US2018033614A1PendingUtilityA1

Compositions and Methods Using Same for Carbon Doped Silicon Containing Films

Assignee: VERSUM MAT US LLCPriority: Jul 27, 2016Filed: Jul 19, 2017Published: Feb 1, 2018
Est. expiryJul 27, 2036(~10 yrs left)· nominal 20-yr term from priority
H10P 14/69433H10P 14/69215H10P 14/6922H10P 14/6682H10P 14/6532H10P 14/6529H10P 14/6522H10P 14/6339H10P 14/683H10P 14/6681C23C 16/56C23C 16/402C23C 16/45553C23C 16/45525C23C 16/308C23C 16/345H10P 95/00H01L 21/02208H01L 21/02118H01L 21/0234H01L 21/02326H01L 21/0228H01L 21/02164H01L 21/0217H01L 21/02126C23C 16/45536C23C 16/401C23C 16/36
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Claims

Abstract

A composition and method for using the composition in the fabrication of an electronic device are disclosed. Compounds, compositions and methods for depositing a low dielectric constant (<4.0) and high oxygen ash resistance silicon-containing film such as, without limitation, a carbon doped silicon oxide, are disclosed.

Claims

exact text as granted — not AI-modified
1 ) A composition comprising:
 (a) at least one silicon precursor compound having one Si—C—Si or two Si—C—Si linkages selected from the group consisting of 1,1,1,3,3,3-hexachloro-1,3-disilapropane, 1,1,1,3,3,3-hexachloro-2-methyl-1,3-disilapropane, 1,1,1,3,3,3-hexachloro-2,2-dimethyl-1,3-disilapropane, 1,1,1,3,3,3-hexachloro-2-ethyl-1,3-disilapropane, 1-chloro-1,3-disilacyclobutane, 1-bromo-1,3-disilacyclobutane, 1,3-dichloro-1,3-1,3-disilacyclobutane, 1,3-dibromo-1,3-disilacyclobutane, 1,1,3-trichloro-1,3-disilacyclobutane, 1,1,3-tribromo-1,3-disilacyclobutane, 1,1,3,3-tetrabromo-1,3-disilacyclobutane, 1,3-dichloro-1,3-dimethyl-1,3-disilacyclobutane, 1,3-bromo-1,3-dimethyl-1,3-disilacyclobutane, 1,1,1,3,3,5,5,5-octachloro-1,3,5-trisilapentane, 1,1,1,3,3,5,5,5-octachloro-1,3,5-trisilapentane, 1,1,1,3,3,5,5,5-octachloro-1,5-dimethyl-1,3,5-trisilapentane, 1,1,1,5,5,5-hexachloro-3,3-dimethyl-1,3,5-trisilapentane, 1,1,3,5,5,5-pentachloro-1,3,5-trimethyl-1,3,5-trisilapentane, 1,1,1,5,5,5-hexachloro-1,3,5-trisilapentane, 1,1,5,5-tetraachloro-1,3,5-trisilapentane; and;   (b) at least one solvent.   
     
     
         2 ) The composition of  claim 1  where in the solvent comprises at least one member selected from the group consisting of ether, tertiary amine, siloxanes, alkyl hydrocarbon, aromatic hydrocarbon, and tertiary aminoether. 
     
     
         3 ) The composition of  claim 1  wherein the difference between the boiling point of the silicon precursor and the boiling point of the solvent is about 40° C. or less. 
     
     
         4 ) The composition of  claim 1  comprising less than 5 ppm of at least one metal ions selected from the group consisting of Al 3+  ions, Fe 2+ , Fe 3+ , Ni 2+ , and Cr 3+ . 
     
     
         5 ) The composition of  claim 1  where in the solvent comprises at least one member selected from the group consisting of heptane, octane, nonane, decane, dodecane, cyclooctane, cyclononane, cyclodecane, toluene, and mesitylene. 
     
