US20020016076A1 - Method of cleaning substrate and method of manufacturing semiconductor device - Google Patents
Method of cleaning substrate and method of manufacturing semiconductor device Download PDFInfo
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- US20020016076A1 US20020016076A1 US09/220,690 US22069098A US2002016076A1 US 20020016076 A1 US20020016076 A1 US 20020016076A1 US 22069098 A US22069098 A US 22069098A US 2002016076 A1 US2002016076 A1 US 2002016076A1
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- acid
- insulating film
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- 239000000758 substrate Substances 0.000 title claims abstract description 88
- 238000000034 method Methods 0.000 title claims abstract description 40
- 238000004140 cleaning Methods 0.000 title claims abstract description 39
- 239000004065 semiconductor Substances 0.000 title claims description 39
- 238000004519 manufacturing process Methods 0.000 title claims description 15
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 claims abstract description 42
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 claims abstract description 40
- 229910005948 SO2Cl Inorganic materials 0.000 claims abstract description 14
- 239000007788 liquid Substances 0.000 claims description 64
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 48
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 32
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 19
- 229910017604 nitric acid Inorganic materials 0.000 claims description 19
- 239000012159 carrier gas Substances 0.000 claims description 10
- 238000005229 chemical vapour deposition Methods 0.000 claims description 8
- 238000000151 deposition Methods 0.000 claims 2
- 239000000126 substance Substances 0.000 abstract description 36
- 230000015572 biosynthetic process Effects 0.000 abstract description 4
- 238000011109 contamination Methods 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 19
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 17
- 229910052710 silicon Inorganic materials 0.000 description 17
- 239000010703 silicon Substances 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 11
- 239000012495 reaction gas Substances 0.000 description 11
- 229910052814 silicon oxide Inorganic materials 0.000 description 11
- 229910001873 dinitrogen Inorganic materials 0.000 description 10
- 238000002230 thermal chemical vapour deposition Methods 0.000 description 8
- 239000000356 contaminant Substances 0.000 description 6
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 5
- 229910052681 coesite Inorganic materials 0.000 description 4
- 229910052906 cristobalite Inorganic materials 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 229910052682 stishovite Inorganic materials 0.000 description 4
- 229910052905 tridymite Inorganic materials 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 3
- 238000004381 surface treatment Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 239000005380 borophosphosilicate glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004518 low pressure chemical vapour deposition Methods 0.000 description 2
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000001312 dry etching Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000005507 spraying Methods 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
- H01L21/02041—Cleaning
- H01L21/02043—Cleaning before device manufacture, i.e. Begin-Of-Line process
- H01L21/02046—Dry cleaning only
-
- 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
- H01L21/02041—Cleaning
- H01L21/02043—Cleaning before device manufacture, i.e. Begin-Of-Line process
- H01L21/02052—Wet cleaning only
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S438/00—Semiconductor device manufacturing: process
- Y10S438/906—Cleaning of wafer as interim step
Definitions
- the present invention relates to a method of cleaning a substrate and a method of manufacturing a semiconductor device and, more particularly, a method of cleaning a substrate and a method of manufacturing a semiconductor device removing contaminants after working a surface of a substrate by chemicals etc. or treating the surface of the substrate by the chemicals, etc. prior to film formation.
- FIGS. 1A and 1B are sectional views showing steps of cleaning a surface of a semiconductor substrate 1 after trench grooves 3 have been formed on the semiconductor substrate 1 .
- the trench grooves 3 are formed on the semiconductor substrate 1 using a resist film 2 as a mask. Then, the resist film 2 is removed by resist removing liquid and, as shown in FIG. 1B, the semiconductor substrate 1 on which the trench grooves 3 are formed is exposed to a liquid such as the sulfuric acid to remove contaminants such as the resist removing liquid.
- FIGS. 2A to 2 C are sectional views showing steps of forming a wiring 13 and then covering the wiring 13 with an insulating film 15 .
- wirings 13 are formed on an underlying insulating film 12 formed on a semiconductor substrate 11 by patterning using the resist film 14 as a mask. Then, as shown in FIG. 2B, the resist film 14 is removed by the resist removing liquid. Then, as shown in FIG. 2C, an insulating film 15 is formed by the CVD method to cover the wirings 13 formed on the underlying insulating film 12 .
- FIGS. 3A and 3B are sectional views showing steps of forming a silicon containing insulating film 23 on an underlying insulating film 22 .
- a surface of the underlying insulating film 22 on a semiconductor substrate 21 is cleaned by a liquid of the sulfuric acid, etc.
- a silicon containing insulating film 23 is deposited on the underlying insulating film 22 by the thermal CVD method with using a reaction gas including TEOS (for exanple, N 2 is employed as the carrier gas) and ozone (which is included in O 2 at a predetermined concentration).
