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酸性电解质中硝酸盐还原过程中Cu(111)和Cu(100)的差异反应性。

Differential reactivity of Cu(111) and Cu(100) during nitrate reduction in acid electrolyte.

作者信息

Bae Sang-Eun, Gewirth Andrew A

机构信息

Department of Chemistry, University of Illinois, Urbana IL 61801, USA.

出版信息

Faraday Discuss. 2008;140:113-23; discussion 185-207. doi: 10.1039/b803088j.

Abstract

The interactions of nitrate with Cu(100) and Cu(111) in acidic solution are studied by cyclic voltammetry (CV) and in situ electrochemical scanning tunneling microscopy (EC-STM). CV results show that reduction of nitrate on Cu(111) commences at 0.0 V vs. Ag/AgCl while the corresponding potential is -0.3 V on Cu(100). EC-STM images show that the terrace of both Cu(111) and Cu(100) are atomically flat at potentials more negative than -0.7 V. The Cu(100) surface exhibits flat terraces throughout the entire cathodic potential range. Close to OCP, step edges start to corrode. In contrast to Cu(100), the first layer of Cu(111) is converted to an atomically rough and defected surface-associated with nascent surface oxidation at potentials positive of -0.7 V. This surface oxidation is correlated with nitrate reduction.

摘要

采用循环伏安法(CV)和原位电化学扫描隧道显微镜(EC-STM)研究了酸性溶液中硝酸盐与Cu(100)和Cu(111)的相互作用。CV结果表明,相对于Ag/AgCl,硝酸盐在Cu(111)上的还原起始于0.0 V,而在Cu(100)上相应的电位为-0.3 V。EC-STM图像显示,在电位比-0.7 V更负时,Cu(111)和Cu(100)的平台在原子尺度上都是平整的。在整个阴极电位范围内,Cu(100)表面呈现出平整的平台。接近开路电位(OCP)时,台阶边缘开始腐蚀。与Cu(100)不同,在电位高于-0.7 V时,Cu(111)的第一层会转变为与新生表面氧化相关的原子粗糙且有缺陷的表面。这种表面氧化与硝酸盐还原相关。

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