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 |
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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.
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•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. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2024.124297 |