US2012070582A1PendingUtilityA1
Deposition of ternary oxide films containing ruthenium and alkali earth metals
Est. expiryMar 26, 2028(~1.7 yrs left)· nominal 20-yr term from priority
C23C 16/40C23C 16/45553C23C 16/56C23C 16/45525C23C 16/44H10P 14/24
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Claims
Abstract
Methods and compositions for the deposition of ternary oxide films containing ruthenium and an alkali earth metal.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for forming a ternary oxide film on one or more substrates; comprising:
a) providing at least one substrate disposed in a reactor; b) introducing a ruthenium precursor in vapor form into the reactor; wherein the ruthenium precursor is selected from the group consisting of: ruthenium tetraoxide; ruthenium(ethylcyclopentadienyl) 2 ; ruthenium(CO) 3 (1-methyl-1,4-cyclohexadiene); (ethylcyclopentadienyl)ruthenium(dimethylpentadienyl); and ruthenium(toluene)(1,4-cyclohexadiene); c) introducing an alkali earth metal precursor in vapor form into the reactor; wherein the alkali earth metal precursor is selected from the group consisting of Ca(iPr 3 Cp) 2 (THF) z ; Sr(iPr 3 Cp) 2 (THF) z ; Ba(iPr 3 Cp) 2 (THF) z ; Ca(iPr 3 Cp) 2 (DME) z ; Sr(iPr 3 Cp) 2 (DME) z ; Ba(iPr 3 Cp) 2 (DME) z ; Ca(iPr 3 Cp) 2 , Sr(iPr 3 Cp) 2 , Ba(iPr 3 Cp) 2 , Ca(tBu 3 Cp) 2 (THF) z ; Sr(tBu 3 Cp) 2 (THF) z ; Ba(tBu 3 Cp) 2 (THF) z ; Ca(tBu 3 Cp) 2 (DME) z ; Sr(tBu 3 Cp) 2 (DME) z ; Ba(tBu 3 Cp) 2 (DME) z ; Ca(tBu 3 CP) 2 , Sr(tBu 3 Cp) 2 , and Ba(tBu 3 Cp) 2 ; and wherein 0≦z≦3 d) depositing through an atomic layer deposition (ALD) process at least part of the ruthenium and alkali earth metal precursors to form a ternary oxide film on at least one of the substrates.
2 . The method of claim 1 , wherein the alkali earth metal precursor has a melting point of less than about 100° C.
3 . The method of claim 4 , wherein the alkali earth metal precursor is a liquid at about 25° C.
4 . The method of claim 1 , wherein the alkali earth metal precursor or the ruthenium precursor is initially supplied dissolved in a solvent, wherein the solvent has a boiling point greater than the melting point of the precursor dissolved therein.
5 . The method of claim 8 , where the solvent has a boiling point greater than about 100° C.
6 . The method of claim 1 , further comprising introducing an oxygen containing reactant into the reactor; wherein the reactant comprises at least one member selected from: O 2 ; O 3 ; H 2 O; H 2 O 2 ; N 2 O; NO; NO 2 ; and mixtures thereof.
7 . The method of claim 1 , further comprising depositing the precursors to form the ternary oxide film through either a chemical vapor deposition (CVD) process or an atomic layer deposition (ALD) process.
8 . The method of claim 7 , wherein the deposition process is performed at temperature between about 100° C. and about 500° C.
9 . The method of claim 8 , further comprising post-treating the ternary film in oxidizing atmosphere, wherein the post treating occurs at a temperature higher than that of the deposition process.Cited by (0)
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