光电流
钒酸铋
材料科学
异质结
分解水
电化学
载流子
纳米技术
光催化
光电子学
化学工程
电极
催化作用
化学
生物化学
物理化学
工程类
作者
Yinhua Jiang,Yilu Su,Imane Ennaji,Amir Khojastehnezhad,Mohamed Siaj
标识
DOI:10.1016/j.cej.2023.147082
摘要
Bismuth vanadate (BiVO4) photoanode shows great potential for photoelectrochemical (PEC) water splitting but still suffers from the sluggish surface reaction kinetic and high charge loss. Further strengthening the intrinsic charge transport for the improvement of solar-to-hydrogen conversion becomes the top priority. Herein, an innovative highly-oriented E-BiVO4/MoS2 heterojunction photoanode is rationally designed and fabricated via directly encapsulating few-layered MoS2 nanosheets on electrochemical-treated BiVO4 (E-BiVO4) nanopyramid arrays. Systematic studies reveal that the electrochemical reduction process can create oxygen vacancies on BiVO4 lattice, thereby increasing the overall carrier concentration, and boosting the bulk and surface charge separation efficiencies. Meanwhile, the introduction of MoS2 as a heterojunction helps build the unidirectional charge transfer channels for further facilitated surface hole extraction and oxidation kinetics, synergistically devoting to the significantly enhanced PEC activity and photostability. As a result, the optimized E-BiVO4/MoS2 photoanode exhibits the highest photocurrent density of 2.11 mA/cm2 at 1.23 VRHE and incident photon-to-electron conversion efficiency (IPCE) of 40.6 %, which are approximately 4.6 and 4.9 times higher than the pristine BiVO4. The present work demonstrates a feasible collaborative strategy to develop photoanodes with simultaneously improved charge separation and hole transport for efficient PEC water splitting application.
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