- TEOS for exanple, N 2 is employed as the carrier gas
- ozone which is included in O 2 at a predetermined concentration
- the chemicals such as EKC (made by the EKC Company, product name) as the particular example is employed as the resist removing liquid, so that the concave portions cannot be buried evenly.
- the reason for this event may be supposed, though not clearly analyzed, such that perhaps the EKC cannot be removed from the surface of the underlying insulating film 12 and thus left thereon, which has a vicious influence upon the growth rate of the SiO 2 film 15 .
- a surface of a substrate is cleaned by use of either a vapor including at least any one of a vapor of sulfuric acid, a vapor of hydrochloric acid, and a vapor of nitric acid or a vapor of chlorosulfonic acid (SO 2 Cl(OH)).
- the chemicals can be supplied as moleculars so that it can enter into the groove which has a narrow opening width and a deep depth. Accordingly, bottoms and side walls of trench grooves each having the opening width of less than 0.3 ⁇ m and the deep depth can be cleaned clearly.
- FIGS. 1A and 1B are sectional views showing steps of a substrate cleaning method according to a first example in the prior art respectively;
- FIGS. 2A to 2 C are sectional views showing steps of a substrate cleaning method according to a second example in the prior art respectively;
- FIGS. 3A and 3B are sectional views showing steps of a substrate cleaning method according to a third example in the prior art respectively;
- FIGS. 4A to 4 D are sectional views showing steps of a substrate cleaning method according to a first embodiment of the present invention respectively;
- FIGS. 5A to 5 C are sectional views showing steps of a substrate cleaning method according to a second embodiment of the present invention respectively;
- FIGS. 6A to 6 D are sectional views showing steps of a substrate cleaning method according to a third embodiment of the present invention respectively.
- FIG. 7 is a side view showing a cleaning chemicals vapor supplying equipment and a substrate processing equipment according to the present invention respectively.
- FIGS. 4A to 4 D are sectional views showing steps of a substrate cleaning method according to a first embodiment of the present invention respectively. For samples processed by four types of the chemicals or liquids of the chemicals and unprocessed samples, growth rates of insulating films on an underlying insulating film are compared to each other.
- a p-type silicon substrate (semiconductor substrate) 31 having a resistivity of 5 ⁇ cm is prepared.
- the silicon substrate 31 is thermally oxidized at a temperature of 1100° C. in oxygen atmosphere to form a silicon oxide film (underlying insulating film) 32 of about 100 nm thickness on a surface of the silicon substrate 31 .
- a substrate 30 can be formed.
- the substrate 30 is cleaned by using cleaning chemicals or vapor of the chemicals.
- cleaning chemicals or vapor of the chemicals four types of the chemicals or vapors of the chemicals described in the following have been employed.
- a first sample has been prepared as follows.
- a liquid 102 of chlorosulfonic acid SO 2 Cl(OH)
- a liquid temperature has been held at a room temperature without heating.
- a nitrogen (N 2 ) gas as a carrier gas has been passed through the liquid 102 of the chiorosulfonic acid (SO 2 Cl (OH)) via a pipe 103 and then introduced via a pipe 105 into a chamber 106 into which the substrate 30 has been loaded. Then, the nitrogen gas including the chiorosulfonic acid has been sprayed onto a surface of the substrate 30 for thirty minutes.
- a temperature of the liquid 102 of chlorosulfonic acid (SO 2 Cl(OH)) may be increased by heating by means of a heater 104 .
- a second sample has been prepared by supplying vapor of sulfuric acid directly from a sulfuric acid bomb and then spraying it onto a surface of the to-be-processed substrate 30 for thirty minutes.
- third and fourth samples have been prepared as follows.
- the liquid of the chlorosulfonic acid of 30 cc has been filled in two beakers.
- the liquid temperature in one beaker is held at a room temperature, while the other beaker has been heated to hold the liquid temperature at 58° C.
- the substrates 30 have been immersed in respective chemicals for thirty minutes.
- the substrates 30 have been cleaned by the flowing pure water after the process has been completed and in turn dried by blowing the nitrogen gas respectively.
- the growth rate on the surface of the insulating film can be improved and therefore a throughput can also be improved.
- either the vapor or liquid of the chlorosulfonic acid or the vapor of the hydrochloric acid has been employed as the cleaning chemicals.
- the cleaning chemicals in addition to only the vapor of sulfuric acid, only the vapor of nitric acid, or the mixed vapor of the vapor of sulfuric acid and the vapor of nitric acid, such vapor including at least any one of the vapor of sulfuric acid, the vapor of hydrochloric acid, and the vapor of nitric acid may be employed.
- FIGS. 5A to 5 C are sectional views showing steps of a substrate cleaning method according to a second embodiment of the present invention respectively.
- a resist film 42 is formed on a silicon substrate (semiconductor substrate) 41 and then opening portions 43 are formed in the resist film 42 .
