光催化
贵金属
猝灭(荧光)
光化学
电子转移
金属
化学工程
催化作用
氧化还原
太阳能燃料
无机化学
化学
荧光
量子力学
物理
工程类
有机化学
生物化学
作者
Yiming Chen,Wenquan Gu,Li Tan,Zhimin Ao,Taicheng An,Shaobin Wang
标识
DOI:10.1016/j.apcata.2021.118127
摘要
Photocatalytic H2O2 production by O2 reduction is an environmental-friendly process for solar light conversion to chemical energy. In this work, Ti3C2 MXene was used as a non-noble metal cocatalyst to load on P25 as Ti3C2/TiO2 (TC/TO) photocatalysts for photocatalytic H2O2 synthesis. A H2O2 formation rate (179.7 μmol L−1 h−1) of the optimized 10 %-TC/TO composite was obtained to be over 21 folds as high as that of P25 under UV light. Radical quenching experiments and superoxide radical detection confirmed the superoxide radical as the primary intermediate, suggesting the O2 reduction in two-step single-electron indirect reaction. The higher activity of TC/TO can be attributed to the functions of Ti3C2 MXene in accelerating the separation and transfer of photogenerated electron-hole pairs, suppressing their recombination, and blocking the surface TiOOH formation. This work proves the promising roles of Ti3C2 MXene in the photocatalytic reaction and further expands their new applications in photocatalysis.
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