Electric Double Layer of Au(100)/Imidazolium-Based Ionic Liquids Interface: Effect of Cation Size

被引:59
|
作者
Su, Yuzhuan
Yan, Jiawei [1 ]
Li, Miangang
Zhang, Meng
Mao, Bingwei
机构
[1] Xiamen Univ, State Key Lab Phys Chem Solid Surfaces, Coll Chem & Chem Engn, Xiamen 361005, Fujian, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2013年 / 117卷 / 01期
关键词
IN-SITU STM; DIFFERENTIAL CAPACITANCE; 1-ALKYL-3-METHYLIMIDAZOLIUM TETRAFLUOROBORATE; GLASSY-CARBON; TEMPERATURE; AU(111); ELECTROCHEMISTRY; ELECTRODEPOSITION; RECONSTRUCTION; CONDUCTIVITY;
D O I
10.1021/jp3079919
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
We have carried out differential capacitance measurements and in-situ scanning tunneling microscope (STM) characterizations to investigate the effect of the length of alkyl side chains on an electric double layer of Au(100)/imidazolium-based ionic liquids interface. In ionic liquids consisting of BMI+ cation (1-butyl-3-methylimidazolium), differential capacitance curves present an obvious bell-shaped feature. In ionic liquids with PMI+ (1-methyl-3-propylimidazolium) or OMI+ (1-methyl-3-octylimidazolium) cations, the rising of capacitance from about -0.5 V disturbs the bell-shaped feature. In-situ STM characterizations reveal the generality of surface etching and micelle-like adsorption of imidazolium cations on Au(100) at potential around the peaks of the bell-shaped feature, demonstrating that the potential of zero charge (PZC) should locate at the potential close to the peaks. Because of the longer side chain length and stronger interaction with Au(100) substrate, an extra capacitance peak appears at the potential as negative as -1.65 V in OMIPF6 and a corresponding order-disorder transformation of OMI+ cation adlayer is revealed by STM, indicating a correlation between differential capacitance curve and STM.
引用
收藏
页码:205 / 212
页数:8
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