IP Library Granted Patent US 6,869,638
Granted Patent B2
US 6,869,638 · App. 09/954,831 · Granted Mar 22, 2005

Source reagent compositions for CVD formation of gate dielectric thin films using amide precursors and method of using same

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Quick Facts
Patent No.
US 6,869,638
App. No.
09/954,831
Granted
Mar 22, 2005
Kind
B2
Abstract

A CVD Method of forming gate dielectric thin films on a substrate using metalloamide compounds of the formula M(NR 1 R 2 ) x , or wherein M is Zr, Hf, Y, La, Lanthanide series elements, Ta, Ti, or Al; N is nitrogen; each of R 1 and R 2 is same or different and is independently selected from H, aryl, perfluoroaryl, C 1 -C 8 alkyl, C 1 -C 8 perfluoroalkyl, alkylsilyl; and x is the oxidation state on metal M; and an aminosilane compound of the formula H x SiA y (NR 1 R 2 ) 4-x-y or wherein H is hydrogen; x is from 0 to 3; Si is silicon; A is a halogen; Y is from 0 to 3; N is nitrogen; each of R 1 and R 2 is same or different and is independently selected from the group consisting of H, aryl, perfluoroaryl, C 1 -C 8 alkyl, and C 1 -C 8 perfluoroalkyl; and n is from 1-6. By comparison with the standard SiO 2 gate dielectric materials, these gate dielectric materials provide low levels of carbon and halide impurity.

Claims (82)

1. A CVD precursor composition for forming a thin film dielectric on a substrate, such precursor composition including a vapor source reagent-mixture including a metalloamide source reagent compound selected from the group consisting of:

M(NR 1 R 2 ) x ; and

wherein M is selected from the group consisting of Zr, Hf, Y, La, Lanthanide series elements, Ta, Ti, Al; N is nitrogen; each of R 1 and R 2 is same or different and is independently selected from the group consisting of H, aryl, perfluoroaryl, C 1 -C 8 alkyl, C 1 -C 8 perfluoroalkyl, alkylsilyl; and x is the oxidation state on metal M; and it is from 1-6; and

an aminosilane source reagent compound selected from the group consisting of:

H x SiA y (NR 1 R 2 ) 4-x-y ; and

wherein H is hydrogen; x is from 0 to 3; Si is silicon; A is a halogen; Y is from 0 to 3; N is nitrogen; each of R 1 and R 2 is same or different and is independently selected from the group consisting of H, aryl, perfluoroaryl, C 1 -C 8 alkyl, and C 1 -C 8 perfluoroalkyl; and n is from 1-6; x is from 0 to 3; Si is silicon; A is a halogen; Y is from 0 to 3; N is nitrogen; n is from 1-6.

2. The CVD precursor composition according to claim 1 , wherein the aminosilane soiree reagent compound is selected from the group consisting of: Si(NMe 2 ) 3 Cl, Si(NEt 2 ) 2 Cl 2 , Si(NMe 2 ) 4 , and Si(NEt 2 ) 4 .

3. The CVD precursor composition according to claim 1 , wherein the metalloamide source reagent compound and the aminosilane source reagent compound are injected by liquid delivery into a chemical vapor deposition chamber.

4. The CVD precursor composition according to claim 1 , wherein the metalloamide source reagent compound and the aminosilane source reagent compound are delivered by bubbler into a chemical vapor deposition chamber.

5. The CVD precursor composition according to claim 1 , wherein the precursor composition further comprises a solvent medium selected from the coup consisting of: ethers, glymes, tetraglymes, amines, polyamines, alcohols, glycols, aliphatic hydrocarbon solvents, aromatic hydrocarbon solvents, cyclic ethers and combinations of two or more of the foregoing.

6. The CVD precursor composition according to claim 1 , wherein the metalloamide source reagent compound is injected by liquid delivery into a chemical vapor deposition chamber.

7. A CVD precursor composition for forming a thin film dielectric on a substrate, such precursor composition including at least one aminosilane source reagent compound selected from the group consisting of:

H x SiA y (NR 1 R 2 ) 4-x-y ; and

wherein H is hydrogen; x is from 0 to 3; Si is silicon; A is a halogen; Y is from 1 to 3; N is nitrogen; each of R 1 and R 2 is same or different and is independently selected from the group consisting of H, aryl, perfluoroaryl, C 1 -C 8 alkyl, and C 1 -C 8 perfluoroalkyl; and n is from 1-6.

