2D/2D/0D TiO2/C3N4/Ti3C2 MXene composite S-scheme photocatalyst with enhanced CO2 reduction activity

[Display omitted] •TiO2/C3N4 forms 2D/2D core–shell van der Waals heterojunction.•0D Ti3C2 MXene quantum dots deposited on van der Waals heterojunction.•TiO2/C3N4/Ti3C2 composite photocatalyst with enhanced CO2 reduction activity.•S-scheme charge transfer mechanism observed between TiO2 and C3N4.•0D...

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Bibliographic Details
Published in:Applied catalysis. B, Environmental Vol. 272; p. 119006
Main Authors: He, Fei, Zhu, Bicheng, Cheng, Bei, Yu, Jiaguo, Ho, Wingkei, Macyk, Wojciech
Format: Journal Article
Language:English
Published: Amsterdam Elsevier B.V 05-09-2020
Elsevier BV
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Summary:[Display omitted] •TiO2/C3N4 forms 2D/2D core–shell van der Waals heterojunction.•0D Ti3C2 MXene quantum dots deposited on van der Waals heterojunction.•TiO2/C3N4/Ti3C2 composite photocatalyst with enhanced CO2 reduction activity.•S-scheme charge transfer mechanism observed between TiO2 and C3N4.•0D Ti3C2 quantum dots extract and trap electrons from C3N4. Herein, two-dimensional (2D) TiO2 mesoporous nanosheets with three to four C3N4 layers grown in situ are employed to design a core–shell 2D/2D van der Waals heterojunction (TiO2/C3N4). Edge-terminated zero-dimensional (0D) Ti3C2 MXene quantum dots (TCQD) are subsequently integrated in the C3N4 surface via electrostatic interactions. The constructed 2D/2D/0D TiO2/C3N4/Ti3C2 composite heterojunction photocatalyst exhibits enhanced CO2 reduction activity compared to TiO2, C3N4, TiO2/C3N4, C3N4/Ti3C2 for CO and CH4 production. A step-scheme (S-scheme) charge transfer mechanism operates for the prepared samples during CO2 reduction, as authenticated by in situ X-ray photoelectron spectroscopy and electron paramagnetic resonance analysis. This study provides a paradigm of a rational structural design for regulating the number and type of heterointerfaces and further insights into the mechanism of multijunction photocatalysts.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2020.119006