Nanoscale electrochemistry

被引:67
|
作者
Schuster, R [1 ]
Kirchner, V [1 ]
Xia, XH [1 ]
Bittner, AM [1 ]
Ertl, G [1 ]
机构
[1] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
关键词
D O I
10.1103/PhysRevLett.80.5599
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
The lateral extension of electrochemically induced surface modifications is usually determined by the macroscopic size of the electrodes and the diffusion length of the reacting species. To overcome this constraint, we conducted an electrochemical reaction far from equilibrium. We applied short voltage pulses (less than or equal to 100 ns, up to +/-4 V) to a scanning tunneling microscope tip while imaging a Au(111) surface in concentrated electrolytes. They lead either to hole formation by anodic dissolution of the Au or to cathodic deposition of Cu islands (in the Cu2+ containing electrolyte), both of nanometer extension.
引用
收藏
页码:5599 / 5602
页数:4
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