US20020090827A1 - Method of processing residue of ion implanted photoresist, and method of producing semiconductor device - Google Patents
Method of processing residue of ion implanted photoresist, and method of producing semiconductor device Download PDFInfo
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- US20020090827A1 US20020090827A1 US09/491,876 US49187600A US2002090827A1 US 20020090827 A1 US20020090827 A1 US 20020090827A1 US 49187600 A US49187600 A US 49187600A US 2002090827 A1 US2002090827 A1 US 2002090827A1
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- 229920002120 photoresistant polymer Polymers 0.000 title claims abstract description 53
- 238000000034 method Methods 0.000 title claims description 57
- 239000004065 semiconductor Substances 0.000 title claims description 9
- 238000004380 ashing Methods 0.000 claims abstract description 54
- 239000007789 gas Substances 0.000 claims description 65
- 239000002019 doping agent Substances 0.000 claims description 37
- 229910052731 fluorine Inorganic materials 0.000 claims description 37
- 239000011737 fluorine Substances 0.000 claims description 37
- 239000001301 oxygen Substances 0.000 claims description 36
- 229910052760 oxygen Inorganic materials 0.000 claims description 36
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 35
- 239000001257 hydrogen Substances 0.000 claims description 22
- 229910052739 hydrogen Inorganic materials 0.000 claims description 22
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 17
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 15
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 claims description 15
- 229910052698 phosphorus Inorganic materials 0.000 claims description 9
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 8
- 229910052785 arsenic Inorganic materials 0.000 claims description 8
- 229910052796 boron Inorganic materials 0.000 claims description 8
- GVGCUCJTUSOZKP-UHFFFAOYSA-N nitrogen trifluoride Chemical compound FN(F)F GVGCUCJTUSOZKP-UHFFFAOYSA-N 0.000 claims description 8
- 239000011574 phosphorus Substances 0.000 claims description 8
- 239000000758 substrate Substances 0.000 claims description 8
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 7
- 229910021529 ammonia Inorganic materials 0.000 claims description 7
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 7
- SFZCNBIFKDRMGX-UHFFFAOYSA-N sulfur hexafluoride Chemical compound FS(F)(F)(F)(F)F SFZCNBIFKDRMGX-UHFFFAOYSA-N 0.000 claims description 6
- 229960000909 sulfur hexafluoride Drugs 0.000 claims description 5
- 239000004020 conductor Substances 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 21
- 239000000463 material Substances 0.000 abstract description 5
- 238000011109 contamination Methods 0.000 abstract description 4
- 239000002245 particle Substances 0.000 abstract description 3
- 238000005260 corrosion Methods 0.000 abstract description 2
- 230000007797 corrosion Effects 0.000 abstract description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 12
- 150000002500 ions Chemical class 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 9
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 7
- 229910001882 dioxygen Inorganic materials 0.000 description 7
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 6
- 238000005468 ion implantation Methods 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 238000003672 processing method Methods 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- -1 fluorine ions Chemical class 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000000295 emission spectrum Methods 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910001868 water Inorganic materials 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 229910000413 arsenic oxide Inorganic materials 0.000 description 1
- 229960002594 arsenic trioxide Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052810 boron oxide Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- KTTMEOWBIWLMSE-UHFFFAOYSA-N diarsenic trioxide Chemical compound O1[As](O2)O[As]3O[As]1O[As]2O3 KTTMEOWBIWLMSE-UHFFFAOYSA-N 0.000 description 1
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 229910052743 krypton Inorganic materials 0.000 description 1
- DNNSSWSSYDEUBZ-UHFFFAOYSA-N krypton atom Chemical compound [Kr] DNNSSWSSYDEUBZ-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 229910052754 neon Inorganic materials 0.000 description 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910001392 phosphorus oxide Inorganic materials 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- VSAISIQCTGDGPU-UHFFFAOYSA-N tetraphosphorus hexaoxide Chemical compound O1P(O2)OP3OP1OP2O3 VSAISIQCTGDGPU-UHFFFAOYSA-N 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- 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
- H01L21/31—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
- H01L21/3105—After-treatment
- H01L21/311—Etching the insulating layers by chemical or physical means
- H01L21/31127—Etching organic layers
- H01L21/31133—Etching organic layers by chemical means
- H01L21/31138—Etching organic layers by chemical means by dry-etching
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/26—Processing photosensitive materials; Apparatus therefor
- G03F7/42—Stripping or agents therefor
- G03F7/427—Stripping or agents therefor using plasma means only
Definitions
- This invention relates to a method of producing a semiconductor device or the like as well as a processing method of removing a photoresist on a substrate used for the method, a residue thereof, or the like and particularly, relates to a processing method of removing a residue which results from ion implantation of a dopant or the like and is difficult to ash (hereinafter simply referred to as “nonashable residue”).
- a photoresist as a photosensitive resin is widely used as a masking material for selective etching and local ion implantation to form a device structure.
- the corresponding photoresist needs to be removed after various processes utilizing this, and in recent years, is generally removed by oxidization and ashing through dry processing with oxidation action mainly using oxygen plasma, oxygen radicals, ozone, and so on.
- dopant ions such as As, P, B, etc. do not form any substance of a high vapor pressure by oxidation, oxides of the ions will remain on the wafer after the resist has been ashed and removed by oxygen-based active species and needs to be removed by subsequent wet processing.
