Abstract
It is facing a tremendous challenge to develop the desirable hybrids for photocatalytic H2 generation by integrating the advantages of a single semiconductor. Herein, an all-sulfide ZnIn2S4/CdS/PdS heterojunction is constructed for the first time, where CdS and PdS nanoparticles anchor in the spaces of ZnIn2S4 micro-flowers due to the confinement effects. The morphology engineering can guarantee rapid charge transfer owing to the short carrier migration distances and the luxuriant reactive sites provided by ZnIn2S4. The S-scheme mechanism between ZnIn2S4 and CdS assisted by PdS cocatalyst is testified by in situ irradiated X-ray photoelectron spectroscopy and electron paramagnetic resonance (EPR), where the electrons and holes move in reverse driven by work function difference and built-in electric field at the interfaces. The optimal ZnIn2S4/CdS/PdS performs a glaring photocatalytic activity of 191.9 µmol h−1 (10 mg of catalyst), and the largest AQE (apparent quantum efficiency) can reach a high value of 26.26%. This work may afford progressive tactics to design multifunctional photocatalysts.
Original language | English |
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Article number | 2207758 |
Journal | Small |
Volume | 19 |
Issue number | 27 |
DOIs | |
State | Published - 5 Jul 2023 |
Keywords
- S-scheme mechanisms
- co-catalysts
- hydrogen generation
- photocatalysis
- water splitting