- the silicon substrate 41 is etched via the opening portions 43 by the dry etching using chlorine (Cl 2 ) to form grooves 44 each having a diameter of about 0.25 ⁇ m and a depth of 1.5 ⁇ m.
- the resultant structure is immersed in the EKC as the resist removing liquid to remove the resist.
- a substrate 40 can be prepared.
- the EKC liquid would remain in the grooves 44 .
- the liquid 102 of the chlorosulfonic acid (SO 2 Cl(OH)) has been filled in the flask 101 and then the liquid temperature has been held at a room temperature or the liquid temperature has been increased by being heated by the heater 104 .
- the nitrogen gas as the carrier gas has been passed through the liquid 102 of chlorosulfonic acid (SO 2 Cl(OH)) to thus form the nitrogen gas including the chlorosulfonic acid.
- such nitrogen gas has been introduced into the chamber 106 via the pipe 105 .
- the nitrogen gas including the chlorosulfonic acid has been sprayed onto a surface of the substrate 40 (FIG. 5C) in the chamber 106 .
- the molecular chlorosulfonic acid can enter easily into the grooves 44 each having a narrow opening portion and a deep depth, it can react with the EKC attached onto the bottoms and sidewalls of the grooves 44 . Hence, all EKC remaining on the bottoms and sidewalls of the grooves 44 can be removed easily.
- the vapor of the chlorosulfonic acid has been employed as the cleaning chemicals.
- the vapor of sulfuric acid in addition to only the vapor of sulfuric acid, only the vapor of nitric acid, or the mixed vapor of the vapor of sulfuric acid and the vapor of nitric acid, the vapor including at least any one of the vapor of sulfuric acid, the vapor of hydrochloric acid, and the vapor of nitric acid may be employed.
- FIGS. 6A to 6 D are sectional views showing steps of a substrate cleaning method according to a third embodiment of the present invention respectively.
- FIG. 6A is a sectional view showing a structure before wirings are formed on the substrate.
- a reference 51 denotes a silicon substrate (semiconductor substrate); 52 , a silicon oxide film (underlying insulating film) formed by thermal oxidation; 53 , a conductive film made of aluminum which is formed on the silicon oxide film 52 to have a thickness of 800 nm; and 54 , a resist film formed on the conductive film to remain on wiring forming regions.
- the conductive film 53 is etched by using the resist film 54 as a mask to form a plurality of wirings 53 a each having a width of 0.5 ⁇ m at a distance 1 ⁇ m between adjacent wirings 53 a.
- a surface of the substrate 50 is cleaned by the vapor of the cleaning chemicals.
- the liquid 102 of the chlorosulfonic acid (SO 2 Cl(OH)) has been filled in the flask 101 , and then held at a room temperature or heated by the heater 104 .
- the nitrogen gas as the carrier gas has been passed through the liquid 102 of chlorosulfonic acid (SO 2 Cl(OH)) to thus form the nitrogen gas including the chlorosulfonic acid.
- the nitrogen gas including the chlorosulfonic acid has been sprayed onto a surface of the substrate 50 for two minutes.
- the substrates 50 have been has been cleaned by the flowing pure water after the process and then dried by blowing the nitrogen gas.
- FIG. 6D is a sectional view showing the sample which has been formed and cleaned by the cleaning method according to the present invention
- FIG. 2C is a sectional view showing the sample which has been formed without treatment.
- the conductive film serving as the upper wirings can be formed normally on the hollow portions on the surface of the insulating film 55 . Also, since the depths of the hollow portions are shallow, the conductive film on the bottoms of the hollow portions can be removed clearly at the time when the conductive film once formed is to be patterned by etching.
- the vapor of chlorosulfonic acid has been employed as the cleaning chemicals.
- the vapor of sulfuric acid in addition to only the liquid of chlorosulfonic acid, only the vapor of sulfuric acid, only the vapor of nitric acid, or the mixed vapor of the vapor of sulfuric acid and the vapor of nitric acid, the vapor including at least any one of the vapor of sulfuric acid, the vapor of hydrochloric acid, and the vapor of nitric acid may be employed.
- the silicon substrate has been employed as the semiconductor substrates 31 , 41 , 51 in the above first to third embodiments, but these substrates are not limited to the silicon substrate.
- the silicon oxide film formed by the thermal oxidation has been employed as the underlying insulating films 32 , 52 , but these underlying insulating films are not limited to the thermal silicon oxide film.
- SiO 2 film, PSG film, BSG film, BPSG film, and others formed by thermal CVD method, and other CVD method may be employed.
- the silicon oxide film has been employed as the insulating films 33 , 55 , but these insulating films are not limited to the silicon oxide film.
- the thermal CVD method using TEOS/O 3 has been employed as the method of forming the insulating films 33 , 55 , but the thermal CVD method using other reaction gas or other CVD method may be employed.
