锐钛矿
金红石
化学
光催化
兴奋剂
相(物质)
原位
化学工程
氢
无机化学
催化作用
材料科学
光电子学
有机化学
工程类
作者
Dandan Peng,Jiaoyang Wang,Le Wang,Qihui Sun,Ying Zhang,Jing‐Jun Ma
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-11-20
卷期号:63 (48): 22806-22818
被引量:10
标识
DOI:10.1021/acs.inorgchem.4c03732
摘要
N-doped anatase/rutile TiO2 (AR-N/TiO2) photocatalysts were prepared by combining the strategy of N-doping and in situ heterophase junction generation, which significantly enhanced the photocatalytic H2 generation (1.68 mmol· h-1·g-1). Under monochromatic light at 400 nm, the light exhibits an apparent quantum efficiency of 8.6%. Moreover, this AR-N/TiO2 heterophase junction demonstrates excellent long-term stability when exposed to visible light irradiation. Through the analysis of the electronic structure, the outstanding photocatalytic activity of AR-N/TiO2 can be attributed to the maximized synergetic effect between rutile and anatase for optimal rutile content (21.6%) and enhanced response to visible light due to N-doping. Additionally, the intimate interface formed by the rutile phase grown in situ from the inner core of the anatase phase establishes well-aligned bands, which promote efficient separation of photoinduced electron-hole pairs. Furthermore, the rough surface and porosity of the as-synthesized heterophase junction facilitate an enlarged specific surface area and exposure of active sites, thereby providing more adsorptive and reactive sites that enhance conversion efficiency. This research offers an alternative approach to phase engineering for developing TiO2-based heterophase junction photocatalysts toward efficient hydrogen evolution.
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