IP Library Granted Patent US 11,152,205
Granted Patent B2
US 11,152,205 · App. 15/913,218 · Granted Oct 19, 2021

Silicon chalcogenate precursors comprising a chemical formula of si(XR1)nR24-n and methods of forming the silicon chalcogenate precursors

Inventors: Timothy A. Quick (Boise, ID); Sumeet C. Pandey (Boise, ID); Stefan Uhlenbrock (Boise, ID)
Assignee: Micron Technology, Inc.
H01L21/02208C01B21/068C07F7/025C09D7/63C23C16/00C23C16/045C23C16/345C23C16/45525H01L21/0217H01L21/0228H01L21/76831
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Quick Facts
Patent No.
US 11,152,205
App. No.
15/913,218
Granted
Oct 19, 2021
Kind
B2
Abstract

A silicon chalcogenate precursor comprising the chemical formula of Si(XR 1 ) n R 2 4-n , where X is sulfur, selenium, or tellurium, R 1 is hydrogen, an alkyl group, a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, each R 2 is independently hydrogen, an alkyl group, a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, and n is 1, 2, 3, or 4. Methods of forming the silicon chalcogenate precursor, methods of forming silicon nitride, and methods of forming a semiconductor structure are also disclosed.

Claims (32)

1. A silicon chalcogenate precursor comprising:

the chemical formula of Si(XR 1 ) n R 2 4-n , where X is sulfur, selenium, or tellurium, R 1 is hydrogen, a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, each R 2 is independently a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, at least one R 2 is different from R 1 , and n is 1, 2, or 3, wherein when R 1 is hydrogen, n is 2, 3, or 4.

2. The silicon chalcogenate precursor of claim 1 , wherein the silicon chalcogenate precursor comprises:

and each of R 3 and R 4 is independently a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, or a halide group.

3. The silicon chalcogenate precursor of claim 2 , wherein R 1 comprises a halogen atom indirectly bonded to the silicon atom and at least one of R 2 , R 3 , or R 4 comprises a halogen atom directly or indirectly bonded to the silicon atom.

4. The silicon chalcogenate precursor of claim 2 , wherein R 1 comprises a halogen atom indirectly bonded to the silicon atom and each of R 2 , R 3 , and R 4 comprises a halogen atom directly or indirectly bonded to the silicon atom.

5. The silicon chalcogenate precursor of claim 1 , wherein the silicon chalcogenate precursor comprises Si(XR 1 )(R 2 )(R 3 )(R 4 ), Si(XR 1 )(XR 2 )(R 3 )(R 4 ), Si(XR 1 )(R 2 )(XR 3 )(R 4 ), Si(XR 1 )(XR 2 )(R 3 )(XR 4 ), Si(XR 1 )(XR 2 )(XR 3 )(R 4 ), Si(XR 1 )(R 2 )(XR 3 )(XR 4 ), or Si(XR 1 )(XR 2 )(XR 3 )(XR 4 ) and each of R 3 and R 4 is independently a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, or a halide group.

6. The silicon chalcogenate precursor of claim 5 , where each X is the same.

7. The silicon chalcogenate precursor of claim 5 , where each X is different.

8. The silicon chalcogenate precursor of claim 1 , wherein the silicon chalcogenate precursor comprises Si(XR 1 )(XR 2 )(XR 3 )(XR 4 ), where X is sulfur or tellurium, each X is the same, and each of R 3 and R 4 is independently a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, or a halide group.

9. The silicon chalcogenate precursor of claim 1 , wherein the silicon chalcogenate precursor comprises at least one halogen atom.

10. The silicon chalcogenate precursor of claim 1 , wherein R 1 comprises a halogen atom indirectly bonded to the silicon atom and R 2 comprises a halogen atom directly or indirectly bonded to the silicon atom.

11. A method of forming a silicon chalcogenate precursor, comprising:

reacting an organolithium reagent with a chalcogen source compound to produce an organolithium chalcogen compound; and

reacting the organolithium chalcogen compound with a silicon halide compound to form a silicon chalcogenate precursor comprising the chemical formula of Si(XR 1 ) n R 2 4-n , where X is sulfur, selenium, or tellurium, R 1 is hydrogen, a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, each R 2 is independently a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, at least one R 2 is different from R 1 , and n is 1, 2, or 3, wherein when R 1 is hydrogen, n is 2, 3, or 4.

12. The method of claim 11 , wherein reacting an organolithium reagent with a chalcogen source compound comprises reacting methyllithium with elemental selenium to form lithium methylselenide.