- the low pressure OVD method (LPCVD method) using an SiH 4 —N 2 O reaction gas the LPCVD method using a TEOS-O 2 reaction gas, the plasma-CVD method using the TEOS-O 2 reaction gas, or the plasma CVD method using an SiH 4 —O 2 reaction gas may be applied.
- the SiO 2 film, the PSG film, the BSG film, the BPSG film, or the like formed by these CVD methods may be employed.
- the surface of the substrate is exposed to either the vapor including at least any one of the vapor of sulfuric acid, the vapor of hydrochloric acid, and the vapor of nitric acid or the vapor of chlorosulfonic acid (SO 2 Cl(OH)).
- the surface of the insulating film is treated by the liquid or vapor of the chlorosulfonic acid (SO 2 Cl(OH)) prior to film formation, the growth rate on the surface of the insulating film can be improved and also a throughput can be improved.
- SO 2 Cl(OH) chlorosulfonic acid
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- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
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Abstract
Description
- 1. Field of the Invention
- The present invention relates to a method of cleaning a substrate and a method of manufacturing a semiconductor device and, more particularly, a method of cleaning a substrate and a method of manufacturing a semiconductor device removing contaminants after working a surface of a substrate by chemicals etc. or treating the surface of the substrate by the chemicals, etc. prior to film formation.
- 2. Description of the Prior Art
- In recent years, mainly a mixed solution consisting of sulfuric acid, hydrochloric acid, ammonium, hydrogen peroxide, etc. has been employed to clean the silicon wafer in the prior art. Since these are effective to remove metals and organic matters, this cleaning method is effective.
- A cleaning method used in various steps to manufacture semiconductors in the prior art will be explained hereunder.
- First, FIGS. 1A and 1B are sectional views showing steps of cleaning a surface of a semiconductor substrate1 after
trench grooves 3 have been formed on the semiconductor substrate 1. - At first, as shown in FIG. 1A, the
trench grooves 3 are formed on the semiconductor substrate 1 using aresist film 2 as a mask. Then, theresist film 2 is removed by resist removing liquid and, as shown in FIG. 1B, the semiconductor substrate 1 on which thetrench grooves 3 are formed is exposed to a liquid such as the sulfuric acid to remove contaminants such as the resist removing liquid. - Second, FIGS. 2A to2C are sectional views showing steps of forming a
wiring 13 and then covering thewiring 13 with aninsulating film 15. - At first, as shown in FIG. 2A,
wirings 13 are formed on an underlyinginsulating film 12 formed on a semiconductor substrate 11 by patterning using theresist film 14 as a mask. Then, as shown in FIG. 2B, theresist film 14 is removed by the resist removing liquid. Then, as shown in FIG. 2C, aninsulating film 15 is formed by the CVD method to cover thewirings 13 formed on the underlyinginsulating film 12. - Third, FIGS. 3A and 3B are sectional views showing steps of forming a silicon containing
insulating film 23 on an underlyinginsulating film 22. - At first, as shown in FIG. 3A, a surface of the underlying
insulating film 22 on asemiconductor substrate 21 is cleaned by a liquid of the sulfuric acid, etc. Then, as shown in FIG. 3B, a silicon containinginsulating film 23 is deposited on the underlyinginsulating film 22 by the thermal CVD method with using a reaction gas including TEOS (for exanple, N2 is employed as the carrier gas) and ozone (which is included in O2 at a predetermined concentration). - In the meanwhile, in the case of FIG. 1, in recent years, with the progress of miniaturized working of the semiconductor, an opening portion has become narrower and thus a ratio of a depth to an opening portion of the trench groove3 (this ratio is called an aspect ratio) has become higher. Such aspect ratio, if being highest, comes up to five to eight. In the case of the groove which has a narrow opening width but a deep depth, according to the chemicals process shown in FIG. 1B, the chemicals has been difficult to enter into a bottom of the
trench groove 3 completely and then the chemicals has become difficult to be replaced next with a pure water, etc. once the chemicals has entered into such groove. In the end, such a problem has existed that it becomes extremely hard to clean the bottom or the side surface of thetrench groove 3 completely. - In the case of FIG. 2, when the
insulating film 15 is formed by the CVD method to cover thewirings 13 after surface treatment, theinsulating film 15 is difficult to be deposited on the portions. As a result, as shown in FIG. 2B, sometimes deep hollows have been produced in the middle portions between the concave portions between thewirings 13. If a conductive film used as the wirings is formed on suchinsulating film 15, such a problem has arisen that the conductive film cannot be deposited satisfactorily on such concave portions or the conductive film entering into the concave portions cannot be removed. If the chemicals such as EKC (made by the EKC Company, product name) as the particular example is employed as the resist removing liquid, the growth rate of the SiO2 film 15 is extremely slow on the concave portion when the film is formed by the CVD method after the pre-treatment prior to film formation has been carried out, so that the concave portions cannot be buried evenly. The reason for this event may be supposed, though not clearly analyzed, such that perhaps the EKC cannot be removed from the surface of the underlyinginsulating film 12 and thus left thereon, which has a vicious influence upon the growth rate of the SiO2film 15. - In the case of FIG. 3, there has been such a problem that, when the film is formed on the
insulating film 22, for example, the silicon thermal oxide film formed on thesemiconductor substrate 21 made of semiconductor by the thermal CVD method using the reaction gas including TEOS, the film forming rate becomes extremely slow on theinsulating film 22 rather than the case where the film is formed directly on the silicon substrate. - As a diameter of the wafer is enlarged from 200 mm to 300 mm, consumption of the chemicals is increased more and more. As a consequence, not only the cost is brought up but also drainage process takes extremely much time, which will create problems for the environmental protection.
