X-ray absorption fine structure study of amorphous metal oxide thin films prepared by photochemical metalorganic deposition

被引:31
作者
Trudel, Simon [1 ,5 ]
Crozier, E. Daryl [2 ]
Gordon, Robert A. [2 ]
Budnik, Peter S. [2 ]
Hill, Ross H. [3 ,4 ]
机构
[1] Univ Calgary, Dept Chem, Calgary, AB T2N 1N4, Canada
[2] Simon Fraser Univ, Dept Phys, Burnaby, BC V5A 1S6, Canada
[3] Simon Fraser Univ, Dept Chem, Burnaby, BC V5A 1S6, Canada
[4] Simon Fraser Univ, LABS 4D, Burnaby, BC V5A 1S6, Canada
[5] SFU Chem 4D LABS, Burnaby, BC, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Amorphous metal oxides; X-ray absorption; Thin films; XANES; EXAFS; XAFS; Solid-state photochemistry; MAGNETIC-PROPERTIES; OXIDATION-STATE; PHOTOLITHOGRAPHIC DEPOSITION; ELECTRONIC-STRUCTURE; ORGANIC DEPOSITION; CRYSTAL-STRUCTURE; TRANSITION-METAL; EDGE XAS; XANES; IRON;
D O I
10.1016/j.jssc.2011.03.015
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The oxidation state and local geometry of the metal centers in amorphous thin films of Fe2O3(Fe3+ oxidation state), CoFe2O4 (Co2+/Fe3+ oxidation states), and Cr2O3 (Cr3+ oxidation state) are determined using K edge X-ray absorption near-edge structure (XANES) spectroscopy and extended X-ray absorption fine structure (EXAFS) spectroscopy. The metal oxide thin films were prepared by the solid-state photochemical decomposition of the relevant metal 2-ethylhexanoates, spin cast as thin films. No peaks are observed in the X-ray diffraction patterns, indicating the metal oxides are X-ray amorphous. The oxidation state of the metals is determined from the edge position of the K absorption edges, and in the case of iron-containing samples, an analysis of the pre-edge peaks. In all cases, the EXAFS analysis indicates the first coordination shell consists of oxygen atoms in an octahedral geometry, with a second shell consisting of metals. No higher shells are observed beyond 3.5 angstrom for all samples, indicating the metal oxides are truly amorphous, consistent with X-ray diffraction results. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:1025 / 1035
页数:11
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