- Japanese Patent Application Laid-Open No. 5-275326 discloses a method in which after processing using oxygen and CF 4 , a further processing is effected using oxygen and nitrogen
- Japanese Patent Application Laid-Open No. 6-104223 discloses a method in which after processing using oxygen and nitrogen, a further processing is effected using oxygen and SF 4
- Japanese Patent Application Laid-Open No. 5-160022 discloses a method in which a photoresist is ashed with an oxygen plasma, and a residue is then ashed with a hydrogen plasma.
- processing article in order to increase the reaction rate, so that the popping phenomenon is apt to take place more easily.
- An object of the present invention is to provide a processing method that can remove a foreign matter on a surface of a processing article at a high efficiency without leaving any residue such as an oxide of an ion implanted dopant.
- a method of removing a residue comprising ashing and removing a dopant-implanted photoresist to expose a surface of a processing article and then removing a dopant-containing residue of the photoresist remaining on the surface of the processing article,
- a method of producing a semiconductor device comprising the steps of:
- FIG. 1 is a flow chart showing the processing method of the present invention
- FIGS. 2A, 2B and 2 C are schematic sectional views showing the processing according to the present invention.
- FIG. 3 is a sectional view showing an example of a plasma processing apparatus used in the present invention.
- FIG. 4 is a sectional view showing another example of a plasma processing apparatus used in the present invention.
- FIGS. 5A, 5B, 5 C, 5 D and 5 E are schematic views showing the method of producing a semiconductor device according to the present invention.
- FIG. 1 is a flow chart showing the processing method of the present invention
- FIGS. 2A, 2B and 2 C are schematic sectional views showing the processing according to the present invention.
- a processing article such as a silicone wafer is denoted as 1
- a photoresist in which a dopant such as phosphorus, arsenic, boron, etc. has been ion implanted is denoted as 2
- a residue containing an oxide of the dopant such as phosphorus oxide and arsenic oxide, boron oxide, etc. is denoted as 3 .
- a step S 1 the dopant-implanted photoresist 2 is ashed and removed so that a surface of the processing article 1 is exposed.
- step S 2 the dopant-containing residue 3 remaining on the surface of the processing article 1 is removed.
- the residue 3 containing the dopant is removed at a temperature T 2 higher than the temperature of the step S 1 , i.e., a temperature T 1 when ashing and removing the photoresist.
- step S 1 Using a low temperature in the step S 1 suppresses popping, while using a high temperature in the step S 2 improves removal efficiency of the dopant oxide.
- the temperature of a processing article in the step S 1 is preferably a temperature lower than 150° C., specifically 130° C. or lower, and more preferably 120° C. or lower.
- the temperature of a processing article in the step S 2 may be any temperature higher than the temperature of the processing article in the step S 1 , and more preferably 150° C. or higher, and most preferably 200° C. or higher.
- an oxidizing gas (a first gas) is used to ash a photoresist. It is preferable to carry out ashing using a plasma of a gas not containing fluorine so as not to damage a surface of the processing article.
- gas not containing fluorine as used herein is intended to encompass those gases to which a fluorine-based gas is not added intentionally. Therefore, those gases in which fluorine is detected at the so-called background level or contamination level may be used in the present invention.
- oxygen gas with an oxygen concentration of 100%, a mixed gas of oxygen gas and an inert gas (with any oxygen concentration), or the like.
- inert gas rare gases such as helium, argon, neon, xenon, krypton, etc. and nitrogen gas are used.
- water, nitrogen oxide, etc. may be added as the occasion demands.
- the gas used in the step S 2 includes a gas containing at least one of fluorine and hydrogen, more specifically carbon fluoride, nitrogen fluoride, ammonia, sulfur fluoride, fluorine, hydrogen, and water. If necessary, they may be mixed with oxygen gas or an inert gas when used. Among others, carbon fluoride, nitrogen fluoride, sulfur fluoride, and ammonia are preferable. Oxygen has not only a function of serving as a diluent gas, but also a function of reacting with carbon or nitrogen generated from carbon fluoride, nitrogen fluoride or ammonia to form carbon dioxide gas or nitrogen oxide gas thus removing remaining carbon or remaining nitrogen from a processing space quickly.
- steps S 1 and S 2 it is preferable to effect plasma processing by use of a microwave plasma of the above mentioned first or second gas.
- CF 4 , C 2 F 6 , C 3 F 8 , C 3 F 6 , NF 3 , SF 6 , NH 3 , etc. are preferably used. These may be mixed with oxygen when used.
- the organic component is oxidized and removed in the first step, and thereafter, in the second step, oxides remaining on the processing article are mainly removed.
- the dopant such as phosphorus, arsenic, boron, or the like is converted by the action of active species such as fluorine ions, fluorine radicals, hydrogen ions, hydrogen radicals, etc.
- a carbon fluoride based gas or nitrogen fluoride based gas does not contain any element to cause undesired contamination and has a good efficiency in generating fluorine active species, which allows desired effects to be exhibited with less addition amount thereof, so that the surface of the processing article will not be damaged seriously.
- ammonia is very effective, since it can be handled more easily than hydrogen and can generate hydrogen active species efficiently because of its low N-H binding energy, and since thus generated NH radicals have long lifetime and can therefore reduce the oxides of the dopant efficiently.
- FIG. 3 is a sectional view showing a configuration of a plasma processing apparatus which generates a plasma using microwaves to plasma process a wafer as the processing article.
- Reference numeral 101 denotes a vacuum container, which together with a dielectric window 107 for microwave introduction forms a processing chamber for plasma generation therein, which is exhausted through an exhaust opening 102 with a vacuum pump (not shown).
