In situ STM investigation of the lithium underpotential deposition on Au(111) in the air- and water-stable ionic liquid 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)amide

被引:52
作者
Gasparotto, L. H. S. [1 ,2 ,3 ]
Borisenko, N. [1 ,2 ]
Bocchi, N. [3 ]
El Abedin, S. Zein [1 ,2 ]
Endres, F. [1 ,2 ]
机构
[1] Clausthal Univ Technol, Inst Mech Verfahrenstech, D-38678 Clausthal Zellerfeld, Germany
[2] EFZN Goslar, D-38640 Goslar, Germany
[3] Univ Fed Sao Carlos, BR-13565 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
TEMPERATURE MOLTEN-SALT; POLYMER ELECTROLYTES; BIS(TRIFLUOROMETHANESULFONYL) IMIDE; ELECTROCHEMICAL PROPERTIES; CYCLING EFFICIENCY; ELECTRODEPOSITION; SOLVENTS; BATTERIES; METALS; ZWITTERION;
D O I
10.1039/b916809e
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
In the present paper the underpotential deposition (UPD) of lithium on Au(111) from 0.5 mol L-1 LiTFSA in the air-and water stable ionic liquid 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)amide, [Py-1,Py-4]TFSA, has been investigated by cyclic voltammetry (CV) and in situ scanning tunneling microscopy (STM). The pure [Py-1,Py-4]TFSA was found to be inert in the potential regime investigated. The results show that the lithium UPD on Au(111) in [Py-1,Py-4]TFSA begins at potentials considerably positive to the electrode potential of bulk deposition and follows a layer-by-layer mechanism with the formation of at least two monolayers. A large number of monoatomically deep pits appear when the potential reaches positive values, which is an indication that a Li-Au alloy was formed.
引用
收藏
页码:11140 / 11145
页数:6
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