Tuning of Silver Catalyst Mesostructure Promotes Selective Carbon Dioxide Conversion into Fuels

被引:268
作者
Yoon, Youngmin [1 ]
Hall, Anthony Shoji [1 ,2 ]
Surendranath, Yogesh [1 ]
机构
[1] MIT, Dept Chem, 77 Massachusetts Ave,18-163, Cambridge, MA 02139 USA
[2] Johns Hopkins Univ, Mat Sci & Engn Dept, 3400 North Charles St, Baltimore, MD 21218 USA
基金
美国国家科学基金会;
关键词
CO2; reduction; electrocatalysis; mass transport; mesoporous materials; renewable energy; ELECTROCHEMICAL CO2 REDUCTION; ELECTRODES; EFFICIENT; COPPER; ELECTROREDUCTION; DEPOSITION; INSIGHTS; METHANE;
D O I
10.1002/anie.201607942
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An electrode's performance for catalytic CO2 conversion to fuels is a complex convolution of surface structure and transport effects. Using well-defined mesostructured silver inverse opal (Ag-IO) electrodes, it is demonstrated that mesostructure-induced transport limitations alone serve to increase the turnover frequency for CO2 activation per unit area, while simultaneously improving reaction selectivity. The specific activity for catalyzed CO evolution systematically rises by three-fold and the specific activity for catalyzed H-2 evolution systematically declines by ten-fold with increasing mesostructural roughness of Ag-IOs. By exploiting the compounding influence of both of these effects, we demonstrate that mesostructure, rather than surface structure, can be used to tune CO evolution selectivity from less than 5% to more than 80%. These results establish electrode mesostructuring as a powerful complementary tool for tuning both catalyst selectivity and efficiency for CO2 conversion into fuels.
引用
收藏
页码:15282 / 15286
页数:5
相关论文
共 29 条
[1]  
BEWICK A, 1977, J ELECTROANAL CHEM, V84, P127, DOI 10.1016/S0022-0728(77)80235-0
[2]   Aqueous CO2 Reduction at Very Low Overpotential on Oxide-Derived Au Nanoparticles [J].
Chen, Yihong ;
Li, Christina W. ;
Kanan, Matthew W. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (49) :19969-19972
[3]   A review of the aqueous electrochemical reduction of CO2 to hydrocarbons at copper [J].
Gattrell, M. ;
Gupta, N. ;
Co, A. .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2006, 594 (01) :1-19
[4]   Calculation for the cathode surface concentrations in the electrochemical reduction of CO2 in KHCO3 solutions [J].
Gupta, N ;
Gattrell, M ;
MacDougall, B .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 2006, 36 (02) :161-172
[5]   Mesostructure-Induced Selectivity in CO2 Reduction Catalysis [J].
Hall, Anthony Shoji ;
Yoon, Youngmin ;
Wuttig, Anna ;
Surendranath, Yogesh .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (47) :14834-14837
[6]  
Hori Y, 2008, MOD ASP ELECTROCHEM, P89
[7]   Effect of Chloride Anions on the Synthesis and Enhanced Catalytic Activity of Silver Nanocoral Electrodes for CO2 Electroreduction [J].
Hsieh, Yu-Chi ;
Senanayake, Sanjaya D. ;
Zhang, Yu ;
Xu, Wenqian ;
Polyansky, Dmitry E. .
ACS CATALYSIS, 2015, 5 (09) :5349-5356
[8]   Finite size effects in ordered macroporous electrodes fabricated by electrodeposition into colloidal crystal templates [J].
Hung, David ;
Liu, Zhu ;
Shah, Neepa ;
Hao, Yaowu ;
Searson, Peter C. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2007, 111 (08) :3308-3313
[9]   Electrochemical CO2 Reduction: Recent Advances and Current Trends [J].
Jones, John-Paul ;
Prakash, G. K. Surya ;
Olah, George A. .
ISRAEL JOURNAL OF CHEMISTRY, 2014, 54 (10) :1451-1466
[10]   Three-dimensional porous hollow fibre copper electrodes for efficient and high-rate electrochemical carbon dioxide reduction [J].
Kas, Recep ;
Hummadi, Khalid Khazzal ;
Kortlever, Ruud ;
de Wit, Patrick ;
Milbrat, Alexander ;
Luiten-Olieman, Mieke W. J. ;
Benes, Nieck E. ;
Koper, Marc T. M. ;
Mul, Guido .
NATURE COMMUNICATIONS, 2016, 7