- It is an object of the present invention to provide a substrate cleaning method capable of cleaning insides of grooves each having a narrow opening width and a deep depth clearly while reducing consumption of chemicals, and removing contaminants such as a resist removing liquid clearly, and forming a film on an insulating film while keeping a film forming rate.
- In the present invention, a surface of a substrate is cleaned by use of either a vapor including at least any one of a vapor of sulfuric acid, a vapor of hydrochloric acid, and a vapor of nitric acid or a vapor of chlorosulfonic acid (SO2Cl(OH)).
- Since the vapor of the chemicals is employed, consumption of the chemicals can be extremely reduced rather than the case where a liquid is employed.
- In addition, since the vapor of the chemicals is employed, the chemicals can be supplied as moleculars so that it can enter into the groove which has a narrow opening width and a deep depth. Accordingly, bottoms and side walls of trench grooves each having the opening width of less than 0.3 μm and the deep depth can be cleaned clearly.
- Further, according to the experiment, contaminants which is hard to remove, for example, the resist removing liquid on the insulating film have been able to be removed clearly by using the liquid or vapor of the chlorosulfonic acid.
- Furthermore, according to the experiment, when the insulating film is formed on the underlying insulating film by the thermal CVD method, the substantially same growth rate as the case where the film is formed directly on the semiconductor substrate, especially the silicon substrate has been able to be maintained by using the liquid or vapor of the chlorosulfonic acid.
- FIGS. 1A and 1B are sectional views showing steps of a substrate cleaning method according to a first example in the prior art respectively;
- FIGS. 2A to2C are sectional views showing steps of a substrate cleaning method according to a second example in the prior art respectively;
- FIGS. 3A and 3B are sectional views showing steps of a substrate cleaning method according to a third example in the prior art respectively;
- FIGS. 4A to4D are sectional views showing steps of a substrate cleaning method according to a first embodiment of the present invention respectively;
- FIGS. 5A to5C are sectional views showing steps of a substrate cleaning method according to a second embodiment of the present invention respectively;
- FIGS. 6A to6D are sectional views showing steps of a substrate cleaning method according to a third embodiment of the present invention respectively; and
- FIG. 7 is a side view showing a cleaning chemicals vapor supplying equipment and a substrate processing equipment according to the present invention respectively.
- Embodiments of the present invention will be explained with reference to the accompanying drawings hereinbelow.
- (1) First Embodiment
- FIGS. 4A to4D are sectional views showing steps of a substrate cleaning method according to a first embodiment of the present invention respectively. For samples processed by four types of the chemicals or liquids of the chemicals and unprocessed samples, growth rates of insulating films on an underlying insulating film are compared to each other.
- First, as shown in FIG. 4A, a p-type silicon substrate (semiconductor substrate)31 having a resistivity of 5 Ωcm is prepared.
- Then, as shown in FIG. 4B, the
silicon substrate 31 is thermally oxidized at a temperature of 1100° C. in oxygen atmosphere to form a silicon oxide film (underlying insulating film) 32 of about 100 nm thickness on a surface of thesilicon substrate 31. With the above, asubstrate 30 can be formed. - Then, as shown in FIG. 4C, the
substrate 30 is cleaned by using cleaning chemicals or vapor of the chemicals. In the experiments, four types of the chemicals or vapors of the chemicals described in the following have been employed. - More particularly, a first sample has been prepared as follows. In other words, as shown in FIG. 7, a
liquid 102 of chlorosulfonic acid (SO2Cl(OH)) has been filled in a flask 101 and then a liquid temperature has been held at a room temperature without heating. A nitrogen (N2) gas as a carrier gas has been passed through the liquid 102 of the chiorosulfonic acid (SO2Cl (OH)) via apipe 103 and then introduced via apipe 105 into achamber 106 into which thesubstrate 30 has been loaded. Then, the nitrogen gas including the chiorosulfonic acid has been sprayed onto a surface of thesubstrate 30 for thirty minutes. A temperature of the liquid 102 of chlorosulfonic acid (SO2Cl(OH)), as the case may be, may be increased by heating by means of aheater 104. - Then, a second sample has been prepared by supplying vapor of sulfuric acid directly from a sulfuric acid bomb and then spraying it onto a surface of the to-
be-processed substrate 30 for thirty minutes. - Then, third and fourth samples have been prepared as follows. The liquid of the chlorosulfonic acid of 30 cc has been filled in two beakers. The liquid temperature in one beaker is held at a room temperature, while the other beaker has been heated to hold the liquid temperature at 58° C. Then, the
substrates 30 have been immersed in respective chemicals for thirty minutes. - For the sake of comparison, a fifth sample which is not treated by the cleaning chemicals or vapor of the chemicals has also been prepared.
