Selective deposition of metal oxide
US-2024282572-A1 · Aug 22, 2024 · US
US9941114B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9941114-B2 |
| Application number | US-201514611691-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 2, 2015 |
| Priority date | Mar 10, 2014 |
| Publication date | Apr 10, 2018 |
| Grant date | Apr 10, 2018 |
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An organometallic precursor is represented by a chemical formula of Xn(M)(R1)m(R2)k. M is a central metal. X is a ligand of M and one of 6,6-dimethylfulvenyl, indenyl, cyclopentadienyl and cyclopentadienyl substituted with an amino group. R1 and R2 are ligands of M, and each independently an amino group or an ethylenediamino group. Each n, m and k is a positive integer, and a sum of n, m and k is equal to 3 or 4.
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What is claimed is: 1. An organometallic precursor represented by Chemical Formula 1: X n (M)(R1) m (R2) k [Chemical Formula 1] wherein M is a central metal, X is a ligand of M and one of 6,6-dimethylfulvenyl, indenyl, cyclopentadienyl and cyclopentadienyl substituted with a first amino group, R1 and R2 are ligands of M, and each independently a second amino group or an ethylenediamino group, each one of n, m and k is a positive integer, and a sum of n, m and k is equal to one of 3 and 4. 2. The organometallic precursor of claim 1 , wherein the central metal is one of zirconium, hafnium and titanium. 3. The organometallic precursor of claim 1 , wherein the second amino group and the ethylenediamino group of R1 and R2 each independently include a C 1 -C 4 alkyl substituent. 4. The organometallic precursor of claim 1 , wherein X is 6,6-dimethylfulvenyl or indenyl, R1 and R2 are each independently the second amino group, n is equal to 1, and m+k is equal to 3. 5. The organometallic precursor of claim 1 , wherein X comprises cyclopentadienyl substituted with the first amino group, and X is a multidendate ligand. 6. The organometallic precursor of claim 5 , wherein the organometallic precursor is represented by Structural Formula 1: wherein M is a central metal, R3 and R4 are each independently methyl or ethyl, and R5 is a C 1 -C 4 alkyl. 7. The organometallic precursor of claim 1 , wherein R1 is the second amino group, R2 is the ethylenediamino group, and each of n, m and k is equal to 1. 8. The organometallic precursor of claim 7 , wherein the organometallic precursor is represented by Structural Formula 2: wherein M is a central metal, R3 and R4 are each independently methyl or ethyl, and R6 is a C1-C4 alkyl. 9. A method of forming a thin layer, comprising: providing a deposition source including an organometallic precursor represented by Chemical Formula 1 on a substrate; and providing a reactive gas on the substrate to react with the deposition source, X n (M)(R1) m (R2) k [Chemical Formula 1] wherein M is a central metal, X is a ligand of M and one of 6,6-dimethylfulvenyl, indenyl, cyclopentadienyl and cyclopentadienyl substituted with a first amino group, R1 and R2 are ligands of M, and each independently a second amino group or an ethylenediamino group, and each of n, m and k is a positive integer, and a sum of n, m and k is equal to one of 3 and 4. 10. The method of claim 9 , wherein the central metal is one of zirconium, hafnium and titanium. 11. The method of claim 10 , wherein the deposition source includes at least two organometallic precursors, the central metals of which are different from each other. 12. The method of claim 9 , wherein the deposition source further includes a silicon compound. 13. The method of claim 9 , wherein the reactive gas includes at least one of an oxidizing agent, a reducing agent and a nitridating agent. 14. The method of claim 9 , wherein the reactive gas and the deposition source are configured to react with each other at a temperature ranging from about 200° C. to about 325° C. 15. The method of claim 9 , wherein the organometallic precursor includes at least one compound from a plurality of compounds represented by Structural Formulas 1 to 4: wherein M is a central metal, R3 and R4 are each independently methyl or ethyl, and R5 and R6 are each independently a C 1 -C 4 alkyl. 16. A deposition structure comprising: a substrate; a deposition layer on the substrate, the deposition layer including an organometallic precursor represented by the following formula: X n (M)(R1) m (R2) k M being a metal, X being a ligand of M and one of 6,6-dimethylfulvenyl, indenyl, cyclopentadienyl and cyclopentadienyl substituted with a first amino group, R1 and R2 being ligands of M, and each independently being a second amino group or an ethylenediamino group, each one of n, m and k being a positive integer, and a sum of n, m and k is equal to one of 3 and 4. 17. The deposition structure of claim 16 , wherein a thickness of the deposition layer is substantially uniform when deposited on a concave surface. 18. The deposition structure of claim 16 , wherein the metal is one of zirconium, hafnium and titanium. 19. The deposition structure of claim 16 , wherein the organometallic precursor is represented by Structural Formula 1: wherein M is a central metal, R3 and R4 are each independently methyl or ethyl, and R5 is a C 1 -C 4 alkyl. 20. The deposition structure of claim 16 , wherein the organometallic precursor is represented by Structural Formula 2: wherein M is a central metal, R3 and R4 are each independently methyl or ethyl, and R6 is a C1-C4 alkyl.
the material containing zirconium, e.g. ZrO2 · CPC title
the encapsulations being directly on the semiconductor body (H10W74/134 takes precedence) · CPC title
comprising oxides, nitrides or carbides, e.g. ceramics or glasses · CPC title
deposition by cyclic CVD, e.g. ALD, ALE or pulsed CVD · CPC title
Electricity · mapped topic
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