钒酸铋
材料科学
钒酸盐
调制(音乐)
铋
光电化学电池
化学工程
纳米技术
无机化学
光催化
冶金
电极
电解质
催化作用
美学
工程类
哲学
物理化学
化学
生物化学
作者
Kaige Tian,Zhuo Xu,Hua Yang,Guilin Chen,Pengfei An,Shouxin Zhang,Shengzhong Liu,Junqing Yan
标识
DOI:10.1002/aenm.202404477
摘要
Abstract BiVO 4 faces significant challenges for widespread application in photoelectrochemical (PEC) water oxidation due to its poor hole transport ability, high surface defect density, and sluggish water oxidation reaction kinetics. Employing interfacial engineering to assist in energy level modulation is an effective strategy to address these challenges. Herein, a CuCrO 2 hole transport layer (HTL) is coupled and further grew NiCo‐MOF in situ to prepare a NiCo‐MOF‐CuCrO 2 ‐BiVO 4 composite photoanode. The novel composite photoanode not only achieves a photocurrent density of 5.75 mA cm −2 at 1.23 V versus a reversible hydrogen electrode (vs RHE) but also maintains stable operation for over 24 h. Comprehensive physicochemical characterization and density‐functional theory calculations confirm that the built‐in electric field generated by the p–n heterojunction formed between the CuCrO 2 HTL and BiVO 4 photoanode enhances the hole transport ability. Moreover, the NiCo‐MOF chelated on the photoanode surface not only passivates the surface defect states but also accelerates the kinetics of the water oxidation reaction. Under the synergistic effect of dual modification, the PEC water oxidation performance of the BiVO 4 photoanode is dramatically improved. This pioneering work presents a MOF/HTL/BiVO 4 configuration that provides a blueprint for the future development of integrated photoanodes for efficient solar energy conversion.
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