4.7 Article

Promoting Charge Separation in Hollow-Structured C/MoS2@ZnIn2S4/Co3O4 Photocatalysts via Double Heterojunctions for Enhanced Photocatalytic Hydrogen Evolution

Journal

INORGANIC CHEMISTRY
Volume 61, Issue 11, Pages 4725-4734

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.2c00045

Keywords

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Funding

  1. Natural Science Foundation of Jiangsu Province [BK20201424]
  2. National Natural Science Foundation of China [21975110]

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In this study, a new core-shell composite material was designed for photocatalytic hydrogen evolution reaction with significant success. The composite material had dual electron collectors, providing a dual electron transfer pathway, leading to enhanced light absorption ability and hydrogen evolution rate.
A reasonable design of samples with efficient spatial separation for photoinduced electron-hole pairs toward the photocatalytic hydrogen evolution reaction (HER) has gained significant attention. Herein, a new C/MoS2@ZnIn2S4/Co3O4 composite with a core-shell structure is designed toward photocatalytic hydrogen production on C/MoS2 and Co3O4 dual electron collectors. Co3O4 nanoparticles as the co-catalyst would form a Schottky junction with ZnIn2S4 nanosheets while the C/MoS2 hollow core would form the step-scheme (S-scheme) heterojunction with ZnIn2S4 sheets, which provides a dual photogenerated electron transfer pathway during the light irradiation process. In addition, the unique core-shell architecture offers large contact interfaces favoring the exposure of rich active sites, which facilitated the separation and the transfer of charges. Consequently, all these factors endowed the C/MoS2@ZnIn2S4/Co3O4 composite with enhanced light absorption ability and an increased hydrogen evolution rate of 6.7 mmol.g(-1).h(-1) under 420 nm light irradiation, which is about 23.4- and 4.5-fold that of ZnIn2S4 and CMZ, respectively. This work offers a guideline for designing efficient composite photocatalysts toward the photocatalytic HER.

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