材料科学
锐钛矿
同质结
X射线光电子能谱
光催化
金红石
表面光电压
光谱学
分解水
化学工程
光电子学
光化学
纳米技术
催化作用
异质结
化学
物理
工程类
量子力学
生物化学
作者
Xiaowen Ruan,Xiaoqiang Cui,Yi Cui,Xiaofeng Fan,Zhi-Yun Li,Tengfeng Xie,Kaikai Ba,Guangri Jia,Haiyan Zhang,Lei Zhang,Wei Zhang,Xiao Zhao,Jing Leng,Shengye Jin,David J. Singh,Weitao Zheng
标识
DOI:10.1002/aenm.202200298
摘要
Developing the technology for high yielding photocatalytic hydrogen evolution reactions is an important challenge. Development and optimization of photocatalytic junctions is a likely route for achieving this if heterojunctions with suitable band alignments can be achieved in sufficiently high-density form. Here, a novel anatase-TiO2/H-rutile-TiO2 heterophase homojunction system with near optimum energy band alignment is reported. The resulting as-prepared catalyst exhibits an excellent photocatalytic hydrogen evolution rate of 29.63 mmol g–1 h–1 under UV–vis light irradiation and an outstanding apparent quantum efficiency of 45.6% at 365 nm. The significant improvement is ascribed to near perfect lattice matching in combination with the rapid separation and transfer of photogenerated carriers in anatase-TiO2/H-rutile-TiO2 heterophase homojunctions. In situ X-ray photoelectron spectroscopy, electron spin resonance spin-trapping tests, femtosecond transient absorption spectroscopy, steady-state surface photovoltage spectroscopy, and transient-state surface photovoltage with additional ex situ characterizations and theoretical calculations show that the mechanism is enhanced transfer of photogenerated carriers in the anatase-TiO2/H-rutile-TiO2 catalyst. This work provides a pathway for enhancing photocatalytic performance through optimization of heterojunctions.
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