电荷密度
电解质
相(物质)
同步加速器
表面电荷
材料科学
电荷(物理)
电化学
过渡金属
Atom(片上系统)
相变
电子密度
电极
散射
分析化学(期刊)
表层
化学
电子
图层(电子)
凝聚态物理
物理化学
纳米技术
光学
物理
生物化学
有机化学
量子力学
色谱法
计算机科学
嵌入式系统
催化作用
作者
Jia Wang,Alison J. Davenport,Hugh S. Isaacs,B. M. Ocko
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1992-03-13
卷期号:255 (5050): 1416-1418
被引量:127
标识
DOI:10.1126/science.255.5050.1416
摘要
Synchrotron surface x-ray scattering (SXS) studies have been carried out at the Au(111)/electrolyte interface to determine the influence of surface charge on the microscopic arrangement of gold surface atoms. At the electrochemical interface, the surface charge density can be continuously varied by controlling the applied potential. The top layer of gold atoms undergoes a reversible phase transition between the (1 × 1) bulk termination and a (23 × √3) reconstructed phase on changing the electrode potential. In order to differentiate the respective roles of surface charge and adsorbates, studies were carried out in 0.1 M NaF, NaCl, and NaBr solutions. The phase transition occurs at an induced surface charge density of 0.07 ± 0.02 electron per atom in all three solutions.
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