- In all cases, the
substrates 30 have been cleaned by the flowing pure water after the process has been completed and in turn dried by blowing the nitrogen gas respectively. - Next, under the conditions set forth in the following, as shown in FIG. 4D, another silicon oxide film (insulating film)33 has been formed on the
silicon oxide film 32 formed by thermal oxidation by virtue of the thermal CVD method using the following reaction gas given in a Table 1.TABLE 1 Reaction gas condition: TEOS: 1 sccm O3 in O2: 120 g (mass of O3 in 1 m3 of O3 + O2), Flow rate of O3 + O2: 7.5 sccm Flow rate of N2 (carrier gas): 18 sccm Film forming temperature: 450° C. - The results are given in a Table 2. In Table 2, a notation “growth rate” signifies a growth rate of the
silicon oxide film 33, and a notation “ratio to Si” signifies a ratio of the growth rate of respective samples to the growth rate obtained when the film is formed directly on the silicon substrate, shown in percentages.TABLE 2 Processing Temp. Process Growth rate Ratio to Chemicals (° C.) Time (min.) (Å/min.) Si (%) chlorosulfonic acid room 30 470 104 vapor temp. hydrochloric acid room 30 398 87 vapor temp. chlorosulfonic acid room 30 491 103 liquid temp. chlorosulfonic acid 58 30 493 104 liquid none — — 355 75 - According to the results shown in Table 2, if surface treatment has been made by both the liquid or vapor of the chlorosulfonic acid, the growth rate has been equal to or higher than the growth rate obtained when the film is formed directly on the silicon substrate.
- As a result, the growth rate on the surface of the insulating film can be improved and therefore a throughput can also be improved.
- In addition, consumption of the chemicals a large amount of which is needed as the liquid can be reduced significantly by employing the vapor of the chemicals.
- In the above first embodiment, either the vapor or liquid of the chlorosulfonic acid or the vapor of the hydrochloric acid has been employed as the cleaning chemicals. However, in addition to only the vapor of sulfuric acid, only the vapor of nitric acid, or the mixed vapor of the vapor of sulfuric acid and the vapor of nitric acid, such vapor including at least any one of the vapor of sulfuric acid, the vapor of hydrochloric acid, and the vapor of nitric acid may be employed.
- (2) Second Embodiment
- FIGS. 5A to5C are sectional views showing steps of a substrate cleaning method according to a second embodiment of the present invention respectively.
- First, as shown in FIG. 5A, a resist
film 42 is formed on a silicon substrate (semiconductor substrate) 41 and then openingportions 43 are formed in the resistfilm 42. - Then, the
silicon substrate 41 is etched via the openingportions 43 by the dry etching using chlorine (Cl2) to formgrooves 44 each having a diameter of about 0.25 μm and a depth of 1.5 μm. - Next, as shown in FIG. 5B, the resultant structure is immersed in the EKC as the resist removing liquid to remove the resist. With the above steps, a
substrate 40 can be prepared. At this time, the EKC liquid would remain in thegrooves 44. - Then, as shown in FIG. 7, the
liquid 102 of the chlorosulfonic acid (SO2Cl(OH)) has been filled in the flask 101 and then the liquid temperature has been held at a room temperature or the liquid temperature has been increased by being heated by theheater 104. The nitrogen gas as the carrier gas has been passed through the liquid 102 of chlorosulfonic acid (SO2Cl(OH)) to thus form the nitrogen gas including the chlorosulfonic acid. Then, such nitrogen gas has been introduced into thechamber 106 via thepipe 105. Then, the nitrogen gas including the chlorosulfonic acid has been sprayed onto a surface of the substrate 40 (FIG. 5C) in thechamber 106. - At that time, since the molecular chlorosulfonic acid can enter easily into the
grooves 44 each having a narrow opening portion and a deep depth, it can react with the EKC attached onto the bottoms and sidewalls of thegrooves 44. Hence, all EKC remaining on the bottoms and sidewalls of thegrooves 44 can be removed easily. - In the above second embodiment, the vapor of the chlorosulfonic acid has been employed as the cleaning chemicals. However, in addition to only the vapor of sulfuric acid, only the vapor of nitric acid, or the mixed vapor of the vapor of sulfuric acid and the vapor of nitric acid, the vapor including at least any one of the vapor of sulfuric acid, the vapor of hydrochloric acid, and the vapor of nitric acid may be employed.
