Embedding Covalency into Metal Catalysts for Efficient Electrochemical Conversion of CO2

被引:207
作者
Lim, Hyung-Kyu [1 ]
Shin, Hyeyoung [1 ]
Goddard, William A., III [2 ]
Hwang, Yun Jeong [3 ]
Min, Byoung Koun [3 ,4 ]
Kim, Hyungjun [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Grad Sch Energy Environm Water & Sustainabil EEWS, Taejon 305701, South Korea
[2] CALTECH, Mat & Proc Simulat Ctr, Beckman Inst, Pasadena, CA 91125 USA
[3] Korea Inst Sci & Technol, Clean Energy Res Ctr, Seoul 136791, South Korea
[4] Korea Univ, Green Sch, Seoul 136713, South Korea
关键词
CARBON-DIOXIDE; REDUCTION; ELECTRODES; SURFACES; DESIGN; FUELS; MEDIA;
D O I
10.1021/ja503782w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CO2 conversion is an essential technology to develop a sustainable carbon economy for the present and the future. Many studies have focused extensively on the electrochemical conversion of CO2 into various useful chemicals. However, there is not yet a solution of sufficiently high enough efficiency and stability to demonstrate practical applicability. In this work, we use first-principles-based high-throughput screening to propose silver-based catalysts for efficient electrochemical reduction of CO2 to CO while decreasing the overpotential by 0.4-0.5 V. We discovered the covalency-aided electrochemical reaction (CAER) mechanism in which p-block dopants have a major effect on the modulating reaction energetics by imposing partial covalency into the metal catalysts, thereby enhancing their catalytic activity well beyond modulations arising from d-block dopants. In particular, sulfur or arsenic doping can effectively minimize the overpotential with good structural and electrochemical stability. We expect this work to provide useful insights to guide the development of a feasible strategy to overcome the limitations of current technology for electrochemical CO2 conversion.
引用
收藏
页码:11355 / 11361
页数:7
相关论文
共 27 条
[11]  
Hon Y., 1989, J CHEM SOC F1, V85, P2309
[12]   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
[13]   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
[14]  
Keene FR., 1993, ELECTROCHEMICAL ELEC, P1
[15]   Efficient iterative schemes for ab initio total-energy calculations using a plane-wave basis set [J].
Kresse, G ;
Furthmuller, J .
PHYSICAL REVIEW B, 1996, 54 (16) :11169-11186
[16]   New insights into the electrochemical reduction of carbon dioxide on metallic copper surfaces [J].
Kuhl, Kendra P. ;
Cave, Etosha R. ;
Abram, David N. ;
Jaramillo, Thomas F. .
ENERGY & ENVIRONMENTAL SCIENCE, 2012, 5 (05) :7050-7059
[17]   STANDARD POTENTIAL AND KINETIC-PARAMETERS OF ELECTROCHEMICAL REDUCTION OF CARBON-DIOXIDE IN DIMETHYLFORMAMIDE [J].
LAMY, E ;
NADJO, L ;
SAVEANT, JM .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1977, 78 (02) :403-407
[18]   VESTA 3 for three-dimensional visualization of crystal, volumetric and morphology data [J].
Momma, Koichi ;
Izumi, Fujio .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2011, 44 :1272-1276
[19]   Origin of the overpotential for oxygen reduction at a fuel-cell cathode [J].
Norskov, JK ;
Rossmeisl, J ;
Logadottir, A ;
Lindqvist, L ;
Kitchin, JR ;
Bligaard, T ;
Jónsson, H .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (46) :17886-17892
[20]  
Perdew JP, 1997, PHYS REV LETT, V78, P1396, DOI 10.1103/PhysRevLett.77.3865