Optical and kinetic properties of cathodically deposited amorphous tungsten oxide films

被引:17
作者
Krasnov, Yu. S. [1 ]
Volkov, S. V. [1 ]
Kolbasov, G. Ya. [1 ]
机构
[1] Natl Acad Sci Ukraine, VI Vernadskii Inst Gen & Inorgan Chem, UA-03680 Kiev 142, Ukraine
关键词
amorphous semiconductors;
D O I
10.1016/j.jnoncrysol.2006.08.007
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Optical properties and the coloration-decoloration kinetics of electrochromic films of amorphous tungsten oxide (a-WO3), produced by cathodic deposition from a sodium tungstate based aqueous peroxide electrolyte, have been investigated. As films color in 1 N H2SO4, sequential appearance of bands with maxima at similar to 1 eV, 1.6 eV, 2 eV, and 2.4 eV is observed in their optical absorption and electrosorption spectra, is the same as in the case of reduction of nanosized hydrated-WO3 colloids with a gradual decrease in their size to that of 12-tungsten polyanions with Keggin structure, indicating the presence of such polytungstates in cathodically deposited a-WO3, too. When polytungstate is reduced by one electron, an absorption band with a maximum at similar to 1.6 eV appears in the optical spectrum of the film. This band corresponds to the optical excitation of charge transfer of the W5+ -> W6+ type between two adjacent tungsten atoms. The reduction of polytungstate by a second electron with potential shift towards more negative values is accompanied by the appearance of an analogous band with a maximum at similar to 2 eV. The reduction of such polytungstates involves participation of the bulk of injected electrons, indicating their dominate role in the nanostructure of the films investigated. The effective co-diffusion coefficient of electrons and protons in cathodically deposited a-WO3 exhibits a potential dependence with a maximum at 0.1 V against a silver-chloride electrode, where its value is similar to 10(-8) cm(2)/s. It has been shown that the decrease in this coefficient at potential values of over 0.1 V is caused by a decrease in electron mobility. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:3995 / 4002
页数:8
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