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Synchrotron-based XPS and NEXAFS study of surface chemical species during electrochemical oxidation of chalcopyrite

机译:基于同步加速器的XPS和NEXAFS研究黄铜矿的电化学氧化过程中表面化学物质

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摘要

The surface chemical information of massive chalcopyrite electrode during electrochemical oxidation was studied by SXPS, NEXAFS and Raman spectroscopy. The electrochemical studies show that there was an activated region for chalcopyrite anodic dissolution between 550 and 630 mV (vs. Ag/AgCI), accompanied by two passive regions nearby. The spectroscopic studies suggest a thin film of non-stoichiometric sulfur-rich layer formed in the first passive region, likely to be responsible for the passivation. In the active region, species and covellite were also found, which could be the cause of the potential surge. When the potential was increased to 650 my, another passive region appeared. At the same time, S-2(2-) and covellite started to dissolve, leaving a highly metal deficient polysulfide and elemental sulfur layer on the chalcopyrite surface. (C) 2015 Elsevier B.V. All rights reserved.
机译:通过SXPS,NEXAFS和拉曼光谱研究了块状黄铜矿电极在电化学氧化过程中的表面化学信息。电化学研究表明,在550至630 mV(vs。Ag / AgCl)之间存在一个黄铜矿阳极溶解的活化区,附近有两个钝化区。光谱研究表明在第一钝化区域中形成的非化学计量的富硫层薄膜很可能是钝化的原因。在活动区域​​,还发现了物种和陨石,这可能是潜在激增的原因。当电势增加到650 my时,出现了另一个无源区域。同时,S-2(2-)和贝壳铝石开始溶解,在黄铜矿表面上留下了高度缺乏金属的多硫化物和元素硫层。 (C)2015 Elsevier B.V.保留所有权利。

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