8. A CVD precursor composition for forming a thin film dielectric on a substrate, such precursor composition including at least one aminosilane source reagent compound selected from the group consisting of Si(NMe 2 ) 2 Cl, Si(NEt 2 ) 2 Cl 2 , Si(NMe 2 ) 4 , and Si(NEt 2 ) 4 .

9. The CVD precursor composition according to claim 7 , wherein R 1 and R 2 of the aminosilane are methyl.

10. The CVD precursor composition according to claim 7 , wherein R 1 and R 2 ethyl.

11. A CVD precursor composition for forming a thin film dielectric on a substrate, such precursor composition including at least one aminosilane source reagent compound having the formula:

H x SiA y (NR 1 R 2 ) 4-r-yt

wherein H is hydrogen; x is from 0 to 3; Si is silicon; A is halogen; Y is from 0 to 3; N is nitrogen; R 1 is methyl, R 2 is ethyl; and n is from 1-6.

12. The CVD precursor composition according to claim 11 , wherein the aminosilane source reagent compound is Si(NMeEt) 4 .

13. A CVD precursor composition for forming a thin film dielectric on a substrate, such precursor composition including at least one aminosilane source reagent compound selected from the group consisting of:

H x SiA y (NR 1 R 2 ) 4-x-y ; and

wherein H is hydrogen; x is from 0 to 3; Si is silicon; A is a halogen; Y is from 0 to 3; N is nitrogen; each of R 1 and R 2 is same or different and is independently selected from the group consisting of H, aryl, perfluoroaryl, C 1 -C 8 alkyl, and C 1 -C 8 perfluoroalkyl; and n is from 1-6 and a solvent medium selected from the group consisting of: ethers, glymes, tetraglymes, amines, polyamines, alcohols, glycols, aliphatic hydrocarbon solvents, aromatic hydrocarbon solvents, cyclic ethers and combinations of two or more of the foregoing.

14. The CVD precursor composition according to claim 13 , wherein the solvent is octane.

15. The CVD precursor composition according to claim 13 , wherein the aminosilane source reagent compound is injected by liquid delivery into a chemical vapor deposition chamber.

16. The CVD precursor of claim 13 , wherein the precursor composition further comprises a metalloamide source reagent compound selected from the group consisting of:

M(NR 1 R 2 ) x ; and

wherein M is selected from the group consisting of: Zr, Hf, Y, La, Lanthanide series elements, Ta, Ti, Al; N is nitrogen each of R 1 and R 2 is same or different and is independently selected from the group consisting of H, aryl, perfluoroaryl, C 1 -C 8 alkyl, C 1 -C 8 perfluoroalkyl, alkylsilyl; and x is the oxidation state on metal M; end n is from 1-6.

17. The CVD precursor composition according to claim 16 , wherein R 1 and R 2 of the metalloamide source reagent are methyl.

18. The CVD precursor composition according to claim 16 , wherein R 1 and R 2 of the metalloamide source reagent compound are ethyl.

19. The CVD precursor composition according to claim 16 , wherein R 1 of the metalloamide source reagent compound is methyl and R 2 of the metalloamide source reagent compound is ethyl.

20. The CVD precursor composition according to claim 16 , wherein M is Zr.

21. The CVD precursor composition according to claim 16 , wherein M is Hf.

22. The CVD precursor composition according to claim 16 , wherein the metalloamide source reagent compound is selected from the group consisting of: Zr(NMe 2 ) 4 , Zr(NMeEt) 4 , Zr(NEt 2 ) 4 , Ta(NEt 2 ) 5 , Ta(NMeEt 2 ) 5 , Ta(NMeEt) 5 , Zr(NiPr 2 ) 4 , Zr(NMe 2 ) 2 (NPr 2 ) 2 , Zr(NC 6 H 12 ) 4 , Zr(NEt 2 ) 2 (NPr 2 ) 2 , Hf(NEt 2 ) 4 , Hf(NMe 2 ) 4 , Hf(NMeEt) 4 , La(NMe 2 ) 3 , La(NEt 2 ) 3 , La(NMeEt) 3 , Al(NMe 2 ) 3 , Al(NEt 2 ) 3 , Y(NMe 2 ) 3 , Y(NEt 2 ) 3 , Y(NMeEt) 3 , Ti(NMe 2 ) 4 , Ti(NEt 3 ) 4 , Ti(NMeEt) 4 , Ta(NMe 2 ) 5 , Ta(NEt 2 ) 5 .

