inside of the
如上述般在本實施型態中,在電漿蝕刻裝置90的蝕刻處理中,以被生成之反應生成物成為能夠乾洗淨者之方式,將蝕刻基板S之氣體僅設為含氟氣體亦即SF6氣體,成為不用使用以往與SF6氣體同時使用的O2氣體。因此,於電漿蝕刻處理之時,不產生蒸氣壓低之MoOx,在腔室產生之堆積物(附著物)僅成為蒸氣壓高的MoFx。因此,比起以往,腔室內之堆積物(附著物)本身減少,同時腔室內之堆積物(附著物)能夠藉由乾洗淨除去,可以明顯地增長開放腔室而進行的腔室洗淨之週期,即是維修週期。
As described above, in the present embodiment, in the etching process of the
再者,因構成電漿蝕刻裝置90中之靜電夾具232之吸附電極246之Al,相對於乾洗淨之時的含氟氣體亦即SF6氣體之電漿具有耐性,故即使進行乾洗淨亦可以確保靜電夾具之壽命。再者,作為靜電夾具232之介電體層245,使用混合熔射膜或Y2O3,依此可以更提高相對於含氟氣體亦即SF6氣體之電漿的耐性。
Furthermore, since Al constituting the
另外,本發明並限定於上述實施型態,能夠在本發明之思想的範圍內做各種變形。例如,在上述實施型態中,雖然針對適用於用以形成TFT之源極電極及汲極電極之含Al金屬膜之蝕刻,及用以形成遮光膜或閘極電極之Mo系材料膜之蝕刻的例予以說明,但是並不限定於此,在電漿蝕刻裝置之電漿蝕刻處理中,若可以使用被生成之反應生成物成為能夠乾洗淨者的處理氣體即可。 In addition, the present invention is not limited to the above-described embodiment, and various modifications can be made within the scope of the idea of the present invention. For example, in the above-mentioned embodiment, although it is suitable for the etching of the Al-containing metal film for forming the source electrode and the drain electrode of the TFT, and the etching of the Mo-based material film for forming the light shielding film or the gate electrode An example will be described, but it is not limited to this. In the plasma etching process of the plasma etching apparatus, the generated reaction product may be used as a process gas capable of being dry cleaned.
再者,在上述實施型態中,雖然表示使用與電漿蝕刻之時之蝕刻氣體相同者,以作為洗淨氣體,但是洗淨氣體即使為與蝕刻氣體不同者亦可。 In addition, in the above-mentioned embodiment, although the same etching gas as the etching gas in the plasma etching is used as the cleaning gas, the cleaning gas may be different from the etching gas.
而且,在上述實施型態中,雖表示使用感應耦合電漿蝕刻裝置以作為電漿蝕刻裝置之例,但是並不限定於此,即使為電容耦合電漿蝕刻裝置或微波電漿蝕刻裝置等之其他電漿蝕刻裝置亦可。 In addition, in the above-mentioned embodiment, although the inductively coupled plasma etching apparatus is used as an example of the plasma etching apparatus, it is not limited to this. Other plasma etching devices may also be used.
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CN108417497B (en) * | 2018-02-07 | 2019-11-15 | 信利(惠州)智能显示有限公司 | A kind of etching technics of LTPS backboard wiring |
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KR20210137395A (en) * | 2020-05-07 | 2021-11-17 | 에이에스엠 아이피 홀딩 비.브이. | Apparatus and methods for performing an in-situ etch of reaction chambers with fluorine-based radicals |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030040191A1 (en) * | 2001-08-23 | 2003-02-27 | Hiroyuki Kitsunai | Process for producing semiconductor device |
JP2003257951A (en) * | 2002-03-07 | 2003-09-12 | Seiko Instruments Inc | Semiconductor manufacturing equipment |
US20080009417A1 (en) * | 2006-07-05 | 2008-01-10 | General Electric Company | Coating composition, article, and associated method |
CN101188207A (en) * | 2006-08-10 | 2008-05-28 | 东京毅力科创株式会社 | Electrostatic sucking electrode, substrate processing apparatus and manufacturing method for electrostatic sucking electrode |
Family Cites Families (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05136101A (en) * | 1991-11-14 | 1993-06-01 | Hitachi Ltd | Manufacture of semiconductor integrated circuit device |
JP3594759B2 (en) * | 1997-03-19 | 2004-12-02 | 株式会社日立製作所 | Plasma processing method |
JP4053112B2 (en) * | 1997-03-27 | 2008-02-27 | 敏夫 淡路 | Exhaust gas treatment method for semiconductor manufacturing process and exhaust gas treatment apparatus for semiconductor manufacturing process |
JP2000012515A (en) * | 1998-06-22 | 2000-01-14 | Hitachi Ltd | Plasma cleaning method for microwave plasma etching apparatus |
US6606234B1 (en) * | 2000-09-05 | 2003-08-12 | Saint-Gobain Ceramics & Plastics, Inc. | Electrostatic chuck and method for forming an electrostatic chuck having porous regions for fluid flow |
KR100450564B1 (en) * | 2001-12-20 | 2004-09-30 | 동부전자 주식회사 | Post treatment method for metal line of semiconductor device |
TWI265636B (en) * | 2002-06-21 | 2006-11-01 | Sanyo Electric Co | Method for producing thin film transistor |
JP2004031410A (en) * | 2002-06-21 | 2004-01-29 | Sanyo Electric Co Ltd | Thin film transistor and its manufacturing method |
