Ag diffusion in amorphous As50Se50 films studied by XPS

被引:11
|
作者
Kalyva, M. [1 ,2 ]
Siokou, A. [1 ]
Yannopoulos, S. N. [1 ]
Wagner, T. [3 ,4 ]
Orava, J. [3 ,4 ]
Frumar, M. [3 ,4 ]
机构
[1] Fdn Res & Technol Hellas, Inst Chem Engn & High Temp Chem Proc FORTH ICE HT, GR-26504 Patras, Greece
[2] Univ Patras, Dept Chem Engn, GR-26504 Patras, Rio, Greece
[3] Univ Pardubice, Dept Gen & Inorgan Chem, Pardubice 53210, Czech Republic
[4] Univ Pardubice, Res Ctr, Pardubice 53210, Czech Republic
关键词
UPS/XPS; Chalcogenides; Photoinduced effects; XPS; CHALCOGENIDES; DISSOLUTION; ELECTRON;
D O I
10.1016/j.jnoncrysol.2009.04.052
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
X-ray photoelectron spectroscopy and depth profile analysis were used to investigate the X-ray-induced silver photodiffusion into an amorphous As50Se50 thin film. At the initial stages of irradiation an induction period was observed while core level spectra analysis revealed the existence of a mixed As-Se-Ag interlayer between the metal and the chalcogenide matrix. It was found that during the induction period this interlayer is enriched in silver and the existing As-Se-Ag intermediate species are transformed to Ag-Se-Ag that form the metal source for the effective silver photodiffusion. With further irradiation photodiffusion proceeds by the disruption of Ag-Se bonds and the recombination of As atoms with Se to stable As-Se units. Ultimately, silver concentration reaches a plateau when the diffusion stops. A separated Ag2Se phase on the film's surface is identified at this stage. Depth profile analysis shows that silver has been homogenously diffused into the chalcogenide matrix and the Ag2Se phase exists only at the top surface layers probably in the form of quasi-crystalline clusters that prohibit further Ag diffusion. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1844 / 1848
页数:5
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