4.7 Article

Photogenerated charge dynamics of CdS nanorods with spatially distributed MoS2 for photocatalytic hydrogen generation

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 420, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2020.127709

Keywords

CdS/MoS2 heterostructures; Spatial distribution; Photocatalytic H-2 evolution; Photogenerated charge dynamics

Funding

  1. Australian Research Council (ARC) [DP170102895]
  2. Hong Kong Research Grant Council (RGC) [GRF1305419]

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A series of MoS2-loaded CdS nanorods have been fabricated, with MoS2 spatially distributed on the tips or both tips and walls of the CdS NRs. The presence of a spatial electric field between CdS NRs and MoS2 tips strongly induces photogenerated electron-hole separation and electron transfer. MoS2 located on the tips of CdS NRs can better separate electron-hole pairs and suppress charge recombination, leading to superior photoactivity.
A series of MoS2-loaded CdS nanorods (NRs) have been successfully fabricated with the MoS2 spatially distributed only on the tips or on the tips and walls of the CdS NRs, which impacted on photocatalytic H-2 evolution activity. MoS2-tipped CdS NRs were found to exhibit a better H-2 evolution performance (31.46 mmol h(-1) g(-1)) than MoS2-coated CdS NRs (7.32 mmol h(-1) g(-1)) and bare CdS NRs (2.96 mmol h(-1) g(-1)). Kelvin probe force microscopy (KPFM) was used to identify the presence of a spatial electric field between the CdS NR and MoS2 tip, with the electric field strongly inducing photogenerated electron-hole separation along the long axis of the CdS NRs and electron transfer to MoS2 tips. The effect of longitudinal transfer of photogenerated electrons was confirmed by Pt photodeposition where it was found that Pt particles were photodeposited on the MoS2 tips, whereas, in the case of pure CdS NRs and MoS2-coated CdS NRs, Pt particles were photodeposited on the walls and tips of the NRs, indicating a lack of spatially directional charge transfer. Time-resolved photoluminescence (TRPL) spectroscopy using band pass and long pass filters was employed to demonstrate that MoS2 located on the tips of CdS NR can better separate photogenerated electron-hole pairs and suppress charge recombination. Consequently, slow charge recombination and spatially separated redox sites, deriving from MoS2 tip engendered long distance of electron separation and transfer within the CdS NRs, give rise to the superior photoactivity by the MoS2-tipped CdS NRs. This study reveals the relationship between the MoS2 distribution and photogenerated charge dynamics, and also provides greater insight into the performance of CdS-MoS2 composites for photocatalytic H-2 evolution.

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