23. The CVD precursor composition according to claim 16 , wherein the metalloamide source reagent compound is selected from the group consisting of Zr(NMe 2 ) 4 , Zr(NEt 2 ) 4 , Zr(NMeEt) 4 , Hf(NEt 2 ) 4 , Hf(NMe 2 ) 4 , and Hf(NMeEt) 4 .

24. A CVD multi-component, single source reagent composition useful for forming a silicate thin film dielectric on a substrate, the source reagent composition comprising at least one metalloamide vapor source reagent compound selected from the group consisting of:

M(NR 1 R 2 ) x ; and

wherein M is selected from the group consisting of: Zr, Hf, Y, La, Lanthanide series elements, Ta, Ti, Al; N is nitrogen; each of R 1 and R 2 is same or different and is independently selected from the group consisting of H, aryl, perfluoroaryl, C 1 -C 8 alkyl, C 1 -C 8 perfluoroalkyl, alkylsilyl; and x is the oxidation state on metal M; and n is from 1-6; and

an aminosilane vapor source reagent compound selected from the group consisting of:

H x SiA y (NR 1 R 2 ) 4-x-y ; and

wherein H is hydrogen; x is from 0 to 3; Si is silicon; A is a halogen; Y is from 0 to 3; N is nitrogen; each of R 1 and R 2 is same or different and is independently selected from the group consisting of H, aryl, perfluoroaryl, C 1 -C 8 alkyl, and C 1 -C 8 perfluoroalkyl; and a is from 1-6; and

a solvent medium in which the metalloamide compound and the aminosilane compound are soluble or suspendable.

25. A CVD method of forming a dielectric thin film on a substrate, comprising the steps of:

vaporizing a source reagent composition comprising at least one metalloamide source reagent compound and at least one aminosilane source reagent compound, to form a source reagent precursor vapor;

transporting the source reagent precursor vapor into a chemical vapor deposition zone, optionally using a carrier gas;

contacting the source reagent precursor vapor with a substrate in said chemical vapor deposition zone at elevated temperature to deposit a dielectric thin film on the substrate.

26. The method according to claim 25 , wherein the metalloamide source reagent compound is selected from the group consisting of:

M(NR 1 R 2 ) x ; and

wherein M is selected from the group consisting of Zr, Hf, Y, La, Lanthanide series elements, Ta, Ti, Al; N is nitrogen; each of R 1 and R 2 is same or different and is independently selected from the group consisting of H, aryl, perfluoroaryl, C 1 -C 8 alkyl, C 1 -C 8 perfluoroalkyl, alkylsilyl; and x is the oxidation state on metal M; and n is from 1-6.

27. The CVD method according to claim 25 , wherein the source reagent composition is vaporized in a liquid delivery apparatus.

28. The CVD method according to claim 25 , wherein the source reagent vapor is transported into the chemical vapor deposition chamber in a pulsed deposition mode.

29. The CVD method according to claim 25 , wherein the dielectric thin film is deposited in the absence of an oxidizer.

30. The CVD method according to claim 25 , wherein the source reagent vapor further comprises a co-reactive gas.

31. The CVD method according to claim 30 , wherein the co-reactive gas is selected from the group consisting of ozone, water vapor and reactive alcohols.

32. The CVD method according to claim 25 , wherein the metalloamide source reagent compound is selected from the group consisting of: Zr(NMe 2 ) 4 , Zr(NEt 2 ) 4, Zr(NMeEt) 4, Hf(NMe 2 ) 4 , Hf(NEt 2 ) 4 , and Hf(NMeEt) 4 .

