Precursors for depositing silicon containing films and processes thereof
View Patent ↗Processes for precursors for silicon dielectric depositions of silicon nitride, silicon oxide and silicon oxynitride on a substrate using a hydrazinosilane of the formula: [R 1 2 N—NH] n Si(R 2 ) 4−n where each R 1 is independently selected from alkyl groups of C 1 to C 6 ; each R 2 is independently selected from the group consisting of hydrogen, alkyl, vinyl, allyl, and phenyl; and n=1–4. Some of the hydrazinosilanes are novel precursors.
1. A process for the chemical vapor deposition of material selected from the group consisting of silicon nitride, silicon oxide, and silicon oxynitride on a substrate using a hydrazinosilane of the formula:
[R 1 2 N—NH] n Si(R 2 ) 4−n
where each R 1 is independently selected from alkyl groups of C 1 to C 6 ; each R 2 is independently selected from the group consisting of hydrogen, alkyl, vinyl, allyl, and phenyl; and n=1–4.
2. The process of claim 1 wherein the hydrazinosilane is selected from the group consisting of: Bis(1,1-dimethylhydrazino)methylsilane, Tris(1,1-dimethylhydrazino)silane, Tris(1,1-dimethylhydrazino)-t-butylsilane, Tris(1,1-dimethylhydrazino)s-butylsilane, Tris(1,1-dimethylhydrazino)ethylsilane, Bis(1,1-dimethylhydrazino)ethylsilane, Bis(1,1-dimethylhydrazino)Iso-propylsilane, Bis(1,1-dimethylhydrazino)allylsilane, Bis(1,1-dimethylhydrazino)silane, Tetrakis(1,1-dimethylhydrazino)silane, N,N′,N″-Tris(dimethylamino)cyclotrisilazane, N,N′,N″,N′″-Tetrakis(dimethylamino)cyclotrisilazane, Tris(1,1-dimethylhydrazino)Iso-propylsilane, Tris(1,1-dimethylhydrazino)allylsilane and mixtures thereof.
3. The process of claim 1 wherein the temperature of the substrate is in the range of approximately 100 to 800° C.
4. The process of claim 1 wherein the pressure is in the range of approximately 10 −5 Torr to 760 Torr.
5. The process of claim 1 wherein the hydrazinosilane is reacted with a nitrogen source selected from the group consisting of nitrogen, ammonia, hydrazine, amines, and mixtures thereof.
6. The process of claim 5 wherein the molar ratio of ammonia to hydrazinosilane can be greater than or equal to zero.
7. The process of claim 1 wherein the substrate is silicon.
8. The process of claim 1 wherein the substrate is an electronic device.
9. The process of claim 1 wherein the substrate is a flat panel display.
10. The process of claim 1 wherein each R 1 is independently selected from the group consisting of methyl and ethyl and each R 2 is independently selected from the group consisting of hydrogen, methyl, ethyl, propyl, iso-propyl, n-butyl, iso-butyl, tert-butyl, allyl and phenyl.
11. The process of claim 1 wherein the material is silicon nitride.
12. The process of claim 1 wherein the material is silicon oxynitride.
13. The process of claim 1 wherein the material is silicon nitride and the chemical vapor deposition is plasma enhanced chemical vapor deposition.
14. The process of claim 1 wherein the material is silicon oxide and the chemical vapor deposition is plasma enhanced chemical vapor deposition.
15. The process of claim 1 wherein the material is silicon oxynitride and the chemical vapor deposition is plasma enhanced chemical vapor deposition.
16. The process of claim 1 wherein the chemical vapor deposition is atomic layer deposition.
17. A low temperature chemical vapor deposition of silicon nitride in a reaction zone, comprising the steps of:
a) heating a substrate to a temperature in the range of approximately 100–800° C. in said zone;
b) maintaining the substrate in a vacuum at a pressure in the range of approximately 10 −5 Torr–760 Torr in said zone;
c) introducing into said zone a hydrazinosilane of the formula:
[R 1 2 N—NH] n Si(R 2 ) 4−n
where each R 1 is independently selected from alkyl groups of C 1 to C 6 ; each R 2 is independently selected from the group consisting of hydrogen, alkyl, allyl, and phenyl; and n=1–4; and
d) maintaining the conditions of a) through c) sufficient to cause a film of silicon nitride to deposit on the substrate.
18. The process of claim 17 wherein the hydrazinosilane is selected from the group consisting of: Bis(1,1-dimethylhydrazino)methylsilane, Tris(1,1-dimethylhydrazino)silane, Tris(1,1-dimethylhydrazino)-t-butylsilane, Tris(1,1-dimethylhydrazino)s-butylsilane, Tris(1,1-dimethylhydrazino)ethylsilane, Bis(1,1-dimethylhydrazino)ethylsilane, Bis(1,1-dimethylhydrazino)Iso-propylsilane, Bis(1,1-dimethylhydrazino)allylsilane, Bis(1,1-dimethylhydrazino)silane, Tetrakis(1,1-dimethylhydrazino)silane, N,N′,N″-Tris(dimethylamino)cyclotrisilazane, N,N′,N″,N′″-Tetrakis(dimethylamino)cyclotrisilazane, Tris(1,1-dimethylhydrazino)Iso-propylsilane, Tris(1,1-dimethylhydrazino)allylsilane and mixtures thereof.
19. The process of claim 17 wherein the hydrazinosilane is reacted with nitrogen source selected from the group consisting of nitrogen, ammonia hydrazine and mixtures thereof.