Assessing the dynamics of O_(2) desorption from cobalt phthalocyanine by in situ electrochemical scanning tunneling microscopy
作者机构:CAS Key Laboratory of Molecular Nanostructure and NanotechnologyCAS Research/Education Center for Excellence in Molecular SciencesBeijing National Laboratory for Molecular Science(BNLMS)Institute of ChemistryChinese Academy of SciencesBeijing 100190China University of Chinese Academy of SciencesBeijing 100049China
出 版 物:《Journal of Energy Chemistry》 (能源化学(英文版))
年 卷 期:2024年第98卷第11期
页 面:144-148页
核心收录:
学科分类:081705[工学-工业催化] 08[工学] 0817[工学-化学工程与技术]
基 金:National Key R&D Program of China (2021YFA1501002) National Natural Science Foundation of China (22132007)
主 题:Electrochemical scanning tunneling microscopy Oxygen evolution reaction Cobalt phthalocyanine
摘 要:We report here the in situ electrochemical scanning tunneling microscopy(ECSTM) study of cobalt phthalocyanine(CoPc)-catalyzed O_(2) evolution reaction(OER) and the dynamics of CoPc-O_(2) *** self-assembled CoPc monolayer is fabricated on Au(111) substrate and resolved by ECSTM in 0.1 M KOH *** OH^(-)adsorption on CoPc prior to OER is observed in ECSTM *** OER,the generated O_(2) adsorbed on Co Pc is observed in the CoPc *** step experiment is employed to monitor the desorption of OER-generated O_(2) from CoPc,which results in the decreasing surface coverage of CoPc-O_(2) with *** rate constant of O_(2) desorption is evaluated through data *** insights into the dynamics of Co-O_(2) dissociation at the molecular level via in situ imaging help understand the role of Co-O_(2) in oxygen reduction reaction(ORR) and OER.