- a microwave wave guide which is denoted as 108 , guides to the vacuum container microwaves generated in a microwave generator (not shown).
- a gas inlet tube which is denoted as 106 , supplies the processing chamber with a gas for plasma processing at a predetermined flow rate supplied from a gas supplying system (not shown).
- W a wafer having a photoresist into which phosphorus (P) has been ion implanted is denoted as W and mounted on a heater 105 .
- the wafer as the processing article is disposed in a position above the heater set at a processing temperature in the ashing apparatus shown in FIG. 3 with a wafer lifting pin or the like to lift the wafer in a floating state.
- a vacuum pump not shown
- the wafer is disposed on the heater by operating the lift pin or the like. This makes it possible to maintain the wafer temperature lower than the heater temperature by the vacuum insulation effect. In the actual determination, the wafer temperature at this time was about 80° C.
- oxygen gas at a predetermined flow rate shown below is introduced into the chamber and the processing is started under the predetermined conditions shown below, and the time taken until the end point of ashing determined by an end point detecting device with a plasma monitor (not shown) is measured. After a period of time about 1.5 to 2 times the measured time has elapsed, the processing is completed. Thereafter, the inside of the chamber is exhausted to a substantial vacuum.
- Active species for ashing can be generated highly efficiently not only with the apparatus shown in FIG. 3 but also with a microwave plasma processing apparatus having a slotted conductor plate.
- a microwave plasma processing apparatus in which a plate-like antenna or radial line slot antenna formed by providing a plurality of slots in a plate-like H-plane of an endless annular waveguide is employed, it is possible to generate the active species more efficiently.
- Such apparatuses are disclosed in Japanese Patent No. 2925535 and U.S. Pat. No. 5,034,086.
- Processing Pressure 1 Torr (approximately 133 Pa)
- the second step is carried out.
- a mixture gas of oxygen/CF 4 mixed at a predetermined ratio is introduced at a predetermined flow rate into the chamber, and the processing is started under the predetermined conditions and is continued for about 15 seconds. This processing removes the residue comprised of oxides of the dopant as left after the first step processing.
- the processing conditions for this second step are, for example, as follows.
- Processing Pressure 0.6 Torr (approximately 80 Pa)
- Wafer Temperature 250° C.
- Processing Time approximately 15 seconds.
- a wafer as the processing article is disposed on the heater set at a processing temperature (a low temperature) in the ashing apparatus as shown in FIG. 3 to allow the wafer temperature to reach the processing temperature, the chamber is sealed and the inside of the chamber is exhausted to substantial vacuum with a vacuum pump (not shown) connected to the chamber.
- a processing temperature a low temperature
- oxygen gas at a predetermined flow rate shown below is introduced into the chamber and the processing is started under the predetermined conditions shown below, and the processing is continued for a period of time which is about twice the time taken until the end point of ashing determined by an end point detecting device with a plasma monitor (not shown).
- Processing Pressure 0.1 Torr (approximately 13.3 Pa)
- Wafer Temperature 80° C.
- Processing Time approximately 1.5 to 2 times the time period until the emission spectrum or the emission intensity changes.
- the chamber is opened to atmosphere and the wafer is taken out.
- the photoresist on the wafer is removed by 5% or more thereof to such clearness that it can no longer be observed with naked eyes.
- the chamber is sealed and the inside of the chamber is exhausted to substantial vacuum with a vacuum pump (not shown) connected to the chamber.
- the processing may either be carried out in another chamber or be carried out in the same chamber with the set temperature changed.
- a mixture gas of oxygen/CF 4 mixed at a predetermined ratio is introduced at a predetermined flow rate into the chamber, and the processing is started under the predetermined conditions and is continued for about 15 seconds. This processing removes the residue comprised of oxides of the dopant to provide a clean surface free from the residue.
- Processing Pressure 0.6 Torr (approximately 80 Pa)
- Wafer Temperature 250° C.
- Processing Time approximately 15 seconds.
- the plasma processing apparatus shown in FIG. 4 is the same as the apparatus of FIG. 3 except that a lift pin 109 is added as a wafer lifting apparatus.
- the wafer as the processing article is disposed in a position above the heater in the ashing apparatus shown in FIG. 4 with the lifting apparatus in a floating state, the chamber is sealed and the inside of the chamber is exhausted to substantial vacuum with a vacuum pump (not shown) connected to the chamber.
- oxygen gas at a predetermined flow rate shown below is introduced into the chamber and the processing is started under the predetermined conditions shown below, and the processing is continued for a period of time which is about twice the time taken until the end point of ashing determined by an. end point detecting device with a plasma monitor (not shown).
- Processing Pressure 0.1 Torr (approximately 13.3 Pa)
- Processing Time approximately 1.5 to 2 times the time period until the emission spectrum or the emission intensity changes.
- the heater temperature at this time is 250° C. However, since the wafer itself is floating above the heater with the lift pin, the temperature of the wafer will be sufficiently lower than 150° C. Thereby, 95% or more of the photoresist can securely be removed.
- the wafer is lowered to be disposed on the heater with the lift apparatus, and a gas such as oxygen, etc. is introduced into the chamber up to approximate atmospheric pressure to heat the wafer to approximately reach 250° C.
- a mixture gas of oxygen/CF 4 mixed at a predetermined ratio is introduced at a predetermined flow rate into the chamber, and the processing is started under the predetermined conditions and is continued for about 15 seconds. This makes it possible to carry out the same processing as that of Embodiment 2 efficiently in a shorter time period.
