Pan Jin-Bo, Wang Bing-Hao, Shen Sheng, Chen Lang, Yin Shuang-Feng
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.
College of Chemical Engineering and Environment, State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Beijing, Changping, 102249, P. R. China.
Angew Chem Int Ed Engl. 2023 Sep 18;62(38):e202307246. doi: 10.1002/anie.202307246. Epub 2023 Aug 8.
Core-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 BiVO 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 BiVO 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 at 1.23 V . 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.
核壳结构光阳极在光电化学(PEC)水氧化方面已显示出巨大潜力。然而,在核与壳之间构建高质量界面以及高催化表面仍然是一项挑战。在此,在计算的指导下,我们展示了一种以吡嗪作为配位剂、涂覆有 ZnCoFe 聚酞菁的 BiVO 光阳极。吡嗪的双向轴向配位通过促进 BiVO 与 ZnCoFe 聚酞菁之间的紧密界面接触以及调节 ZnCoFe 酞菁中金属位点的电子密度和自旋构型发挥双重作用,从而促进*OOH 解吸的限速步骤。所得光阳极在 1.23 V 时显示出 5.7±0.1 mA cm 的高光电流密度。本研究介绍了一种构建核壳结构光阳极的新方法,并揭示了吡嗪轴向配位在调节金属酞菁催化活性中的关键作用。