An In Situ Scanning Tunneling Microscopy Study on the Electrochemical Interface between Au(111) and Ethaline Deep Eutectic Solvent

被引:19
|
作者
Tan, Zhuo [1 ,2 ]
Peng, Yu [1 ,2 ]
Liu, Jingli [1 ,2 ]
Yang, Yun [3 ]
Zhang, Zhisen [3 ]
Chen, Zhaobin [1 ,2 ]
Mao, Bingwei [1 ,2 ]
Yan, Jiawei [1 ,2 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, Xiamen 361005, Peoples R China
[3] Xiamen Univ, Coll Phys Sci & Technol, Res Inst Biomimet & Soft Matter, Fujian Prov Key Lab Soft Funct Mat,Res Inst, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
scanning tunneling microscopy; electrical double layer; ethaline; deep eutectic solvents; reconstruction; IONIC-LIQUID; CHOLINE CHLORIDE; QUATERNARY AMMONIUM; DOUBLE-LAYER; ELECTRODEPOSITION; EXTRACTION; SURFACES; NANOSTRUCTURES; RECONSTRUCTION; MICELLIZATION;
D O I
10.1002/celc.202001264
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Deep eutectic solvents (DESs) possess excellent properties that make them promising candidates for electrolytes in electrochemical fields. However, information about the electrical double layer, particularly the potential-dependent innermost layer structure and electrode surface structure, is still lacking. In this work, we investigated the Au(111) surface structure and adsorption behaviors of DES components on a Au(111) surface in ethaline (choline chloride and ethylene glycol in a 1 : 2 molar ratio) by using in situ scanning tunneling microscopy and cyclic voltammetry. The surface reconstruction of Au(111) and its lifting are disclosed, and the potential-dependent adsorption behavior of chloride ions is analyzed with emphasis on their strong interactions with the Au surface. The results provide new insights into the electrical double layer structure in ethaline DES with atomic-level resolution.
引用
收藏
页码:4601 / 4605
页数:5
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