Single Atom Bi Decorated Copper Alloy Enables C−C Coupling for Electrocatalytic Reduction of CO2 into C2+ Products**

Author:

Cao Yucheng12,Chen Suya3,Bo Shuowen4,Fan Wenjun1,Li Jiangnan12,Jia Chunmei1,Zhou Zhen3,Liu Qinghua4,Zheng Lirong5,Zhang Fuxiang1ORCID

Affiliation:

1. State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian National Laboratory for Clean Energy Dalian 116023 Liaoning China

2. Center of Materials Science and Optoelectronics Engineering University of Chinese Academy of Sciences Beijing 100049 China

3. School of Materials Science and Engineering Institute of New Energy Material Chemistry Renewable Energy Conversion and Storage Center (ReCast) Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education) Nankai University Tianjin 300350 China

4. National Synchrotron Radiation Laboratory University of Science and Technology of China Hefei 230029 Anhui China

5. Beijing Synchrotron Radiation Facility Institute of High Energy Physics Chinese Academy of Sciences Beijing 100049 China

Abstract

AbstractSingle atom alloy (SAA) catalysts have been recently explored for promotion of various heterogeneous catalysis, but it remains unexplored for selective electrocatalytic reduction of carbon dioxide (CO2) into multi‐carbon (C2+) products involving C−C coupling. Herein we report a single‐atomic Bi decorated Cu alloy (denoted as BiCu‐SAA) electrocatalyst that could effectively modulate selectivity of CO2 reduction into C2+ products instead of previous C1 ones. The BiCu‐SAA catalyst exhibits remarkably superior selectivity of C2+ products with optimal Faradaic efficiency (FE) of 73.4 % compared to the pure copper nanoparticle or Bi nanoparticles‐decorated Cu nanocomposites, and its structure and performance can be well maintained at current density of 400 mA cm−2 under the flow cell system. Based on our in situ characterizations and density functional theory calculations, the BiCu‐SAA is found to favor the activation of CO2 and subsequent C−C coupling during the electrocatalytic reaction, as should be responsible for its extraordinary C2+ selectivity.

Funder

National Natural Science Foundation of China

Ministry of Science and Technology of the People's Republic of China

Chinese Academy of Sciences

Publisher

Wiley

Subject

General Chemistry,Catalysis

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3