Precursors and methods for atomic layer deposition of transition metal oxides
US-10344378-B2 · Jul 9, 2019 · US
US11555242B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11555242-B2 |
| Application number | US-201916460139-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 2, 2019 |
| Priority date | Feb 25, 2010 |
| Publication date | Jan 17, 2023 |
| Grant date | Jan 17, 2023 |
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Methods are provided herein for forming transition metal oxide thin films, preferably Group IVB metal oxide thin films, by atomic layer deposition. The metal oxide thin films can be deposited at high temperatures using metalorganic reactants. Metalorganic reactants comprising two ligands, at least one of which is a cycloheptatriene or cycloheptatrienyl (CHT) ligand are used in some embodiments. The metal oxide thin films can be used, for example, as dielectric oxides in transistors, flash devices, capacitors, integrated circuits, and other semiconductor applications.
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We claim: 1. A method for synthesizing a Zr or Hf compound, comprising: combining a catalyst and cycloheptatriene in a container comprising magnesium to form a reaction mixture; and adding a transition metal precursor comprising Zr or Hf to the reaction mixture, wherein the Zr or Hf compound is (MeCp)ZrCHT, where Cp is cyclopentadienyl and CHT is cycloheptatrienyl, wherein the Zr or Hf compound has the formula (R 1 R 2 R 3 R 4 R 5 R 6 R 7 )CHT-M-CHT(R 8 R 9 R 10 R 11 R 12 R 13 R 14 ), where M is Zr or Hf, and R 1-14 are independently H or an alkyl group, wherein the Zr or Hf compound has the formula (R 1 R 2 R 3 R 4 R 5 R 6 R 7 )CHT-M-CHD(R 8 R 9 R 10 R 11 R 12 R 13 R 14 R 15 R 16 ), where M is Zr or Hf, CHD is cycloheptadienyl, and R 1-16 are independently H or an alkyl group, or wherein the Zr or Hf compound has the formula (R 1 R 2 R 3 R 4 R 5 R 6 R 7 R 8 )X-M-X(R 9 R 10 R 11 R 12 R 13 R 14 R 15 R 16 ), where M is Zr or Hf, R 1-16 are independently H or an alkyl group, and X is cycloheptatriene. 2. The method of claim 1 , wherein the transition metal precursor is a transition metal halide. 3. The method of claim 2 , wherein the transition metal precursor is a transition metal chloride. 4. The method of claim 1 , wherein the transition metal precursor is a transition metal halide THF adduct. 5. The method of claim 1 , wherein the transition metal precursor is in solution with THF. 6. The method of claim 1 , wherein the transition metal precursor is added to the reaction mixture over a one hour period. 7. The method of claim 1 , wherein tetrahydrofuran is combined with the catalyst and cycloheptatriene in forming the reaction mixture. 8. The method of claim 1 , wherein the catalyst is ferric chloride. 9. The method of claim 1 , wherein the magnesium is in the form of magnesium chips or turnings. 10. The method of claim 1 , wherein the Zr of Hf compound is a liquid. 11. The method of claim 1 , wherein the Zr of Hf compound is a solid. 12. The method of claim 1 , wherein the Zr or Hf compound has the formula C 7 H 7 -M-L or ((CH 3 ) 3 C 7 H 4 )-M-L.
characterized by the ALD cycle, e.g. different flows or temperatures during half-reactions, unusual pulsing sequence, use of precursor mixtures or auxiliary reactants or activations · CPC title
Oxides · CPC title
Producing by vapour phase processes, e.g. halide oxidation · CPC title
of refractory metals or yttrium · CPC title
characterized by the use of precursors specially adapted for ALD · CPC title
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