Effect of solution pH on CO: formate formation rates during electrochemical reduction of aqueous CO2 at Sn cathodes

被引:81
作者
Bumroongsakulsawat, P. [1 ]
Kelsall, G. H. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem Engn, London SW7 2AZ, England
关键词
CO2; Electrochemical reduction; Sn; formate; CO; CARBON-DIOXIDE; ELECTRO-REDUCTION; CONTINUOUS REACTOR; DIFFUSION-COEFFICIENT; MERCURY-ELECTRODE; COPPER ELECTRODE; WATER; HYDROCARBONS; PRESSURE; OXIDE;
D O I
10.1016/j.electacta.2014.07.057
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The dependence of the molar ratios of CO:formate products formed by electrochemical reduction of CO2 at Sn electrodes was studied in aqueous buffer solutions as a function of pH, with values of those ratios ranging from 1 to 0.15 over the pH range 2.9 to 7.8. However, decreasing pH led to decreased charge yields of CO2 reduction, due to increasing rates of the competing hydrogen evolution reaction. A reaction scheme was proposed to explain the observed relationship and a mathematical model was developed to quantify the dependence of the product ratios on pH and to predict the observed partial current densities of product formation at different pHs and electrode potentials. The reaction scheme was based on multiple protonation states of the intermediate in CO2 reduction; the higher the protonation state, the higher was the tendency of the intermediate to form CO. A generalised reaction mechanism for other electrode materials was also proposed. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:216 / 225
页数:10
相关论文
共 31 条
[1]  
Bard A. J., 1985, STANDARD POTENTIALS
[2]   THE SOLUBILITY OF CARBON-DIOXIDE IN WATER AT LOW-PRESSURE [J].
CARROLL, JJ ;
SLUPSKY, JD ;
MATHER, AE .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1991, 20 (06) :1201-1209
[3]  
Cussler E.L., 2008, Diffusion Mass Transfer in Fluid Systems
[4]   TRACER DIFFUSION STUDIES IN THE SYSTEM PHOSPHORIC ACID-DISODIUM HYDROGEN PHOSPHATE-WATER BY A RADIOACTIVE METHOD [J].
DAS, A ;
CHANGDAR, SN .
RADIATION PHYSICS AND CHEMISTRY, 1995, 45 (05) :773-778
[5]   Mathematical Modeling of CO2 Reduction to CO in Aqueous Electrolytes I. Kinetic Study on Planar Silver and Gold Electrodes [J].
Delacourt, Charles ;
Ridgway, Paul L. ;
Newman, John .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2010, 157 (12) :B1902-B1910
[6]   Electrochemical conversion of CO2 to C2 hydrocarbons using different ex situ copper electrodeposits [J].
Goncalves, M. R. ;
Gomes, A. ;
Condeco, J. ;
Fernandes, T. R. C. ;
Pardal, T. ;
Sequeira, C. A. C. ;
Branco, J. B. .
ELECTROCHIMICA ACTA, 2013, 102 :388-392
[7]  
Greenwood N. N., 2012, Chemistry of the Elements
[8]   ELECTROCATALYTIC PROCESS OF CO SELECTIVITY IN ELECTROCHEMICAL REDUCTION OF CO2 AT METAL-ELECTRODES IN AQUEOUS-MEDIA [J].
HORI, Y ;
WAKEBE, H ;
TSUKAMOTO, T ;
KOGA, O .
ELECTROCHIMICA ACTA, 1994, 39 (11-12) :1833-1839
[9]   FORMATION OF HYDROCARBONS IN THE ELECTROCHEMICAL REDUCTION OF CARBON-DIOXIDE AT A COPPER ELECTRODE IN AQUEOUS-SOLUTION [J].
HORI, Y ;
MURATA, A ;
TAKAHASHI, R .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1989, 85 :2309-2326
[10]   Deactivation of copper electrode in electrochemical reduction of CO2 [J].
Hori, Y ;
Konishi, H ;
Futamura, T ;
Murata, A ;
Koga, O ;
Sakurai, H ;
Oguma, K .
ELECTROCHIMICA ACTA, 2005, 50 (27) :5354-5369