JP4131813B2 (en) * | 2002-10-24 | 2008-08-13 | 株式会社半導体エネルギー研究所 | Plasma etching method and semiconductor device manufacturing method |
JP2003347276A (en) * | 2003-06-30 | 2003-12-05 | Hitachi Ltd | Plasma treatment method and method for manufacturing semiconductor device |
US7220497B2 (en) * | 2003-12-18 | 2007-05-22 | Lam Research Corporation | Yttria-coated ceramic components of semiconductor material processing apparatuses and methods of manufacturing the components |
CN101101887A (en) * | 2006-07-06 | 2008-01-09 | 通用电气公司 | Corrosion resistant wafer processing apparatus and method for making thereof |
JP4992389B2 (en) * | 2006-11-06 | 2012-08-08 | 東京エレクトロン株式会社 | Mounting apparatus, plasma processing apparatus, and plasma processing method |
JP5248038B2 (en) * | 2007-05-22 | 2013-07-31 | 東京エレクトロン株式会社 | Mounting table and plasma processing apparatus using the same |
TW200935555A (en) * | 2007-12-20 | 2009-08-16 | Saint Gobain Ceramics & Plastics Inc | Electrostatic chuck and method of forming |
JP2009188257A (en) * | 2008-02-07 | 2009-08-20 | Tokyo Electron Ltd | Plasma etching method, plasma etching apparatus, and storage medium |
JP2009193989A (en) * | 2008-02-12 | 2009-08-27 | Tokyo Electron Ltd | Plasma-etching method and apparatus, and computer storage medium |
JP2010084939A (en) * | 2008-09-08 | 2010-04-15 | Fuji Koki Corp | Four-way switch valve |
JP5390846B2 (en) * | 2008-12-09 | 2014-01-15 | 東京エレクトロン株式会社 | Plasma etching apparatus and plasma cleaning method |
JP5364514B2 (en) * | 2009-09-03 | 2013-12-11 | 東京エレクトロン株式会社 | Cleaning method in chamber |
KR101506303B1 (en) * | 2011-09-29 | 2015-03-26 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | Semiconductor device and method for manufacturing the same |
US9419211B2 (en) * | 2012-10-30 | 2016-08-16 | Tokyo Electron Limited | Etching method and substrate processing apparatus |
US10557190B2 (en) * | 2013-01-24 | 2020-02-11 | Tokyo Electron Limited | Substrate processing apparatus and susceptor |
JP5704192B2 (en) * | 2013-06-14 | 2015-04-22 | 東京エレクトロン株式会社 | Plasma etching method, plasma etching apparatus, and storage medium |
US9789444B2 (en) * | 2014-03-04 | 2017-10-17 | The Texas A&M University System | Methods to enhance separation performance of metal-organic framework membranes |
US9944561B2 (en) * | 2014-03-10 | 2018-04-17 | Sumitomo Osaka Cement Co., Ltd. | Dielectric material and electrostatic chucking device |
JP6349796B2 (en) * | 2014-03-11 | 2018-07-04 | 東京エレクトロン株式会社 | Plasma processing apparatus, thin film transistor manufacturing method, and storage medium |
KR101870491B1 (en) * | 2014-03-11 | 2018-06-22 | 도쿄엘렉트론가부시키가이샤 | Plasma processing appratus, substrate processing system, fabrication method of thin film transistor, and storage medium |
JP2016048286A (en) | 2014-08-27 | 2016-04-07 | 株式会社ジャパンディスプレイ | Display device and manufacturing method of the same |
-
2016
- 2016-07-15 JP JP2016140043A patent/JP6854600B2/en active Active
-
2017
- 2017-06-30 TW TW106122062A patent/TWI767918B/en active
- 2017-07-13 KR KR1020170088761A patent/KR102049146B1/en active IP Right Grant
- 2017-07-14 CN CN201710574737.8A patent/CN107622945B/en active Active
- 2017-07-14 CN CN202011136319.9A patent/CN112259457B/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030040191A1 (en) * | 2001-08-23 | 2003-02-27 | Hiroyuki Kitsunai | Process for producing semiconductor device |
JP2003068705A (en) * | 2001-08-23 | 2003-03-07 | Hitachi Ltd | Manufacturing method of semiconductor element |
JP2003257951A (en) * | 2002-03-07 | 2003-09-12 | Seiko Instruments Inc | Semiconductor manufacturing equipment |
US20080009417A1 (en) * | 2006-07-05 | 2008-01-10 | General Electric Company | Coating composition, article, and associated method |
CN101188207A (en) * | 2006-08-10 | 2008-05-28 | 东京毅力科创株式会社 | Electrostatic sucking electrode, substrate processing apparatus and manufacturing method for electrostatic sucking electrode |
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