- Processing Pressure 0.6 Torr (approximately 80 Pa)
- Processing Time approximately 15 seconds.
- Fluorine active species generated when a gas containing fluorine is subjected to plasma formation will corrode silicon constituting the processing article and silicon oxides if the processing takes a long time. Moreover, if ashing is carried out with addition of a gas containing fluorine, the resist may be fluorinated to be difficult to ash.
- the Embodiments described above do not give rise to such problems.
- a semiconductor substrate such as an Si wafer is prepared as the processing article 1 .
- a surface of the processing article 1 is coated with a photoresist material 4 .
- the photoresist material is exposed to be developed, thus providing a photoresist pattern 2 .
- a dopant such as phosphorus, arsenic, boron, or the like is implanted using the photoresist pattern 2 as a mask. In a portion not covered with the photoresist pattern, a doped layer 5 is formed. In addition, the dopant is incorporated into the photoresist pattern.
- the doped layer 5 of the semiconductor device can be formed.
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Abstract
In order to carry out ashing at a high efficiency without leaving any residue and also to inhibit corrosion of an underlying material of a resist and further to prevent particle contamination, a photoresist is ashed at a low temperature to be removed and a residue of the photoresist is removed at a high temperature.
Description
- 1. Field of the Invention
- This invention relates to a method of producing a semiconductor device or the like as well as a processing method of removing a photoresist on a substrate used for the method, a residue thereof, or the like and particularly, relates to a processing method of removing a residue which results from ion implantation of a dopant or the like and is difficult to ash (hereinafter simply referred to as “nonashable residue”).
- 2. Related Background Art
- In the production process for a semiconductor device, a photoresist as a photosensitive resin is widely used as a masking material for selective etching and local ion implantation to form a device structure. The corresponding photoresist needs to be removed after various processes utilizing this, and in recent years, is generally removed by oxidization and ashing through dry processing with oxidation action mainly using oxygen plasma, oxygen radicals, ozone, and so on.
- As a method of removing a photoresist as an organic substance consisting mainly of carbon and hydrogen, a technique is widely used in which the photoresist is exposed to oxygen as activated by electric discharge or irradiation with ultra violet and is gasified through the oxidation action into steam, carbon dioxide, carbon monoxide, etc., thus effecting ashing and removal.
- On the other hand, in the case where a photoresist is used as a mask for ion implantation of a dopant, etc., the resist, the surface of which is modified by the energy of implanted ions, will be difficult to remove by oxidation, so that the processing efficiency decreases significantly. In addition, it is known that, when an ion implanted photoresist is heated to 150° C. to 250° C. as the normal ashing temperature, the phenomena (popping) that the surface modified layer bursts by steam of an organic solvent generated from an unmodified layer in a lower portion of the photoresist to form flake-shaped particles to be scattered around, is observed, so that the wafer is contaminated. Moreover, since dopant ions such as As, P, B, etc. do not form any substance of a high vapor pressure by oxidation, oxides of the ions will remain on the wafer after the resist has been ashed and removed by oxygen-based active species and needs to be removed by subsequent wet processing.
- For the purpose of removing the above mentioned resist which is generated after ion implantation and is difficult to ash, there have hitherto been proposed a method in which after a modified layer of the resist surface is removed while hydrogenating and removing the dopant ions with a hydrogen plasma or steam plasma, an underlying unmodified layer is ashed and removed with an oxygen plasma, a method in which the resist is ashed and remove with a plasma of a mixed gas obtained by adding to oxygen gas a gas containing fluorine having a function to increase the ashing rate and to remove the implanted ion species, or the like.
- In addition, Japanese Patent Application Laid-Open No. 5-275326 discloses a method in which after processing using oxygen and CF4, a further processing is effected using oxygen and nitrogen, and Japanese Patent Application Laid-Open No. 6-104223 discloses a method in which after processing using oxygen and nitrogen, a further processing is effected using oxygen and SF4. Moreover, Japanese Patent Application Laid-Open No. 5-160022 discloses a method in which a photoresist is ashed with an oxygen plasma, and a residue is then ashed with a hydrogen plasma.
- However, in the case where a modified layer generated by ion implantation is removed with a hydrogen plasma or steam plasma, the processing efficiency generally becomes small due to its low reaction rate. Moreover, it is necessary to sufficiently raise the temperature of an article to be processed (hereinafter referred to as “processing article”) in order to increase the reaction rate, so that the popping phenomenon is apt to take place more easily.
- In a processing with a plasma of a mixed gas formed by adding to oxygen a gas containing fluorine as a halogen which is an example of the gas containing halogen, the processing efficiency is improved by the function of generated fluorine ions and fluorine radicals, compared with the case of using an oxygen plasma only. However, since low temperature processing is apt to give rise to a photoresist residue, in order to avoid this, it is necessary to effect processing at a high temperature which is apt to cause the popping.
- In view of the problems as described above, in the actual producing process, after ashing with oxygen has been effected, oxides of a dopant remaining on a wafer as a processing article are cleaned and removed in a subsequent wet processing.
- An object of the present invention is to provide a processing method that can remove a foreign matter on a surface of a processing article at a high efficiency without leaving any residue such as an oxide of an ion implanted dopant.
- According to a first aspect of the present invention, there is provided a method of removing a residue comprising ashing and removing a dopant-implanted photoresist to expose a surface of a processing article and then removing a dopant-containing residue of the photoresist remaining on the surface of the processing article,
- wherein the dopant-containing residue is removed at a temperature higher than the temperature at which the photoresist is ashed and removed.
