BiVO4 , which is a representative photoanode material for photoelectrochemical water splitting, intrinsically restricts high conversion efficiency, owing to faster recombination, low electron mobility, and short electron diffusion length. While the photocurrent density of typical BiVO4 corresponds to only 21.3% of the maximum photocurrent density (4.68 mA cm-2 ), decoration of the BiVO4 photoanode with zeolitic imidazolate framework-67 (ZIF-67) exhibits a synergetic effect to raise the overall photocatalytic ability at the BiVO4 surface region to a higher level via the energy-transfer process from BiVO4 to ZIF-67. The hybrid ZIF-67/BiVO4 photoanode follows two convenient photoelectrochemical pathways: 1) energy-transfer-induced water oxidation reaction in ZIF-67 and 2) water oxidation reaction by direct contact between the BiVO4 surface and electrolytes. Compared to the moderate photocurrent density (≈1 mA cm-2 ) of single-layer BiVO4 , the proposed ZIF-67/BiVO4 photoanodes show a remarkably high photocurrent (2.25 mA cm-2 ) with high stability, despite the lack of hole scavengers in the electrolyte. Furthermore, the absorbed photon-to-current efficiency of the ZIF-67/BiVO4 photoanode is ≈2.5 times greater than that of BiVO4 . This work proposes a promising solution for efficient water oxidation that overcomes the intrinsic material limitations of BiVO4 photoelectrodes by using energy transfer-induced photon recycling and the decoration of porous ZIFs.
Keywords: bismuth vanadate; energy transfer; photoanodes; photoelectrochemical reactions; zeolitic imidazolate frameworks.
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