13. The method of claim 11 , wherein reacting an organolithium reagent with a chalcogen source compound comprises reacting the organolithium reagent with a chalcogen source compound comprising sulfur, selenium, tellurium, or combinations thereof.

14. The method of claim 11 , wherein reacting the organolithium chalcogen compound with a silicon halide compound comprises reacting the organolithium chalcogen compound and the silicon halide compound at below room temperature.

15. The method of claim 11 , wherein reacting the organolithium chalcogen compound with a silicon halide compound comprises reacting the organolithium chalcogen compound and the silicon halide compound at below 0° C.

16. The method of claim 11 , wherein reacting the organolithium chalcogen compound with a silicon halide compound comprises reacting the organolithium chalcogen compound and the silicon halide compound at below −76° C.

17. The method of claim 11 , wherein reacting the organolithium chalcogen compound with a silicon halide compound comprises reacting the organolithium chalcogen compound with a compound of silicon and fluorine, a compound of silicon and chlorine, a compound of silicon and bromine, or a compound of silicon and iodine.

18. The method of claim 11 , wherein reacting the organolithium chalcogen compound with a silicon halide compound comprises reacting the organolithium chalcogen compound with silicon tetrachloride to form the silicon chalcogenate precursor.

19. A method of forming a silicon chalcogenate precursor, comprising:

reacting a Grignard reagent with a chalcogen source compound to produce an organometallic chalcogen compound; and

reacting the organometallic chalcogen compound with a silicon halide compound to form a silicon chalcogenate precursor comprising the chemical formula of Si(XR 1 ) n (R 2 ) 4-n , where X is sulfur, selenium, or tellurium, R 1 is hydrogen, an alkyl group, a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, R 2 is independently hydrogen, an alkyl group, a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, n is 1, 2, 3, or 4, R 1 comprises a halogen atom indirectly bonded to the silicon atom, and at least one R 2 comprises a halogen atom indirectly or directly bonded to the silicon atom.

20. A silicon chalcogenate precursor comprising:

the chemical formula of Si(XR 1 ) n R 2 4-n , where X is sulfur, selenium, or tellurium, R 1 is hydrogen, an alkyl group, a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, R 2 is independently hydrogen, an alkyl group, a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, n is 1, 2, 3, or 4, R 1 comprises a halogen atom indirectly bonded to the silicon atom, and at least one R 2 comprises a halogen atom directly or indirectly bonded to the silicon atom.

21. The silicon chalcogenate precursor of claim 20 , wherein only one R 1 comprises a halogen atom indirectly bonded to the silicon atom.

22. A silicon chalcogenate precursor comprising:

the chemical formula of Si(XR 1 )(R 2 )(R 3 )(R 4 ), where X is sulfur, selenium, or tellurium, R 1 is hydrogen, an alkyl group, a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, R 2 , R 3 , and R 4 are independently hydrogen, an alkyl group, a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, and at least one of R 2 , R 3 , or R 4 comprises a halogen atom directly bonded to the silicon atom.

23. A silicon chalcogenate precursor comprising:

the chemical formula of Si(XR 1 )(R 2 )(R 3 )(R 4 ), where X is sulfur, selenium, or tellurium, R 1 is hydrogen, an alkyl group, a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, R 2 , R 3 , and R 4 are independently hydrogen, an alkyl group, a substituted alkyl group, an alkoxide group, a substituted alkoxide group, an amide group, a substituted amide group, an amine group, a substituted amine group, or a halogen group, and each of R 2 , R 3 , or R 4 comprises a halogen atom directly bonded to the silicon atom.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Nov 12, 2019
From: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
To: MICRON TECHNOLOGY, INC.; MICRON SEMICONDUCTOR PRODUCTS, INC.
Reel/Frame 051028/0001 →
RELEASE OF SECURITY INTEREST Recorded Oct 10, 2019
From: MORGAN STANLEY SENIOR FUNDING, INC., AS COLLATERAL AGENT
To: MICRON TECHNOLOGY, INC.
Reel/Frame 050709/0965 →
SECURITY INTEREST Recorded Jul 13, 2018
From: MICRON TECHNOLOGY, INC.; MICRON SEMICONDUCTOR PRODUCTS, INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 047540/0001 →
SUPPLEMENT NO. 8 TO PATENT SECURITY AGREEMENT Recorded May 7, 2018
From: MICRON TECHNOLOGY, INC.
To: MORGAN STANLEY SENIOR FUNDING, INC., AS COLLATERAL AGENT
Reel/Frame 046084/0955 →
Continuity (2)
Division 15215102 · Jul 20, 2016
Related Publication 20180197735A1 · Jul 12, 2018