SURFACE-ANALYSIS STUDIES OF COPPER CHEMICAL VAPOR-DEPOSITION FROM 1,5-CYCLOOCTADIENE-COPPER(I)-HEXAFLUOROACETYLACETONATE

被引:35
作者
COHEN, SL
LIEHR, M
KASI, S
机构
来源
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS | 1992年 / 10卷 / 04期
关键词
D O I
10.1116/1.577685
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The chemical vapor deposition of Cu from the 1,5-cyclooctadiene copper(I) hexafluoroacetylacetonate (COD-Cu-hfac) precursor has been studied using x-ray photoelectron spectroscopy, high-resolution electron energy-loss spectroscopy, and in situ reactor growth. Cu films are reproducibly grown on a Ag seed layer with resistivities of 2.0-2.4-mu-OMEGA cm with a deposition rate of 30-80 angstrom/min at 180-degrees-C. After deposition, the surface of the Cu is covered by some adsorbed precursor fragments and residual hydrocarbon. Upon heating in vacuum, the precursor desorbs leaving behind about 3-5 angstrom carbon. Incorporation of carbon, oxygen, and fluorine into the bulk of the Cu films is limited to 1% or less. The reactive sticking coefficient of the COD-Cu-hfac molecule during deposition is estimated to be approximately 1 X 10(-3) at 180-degrees-C. Cu grows somewhat selectively on metal relative to oxide surfaces at 180-degrees-C. Room temperature adsorption of the precursor on Ag leads to dissociation of the molecule and loss of the COD ligand. The stoichiometry of the surface complex corresponds to Cu(I)-hfac. Heating the surface to > 170-degrees-C leads to desorption of the surface hfac ligand. This is consistent with a bimolecular disproportionation reaction in which 2 Cu(I)-hfac species react to form a volatile Cu(hfac)2 complex and a reduced Cu atom.
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页码:863 / 868
页数:6
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