- (3) Third Embodiment
- FIGS. 6A to6D are sectional views showing steps of a substrate cleaning method according to a third embodiment of the present invention respectively.
- FIG. 6A is a sectional view showing a structure before wirings are formed on the substrate. In FIG. 6A, a
reference 51 denotes a silicon substrate (semiconductor substrate); 52, a silicon oxide film (underlying insulating film) formed by thermal oxidation; 53, a conductive film made of aluminum which is formed on thesilicon oxide film 52 to have a thickness of 800 nm; and 54, a resist film formed on the conductive film to remain on wiring forming regions. - First, as shown in FIG. 6B, the
conductive film 53 is etched by using the resistfilm 54 as a mask to form a plurality ofwirings 53 a each having a width of 0.5 μm at a distance 1 μm betweenadjacent wirings 53 a. - Then, as shown in FIG. 6C, a surface of the
substrate 50 is cleaned by the vapor of the cleaning chemicals. In other words, as shown in FIG. 7, theliquid 102 of the chlorosulfonic acid (SO2Cl(OH)) has been filled in the flask 101, and then held at a room temperature or heated by theheater 104. The nitrogen gas as the carrier gas has been passed through the liquid 102 of chlorosulfonic acid (SO2Cl(OH)) to thus form the nitrogen gas including the chlorosulfonic acid. Then, the nitrogen gas including the chlorosulfonic acid has been sprayed onto a surface of thesubstrate 50 for two minutes. - For the sake of comparison, a sample which is not treated by the cleaning. chemicals or the vapor of the chemicals has also been prepared.
- In all cases, the
substrates 50 have been has been cleaned by the flowing pure water after the process and then dried by blowing the nitrogen gas. - Next, under the conditions set forth in the following, as shown in FIG. 6D, according to thermal oxidation by virtue of the thermal CVD method using the following reaction gas given in a Table 3, another silicon oxide film (insulating film)55 has been formed to cover the
wirings 53 a.TABLE 3 Reaction gas condition: TEOS: 1 sccm O3 in O2: 120 g (mass of O3 in 1 m3 of O3 + O2), Flow rate of O3 + O2: 7.5 sccm Flow rate of N2 (carrier gas): 18 sccm Film forming temperature: 450° C. - Sectional shapes of the insulating films obtained as above to cover the wirings have been compared to each other with reference to FIGS. 6D and 2C. FIG. 6D is a sectional view showing the sample which has been formed and cleaned by the cleaning method according to the present invention, and FIG. 2C is a sectional view showing the sample which has been formed without treatment.
- According to the results, in the case where surface treatment has been carried out by the vapor of chlorosulfonic acid as shown in FIG. 6D, hollows of the concave portions between the wirings53 a have been able to be made shallower in the sectional shape of the insulating
film 55 to cover the wirings than the case where no treatment has been applied as shown in FIG. 2C. - Consequently, the conductive film serving as the upper wirings can be formed normally on the hollow portions on the surface of the insulating
film 55. Also, since the depths of the hollow portions are shallow, the conductive film on the bottoms of the hollow portions can be removed clearly at the time when the conductive film once formed is to be patterned by etching. - In the above third embodiment, the vapor of chlorosulfonic acid has been employed as the cleaning chemicals. However, in addition to only the liquid of chlorosulfonic acid, only the vapor of sulfuric acid, only the vapor of nitric acid, or the mixed vapor of the vapor of sulfuric acid and the vapor of nitric acid, the vapor including at least any one of the vapor of sulfuric acid, the vapor of hydrochloric acid, and the vapor of nitric acid may be employed.
- The silicon substrate has been employed as the
semiconductor substrates - In addition, the silicon oxide film formed by the thermal oxidation has been employed as the underlying insulating
films - The silicon oxide film has been employed as the insulating
films films - As discussed above, in the present invention, the surface of the substrate is exposed to either the vapor including at least any one of the vapor of sulfuric acid, the vapor of hydrochloric acid, and the vapor of nitric acid or the vapor of chlorosulfonic acid (SO2Cl(OH)).
- Since the vapor is employed, molecular chemicals are ready to enter into the insides of the grooves each having the narrow width and the deep depth, so that they can achieve a noticeable effect of removing the contaminants.
- Since the vapor is employed, consumption of the chemicals, a large quantity of which is needed as the liquid, can be extremely reduced.
- Since the surface of the insulating film is treated by the liquid or vapor of the chlorosulfonic acid (SO2Cl(OH)) prior to film formation, the growth rate on the surface of the insulating film can be improved and also a throughput can be improved.
- Since the surface of the substrate is treated by the liquid or vapor of the chlorosulfonic acid (SO2Cl(OH)) before the insulating film to cover the wirings is formed, contaminants on the underlying insulating film can be removed, otherwise the growth rate of the insulating film to the surface of the underlying insulating film can be put close to the growth rate of the insulating film to the surface of the silicon substrate.