33. The CVD method according to claim 25 , wherein the metalloamide source reagent compound is Hf(NMe 2 ) 4 .

34. A CVD method of forming a dielectric thin film on a substrate, comprising the steps of:

vaporizing a source reagent composition comprising at least one metalloamide precursor dissolved or suspended in octane, to form a source reagent precursor vapor;

transforming the source reagent precursor vapor into a chemical vapor deposition zone, optionally using a carrier gas;

contacting the source reagent precursor vapor with a substrate in the chemical vapor deposition zone at elevated temperature, to deposit a dielectric thin film on the substrate.

35. The CVD method according to claim 25 , wherein the metalloamide source reagent compound is solubilized or suspended in a solvent.

36. The CVD method according to claim 25 , wherein the metalloamide source reagent compound is Zr(NMe 2 ) 4 .

37. A method of forming a dielectric thin film a substrate, comprising the steps of:

vaporizing a source reagent composition comprising La(NMe 2 ) and Zr(NMe 2 ) 4 to form a source reagent precursor vapor;

transporting the source reagent precursor vapor into a chemical vapor deposition zone, optionally using a carrier gas;

contacting the source reagent precursor vapor with a substrate in the chemical vapor deposition zone at elevated temperature to deposit a dielectric thin film on the substrate.

38. A CVD method of forming a dielectric thin film on a substrate, comprising the steps of:

vaporizing a source reagent composition comprising a X(NMe 2 ) 3 , to form a source reagent precursor vapor;

transporting the source reagent precursor vapor into a chemical vapor deposition zone, optionally using a carrier gas;

contacting the source reagent precursor vapor with a substrate in said chemical vapor deposition zone at elevated temperature to deposit a dielectric thin film on the substrate.

39. A CVD method of forming a dielectric thin film on a substrate, comprising the steps of:

vaporizing a source reagent composition comprising Hf(N(CH 3 ) 2 ) 4 and La(N(CH 3 ) 2 ) 3 , to form a source reagent precursor vapor;

transporting the source reagent precursor vapor into a chemical vapor deposition zone, optionally using a carrier gas;

contacting the source reagent precursor vapor with a substrate in the chemical vapor deposition zone at elevated temperature to deposit a dielectric thin film on the substrate.

40. The CVD method according to claim 25 , wherein the metalloamide source reagent compound is Hf(NMe 2 ) 4 and the aminosilane source reagent compound is Si(NMe 2 ) 3 Cl.

41. The CVD method according to claim 25 , wherein the carrier gas is selected from the group consisting of: He, Ar, H 2 , N 2 and O 2 .

42. The CVD method according to claim 25 , further comprising an oxidizing gas selected from the group consisting of: O 2 , N 2 O, NO and O 3 .

43. The CVD method according to claim 42 , wherein the oxidizing gas is N 2 O.

44. The CVD method according to claim 25 , further comprising an oxidizing gas, wherein the oxidizing gas is N 2 O.

45. The CVD method according to claim 25 , wherein the metalloamide source reagent compound is vaporized at a temperature in a range of from about 100° C. to about 300° C.

46. The CVD method according to claim 25 , wherein the temperature in the chemical vapor deposition zone is between about 350° C. to about 750° C.

Assignments (4)
ASSIGNMENT OF PATENT SECURITY INTEREST RECORDED AT REEL/FRAME 048811/0679 Recorded Nov 5, 2019
From: GOLDMAN SACHS BANK USA
To: MORGAN STANLEY SENIOR FUNDING, INC.
Reel/Frame 050965/0035 →
SECURITY INTEREST Recorded Nov 13, 2018
From: ENTEGRIS, INC.; SAES PURE GAS, INC.
To: GOLDMAN SACHS BANK USA
Reel/Frame 048811/0679 →
RELEASE OF SECURITY INTEREST Recorded Nov 8, 2018
From: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
To: ENTEGRIS, INC.; POCO GRAPHITE, INC.; ATMI, INC.; ATMI PACKAGING, INC.; ADVANCED TECHNOLOGY MATERIALS, INC.
Reel/Frame 047477/0032 →
RELEASE OF SECURITY INTEREST Recorded Nov 8, 2018
From: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
To: ENTEGRIS, INC.; POCO GRAPHITE, INC.; ATMI, INC.; ATMI PACKAGING, INC.; ADVANCED TECHNOLOGY MATERIALS, INC.
Reel/Frame 047477/0151 →