期刊
APPLIED CATALYSIS B-ENVIRONMENTAL
卷 258, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.apcatb.2019.117956
关键词
-
资金
- Program for the National Natural Science Foundation of China [81773333, 51521006, 51879101, 51579098, 51779090, 51709101, 51809090, 51278176, 51378190]
- National Program of Top-Notch Young Professionals of China (2014)
- Program for Changjiang Scholars and Innovative Research Team in University [IRT-13R17]
- Hunan Provincial Science and Technology Plan Project [2018SK20410, 2017SK2243, 2016RS3026]
- Fundamental Research Funds for the Central Universities [531119200086, 531118010114, 531107050978]
The development of efficient photocatalysts for the production of hydrogen peroxide (H2O2) is a promising strategy to realize solar-to-chemical energy conversion. Graphitic carbon nitride (g-C3N4) presents giant potential for photocatalytic H2O2 production, but the sluggish charge separation depresses its photocatalytic performance. Herein, an interfacial Schottky junction composed of Ti3C2 nanosheets and porous g-C3N4 nanosheets (TC/pCN) is constructed by a facile electrostatic self-assembly route to significantly boost the spatial charge separation to promote the activation of molecular oxygen for H2O2 production. As the optimal sample, TC/pCN-2 possesses the highest H2O2 production rate (2.20 mu mol L-1 min(-1)) under visible light irradiation (lambda > 420 nm), which is about 2.1 times than that of the porous g-C3N4. The results of superoxide radical detection and rotating disk electrode measurement suggest that the two-step single-electron reduction of oxygen is the predominant reaction step during this photocatalytic H2O2 production process. The enhanced photocatalytic performance is ascribed to the formation of Schottky junction and subsequent built-in electric field at their interface, which accelerate the spatial charge separation and restrain the charge recombination. This work provides an in-depth understanding of the mechanism of photocatalytic H2O2 production, and gives ideas for the design of highly active materials for photocatalytic H2O2 production.
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