Hydrogen bond-assisted construction of MOF/semiconductor heterojunction photocatalysts for highly efficient electron transfer

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 (labe...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2024-11, Vol.357, p.124297, Article 124297
Hauptverfasser: Dong, Pengyu, Gao, Kangjie, Zhang, Lihua, Huan, Hengke, Xie, Ming-Hua, Yang, Xiu-Li, Zhang, Jinlong
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Sprache:eng
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Zusammenfassung: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. [Display omitted] •MOF/semiconductor heterojunction photocatalyst was firstly constructed.•Hydrogen-bonded combination between the –OOH groups and the –NH2 group in MOF.•The significantly enhanced photocatalytic property of the H-T/M heterojunction for reducing Cr(VI).•The built-in electric field could provide the driving force for charge transfer.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2024.124297