Janus Flower-Like Hollow TiO2 Photocatalysts Bearing RuO2 and Pt Nanoparticles for Solar-Light-Driven Catalytic H2 Evolution

被引:0
作者
Li, Bowen [3 ]
Zhu, Huihui [1 ]
Zhang, Hao [2 ]
Xiao, Lina [2 ]
He, Siyuan [4 ]
机构
[1] Henan Univ, Sch Energy Sci & Technol, Kaifeng 475004, Peoples R China
[2] Xinyang Univ, Coll Technol, Xinyang 464000, Peoples R China
[3] Zhoukou Normal Univ, Coll Phys & Telecommiunicat Engn, Zhoukou 466001, Peoples R China
[4] Zhoukou Normal Univ, Lib, Zhoukou 466001, Peoples R China
基金
中国国家自然科学基金;
关键词
flower-like hollow TiO2; spatiallyseparateddual cocatalysts; Janus structure; position control; H-2; evolution; CONSTRUCTION; HETEROJUNCTIONS; DEGRADATION; REDUCTION; SPECTRUM; WATER;
D O I
10.1021/acsanm.3c03453
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The reaction efficiency of TiO2-based photocatalysts can be improved through the effective utilization of light and separation of carriers, which can be achieved via material structure designing. Herein, the synthesis of a novel hollow flower-like TiO2-based nanomaterial by regulating the positions of dual cocatalysts on a Janus surface is reported. The dual cocatalysts (RuO2 and Pt NPs) with redox capability were selectively deposited on different surfaces (constructed Janus surface) of TiO2 materials to achieve directional transfer and spatial separation of photogenerated charges. Furthermore, the presence of dual cocatalysts may reduce the activation energy necessary for the reaction, enable the catalytic reaction to progress in a favorable direction, and increase the catalyst capability. Additionally, hollow nanostructures significantly shorten the migration distance of photogenerated carriers, owing to their thin-shell structure, further improving the separation of electron-hole pairs and migration efficiency. The results indicate that the deposition positions of the dual cocatalysts significantly affect the H-2-evolution rate. Further studies reveal that macromolecule OH- exhibits a lower probability of entering the inner surface of the catalyst to participate in the reaction, whereas micromolecule H+ demonstrates a higher probability of entering the inner surface of the catalyst, leading to differences in catalyst activity. Among the analyzed samples, PTR demonstrates the most notable H-2-evolution rate, reaching 4,024 mu mol g(-1) h(-1), which is higher than those of pure TiO2 and RTP by 60.96- and 1.22-fold, respectively. Furthermore, the mechanism of the charge migration pathway was analyzed via ultraviolet photoelectron spectroscopy, Mott-Schottky plots, and ultraviolet-visible diffusive reflectance spectroscopy. Catalyst activity increased substantially under illumination owing to the synergy between the special hollow Janus structure and the spatially separated dual cocatalysts.
引用
收藏
页码:18978 / 18987
页数:10
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