A review on the electrochemical reduction of CO2 in fuel cells, metal electrodes and molecular catalysts

被引:392
作者
Lim, Rern Jern [1 ]
Xie, Mingshi [1 ]
Sk, Mahasin Alam [1 ]
Lee, Jong-Min [1 ]
Fisher, Adrian [2 ]
Wang, Xin [1 ]
Lim, Kok Hwa [1 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Div Chem & Biomol Engn, Singapore 637459, Singapore
[2] Univ Cambridge, Dept Chem Engn & Biotechnol, Cambridge CB2 3RA, England
关键词
CO2; reduction; Electrochemistry; Fuel cells; Metal electrodes; Molecular catalysts; HYDROGEN-STORING MATERIALS; CARBON-DIOXIDE REDUCTION; COPPER SINGLE-CRYSTAL; ELECTROCATALYTIC REDUCTION; PULSED ELECTROREDUCTION; HIGH-PRESSURE; ELECTRODE/ELECTROLYTE INTERFACE; PHOTOELECTROCHEMICAL REDUCTION; ELECTROPOLYMERIZED FILMS; ALLOY ELECTROCATALYSTS;
D O I
10.1016/j.cattod.2013.11.037
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In this review article, we report the development and utilisation of fuel cells, metal electrodes in aqueous electrolyte and molecular catalysts in the electrochemical reduction of CO2. Fuel cells are able to function in both electrolyser and fuel cell mode and could potentially reduce CO2 and produce energy at the same time. However, it requires considerably high temperatures for efficient operation. Direct reduction using metal electrodes and molecular catalysts are possible at room temperatures but require an additional applied potential and generally have low current densities. Density functional theory (DFT) studies have been used and have begun to unveil possible mechanisms involved which could lead to improvements and development of more efficient catalysts. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 180
页数:12
相关论文
共 140 条
[61]   Electrochemical reduction of CO2 mediated by poly-M-aminophthalocyanines (M = Co, Ni, Fe):: poly-Co-tetraaminophthalocyanine, a selective catalyst [J].
Isaacs, M ;
Armijo, F ;
Ramírez, G ;
Trollund, E ;
Biaggio, SR ;
Costamagna, J ;
Aguirre, MJ .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2005, 229 (1-2) :249-257
[62]   Pulsed electroreduction of CO2 on Cu-Ag alloy electrodes [J].
Ishimaru, S ;
Shiratsuchi, R ;
Nogami, G .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2000, 147 (05) :1864-1867
[63]   Catalytic reduction of carbon dioxide with atomic hydrogen permeating through palladized Pd sheet electrodes [J].
Iwakura, C ;
Takezawa, S ;
Inoue, H .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1998, 459 (01) :167-169
[64]   Electrochemical reduction of carbon dioxide on flat metallic cathodes [J].
Jitaru, M ;
Lowy, DA ;
Toma, M ;
Toma, BC ;
Oniciu, L .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1997, 27 (08) :875-889
[65]  
Keeling CD, 2005, ECOL STU AN, V177, P83
[66]   Electrochemical reactivities of pyridinium in solution: consequences for CO2 reduction mechanisms [J].
Keith, John A. ;
Carter, Emily A. .
CHEMICAL SCIENCE, 2013, 4 (04) :1490-1496
[67]   Theoretical Insights into Pyridinium-Based Photoelectrocatalytic Reduction of CO2 [J].
Keith, John A. ;
Carter, Emily A. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (18) :7580-7583
[68]   REDUCTION OF CO2 AND CO TO METHANE ON CU FOIL ELECTRODES [J].
KIM, JJ ;
SUMMERS, DP ;
FRESE, KW .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1988, 245 (1-2) :223-244
[69]   Internal carbon dioxide reforming by methane over Ni-YSZ-CeO2 catalyst electrode in electrochemical cell [J].
Kim, T ;
Moon, S ;
Hong, SI .
APPLIED CATALYSIS A-GENERAL, 2002, 224 (1-2) :111-120
[70]   Adsorbate formation during the electrochemical reduction of carbon dioxide at palladium - A DEMS study [J].
Kolbe, D ;
Vielstich, W .
ELECTROCHIMICA ACTA, 1996, 41 (15) :2457-2460