Dealloying of CuxAu studied by hard X-ray photoelectron spectroscopy

被引:3
|
作者
Rajput, Parasmani [1 ]
Gupta, Ajay [2 ]
Detlefs, Blanka [1 ]
Kolb, Dieter M. [3 ]
Potdar, Satish [2 ]
Zegenhagen, Joerg [1 ]
机构
[1] European Synchrotron Radiat Facil, F-38043 Grenoble, France
[2] UGC DAE Consortium Sci Res, Indore 452017, Madhya Pradesh, India
[3] Univ Ulm, Inst Elect, D-89069 Ulm, Germany
关键词
Photoelectron spectroscopy; Hard X-ray; HAXPES; Corrosion of alloys; BINDING-ENERGY SHIFT; CU-AU ALLOYS; SURFACE SEGREGATION; ANODIC-DISSOLUTION; CORROSION; DEPENDENCE; COPPER;
D O I
10.1016/j.elspec.2013.01.003
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
We studied pristine and leached ultra-thin CuxAu (x approximate to 4)) films by hard X-ray photoelectron spectroscopy. The Au 4f and Cu 3s core levels show a shift in binding energy which is opposite to expected from the nobility of the elements, which is explained by charge transfer involving differently screening s and d valence levels of the elements [W. Eberhardt, S.C. Wu, R. Garrett, D. Sondericker, F. Jona, Phys. Rev. B 31 (1985) 8285]. The magnitude of the chemical shifts of the metal lines is strongly influenced by the finite size and disorder of the films. Angular dependent photoelectron emission allowed to assess the alloy composition as a function of depth larger than 5 nm. The potential controlled dealloying proceeds into depth like a spinodal decomposition with Cu going into solution and the remaining Au accumulating in the surface region. The compositional gradient did not lead to a significant broadening of the metal photoelectron lines suggesting a non-local screening mechanism. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:289 / 294
页数:6
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