- According to a second aspect of the present invention, there is provided a method of processing an article comprising the steps of:
- ashing and removing a dopant-implanted photoresist on a surface of an article at a first temperature; and
- removing a dopant-containing residue of the photoresist at a second temperature higher than the first temperature.
- According to a third aspect of the present invention, there is provided a method of producing a semiconductor device comprising the steps of:
- forming a photoresist pattern on a surface of a substrate;
- implanting a dopant in the substrate using the photoresist pattern as a mask;
- ashing and removing a dopant-implanted photoresist on the surface of the substrate at a first temperature; and
- removing a dopant-containing residue of the photoresist at a second temperature higher than the first temperature.
- FIG. 1 is a flow chart showing the processing method of the present invention;
- FIGS. 2A, 2B and2C are schematic sectional views showing the processing according to the present invention;
- FIG. 3 is a sectional view showing an example of a plasma processing apparatus used in the present invention;
- FIG. 4 is a sectional view showing another example of a plasma processing apparatus used in the present invention; and
- FIGS. 5A, 5B,5C, 5D and 5E are schematic views showing the method of producing a semiconductor device according to the present invention.
- FIG. 1 is a flow chart showing the processing method of the present invention, and FIGS. 2A, 2B and2C are schematic sectional views showing the processing according to the present invention.
- A processing article such as a silicone wafer is denoted as1, a photoresist in which a dopant such as phosphorus, arsenic, boron, etc. has been ion implanted is denoted as 2, and a residue containing an oxide of the dopant such as phosphorus oxide and arsenic oxide, boron oxide, etc. is denoted as 3.
- In a step S1, the dopant-implanted
photoresist 2 is ashed and removed so that a surface of theprocessing article 1 is exposed. - Thereafter, in a step S2, the dopant-containing
residue 3 remaining on the surface of theprocessing article 1 is removed. - At this time, the
residue 3 containing the dopant is removed at a temperature T2 higher than the temperature of the step S1, i.e., a temperature T1 when ashing and removing the photoresist. - Thus, a highly clean surface of the processing article is obtained.
- Using a low temperature in the step S1 suppresses popping, while using a high temperature in the step S2 improves removal efficiency of the dopant oxide.
- The temperature of a processing article in the step S1 is preferably a temperature lower than 150° C., specifically 130° C. or lower, and more preferably 120° C. or lower.
- The temperature of a processing article in the step S2 may be any temperature higher than the temperature of the processing article in the step S1, and more preferably 150° C. or higher, and most preferably 200° C. or higher.
- In the step S1, an oxidizing gas (a first gas) is used to ash a photoresist. It is preferable to carry out ashing using a plasma of a gas not containing fluorine so as not to damage a surface of the processing article. The term “gas not containing fluorine” as used herein is intended to encompass those gases to which a fluorine-based gas is not added intentionally. Therefore, those gases in which fluorine is detected at the so-called background level or contamination level may be used in the present invention. As the first gas used in the step S1, there may be included oxygen gas with an oxygen concentration of 100%, a mixed gas of oxygen gas and an inert gas (with any oxygen concentration), or the like., As the inert gas, rare gases such as helium, argon, neon, xenon, krypton, etc. and nitrogen gas are used. In addition, water, nitrogen oxide, etc. may be added as the occasion demands.
- The gas used in the step S2 includes a gas containing at least one of fluorine and hydrogen, more specifically carbon fluoride, nitrogen fluoride, ammonia, sulfur fluoride, fluorine, hydrogen, and water. If necessary, they may be mixed with oxygen gas or an inert gas when used. Among others, carbon fluoride, nitrogen fluoride, sulfur fluoride, and ammonia are preferable. Oxygen has not only a function of serving as a diluent gas, but also a function of reacting with carbon or nitrogen generated from carbon fluoride, nitrogen fluoride or ammonia to form carbon dioxide gas or nitrogen oxide gas thus removing remaining carbon or remaining nitrogen from a processing space quickly.
- In the steps S1 and S2, it is preferable to effect plasma processing by use of a microwave plasma of the above mentioned first or second gas.
- As the second gas, among others, CF4, C2F6, C3F8, C3F6, NF3, SF6, NH3, etc. are preferably used. These may be mixed with oxygen when used. Of the photoresist into which phosphorus, arsenic, boron, etc. have been implanted, the organic component is oxidized and removed in the first step, and thereafter, in the second step, oxides remaining on the processing article are mainly removed. The dopant such as phosphorus, arsenic, boron, or the like is converted by the action of active species such as fluorine ions, fluorine radicals, hydrogen ions, hydrogen radicals, etc. into a volatile fluoride or hydride to be removed from the surface of the processing article. A carbon fluoride based gas or nitrogen fluoride based gas does not contain any element to cause undesired contamination and has a good efficiency in generating fluorine active species, which allows desired effects to be exhibited with less addition amount thereof, so that the surface of the processing article will not be damaged seriously. In addition, ammonia is very effective, since it can be handled more easily than hydrogen and can generate hydrogen active species efficiently because of its low N-H binding energy, and since thus generated NH radicals have long lifetime and can therefore reduce the oxides of the dopant efficiently.
- (Embodiment 1)
- FIG. 3 is a sectional view showing a configuration of a plasma processing apparatus which generates a plasma using microwaves to plasma process a wafer as the processing article.
