非阻塞I/O
分解水
材料科学
制氢
可见光谱
兴奋剂
析氧
电子转移
化学工程
光催化
氢
电极
纳米技术
光电子学
光化学
电化学
催化作用
化学
物理化学
生物化学
工程类
有机化学
作者
Shilei Xie,Teng Zhai,Yongjie Zhu,Wei Li,Rongliang Qiu,Yexiang Tong,Xihong Lu
标识
DOI:10.1016/j.ijhydene.2014.01.072
摘要
Photoelectrochemical water splitting has attracted increasing attention recently in the perspective of clean and sustainable energy economy. Herein, we reported the synthesis of NiO functionalized Mo doped BiVO4 (denoted as NiO/Mo:BiVO4) nanobelts and their enhanced photoelectrochemical activity for efficient water oxidation. The prepared NiO/Mo:BiVO4 p–n junction structure showed much higher water splitting activity than the pristine BiVO4 and Mo:BiVO4. Such obvious enhancement are due to the increased donor density by doping with Mo and fast separation of the photoexcited electron–hole pairs by the novel p–n junction composite structure. Under light irradiation, photoexcited holes in the conduction band (CB) of Mo:BiVO4 will conveniently transfer to the p-type NiO with the effect of the inner electric field. Meanwhile, the holes would oxidize the water into oxygen and the electrons transfer to the counter electrode (Pt electrode) to produce hydrogen. This novel p–n junction structure could open up new opportunities to develop high-performance photoanode for water splitting.
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