     
         6 ) A method for forming a carbon doped silicon oxide film having carbon content ranging from 15 at. % to 30 at. % via a thermal ALD process, the method comprising:
 a) placing one or more substrates comprising a surface feature into a reactor;   b) heating to reactor to one or more temperatures ranging from ambient temperature to about 550° C. and optionally maintaining the reactor at a pressure of 100 torr or less;   c) introducing into the reactor at least one silicon precursor having two Si—C—Si linkages selected from the group consisting of 1-chloro-1,3-disilacyclobutane, 1-bromo-1,3-disilacyclobutane, 1,3-dichloro-1,3-1,3-disilacyclobutane, 1,3-dibromo-1,3-disilacyclobutane, 1,1,3-trichloro-1,3-disilacyclobutane, 1,1,3-tribromo-1,3-disilacyclobutane, 1,1,3,3-tetrachloro-1,3-disilacyclobutane, 1,1,3,3-tetrabromo-1,3-disilacyclobutane, 1,3-dichloro-1,3-dimethyl-1,3-disilacyclobutane, 1,3-bromo-1,3-dimethyl-1,3-disilacyclobutane, 1,1,1,3,3,5,5,5-octachloro-1,3,5-trisilapentane, 1,1,1,3,3,5,5,5-octachloro-1,3,5-trisilapentane, 1,1,1,3,3,5,5,5-octachloro-1,5-dimethyl-1,3,5-trisilapentane, 1,1,1,5,5,5-hexachloro-3,3-dimethyl-1,3,5-trisilapentane, 1,1,3,5,5,5-pentachloro-1,3,5-trimethyl-1,3,5-trisilapentane, 1,1,1,5,5,5-hexachloro-1,3,5-trisilapentane, 1,1,5,5-tetraachloro-1,3,5-trisilapentane;   d) purge with an inert gas;   e) providing a nitrogen source into the reactor to react with the surface to form a carbon doped silicon nitride film;   f) purge with inert gas to remove reaction by-products;   g) steps c to f are repeated to provide a desired thickness of carbon doped silicon nitride;   h) treating the resulting carbon doped silicon nitride film with an oxygen source at one or more temperatures ranging from about ambient temperature to 1000° C. or from about 100° to 400° C. to convert the carbon doped silicon nitride film into a carbon doped silicon oxide film; and   i) providing post-deposition exposing the carbon doped silicon oxide film to a plasma comprising hydrogen.   
     
     
         7 ) method of  claim 6  wherein the silicon precursor comprises the composition of  claim 1 . 
     
     
         8 ) A film formed according to the method of  claim 6  having a k of less than about 4, a carbon content of at least about 10 at. %. 
     
     
         9 ) A film formed according to the method of  claim 6  having an etch rate of at least 0.5 times less than thermal silicon oxide. 
     
     
         10 ) A film formed according to the method of  claim 6  having an etch rate of at least 0.1 times less than thermal silicon oxide. 
     
     
         11 ) A film formed according to the method of  claim 6  having an etch rate of at least 0.05 times less than thermal silicon oxide. 
     
     
         12 ) A film formed according to the method of  claim 6  having an etch rate of at least 0.01 times less than thermal silicon oxide. 
     
     
         13 ) A film formed according to the method of  claim 6  having less damage layer (50 Å or less) when exposing to oxygen ashing process. 
     
     
         14 ) A film formed according to the method of  claim 6  having less damage layer (20 Å or less) when exposing to oxygen ashing process. 
     
     
         15 ) A film formed according to the method of  claim 6  having less damage layer (10 Å or less) when exposing to oxygen ashing process. 
     
     
         16 ) A film formed according to the method of  claim 6  having less damage layer (5 Å or less) when exposing to oxygen ashing process. 
     
     
         17 ) A stainless steel container housing the composition of  claim 1 . 
     
     
         18 ) A method for forming a carbon doped silicon oxide film having carbon content ranging from 15 at % to 30 at. % via a thermal ALD process, the method comprising the method comprising:
 a. placing one or more substrates comprising a surface feature into a reactor;   b. heating the reactor to one or more temperatures ranging from ambient temperature to about 150° C. and optionally maintaining the reactor at a pressure of 100 torr or less;   c. introducing into the reactor at least precursor having two Si—C—Si linkages selected from the group consisting of 1-chloro-1,3-disilacyclobutane, 1-bromo-1,3-disilacyclobutane, 1,3-dichloro-1,3-1,3-disilacyclobutane, 1,3-dibromo-1,3-disilacyclobutane, 1,1,3-trichloro-1,3-disilacyclobutane, 1,1,3-tribromo-1,3-disilacyclobutane, 1,1,3,3-tetrachloro-1,3-disilacyclobutane, 1,1,3,3-tetrabromo-1,3-disilacyclobutane, 1,3-dichloro-1,3-dimethyl-1,3-disilacyclobutane, 1,3-bromo-1,3-dimethyl-1,3-disilacyclobutane, 1,1,1,3,3,5,5,5-octachloro-1,3,5-trisilapentane, 1,1,1,3,3,5,5,5-octachloro-1,3,5-trisilapentane, 1,1,1,3,3,5,5,5-octachloro-1,5-dimethyl-1,3,5-trisilapentane, 1,1,1,5,5,5-hexachloro-3,3-dimethyl-1,3,5-trisilapentane, 1,1,3,5,5,5-pentachloro-1,3,5-trimethyl-1,3,5-trisilapentane, 1,1,1,5,5,5-hexachloro-1,3,5-trisilapentane, 1,1,5,5-tetraachloro-1,3,5-trisilapentane and a catalyst;   d. purge with an inert gas   e. providing vapors of water into the reactor to react with the precursor as well as a catalyst to form a carbon doped silicon oxide as-deposited film;   f. purge with inert gas to remove reaction by-products;   g. steps c to f are repeated to provide a desired thickness of carbon doped silicon oxide;   
     
     
         19 ) The method of  claim 18  further comprising post-deposition treatment of the carbon doped silicon oxide film with a thermal anneal at temperatures from 300 to 700° C. 
     
     
         20 ) The method of  claim 18  further comprising hydrogen plasma treatment of the carbon doped silicon oxide film with a plasma comprising hydrogen.

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