Your browser doesn't support javascript.
loading
Axial Phosphate Coordination in Co Single Atoms Boosts Electrochemical Oxygen Evolution.
Liu, Yan; Zhang, Shuangshuang; Jiao, Chi; Chen, Huimei; Wang, Gang; Wu, Wenjie; Zhuo, Zhiwen; Mao, Junjie.
Afiliação
  • Liu Y; Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University, Wuhu, 241002, P. R. China.
  • Zhang S; Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University, Wuhu, 241002, P. R. China.
  • Jiao C; Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University, Wuhu, 241002, P. R. China.
  • Chen H; Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University, Wuhu, 241002, P. R. China.
  • Wang G; Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University, Wuhu, 241002, P. R. China.
  • Wu W; Institute of Chemistry, Chinese Academy of Sciences (CAS), Beijing, 100190, P. R. China.
  • Zhuo Z; Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University, Wuhu, 241002, P. R. China.
  • Mao J; Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University, Wuhu, 241002, P. R. China.
Adv Sci (Weinh) ; 10(5): e2206107, 2023 Feb.
Article em En | MEDLINE | ID: mdl-36494096
Cobalt single atoms coordinated with planar four nitrogen atoms (Co1 N4 ) represent an efficient electrocatalyst for oxygen evolution reaction (OER), whereas the large energy barrier of CoOH dehydrogenation limits the OER activity. Herein, axial phosphate (PO4 ) coordination is incorporated in Co1 N4 single atoms of cobalt phthalocyanine@carbon nanotubes (P-CoPc@CNT), so as to boost the intrinsic OER performance through manipulating the reaction pathway. With a relative low mass loading of Co (2.7%), the P-CoPc@CNT shows remarkable alkaline OER activity with the overpotential of 300 mV and Tafel slope of 41.7 mV dec-1 , which dramatically outperforms the CoPc@CNT without axial PO4 coordination. Based on mechanistic analysis, the axial PO4 coordination directly participates in the OER cycle by the transformation of axial ligand. Specially, the CoOH dehydrogenation process is replaced by the dehydrogenation of HPO4 -Co1 N4 intermediate, which largely decreases the energy barrier and thus benefits the whole OER process.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article