Formation of Enriched Vacancies for Enhanced CO2 Electrocatalytic Reduction over AuCu Alloys

被引:107
作者
Zhu, Wenjin [1 ]
Zhang, Lei [1 ]
Yang, Piaoping [1 ]
Hu, Congling [1 ]
Dong, Hao [1 ]
Zhao, Zhi-Jian [1 ]
Mu, Rentao [1 ]
Gong, Jinlong [1 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Minist Educ,Key Lab Green Chem Technol, Tianjin 300072, Peoples R China
基金
美国国家科学基金会; 中国博士后科学基金;
关键词
ULTRAHIGH MASS ACTIVITY; ELECTROCHEMICAL REDUCTION; CARBON-DIOXIDE; HIGH-EFFICIENCY; AQUEOUS CO2; ELECTROREDUCTION; SIZE; CONVERSION; NANOWIRES;
D O I
10.1021/acsenergylett.8b01286
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electroreduction (ER) of carbon dioxide (CO2) is a promising way to curb excessive CO2 emission and produce value-added products. Gold-copper (AuCu) alloys are known to exhibit eminent CO production performance toward CO2ER. However, it still remains a grand challenge to balance *COOH and *CO bonding and to further decrease CO onset potential. This Letter describes the construction of Cu vacancies at an abrupt surface over a dealloyed AuCu catalyst to effectively decrease the overpotential and increase CO faradaic efficiency. Dealloyed Au3Cu exhibited a 90.2% CO faradaic efficiency at -0.38 V vs RHE and a 418.60 A/g CO mass current density at -0.8 V. vs RHE, achieving the record for CO production among AuCu catalysts. Combining the experimental and theoretical results, we concluded that the improved performance primarily results from the enhanced *COOH absorption.
引用
收藏
页码:2144 / 2149
页数:11
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