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作 者:XIAO Long WU Huirong ZHANG Yong SUN Hao ZHANG Wenchao LYU Fenglei DENG Zhao PENG Yang
机构地区:[1]Soochow Institute for Energy and Material Innovations,College of Energy,Soochow University,Suzhou,215006,P.R.China [2]School of Chemistry and Life Science,Suzhou University of Science and Technology,Suzhou,215009,P.R.China
出 处:《Chemical Research in Chinese Universities》2023年第2期219-223,共5页高等学校化学研究(英文版)
基 金:National Key R&D Program of China(No.2020YFB1505703);National Natural Science Foundation of China(Nos.22072101,22075193);Natural Science Foundation of Jiangsu Province,China(Nos.BK20211306,BK20220483);Fund of the Key Technology Initiative of Suzhou Municipal Science and Technology Bureau,China(No.SYG201934);Six Talent Peaks Project in Jiangsu Province,China(No.TD-XCL-006);Priority Academic Program Development(PAPD)of Jiangsu Higher Education Institutions,China.
摘 要:Oxygen evolution reaction(OER)plays a key role in the electrochemical conversion and storage processes,but the sluggish kinetics of OER strongly impedes its large-scale applications.We herein reported the in situ growth of Fe-benzenedicarboxylate(Fe-BDC)on Co(OH)_(2) nanoplates[Fe-BDC/Co(OH)_(2)]that showed remarkably enhanced OER activity than the pristine Co(OH)_(2).The incorporation of Fe species could enhance the intrinsic OER activity of Co and BDC could increase the electrochemically active surface area(ECSA),thus resulting in dramatically enhanced OER activity.In situ Raman spectroscopy characterization disclosed that Fe-CoOOH reconstructed from Fe-BDC/Co(OH)_(2) was the real active site for OER.This work highlights the significance of rational tailoring of the nanostructure and electronic structure of Co(OH)_(2) and provides more opportunities for its widespread applications.
关 键 词:Co(OH)_(2)nanoplate Oxygen evolution reaction Electronic structure Nanostructure In situ Raman spectroscopy
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