Electrodeposition of magnesium film from BMIMBF4 ionic liquid

被引:61
|
作者
NuLi, Yanna [1 ]
Yang, Jun [1 ]
Wang, Pu [1 ]
机构
[1] Shanghai Jiao Tong Univ, Dept Chem Engn, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
electrodeposition and dissolution; electrochemical reversibility; magnesium; ionic liquids; BMIMBF4;
D O I
10.1016/j.apsusc.2005.10.022
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 this paper, we reported for the first time magnesium electrodeposition and dissolution processes in the ionic liquid of BMIMBF4 with 1 M Mg(CF3SO3)(2) at room temperature. Our study found that complete electrochemical reoxidation of the electrodeposited magnesium film was feasible only on Ag substrate, comparing with the Pt, Ni, and stainless-steel. Scanning electron microscope (SEM) and energy dispersive spectroscopy (EDS) results showed that magnesium was found in the deposited film and the deposits were dense. The electrodeposition of magnesium on Ag substrate in the ionic liquid was considered to be a reversible process by cyclic voltammetry. Plots of peak current versus the square root of the scan rate were found to be linear, which indicates that the mass-transport process of electroactive species was mainly diffusion controlled. The diffusion coefficient D values of electroactive species were calculated from cyclic voltammetry and chronoamperometry, respectively. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:8086 / 8090
页数:5
相关论文
共 50 条
  • [21] Electrochemical activation of CO2 in ionic liquid ( BMIMBF4):: synthesis of organic carbonates under mild conditions
    Zhang, Li
    Niu, Dongfang
    Zhang, Kai
    Zhang, Guirong
    Luo, Yiwen
    Lu, Jiaxing
    GREEN CHEMISTRY, 2008, 10 (02) : 202 - 206
  • [22] Evaluation of band structure and concentration of ionic liquid BMImBF4 in molecular mixtures by using second derivatives of FTIR spectra
    Wu, Jianping
    Wang, Meng-Jiy
    Stark, John P. W.
    JOURNAL OF QUANTITATIVE SPECTROSCOPY & RADIATIVE TRANSFER, 2006, 102 (02): : 228 - 235
  • [23] Leakage free electrolyte engraved flexible supercapacitors from Chitosan/GO@MnCO3 polymer hydrogel chelate film under BMIMBF4 ionic liquid assistance
    Selvam, Samayanan
    Yim, Jin-Heong
    JOURNAL OF ENERGY STORAGE, 2021, 43
  • [24] Nanoporous copper incorporated platinum composites for electrocatalytic reduction of CO2 in ionic liquid BMIMBF4
    Feng, Qiuju
    Liu, Suqin
    Wang, Xuanyun
    Jin, Ganhua
    APPLIED SURFACE SCIENCE, 2012, 258 (12) : 5005 - 5009
  • [25] Gold nanoparticles optical properties induced by water and an ionic liquid (bmimBF4) inside cationic reverse micelles
    Blach, Diana
    Martinez, Fernando O.
    NEW JOURNAL OF CHEMISTRY, 2017, 41 (21) : 13104 - 13113
  • [26] Electrocatalysis of CO2 Reduction on Nano Silver Cathode in Ionic Liquid BMIMBF4: Synthesis of Dimethylcarbonate
    Luo, Yafeng
    Xia, Chuibo
    Abulizi, Reyisha
    Feng, Qiuju
    Liu, Wenping
    Zhang, Aihua
    INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE, 2017, 12 (06): : 4828 - 4834
  • [27] Second virial coefficient of bmimBF4/Triton X-100/cyclohexane ionic liquid microemulsion as investigated by microcalorimetry
    Li, Na
    Zhang, Shaohua
    Zheng, Liqiang
    Gao, Yan'an
    Yu, Li
    LANGMUIR, 2008, 24 (07) : 2973 - 2976
  • [28] Electrocatalytic dimerisation of benzyl bromides and phenyl bromide at silver cathode in ionic liouid BMIMBF4
    Niu, Dongfang
    Zhang, Aijian
    Xue, Teng
    Zhang, Jingbo
    Zhao, Shufeng
    Lu, Jiaxing
    ELECTROCHEMISTRY COMMUNICATIONS, 2008, 10 (10) : 1498 - 1501
  • [29] Studies on the micropolarities of bmimBF4/TX-100/toluene ionic liquid microemulsions and their behaviors characterized by UV-visible spectroscopy
    Li, Na
    Gao, Yan'an
    Zheng, Liqiang
    Zhang, Jin
    Yu, Li
    Li, Xinwei
    LANGMUIR, 2007, 23 (03) : 1091 - 1097
  • [30] Electrochemical Reduction Behaviour of CO2 on Cu Electrode in Ionic Liquid (BMIMBF4) During Synthesis of Dimethyl Carbonate
    Feng, Qiuju
    Liu, Suqin
    ASIAN JOURNAL OF CHEMISTRY, 2011, 23 (11) : 4823 - 4826