Reference numeral 101 denotes a vacuum container, which together with adielectric window 107 for microwave introduction forms a processing chamber for plasma generation therein, which is exhausted through anexhaust opening 102 with a vacuum pump (not shown). A microwave wave guide, which is denoted as 108, guides to the vacuum container microwaves generated in a microwave generator (not shown). A gas inlet tube, which is denoted as 106, supplies the processing chamber with a gas for plasma processing at a predetermined flow rate supplied from a gas supplying system (not shown). In the drawing, a wafer having a photoresist into which phosphorus (P) has been ion implanted is denoted as W and mounted on aheater 105. - The wafer as the processing article is disposed in a position above the heater set at a processing temperature in the ashing apparatus shown in FIG. 3 with a wafer lifting pin or the like to lift the wafer in a floating state. Specifically, after the chamber has been sealed and the inside thereof has been exhausted to substantial vacuum with a vacuum pump (not shown) connected to the chamber, the wafer is disposed on the heater by operating the lift pin or the like. This makes it possible to maintain the wafer temperature lower than the heater temperature by the vacuum insulation effect. In the actual determination, the wafer temperature at this time was about 80° C.
- For the purpose of removing organic components of the resist, oxygen gas at a predetermined flow rate shown below is introduced into the chamber and the processing is started under the predetermined conditions shown below, and the time taken until the end point of ashing determined by an end point detecting device with a plasma monitor (not shown) is measured. After a period of time about 1.5 to 2 times the measured time has elapsed, the processing is completed. Thereafter, the inside of the chamber is exhausted to a substantial vacuum.
- This will completely remove 95% or more of the photoresist on the wafer to such an extent that no photoresist can be observed with naked eyes.
- Active species for ashing can be generated highly efficiently not only with the apparatus shown in FIG. 3 but also with a microwave plasma processing apparatus having a slotted conductor plate. When a microwave plasma processing apparatus is used in which a plate-like antenna or radial line slot antenna formed by providing a plurality of slots in a plate-like H-plane of an endless annular waveguide is employed, it is possible to generate the active species more efficiently. Such apparatuses are disclosed in Japanese Patent No. 2925535 and U.S. Pat. No. 5,034,086.
- The typical processing conditions for this first step are as follows.
- Gas/Flow Rate: O2/1000 sccm
- Processing Pressure: 1 Torr (approximately 133 Pa)
- Wafer Temperature of 80° C.<Heater Temperature of 250° C.
- Next, in order to break the vacuum insulation and to heat the wafer to the heater temperature, oxygen is introduced into the chamber until the inside pressure reaches substantially atmospheric pressure. However, introduction of any other gas instead of oxygen will not give rise to any particular problem.
- Next, after the inside of the chamber has been exhausted again, the second step is carried out. Here, for the purpose of removing a residue not removed only by oxygen and remaining on the wafer, a mixture gas of oxygen/CF4 mixed at a predetermined ratio is introduced at a predetermined flow rate into the chamber, and the processing is started under the predetermined conditions and is continued for about 15 seconds. This processing removes the residue comprised of oxides of the dopant as left after the first step processing.
- The processing conditions for this second step are, for example, as follows.
- Gas/Flow Rate: O2+CF4/500 sccm+2 sccm
- Processing Pressure: 0.6 Torr (approximately 80 Pa)
- Wafer Temperature: 250° C.
- Microwave Output: 1500 W
- Processing Time: approximately 15 seconds.
- (Embodiment 2)
- After a wafer as the processing article is disposed on the heater set at a processing temperature (a low temperature) in the ashing apparatus as shown in FIG. 3 to allow the wafer temperature to reach the processing temperature, the chamber is sealed and the inside of the chamber is exhausted to substantial vacuum with a vacuum pump (not shown) connected to the chamber.
- For the purpose of removing organic components of the resist, oxygen gas at a predetermined flow rate shown below is introduced into the chamber and the processing is started under the predetermined conditions shown below, and the processing is continued for a period of time which is about twice the time taken until the end point of ashing determined by an end point detecting device with a plasma monitor (not shown).
- The processing conditions for the first step are as follows.
- Gas/Flow Rate: O2/100 sccm
- Processing Pressure: 0.1 Torr (approximately 13.3 Pa)
- Wafer Temperature: 80° C.
- Microwave Output: 1500 W
- Processing Time: approximately 1.5 to 2 times the time period until the emission spectrum or the emission intensity changes.
- Afterwards, the chamber is opened to atmosphere and the wafer is taken out. The photoresist on the wafer is removed by 5% or more thereof to such clearness that it can no longer be observed with naked eyes.
- After the wafer as the processing article is disposed on the heater set at a processing temperature (a high temperature) in the ashing apparatus as shown in FIG. 3 to allow the wafer temperature to reach the processing temperature, the chamber is sealed and the inside of the chamber is exhausted to substantial vacuum with a vacuum pump (not shown) connected to the chamber. At this time, the processing may either be carried out in another chamber or be carried out in the same chamber with the set temperature changed.
- For the purpose of removing a residue left after the removal of the organic components in the resist in the first step processing, a mixture gas of oxygen/CF4 mixed at a predetermined ratio is introduced at a predetermined flow rate into the chamber, and the processing is started under the predetermined conditions and is continued for about 15 seconds. This processing removes the residue comprised of oxides of the dopant to provide a clean surface free from the residue.
- The processing conditions for the second step are as follows.
