Efficient Electrochemical Co‐Reduction of Carbon Dioxide and Nitrate to Urea with High Faradaic Efficiency on Cobalt‐Based Dual‐Sites

Author:

Fan Xiaoya1234,Liu Chaozhen5,He Xun3,Li Zixiao3,Yue Luchao3,Zhao Wenxi3,Li Jun3,Wang Yan3,Li Tingshuai3,Luo Yongsong4,Zheng Dongdong4,Sun Shengjun4,Liu Qian6,Li Luming6,Chu Wei6,Gong Feng5,Tang Bo47,Yao Yongchao2,Sun Xuping134ORCID

Affiliation:

1. Center for High Altitude Medicine, West China Hospital Sichuan University Chengdu Sichuan 610041 China

2. Precision Medicine Translational Research Center, West China Hospital Sichuan University Chengdu Sichuan 610041 China

3. Institute of Fundamental and Frontier Sciences University of Electronic Science and Technology of China Chengdu Sichuan 610054 China

4. College of Chemistry, Chemical Engineering and Materials Science Shandong Normal University Jinan Shandong 250014 China

5. MOE Key Laboratory of Energy Thermal Conversion and Control, School of Energy and Environment Southeast University Nanjing Jiangsu 211189 China

6. Institute for Advanced Study Chengdu University Chengdu Sichuan 610106 China

7. Laoshan Laboratory Qingdao Shandong 266237 China

Abstract

AbstractRenewable electricity‐powered nitrate/carbon dioxide co‐reduction reaction toward urea production paves an attractive alternative to industrial urea processes and offers a clean on‐site approach to closing the global nitrogen cycle. However, its large‐scale implantation is severely impeded by challenging C–N coupling and requires electrocatalysts with high activity/selectivity. Here, cobalt‐nanoparticles anchored on carbon nanosheet (Co NPs@C) are proposed as a catalyst electrode to boost yield and Faradaic efficiency (FE) toward urea electrosynthesis with enhanced C–N coupling. Such Co NPs@C renders superb urea‐producing activity with a high FE reaching 54.3% and a urea yield of 2217.5 µg h−1 mgcat.−1, much superior to the Co NPs and C nanosheet counterparts, and meanwhile shows strong stability. The Co NPs@C affords rich catalytically active sites, fast reactant diffusion, and sufficient catalytic surfaces‐electrolyte contacts with favored charge and ion transfer efficiencies. The theoretical calculations reveal that the high‐rate formation of *CO and *NH2 intermediates is crucial for facilitating urea synthesis.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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