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Erschienen in: Journal of Materials Science 23/2018

03.08.2018 | Chemical routes to materials

In-situ construction of 2D direct Z-scheme g-C3N4/g-C3N4 homojunction with high photocatalytic activity

verfasst von: Qing Qiao, Wei-Qing Huang, Yuan-Yuan Li, Bo Li, Wangyu Hu, Wei Peng, Xiaoxing Fan, Gui-Fang Huang

Erschienen in: Journal of Materials Science | Ausgabe 23/2018

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Abstract

Constructing all-solid-state Z-scheme junction is a very effective strategy to design highly active photocatalysts for solar energy conversion and environmental purification. We herein firstly construct 2D g-C3N4/g-C3N4 Z-scheme homojunction by using a bottom-up approach, during which the supramolecular complex is initially formed, followed by a facile thermal polycondensation. Based on the active species trapping experiments, Mott–Schottky test and band edge position analysis, the prepared 2D nanosheet g-C3N4/g-C3N4 homojunctions are found to be Z-scheme type, different from those available reported ones with a type-II energy alignment. Benefiting from the specific 2D morphology with large exposed surface area and Z-scheme junction with efficient separation and high redox abilities of the photoinduced electrons and holes, the obtained 2D g-C3N4/g-C3N4 homojunctions are much more active than the conventional g-C3N4/g-C3N4 homojunction (CN-MT) and bulk g-C3N4 (CN-M) under visible light irradiation, validating by the high rhodamine degradation rate of 0.833 h1, which is about 3.9 and 15.4 times higher than that of CN-MT (0.214 h1) and CN-M (0.054 h1), respectively. The present work sheds light on design of novel Z-scheme photocatalysts with specific morphology and thus further application in the field of environment or energy.

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Metadaten
Titel
In-situ construction of 2D direct Z-scheme g-C3N4/g-C3N4 homojunction with high photocatalytic activity
verfasst von
Qing Qiao
Wei-Qing Huang
Yuan-Yuan Li
Bo Li
Wangyu Hu
Wei Peng
Xiaoxing Fan
Gui-Fang Huang
Publikationsdatum
03.08.2018
Verlag
Springer US
Erschienen in
Journal of Materials Science / Ausgabe 23/2018
Print ISSN: 0022-2461
Elektronische ISSN: 1573-4803
DOI
https://doi.org/10.1007/s10853-018-2762-x

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