Enhanced charge separation by continuous homojunction with spatially separated redox sites for hydrogen evolution

被引:3
|
作者
Yu, Mingyuan [1 ]
Wang, Tongyu [1 ]
Huang, Chengxi [1 ]
Wu, Fang [2 ]
Liu, Xuan [1 ]
Huo, Hailing [1 ]
Jian, Hanwen [1 ]
Liang, Zikun [1 ]
Ma, Jingjing [3 ]
Kan, Erjun [1 ]
Li, Ang [1 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Sci, MIIT Key Lab Semicond Microstruct & Quantum Sensin, Nanjing 210094, Peoples R China
[2] Nanjing Forestry Univ, Coll Informat Sci & Technol, Nanjing 210037, Peoples R China
[3] Ningxia Univ, State Key Lab High Efficiency Utilizat Coal & Gree, Yinchuan 750021, Ningxia, Peoples R China
基金
中国国家自然科学基金;
关键词
continuous homojunction; spatially separated reaction sites; charge separation; hydrogen evolution; SEMICONDUCTORS; ANATASE; SPHERES; SIZE;
D O I
10.1007/s12274-023-5976-4
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photocatalytic hydrogen generation represents a promising strategy for the establishment of a sustainable and environmentally friendly energy reservoir. However, the current solar-to-hydrogen conversion efficiency is not yet sufficient for practical hydrogen production, highlighting the need for further research and development. Here, we report the synthesis of a Sn-doped TiO2 continuous homojunction hollow sphere, achieved through controlled calcination time. The incorporation of a gradient doping profile has been demonstrated to generate a gradient in the band edge energy, facilitating carrier orientation migration. Furthermore, the hollow sphere's outer and inner sides provide spatially separated reaction sites allowing for the separate acceptance of holes and electrons, which enables the rapid utilization of carriers after separation. As a result, the hollow sphere TiO2 with gradient Sn doping exhibits a significantly increased hydrogen production rate of 20.1 mmol & BULL;g-1 & BULL;h-1. This study offers a compelling and effective approach to the designing and fabricating highly efficient nanostructured photocatalysts for solar energy conversion applications.
引用
收藏
页码:12323 / 12330
页数:8
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