- As a result, since the growth rate of the insulating film to the underlying insulating film in the concave portions between the wirings can be improved and thus hollows of the insulating film on the concave portions can be reduced as small as possible, the upper wirings can be formed regularly on the insulating film.
Claims (16)
Priority Applications (2)
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JP9243937A JP3037915B2 (en) | 1997-09-09 | 1997-09-09 | Method for manufacturing semiconductor device |
US09/220,690 US6372650B2 (en) | 1997-09-09 | 1998-12-28 | Method of cleaning substrate and method of manufacturing semiconductor device |
Applications Claiming Priority (2)
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JP9243937A JP3037915B2 (en) | 1997-09-09 | 1997-09-09 | Method for manufacturing semiconductor device |
US09/220,690 US6372650B2 (en) | 1997-09-09 | 1998-12-28 | Method of cleaning substrate and method of manufacturing semiconductor device |
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US20020016076A1 true US20020016076A1 (en) | 2002-02-07 |
US6372650B2 US6372650B2 (en) | 2002-04-16 |
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US09/220,690 Expired - Fee Related US6372650B2 (en) | 1997-09-09 | 1998-12-28 | Method of cleaning substrate and method of manufacturing semiconductor device |
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JP (1) | JP3037915B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070295357A1 (en) * | 2006-06-27 | 2007-12-27 | Lovejoy Michael L | Removing metal using an oxidizing chemistry |
US20130068248A1 (en) * | 2011-09-15 | 2013-03-21 | Taiwan Semiconductor Manufacturing Company, Ltd., ("Tsmc") | Semiconductor device cleaning method |
US11355362B2 (en) | 2017-04-25 | 2022-06-07 | Tokyo Ohka Kogyo Co., Ltd. | Washing method, washing device, storage medium, and washing composition |
Families Citing this family (5)
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JP3037915B2 (en) * | 1997-09-09 | 2000-05-08 | キヤノン販売株式会社 | Method for manufacturing semiconductor device |
US7560337B2 (en) * | 2006-01-09 | 2009-07-14 | Macronix International Co., Ltd. | Programmable resistive RAM and manufacturing method |
US7879643B2 (en) * | 2008-01-18 | 2011-02-01 | Macronix International Co., Ltd. | Memory cell with memory element contacting an inverted T-shaped bottom electrode |
US7879645B2 (en) * | 2008-01-28 | 2011-02-01 | Macronix International Co., Ltd. | Fill-in etching free pore device |
JP2013012566A (en) * | 2011-06-29 | 2013-01-17 | Kyocera Corp | Method of forming oxide film, method of manufacturing semiconductor device, semiconductor device, and formation device for oxide film |
Family Cites Families (7)
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US3775176A (en) * | 1971-02-23 | 1973-11-27 | Amicon Corp | Method of forming an electroplatable microporous film with exposed metal particles within the pores |
JPH02184311A (en) | 1989-01-09 | 1990-07-18 | Toray Ind Inc | Method for cleaning filter and filter device |
JPH05304126A (en) | 1992-04-28 | 1993-11-16 | Dainippon Screen Mfg Co Ltd | Method and system for removing organic compound from surface of substrate in vapor phase |
JP3040307B2 (en) | 1994-04-12 | 2000-05-15 | 新日本製鐵株式会社 | Steam cleaning method |
US5516730A (en) * | 1994-08-26 | 1996-05-14 | Memc Electronic Materials, Inc. | Pre-thermal treatment cleaning process of wafers |
JP3076270B2 (en) * | 1997-06-24 | 2000-08-14 | キヤノン販売株式会社 | Method for removing resist film and method for manufacturing semiconductor device |
JP3037915B2 (en) * | 1997-09-09 | 2000-05-08 | キヤノン販売株式会社 | Method for manufacturing semiconductor device |
-
1997
- 1997-09-09 JP JP9243937A patent/JP3037915B2/en not_active Expired - Lifetime
-
1998
- 1998-12-28 US US09/220,690 patent/US6372650B2/en not_active Expired - Fee Related
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070295357A1 (en) * | 2006-06-27 | 2007-12-27 | Lovejoy Michael L | Removing metal using an oxidizing chemistry |
US20130068248A1 (en) * | 2011-09-15 | 2013-03-21 | Taiwan Semiconductor Manufacturing Company, Ltd., ("Tsmc") | Semiconductor device cleaning method |
US11355362B2 (en) | 2017-04-25 | 2022-06-07 | Tokyo Ohka Kogyo Co., Ltd. | Washing method, washing device, storage medium, and washing composition |
Also Published As
Publication number | Publication date |
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JPH1187291A (en) | 1999-03-30 |
JP3037915B2 (en) | 2000-05-08 |
US6372650B2 (en) | 2002-04-16 |
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