- Gas/Flow Rate: O2+CF4/500 sccm+2 sccm
- Processing Pressure: 0.6 Torr (approximately 80 Pa)
- Wafer Temperature: 250° C.
- Microwave Output: 1500 W
- Processing Time: approximately 15 seconds.
- In this method, since the processing temperature in the first step carried out with a non-fluoride oxidizing gas is set at a temperature lower than the temperature in the second step, namely a temperature sufficiently lower than 150° C., popping was suppressed.
- (Embodiment 3)
- The plasma processing apparatus shown in FIG. 4 is the same as the apparatus of FIG. 3 except that a
lift pin 109 is added as a wafer lifting apparatus. - The wafer as the processing article is disposed in a position above the heater in the ashing apparatus shown in FIG. 4 with the lifting apparatus in a floating state, the chamber is sealed and the inside of the chamber is exhausted to substantial vacuum with a vacuum pump (not shown) connected to the chamber.
- For the purpose of removing organic components of the resist, oxygen gas at a predetermined flow rate shown below is introduced into the chamber and the processing is started under the predetermined conditions shown below, and the processing is continued for a period of time which is about twice the time taken until the end point of ashing determined by an. end point detecting device with a plasma monitor (not shown).
- The processing conditions. for the first step are as follows.
- Gas/Flow Rate: O2/100 sccm
- Processing Pressure: 0.1 Torr (approximately 13.3 Pa)
- Heater Temperature: 250° C.
- Microwave Output: 1500 W
- Processing Time: approximately 1.5 to 2 times the time period until the emission spectrum or the emission intensity changes.
- The heater temperature at this time is 250° C. However, since the wafer itself is floating above the heater with the lift pin, the temperature of the wafer will be sufficiently lower than 150° C. Thereby, 95% or more of the photoresist can securely be removed.
- After the first step, the wafer is lowered to be disposed on the heater with the lift apparatus, and a gas such as oxygen, etc. is introduced into the chamber up to approximate atmospheric pressure to heat the wafer to approximately reach 250° C.
- For the purpose of removing a residue left after the removal of the organic components in the resist in the preceding step processing, a mixture gas of oxygen/CF4 mixed at a predetermined ratio is introduced at a predetermined flow rate into the chamber, and the processing is started under the predetermined conditions and is continued for about 15 seconds. This makes it possible to carry out the same processing as that of
Embodiment 2 efficiently in a shorter time period. - The processing conditions for the second step are as follows.
- Gas/Flow Rate: O2+CF4/500 sccm+2 sccm
- Processing Pressure: 0.6 Torr (approximately 80 Pa)
- Heater Temperature (Processing Article Temperature): 250° C.
- Microwave Output: 1500 W
- Processing Time: approximately 15 seconds.
- Fluorine active species generated when a gas containing fluorine is subjected to plasma formation will corrode silicon constituting the processing article and silicon oxides if the processing takes a long time. Moreover, if ashing is carried out with addition of a gas containing fluorine, the resist may be fluorinated to be difficult to ash. The Embodiments described above do not give rise to such problems.
- (Embodiment 4)
- Next, the producing method of a semiconductor device according to the present invention will be described.
- A semiconductor substrate such as an Si wafer is prepared as the
processing article 1. - As shown in FIG. 5A, a surface of the
processing article 1 is coated with aphotoresist material 4. - As shown in FIG. 5B, the photoresist material is exposed to be developed, thus providing a
photoresist pattern 2. - As shown in FIG. 5C, a dopant such as phosphorus, arsenic, boron, or the like is implanted using the
photoresist pattern 2 as a mask. In a portion not covered with the photoresist pattern, adoped layer 5 is formed. In addition, the dopant is incorporated into the photoresist pattern. - The processing in the first step as described in
Embodiments 1 to 3 is carried out to ash and remove thephotoresist pattern 2. This leaves aresidue 3 consisting of oxides of the dopant on the surface of theprocessing article 1 as shown in FIG. 5D - Subsequently, performing the above described second step results in removal of the
residue 3 as shown in FIG. 5E. - Thus, the doped
layer 5 of the semiconductor device can be formed. - [Example]
- According to the procedure described in
Embodiment 3, the photoresist having P ions implanted therein was ashed and the residue was then removed, with the result that the residue consisting of dopant oxides was scarcely left. - According to the Embodiments as described, without leaving any residue of modified organic components, highly efficient ashing for removal can be performed, and corrosion of a surface of the processing article as the underlying material of the organic substance to ash can be suppressed and the cause of particle contamination can be also suppressed. In addition, wet cleaning for removal of a residue required for the conventional processing can be omitted.
Claims (36)
1. A method of removing a residue comprising ashing and removing a dopant-implanted photoresist to expose a surface of a processing article and then removing a dopant-containing residue of the photoresist remaining on the surface of the processing article,
wherein the dopant-containing residue is removed at a temperature higher than the temperature at which the photoresist is ashed and removed.
2. The method according to claim 1 , wherein the ashing and removal of the dopant-implanted photoresist comprises ashing using a plasma of a gas not containing fluorine.
3. The method according to claim 1 , wherein the removal of the dopant-containing residue comprises a processing using a gas containing at least one of fluorine and hydrogen.
4. The method according to claim 1 , wherein the removal of the dopant-containing residue comprises a processing using a gas containing oxygen and at least one of fluorine and hydrogen.
5. The method according to claim 1 , wherein the ashing and removal of the dopant-implanted photoresist comprises ashing using a plasma of a first gas not containing fluorine, and wherein the removal of the dopant-containing residue comprises a processing using a second gas containing at least one of fluorine and hydrogen.
