异质结
半导体
电子转移
材料科学
光催化
光电子学
氢键
氢
纳米技术
化学工程
光化学
化学
分子
工程类
催化作用
有机化学
作者
Pengyu Dong,Kangjie Gao,Lihua Zhang,Hengke Huan,Ming-Hua Xie,Xiu‐Li Yang,Jinlong Zhang
标识
DOI:10.1016/j.apcatb.2024.124297
摘要
It remains challenging for the fabrication of metal-organic framework (MOF)/semiconductor heterojunction photocatalysts with close contact interfaces. In this work, a novel MOF/semiconductor heterojunction photocatalyst consisting of H2O2-modified TiO2 nanotubes (H2O2-TNTs) and MIL-88B(Fe)-NH2 (labeled as H-T/M) was firstly constructed based on the hydrogen-bonded combination between the O atoms from –OOH groups resulting from H2O2 absorbed on the surface of TiO2 nanotubes and the H atoms of the –NH2 group in MOF. The significantly enhanced photocatalytic property of the H-T/M heterojunction for reducing Cr(VI) could be ascribed to the accelerated interfacial electron transfer dynamics by a channel of hydrogen bonds (N···H–O–O–Ti), which could be extracted from the femtosecond transient absorption spectroscopy (fs-TAS). Moreover, the built-in electric field and the differences in charge density based on density functional theory (DFT) calculations could provide the driving force for charge transfer.
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