4.7 Article

Emb e dding laser-generate d CdTe nanocrystals into ultrathin ZnIn 2 S 4 nanosheets with sulfur vacancies for boosted photocatalytic H 2 evolution

Journal

JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
Volume 166, Issue -, Pages 113-122

Publisher

JOURNAL MATER SCI TECHNOL
DOI: 10.1016/j.jmst.2023.02.066

Keywords

Photocatalysis; Hydrogen evolution; Laser irradiation; Heterostructure; Sulfur vacancies

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CdTe nanocrystals are embedded into ultrathin ZnIn2S4 nanosheets to construct ZnIn2S4/CdTe heterostructures, which exhibit excellent catalytic activity. The enhancement is attributed to nanoscale heterojunctions and sulfur vacancies, promoting charge separation and facilitating the H2 generation reaction. The research provides new insights into the regulation of charge transfer through embedding nanocrystals.
To suppress the inner charge recombination and inject vast electrons, CdTe nanocrystals are embedded into ultrathin ZnIn2S4 nanosheets to construct ZnIn2S4/CdTe heterostructures, where the nanocrystals are generated by a laser irradiation method. The optimal ZnIn2S4/CdTe heterojunction exhibits an excellent catalytic activity of 24.3 mmol/h/g, which is relatively high among the ZnIn2S4-based photocatalysts with-out noble metals. This enhancement is ascribed to a win-win mechanism of nanoscale heterojunctions and sulfur vacancies. The strong electron coupling effect, which is verified by density functional the-ory (DFT) calculations, impels the photo-generated electrons transfer from CdTe to ZnIn2S4, boosting the charge separation. Meanwhile, the sulfur vacancies existing in ZnIn2S4 can capture photoelectrons and act as active sites, facilitating the H 2 generation reaction. In addition, the ZnIn2S4 base and the ZnIn2S4/CdTe heterojunction also possess an evident photothermal effect and renewable cycle phenomena, enhancing the photocatalytic performance. This research provides new insights into the regulation of charge transfer through embedding nanocrystals.& COPY; 2023 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.

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