光催化
催化作用
材料科学
聚合
纳米晶
电子转移
吸附
化学工程
环境友好型
氧化还原
降级(电信)
可见光谱
纳米技术
光化学
化学
有机化学
光电子学
聚合物
复合材料
冶金
工程类
生态学
生物
电信
计算机科学
作者
Chengcheng Chu,Wei Miao,Qiuju Li,Dandan Wang,Ying Liu,Shun Mao
标识
DOI:10.1016/j.cej.2021.132531
摘要
Light-driven molecular oxygen reduction to H2O2 from water is an emerging environmentally friendly approach that can convert solar energy into green chemical. In this work, the photocatalytic properties of g-C3N4 for H2O2 production was enhanced by co-modification with cyano group and SnO2 nanocrystal through a facile one-step thermal polymerization method. The cyano group and SnO2 nanocrystal broaden the photo-absorption range of g-C3N4, enhance the electron generation and transfer ability, and provide more active sites for O2 and H+ adsorption. Significantly, this structure modification strategy leads to excellent H2O2 production performance, and the H2O2 yield rate reaches 703.4 μM g-1h−1 under visible light illumination, which is superior among g-C3N4-based photocatalysts. Moreover, the reaction mechanism study indicates that the photocatalytic H2O2 production proceeds through a two-step single-electron reaction and the catalyst shows good cyclability for long-term use. This work demonstrates a novel and feasible modification approach to improve the photocatalytic activity of g-C3N4, and will promote the development of advanced semiconducting catalysts for photocatalytic H2O2 evolution.
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