光催化
异质结
铟
材料科学
氧化物
煅烧
电子转移
化学工程
载流子
氢
光电子学
多孔性
光化学
化学
催化作用
复合材料
冶金
生物化学
工程类
有机化学
作者
Xing Liu,Lu Zhang,Yudong Li,Xianzhu Xu,Yunchen Du,Yanqiu Jiang,Kaifeng Lin
标识
DOI:10.1016/j.materresbull.2020.111078
摘要
The construction of heterojunction structures is considered as a promising method in the field of photocatalytic hydrogen evolution. Here, In-MOF precursor and melamine were mixed, then calcined and annealed to synthesize a series of In2O3/g-C3N4 heterojunction composites with multi-porosity. Porous and fluffy In2O3 provide a transmission channel, and the heterostructures can further accelerate electron transport due to the potential difference, thereby inhibiting the reorganization of electron-hole pairs. The In2O3/g-C3N4 photocatalytic hydrogen evolution average rate can reach 68.7 μmol h−1, which is almost 9.3 times that of pristine g-C3N4 (7.4 μmol h−1). Notably, the charge transfer process between In2O3/g-C3N4 heterostructure is investigated by DFT calculation. The results show that the polarization field prevents the recombination of electron-hole pairs and accelerates the transfer of photogenerated electrons so that the lifetime of photogenerated carriers is increased, ultimately enhancing the photocatalytic activity.
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