Chem. J. Chinese Universities

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Electrochemical Behavior of CO2 on Copper Electrode

ZHANG Li, LUO Yi-Wen, NIU Dong-Fang, XIAO Li-Ping, LU Jia-Xing*   

  1. Department of Chemistry, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, East China Normal University, Shanghai 200062, China
  • Received:2006-12-27 Revised:1900-01-01 Online:2007-09-10 Published:2007-09-10
  • Contact: LU Jia-Xing

Abstract: The electrochemical reduction of CO2 on copper electrode was investigated in acetonitrile(MeCN), dimethyl formamide(DMF) and dimethyl sulfoxide(DMSO) containing 0.1 mol/L tetraethylammonium bromioe(TEABr) by cyclic voltammetry and chronocoulometry at 298 K and under atmospheric pressure. There were obviously irreversible one-electron reduction peaks after saturated with CO2 on copper electrode in three solvents, which generated anion radical of CO2. The influence of scan rate was also studied by cyclic voltammetry. The diffusion coefficients of CO2 in MeCN, DMF and DMSO were 8.981×10-6, 1.019×10-6 and 1.032×10-6 cm2/s and the transfer coefficients were 0.064, 0.042 and 0.059, respectively. These results show that the electroreduction of CO2 was an irreversible diffusion controlled process.

Key words: Carbon dioxide, Copper electrode, Cyclic voltammetry, Chronocoulometry

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