标题:Atomic Modulation and Structure Design of Carbons for Bifunctional Electrocatalysis in Metal–Air Batteries
作者:Huang Y.; Wang Y.; Tang C.; Wang J.; Zhang Q.; Wang Y.; Zhang J.
作者机构:[Huang, Y] CAS Key Laboratory of Design and Assembly of Functional Nanostructures, and Fujian Provincial Key Laboratory of Nanomaterials, State Key La 更多
通讯作者:Zhang, Q(zhang-qiang@mails.tsinghua.edu.cn)
通讯作者地址:[Zhang, Q] Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology, Department of Chemical Engineering, Tsinghua UniversityChina;
来源:Advanced Materials
出版年:2018
DOI:10.1002/adma.201803800
关键词:bifunctional electrocatalysts; metal-free carbon; metal–air batteries; oxygen evolution reaction; oxygen reduction reaction
摘要:With the extensive research and development of renewable energy technologies, there is an increasing interest in developing metal-free carbons as a new class of bifunctional electrocatalysts for boosting the performance of metal–air batteries. Along with significant understanding of the electrocatalytic nature and the rapid development of techniques, the activities of carbon electrocatalysts are well-tailored by introducing particular dopants/defects and structure regulation. Herein, the recent advances regarding the rational design of carbon-based electrocatalysts for the oxygen reduction reaction and oxygen evolution reaction are summarized, with a special focus on the bifunctional applications in Zn–air and Li–air batteries. Specifically, the atomic modulation strategies to regulate the electrocatalytic activities of carbons and structure modification are summarized to gain deep insights into bifunctional mechanisms and boost advanced Zn–air and Li–air batteries. The current challenges and future perspectives are also addressed to accelerate the exploration of promising bifunctional carbon catalysts for renewable energy technologies, particularly metal–air batteries. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
收录类别:SCOPUS
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053833254&doi=10.1002%2fadma.201803800&partnerID=40&md5=ebbb64db81079a9214188c76cca35004
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