Zhengbo Jiao1,2, Jingjing Zheng3, Chenchen Feng2, Zeli Wang1, X.‐S. Wang1, Gongxuan Lü2, Yingpu Bi2
1Department of Physics, National University of Singapore, Singapore, 117542, Singapore
2State Key Laboratory for Oxo Synthesis and Selective Oxidation National Engineering Research Center for Fine Petrochemical Intermediates Lanzhou Institute of Chemical Physics CAS Lanzhou 730000 China
3Department of Chemical Engineering, Binzhou University, Binzhou 256603, China
Tóm tắt
AbstractBiVO4 has been identified as one of the excellent visible light responsive photoanodes for use in photoelectrochemical (PEC) water splitting. However, pristine BiVO4 usually exhibits relative low photocatalytic properties owing to insufficient charge separation and transport characteristics. Although the marginal n‐type doping of higher valence ions can obviously raise the photocurrent value, it by no means improves the PEC stability. In this work, we successfully enhanced the PEC stability of BiVO4 by doping Fe ions in substitution of Bi. Density functional theory calculations have illustrated that Fe‐doping would result in an impurity band in the forbidden gap, and thus narrow its energy gap. More importantly, Fe‐doping can synergize with other means to further improve the PEC activities of BiVO4. Therefore, we fabricated a nanoporous Fe/W co‐doped BiVO4 photoelectrode, and then loaded the metal–organic framework (MOF) MIL‐100(Fe) as cocatalyst to further promote the separation of charge carriers. To the best of our knowledge, MOFs have not yet been utilized as a cocatalyst to facilitate the charge separation, which could increase the photocurrent density of Fe/W co‐doped BiVO4.
