异质结
光降解
范德瓦尔斯力
光催化
光电子学
电场
光化学
载流子
氧化还原
化学
化学物理
材料科学
分子
物理
有机化学
催化作用
量子力学
冶金
作者
Yi Zhong,Chenglin Wu,Daimei Chen,Jinzhong Zhang,Yanmei Feng,Kang Xu,Weichang Hao,Hao Ding,Guocheng Lv,Yi Du,Lianzhou Wang
标识
DOI:10.1016/j.apcatb.2023.122554
摘要
As 2D heterojunction photocatalysts, lateral heterojunctions (LHs) formed based on chemical bonding generally exhibit much higher photocarrier separation efficiency than vertical heterojunctions (VHs) formed by van der Waals bonds. However, little is known about the different detailed interfacial structures and photocarrier separation mechanisms of the two heterojunctions. Herein, 2D BiOCl and Bi4O5I2 were selected as model building blocks to construct BiOCl/Bi4O5I2 VHs and LHs. The LHs with direct charge carrier transport channels show stronger interfacial electric field and higher charge transfer efficiency than the VHs. The photogenerated charge carrier migration pathway in the LHs follows a Z-scheme model, while the VHs fits a type II model. As a result, the BiOCl/Bi4O5I2 LHs exhibited higher redox performance than the VHs, which is 1.55, 1.56 and 2.1 times better for H2 production, Cr(VI) photoreduction and phenol photodegradation, respectively. This study demonstrates a new approach to constructing highly efficient facet-dependent 2D heterojunction photocatalysts.
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