4.6 Article

The influence of halides on the initial selective dissolution of Cu3Au (111)

期刊

ELECTROCHIMICA ACTA
卷 85, 期 -, 页码 384-392

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2012.08.059

关键词

Dealloying; Selective dissolution; Solid-electrolyte interface; Halide additives; Electrochemistry

资金

  1. International Max Planck Research School for Surface and Interface Engineering in Advanced Materials (IMPRS-SurMat)

向作者/读者索取更多资源

We report an electrochemical in situ X-ray diffraction (XRD) and ex situ atomic force microscopy (AFM) study on the influence of the halide additives bromide and iodide in comparison to chloride in 0.1 M H2SO4 solution on the selective dissolution of Cu3Au (1 1 1). Our results suggest that the addition of these halides have a pronounced effect on the dealloying process and lead to peculiar changes in the resulting surface morphologies. For an additive of bromide we observed (similar to an earlier study with chloride) a sequence of specific Au surface layers with an initial ultra-thin stacking-inverted Au-rich layer, subsequent pure Au islands, and finally substrate oriented nanometer-scale ligaments (nanoporosity). These structures occur with a negative shift in the transformation potentials compared to pure sulfuric acid solution. With an additive of iodide no stable passive Au film is formed and a porous surface was observed at relatively short times and low potentials. A precipitation of copper iodide (CuI) visible in the ex situ AFM images leads to the formation of surface porosity with bimodal length scales. (C) 2012 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据