Affiliation:
1. College of Chemistry and Chemical Engineering, State Key Laboratory of Chemo/Biosensing and Chemometrics, Ministry of Education of Advanced Engineering Research Center for Catalysis Hunan University Changsha 410082 P. R. China
2. College of Chemical Engineering and Environment, State Key Laboratory of Heavy Oil Processing China University of Petroleum Beijing, Changping 102249 P. R. China
Abstract
AbstractCore‐shell photoanodes have shown great potential for photoelectrochemical (PEC) water oxidation. However, the construction of a high‐quality interface between the core and shell, as well as a highly catalytic surface, remains a challenge. Herein, guided by computation, we present a BiVO4 photoanode coated with ZnCoFe polyphthalocyanine using pyrazine as a coordination agent. The bidirectional axial coordination of pyrazine plays a dual role by facilitating intimate interfacial contact between BiVO4 and ZnCoFe polyphthalocyanine, as well as regulating the electron density and spin configuration of metal sites in ZnCoFe phthalocyanine, thereby promoting the potential‐limiting step of *OOH desorption. The resulting photoanode displayed a high photocurrent density of 5.7±0.1 mA cm−2 at 1.23 VRHE. This study introduces a new approach for constructing core–shell photoanodes, and uncovers the key role of pyrazine axial coordination in modulating the catalytic activity of metal phthalocyanine.
Funder
National Natural Science Foundation of China