异质结
分解水
工作职能
材料科学
钒酸铋
兴奋剂
光电子学
半导体
光电化学电池
纳米技术
电极
光催化
化学
催化作用
电解质
图层(电子)
物理化学
生物化学
作者
Kai‐Hang Ye,Haibo Li,Duan Huang,Shuang Xiao,Weitao Qiu,Mingyang Li,Yuwen Hu,Wenjie Mai,Hongbing Ji,Shihe Yang
标识
DOI:10.1038/s41467-019-11586-y
摘要
Abstract We herein demonstrate the unusual effectiveness of two strategies in combination to enhance photoelectrochemical water splitting. First, the work function adjustment via molybdenum (Mo) doping significantly reduces the interfacial energy loss and increases the open-circuit photovoltage of bismuth vanadate (BiVO 4 ) photoelectrochemical cells. Second, the creation and optimization of the heterojunction of boron (B) doping carbon nitride (C 3 N 4 ) and Mo doping BiVO 4 to enforce directional charge transfer, accomplished by work function adjustment via B doping for C 3 N 4 , substantially boost the charge separation of photo-generated electron-hole pairs at the B-C 3 N 4 and Mo-BiVO 4 interface. The synergy between the above efforts have significantly reduced the onset potential, and enhanced charge separation and optical properties of the BiVO 4 -based photoanode, culminating in achieving a record applied bias photon-to-current efficiency of 2.67% at 0.54 V vs. the reversible hydrogen electrode. This work sheds light on designing and fabricating the semiconductor structures for the next-generation photoelectrodes.
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