An in Situ STM and DTS Study of the Extremely Pure [EMIM]FAP/Au(111) Interface

被引:22
作者
Borisenko, Natalia [1 ,2 ]
El Abedin, Sherif Zein [1 ,2 ,3 ]
Endres, Frank [1 ,2 ]
机构
[1] Clausthal Univ Technol, Inst Particle Technol, D-38678 Clausthal Zellerfeld, Germany
[2] EFZN Goslar, D-38640 Goslar, Germany
[3] Natl Res Ctr, Electrochem & Corros Lab, Cairo, Egypt
关键词
cyclic voltammetry; interfaces; ionic liquids; scanning tunneling microscopy; surface analysis; ELECTRICAL DOUBLE-LAYER; STABLE IONIC LIQUIDS; ELECTRODEPOSITION; CAPACITANCE; AIR; TEMPERATURE; MICROSCOPY; ALUMINUM; AU(111); SURFACE;
D O I
10.1002/cphc.201100873
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Herein the structure of the interfacial layer between the air- and water-stable ionic liquid 1-ethyl-3-methylimidazolium tris(pentafluoroethyl)trifluorophosphate ([EMIM]FAP) and Au(111) is investigated using in situ scanning tunneling microscopy (STM), distance tunneling spectroscopy (DTS) and cyclic voltammetry (CV) measurements. The in situ STM measurements reveal that structured interfacial layers can be probed in both cathodic and anodic regimes at the IL/Au(111) interface. The structure of these layers is dependent on the applied electrode potential, the number of subsequent STM scans and the scan rate. Furthermore, first DTS results show that the tunneling barrier during the 1st STM scan does not seem to change significantly in the cathodic potential regime between the ocp (-0.2 V) and -2.0 V.
引用
收藏
页码:1736 / 1742
页数:7
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