Precursors for CVD silicon carbo-nitride and silicon nitride films
View Patent ↗Classes of liquid aminosilanes have been found which allow for the production of silicon carbo-nitride films of the general formula Si x C y N z . These aminosilanes, in contrast, to some of the precursors employed heretofore, are liquid at room temperature and pressure allowing for convenient handling. In addition, the invention relates to a process for producing such films. The classes of compounds are generally represented by the formulas: and mixtures thereof, wherein R and R 1 in the formulas represent aliphatic groups typically having from 2 to about 10 carbon atoms, e.g., alkyl, cycloalkyl with R and R 1 in formula A also being combinable into a cyclic group, and R 2 representing a single bond, (CH 2 ) n , a ring, or SiH 2 .
1. A process for forming silicon nitride or silicon carbo-nitride films on a substrate through chemical vapor deposition of a silicon nitride or silicon carbo-nitride film forming precursor which comprises:
using a precursor selected from the group consisting of an aminosilane represented by the formulas:
and mixtures thereof, wherein R is selected from C 1 -C 10 alkyl groups, linear, branched, or cyclic, saturated or unsaturated; aromatic, heterocyclic, amine groups, or silyl in formula C, R 1 is selected from C 3 -C 10 alkyl groups, branched, or cyclic, saturated or unsaturated;
aromatic, heterocyclic, hydrogen, silyl groups with or without substituents with R and R 1 in formula A also being combinable into a cyclic group (CH 2 ) n , wherein n is from 2-6, R and R in formula C also being combinable into a cyclic group and R 2 representing a single bond, (CH 2 ) m chain, a ring, SiR 2 , or SiH 2 and wherein R and R 1 in Formula A are each independently C 3 -C 10 branched alkyl groups.
2. The process of claim 1 wherein R and R 1 are cyclic.
3. The process of claim 1 wherein R and R 1 are combined into a ring in the form of (CH 2 ) n where n is from 4-5.
4. The process of claim 1 wherein R and R 1 are isopropyl.
5. The process of claim 1 wherein the using step further comprises a nitrogen source selected from the group consisting of ammonia, nitrogen and hydrazine.
6. The process of claim 5 wherein the temperature of the substrate during chemical vapor deposition is within the range of approximately 500 to 700° C.
7. The process of claim 6 wherein the pressure during chemical vapor deposition is in the range of approximately 20 mTorr to 20 Torr.
8. The process of claim 5 wherein the nitrogen source is ammonia or nitrogen and the nitrogen source is present in a nitrogen source:precursor range of from 0.1 to 4:1.
9. The process of claim 1 wherein the precursor aminosilane is represented by the formula A and within that class, is selected from the aminosilanes having the formula:
and where m is 1-6.
10. The process of claim 1 wherein the precursor is represented by the formula B and within that class, the precursor is selected from the group having the formula:
11. The process of claim 10 wherein a nitrogen source selected from the group consisting of ammonia or nitrogen is included as precursor and the nitrogen source is present in a nitrogen source:precursor range of from 0.1 to 4:1.
12. The process of claim 1 wherein the precursor is represented by the formula C and within that class, the precursor is selected from the group having the formulas:
13. In a process for forming a silicon nitride or silicon carbo-nitride film wherein such film is formed by the chemical vapor deposition of a silane precursor, the improvement which comprises:
employing an aminosilane as the silane precursor which is represented by the formula:
wherein R and R 1 are each independently selected from a C 3 -C 10 alkyl groups branched, cyclic, saturated, or unsaturated; aromatic group; heterocyclic; or silyl groups with R and R 1 also being combinable into a cyclic group (CH 2 ) n , wherein n is from 2-6.
14. The process of claim 13 wherein R and R 1 are isopropyl.
15. The process of claim 14 wherein the chemical vapor deposition further comprises a nitrogen source selected from the group consisting of ammonia or nitrogen in employed in a nitrogen source:silane precursor ratio of from 0.1 to 4:1.
16. The process of claim 15 wherein the temperature of the substrate is maintained with a range of 500 to 700° C. and the pressure is from 20 mTorr to 20 Torr.
17. The process of claim 10 wherein the precursor has the formula:
18. The process of claim 10 wherein the precursor has the formula:
19. The process of claim 12 wherein the precursor has the formula:
20. The process of claim 12 wherein the precursor has the formula:
21. The process of claim 1 wherein R and R 1 are combined into a ring in the form of (CH 2 ) n where n is from 2-6.
22. A process for forming a silicon carbo-nitride film on a substrate through chemical vapor deposition comprising:
using a precursor selected from the group consisting of an aminosilane represented by the formula:
and mixtures thereof, wherein R is selected from C 1 -C 10 alkyl groups, linear, branched, or cyclic, saturated or unsaturated and aromatic or heterocyclic amine groups
wherein the precursor is selected from the group having the formula:
23. A process for forming a silicon carbo-nitride film on a substrate through chemical vapor deposition which comprises:
using a precursor selected from the group consisting of an aminosilane represented by the formulas:
and mixtures thereof, wherein R is selected from C 1 -C 10 alkyl groups, linear, branched, or cyclic, saturated or unsaturated; aromatic, heterocyclic, amine groups, or silyl in formula C, R and R in formula C also being combinable into a cyclic group and R 2 representing a single bond, (CH 2 ) m chain, a ring, SiR 2 , or SiH 2 ,
wherein the precursor is selected from the group having the formulas:
24. A process for forming silicon nitride or silicon carbo-nitride films on a substrate through chemical vapor deposition of a silicon nitride or silicon carbo-nitride film forming precursor which comprises:
using a precursor selected from the group consisting of an aminosilane represented by the formulas:
and mixtures thereof, wherein R is selected from C 1 -C 10 alkyl groups, linear, branched, or cyclic, saturated or unsaturated; aromatic, heterocyclic, amine groups, or silyl in formula C, wherein R and R in formula C also being combinable into a cyclic group and R 2 representing a single bond, (CH 2 ) m chain, a ring, SiR 2 , or SiH 2 .