6. The method according to claim 1 , wherein the ashing and removal of the dopant-implanted photoresist comprises ashing using a plasma of a first gas not containing fluorine, and wherein the removal of the dopant-containing residue comprises a processing using a second gas containing oxygen and at least one of fluorine and hydrogen.
7. The method according to claim 1 , wherein the ashing and removal of the dopant-implanted photoresist comprises ashing using a plasma of oxygen, and wherein the removal of the dopant-containing residue comprises a processing using a gas containing oxygen and at least one of carbon fluoride, nitrogen fluoride, sulfur fluoride, and ammonia.
8. The method according to claim 1 , wherein the dopant is at least one of phosphorus, arsenic and boron.
9. The method according to claim 1 , wherein the ashing comprises a plasma processing using a microwave plasma.
10. The method according to claim 1 , wherein the removal of the residue comprises a plasma processing using a microwave plasma.
11. The method according to claim 9 or 10, wherein the microwave plasma is generated by radiating microwaves via a microwave antenna having a plurality of slots provided in a conductor plate.
12. The method according to claim 1 , wherein the ashing is carried out in such a state that the processing article is not in contact with a heater, and wherein the removal of the residue is carried out in such a state that the processing article is in contact with a heater.
13. A method of processing an article comprising the steps of:
ashing and removing a dopant-implanted photoresist on a surface of an article at a first temperature; and
removing a dopant-containing residue of the photoresist at a second temperature higher than the first temperature.
14. The method according to claim 13 , wherein the step of ashing and removal comprises ashing using a plasma of a gas not containing fluorine.
15. The method according to claim 13 , wherein the step of removal of the residue comprises a processing using a gas containing at least one of fluorine and hydrogen.
16. The method according to claim 13 , wherein the step of removal of the residue comprises a processing using a gas containing oxygen and at least one of fluorine and hydrogen.
17. The method according to claim 13 , wherein the step of ashing and removal comprises ashing using a plasma of a first gas not containing fluorine, and wherein the step of removal of the residue comprises a processing using a second gas containing at least one of fluorine and hydrogen.
18. The method according to claim 13 , wherein the step of ashing and removal comprises ashing using a plasma of a first gas not containing fluorine, and wherein the step of removal of the residue comprises a processing using a second gas containing oxygen and at least one of fluorine and hydrogen.
19. The method according to claim 13 , wherein the step of ashing and removal comprises ashing using a plasma of oxygen, and wherein the step of removal of the residue comprises a processing using a gas containing oxygen and at least one of carbon fluoride, nitrogen fluoride, sulfur fluoride, and ammonia.
20. The method according to claim 13 , wherein the dopant is at least one of phosphorus, arsenic and boron.
21. The method according to claim 13 , wherein the ashing comprises a plasma processing using a microwave plasma.
22. The method according to claim 13 , wherein the removal of the residue comprises a plasma processing using a microwave plasma.
23. The method according to claim 21 or 22, wherein the microwave plasma is generated by radiating microwaves via a microwave antenna having a plurality of slots provided in a conductor plate.
24. The method according to claim 13 , wherein the step of ashing is carried out in such a state that the processing article is not in contact with a heater, and wherein the step of removal of the residue is carried out in such a state that the processing article is in contact with a heater.
25. A method of producing a semiconductor device comprising the steps of:
forming a photoresist pattern on a surface of a substrate;
implanting a dopant in the substrate using the photoresist pattern as a mask;
ashing and removing a dopant-implanted photoresist on the surface of the substrate at a first temperature; and
removing a dopant-containing residue of the photoresist at a second temperature higher than the first temperature.
26. The method according to claim 25 , wherein the step of ashing and removal comprises ashing using a plasma of a gas not containing fluorine.
27. The method according to claim 25 , wherein the step of removal of the residue comprises a processing using a gas containing at least one of fluorine and hydrogen.
28. The method according to claim 25 , wherein the step of removal of the residue comprises a processing using a gas containing oxygen and at least one of fluorine and hydrogen.
29. The method according to claim 25 , wherein the step of ashing and removal comprises ashing using a plasma of a first gas not containing fluorine, and wherein the step of removal of the residue comprises a processing using a second gas containing at least one of fluorine and hydrogen.
30. The method according to claim 25 , wherein the step of ashing and removal comprises ashing using a plasma of a first gas not containing fluorine, and wherein the step of removal of the residue comprises a processing using a second gas containing oxygen and at least one of fluorine and hydrogen.
31. The method according to claim 25 , wherein the step of ashing and removal comprises ashing using a plasma of oxygen, and wherein the step of removal of the residue comprises a processing using a gas containing oxygen and at least one of carbon fluoride, nitrogen fluoride, sulfur fluoride, and ammonia.
32. The method according to claim 25 , wherein the dopant is at least one of phosphorus, arsenic and boron.
33. The method according to claim 25 , wherein the ashing comprises a plasma processing using a microwave plasma.
34. The method according to claim 25 , wherein the removal of the residue comprises a plasma processing using a microwave plasma.
35. The method according to claim 33 or 34, wherein the microwave plasma is generated by radiating microwaves via a microwave antenna having a plurality of slots provided in a conductor plate.
36. The method according to claim 25 , wherein the step of ashing is carried out in such a state that the processing article is not in contact with a heater, and wherein the step of removal of the residue is carried out in such a state that the processing article is in contact with a heater.
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