Electrochemical reduction of carbon dioxide at low overpotential on a polyaniline/Cu2O nanocomposite based electrode

被引:102
作者
Grace, Andrews Nirmala [1 ,2 ]
Choi, Song Yi [1 ]
Vinoba, Mari [1 ]
Bhagiyalakshmi, Margandan [3 ]
Chu, Dae Hyun [1 ]
Yoon, Yeoil [1 ]
Nam, Sung Chan [1 ]
Jeong, Soon Kwan [1 ]
机构
[1] Korea Inst Energy Res, Taejon 305343, South Korea
[2] VIT Univ, Ctr Nanotechnol Res, Vellore 632014, Tamil Nadu, India
[3] Cent Univ Kerala, Dept Chem, Kasaragod 671314, India
关键词
Electrochemical CO2 reduction; Polyaniline; Cu2O; H-Type cell; Membrane cell; Faradaic efficiency; CO2; REDUCTION; HIGH-PRESSURE; FORMIC-ACID; ACETIC-ACID; POLYPYRROLE ELECTRODE; CU2O; CONVERSION; METHANOL; ELECTROREDUCTION; COMPOSITE;
D O I
10.1016/j.apenergy.2014.01.022
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The electrochemical reduction of CO2 using Cu2O nanoparticle decorated polyaniline matrix (PANI/Cu2O) in 0.1 M tetrabutylammonium perchlorate (TBAP) and methanol electrolyte was investigated under ambient conditions. The experiment was carried out in a divided H-type two-compartment cell with a Nafion membrane as diaphragm separating the cathodic and anodic compartments. The catalyst was synthesized electrochemically as a thin film by using cyclic voltammetry and constant current mode deposition technique. The as-fabricated electrode was analyzed with various techniques to probe the nature and composition of the nanoparticles deposited onto the polyaniline matrix, which confirmed the presence of well-defined Cu (I) species in the film. The reduction of CO2 was carried out at various polarization potentials; the main products were formic and acetic acid with faradaic efficiencies of 30.4% and 63.0% at a polarization potential of -0.3 V vs. SCE (sat. KCl). A possible reduction pathway is through the formation of Had atoms and subsequent transfer to CO2 through the polymer film to form the products. An appreciable efficiency was achieved in the formation of formic acid and acetic acid with the developed catalyst. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:85 / 94
页数:10
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