纳米片
材料科学
异质结
光电流
载流子
电解质
可逆氢电极
化学工程
氧气
分解水
基质(水族馆)
光催化
光电子学
纳米技术
催化作用
兴奋剂
物理化学
工作电极
电极
海洋学
地质学
工程类
有机化学
化学
生物化学
作者
Wei Tian,Cheng Chen,Linxing Meng,Weiwei Xu,Fengren Cao,Liang Li
标识
DOI:10.1002/aenm.201903951
摘要
Abstract The photoelectrochemical performance of the WO 3 photoanode is limited by the severe charge recombination in the bulk phase and at the WO 3 /electrolyte interface. Herein, In 2 S 3 nanosheets are integrated onto the surface of the WO 3 nanowall array photoanode, followed by a facile polyvinylpyrrolidone (PVP) solution treatment. The PVP treatment results in sulfur vacancies and a gradient oxygen doping into In 2 S 3 from surface to interior, which induces the formation of a gradient energy band distribution. The gradient band structured In 2 S 3 and type II band alignment at the WO 3 /In 2 S 3 interface simultaneously create a channel that favors photogenerated electrons to migrate from the surface to the conductive substrate, thereby suppressing bulk carrier recombination. Meanwhile, the sulfur vacancies and oxygen doping contribute to increased charge carrier concentration, prolonged carrier lifetime, more active sites, and small interfacial transfer impedance. As a consequence, the PVP treated WO 3 /In 2 S 3 heterostructure photoanode exhibits a significantly enhanced photocurrent of 1.61 mA cm −2 at 1.23 V versus reversible hydrogen electrode (RHE) and negative onset potential of 0.02 V versus RHE.
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