Purified surface region of an oxide semiconductor, and method of near-surface purification
US-2024355884-A1 · Oct 24, 2024 · US
US9704713B1 · US · B1
| Field | Value |
|---|---|
| Publication number | US-9704713-B1 |
| Application number | US-201615091798-A |
| Country | US |
| Kind code | B1 |
| Filing date | Apr 6, 2016 |
| Priority date | Nov 26, 2008 |
| Publication date | Jul 11, 2017 |
| Grant date | Jul 11, 2017 |
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In one aspect, the present invention provides undoped and doped siloxanes, germoxanes, and silagermoxanes that are substantially free from carbon and other undesired contaminants. In a second aspect, the present invention provides methods for making such undoped and doped siloxanes, germoxanes, and silagermoxanes. In still another aspect, the present invention provides compositions comprising undoped and/or doped siloxanes, germoxanes, and silagermoxanes and a solvent, and methods for forming undoped and doped dielectric films from such compositions. Undoped and/or doped siloxane compositions as described advantageously provide undoped and/or doped dielectric precursor inks that may be employed in forming substantially carbon-free undoped and/or doped dielectric films.
Opening claim text (preview).
What is claimed is: 1. A siloxane, germoxane, or silagermoxane compound, comprising at least 7 units of the formula —(OA[O d H] 2 )— or —(OA[O d H] 3 ), where each instance of A is independently Si or Ge, and each instance of d is independently 0 or 1, and one or more units of the formula O c DR 1 p , where each instance of D is independently Sb, As, P, B or Al, each instance of p is independently an integer from 0 to 2, and each instance of R 1 is independently alkyl, aryl, aralkyl, H, OH or AR 2 , where R 2 is H, OH or —(OA) y (O c H) 2y+1 , y is an integer from 1 to 4, and each instance of c independently 0 or 1. 2. The compound of claim 1 , wherein A is Si. 3. The compound of claim 2 , having the formula -(c-(OA) q [O d H] 2q-x )—, where q is an integer from 7 to 12, and x is an integer from 0 to q. 4. The compound of claim 3 , wherein d=0. 5. The compound of claim 2 , having at least 15 units of the formula ═(OSi[O d H])—, —(OSi[O d H] 2 )— or —(OSi[O d H] 3 ). 6. The compound of claim 5 , wherein d=0. 7. The compound of claim 1 , wherein d=0. 8. The compound of claim 1 , having at least 15 units of the formula ═(OA[O d H])—, —(OA[O d H] 2 )— or —(OA[O d H] 3 ). 9. The compound of claim 8 , wherein d=0. 10. The compound of claim 8 , wherein D is B. 11. The compound of claim 8 , wherein D is P. 12. The compound of claim 8 , wherein R 1 is C 1 -C 6 alkyl or C 6 -C 12 aryl. 13. The compound of claim 8 , wherein R 1 is H or OH. 14. The compound of claim 1 , wherein D is B and c=0, or D is P and c=1. 15. The compound of claim 1 , wherein D is B. 16. The compound of claim 1 , wherein D is P. 17. The compound of claim 1 , wherein R 1 is C 1 -C 6 alkyl. 18. The compound of claim 1 , wherein R 1 is C 6 -C 12 aryl. 19. The compound of claim 18 , wherein R 1 is phenyl. 20. The compound of claim 1 , wherein R 1 is H or OH.
Thermal treatments, e.g. annealing or sintering · CPC title
the material containing Si, O and at least one of H, N, C, F or other non-metal elements, e.g. SiOC, SiOC:H or SiONC · CPC title
of treatments performed after formation of the materials · CPC title
using printing, e.g. ink-jet printing · CPC title
Liquid deposition, e.g. spin-coating, sol-gel techniques or spray coating · CPC title
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