Precursors for chemical vapor deposition
Ti, Zr Hf and La precursors for use in MOCVD techniques have a ligand of the general formula OCR 1 (R 2 )CH 2 X, wherein R 1 is H or an alkyl group, R 2 is an optionally substituted alkyl group and X is selected from OR and NR 2 , wherein R is an alkyl group or a substituted alkyl group.
1. A precursor for use in a MOCVD process having the following general formula:
M(L) x [OCR 1 (R 2 )CH 2 X] 4-x
wherein M is a metal selected from Ti, Zr and Hf, L is a ligand, x is a number from 0 through 3 inclusive, R 1 is H or an alkyl group, R 2 is an optionally substituted alkyl group, and X is OR, wherein R is an alkyl group or a substituted alkyl group.
2. The precursor according to claim 1 , wherein the ligand L is an alkoxy group having from 1 to 4 carbon atoms.
3. precursor according to claim 2 , wherein the ligand L is selected from tertiary-butoxide and iso-propoxide.
4. The precursor according to claim 1 , wherein [OCR 1 (R 2 )CH 2 X] is 1-methoxy-2-methyl-2-propanolate.
5. The precursor according to claim 1 , wherein [OCR 1 (R 2 )CH 2 X] is selected from the group consisting of OCH(Me)CH 2 OMe, OCEt 2 CH 2 OMe, OCH(Bu t )CH 2 OEt, OC(Bu t ) 2 CH 2 OEt, OC(Pr i ) 2 CH 2 OEt, OC(Pr i ) 2 CH 2 OC 2 H 4 OMe and OC(Bu t )(CH 2 Opr i ) 2 .
6. The precursor according to claim 1 , wherein said precursor is Zr(OBu t ) 2 (mmp) 2 .
7. The precursor according to claim 1 , wherein said precursor is Zr(mmp) 4 .
8. The precursor according to claim 1 , wherein said precursor is Hf(OBu t ) 2 (mmp) 2 .
9. The precursor according to claim 1 , wherein said precursor is Hf(mmp) 4 .
10. A method of making a Ti-. Zr- or Hf-based precursor for use in a MOCVD process comprising reacting HOCR 1 (R 2 )CH 2 X with the corresponding metal alkoxide or metal alkylamide in appropriate molar proportions; wherein R 1 is H or an alkyl group, R 2 is an optionally substituted alkyl group and X is selected from OR and NR 2 wherein R is an alkyl group or a substituted alkyl group.
11. A precursor for use in a MOCVD process having the following general formula:
La[OCR 1 (R 2 )CH 2 X] 3
wherein R 1 is H or an alkyl group, R 2 is an optionally substituted alkyl group and X is selected from OR and NR 2 , wherein R is an alkyl group or a substituted alkyl group.
12. The precursor according to claim 11 , wherein [OCR 1 (R 2 )CH 2 X] is 1-methoxy-2-methyl-2-propanolate.
13. The precursor according to claim 12 , wherein [OCR 1 (R 2 )CH 2 X] is selected from the group consisting of OCH(Me)CH 2 OMe, OCEt 2 CH 2 OMe, OCH(Bu t )CH 2 OEt, OC(Bu t ) 2 CH 2 OEt, OC(Pr i ) 2 CH 2 OEt, OCH(Bu t )CH 2 NEt 2 , OC(Pr i ) 2 CH 2 OC 2 H 4 OMe and OC(Bu t )(CH 2 OPr i ) 2 .
14. A method of making a precursor as claimed in claim 11 comprising reacting HOCR 1 (R 2 )CH 2 X with La{N(SiMe 3 ) 2 } 3 in appropriate molar proportions.
15. A method of depositing single or mixed oxide layers or films by MOCVD, in which a precursor is contained in a metalorganic bubbler; or by liquid injection MOCVD, in which a precursor is dissolved in an appropriate inert organic solvent and then evaporated into the vapor phase using a heated evaporator, wherein at least one of the precursors is as defined in claim 1 .
16. A method of providing a ZrO 2 , ZrSO, HfO 2 , HfSO, TiO 2 , or TiSO film on a silicon substrate, the method comprising using metalorganic chemical vapor deposition to deposit the metal oxide, wherein the deposition utilizes a precursor material of the formula:
M(L) x [OCR 1 (R 2 )CH 2 X] 4-x
wherein M is a metal selected from Ti, Zr and Hf, L is a ligand, x is a number from 0 through 3 inclusive, R 1 is H or an alkyl group, R 2 is an optionally substituted alkyl group, and X is selected from OR and NR 2 , wherein R is an alkyl group or a substituted alkyl group.
17. A method according to claim 16 , wherein the ligand L is an alkoxy group having from 1 to 4 carbon atoms.
18. A method of providing a LaO 2 or LaSO film on a silicon substrate, the method comprising using metalorganic chemical vapor deposition to deposit the metal oxide, wherein the deposition utilizes a precursor material of the formula:
La[OCR 1 (R 2 )CH 2 X ] 3
wherein R 1 is H or an alkyl group, R 2 is an optionally substituted alkyl group and X is selected from OR and NR 2 , wherein R is an alkyl group or a substituted alkyl group.
19. The method according to claim 18 , wherein said precursor is La(mmp) 3 .