Light-Induced Formation of MoOS Clusters on CdS Nanorods as Cocatalyst for Enhanced Hydrogen Evolution.

Metal and metal-oxide particles are commonly photodeposited on photocatalysts by reduction and oxidation reactions, respectively, consuming charges that are generated under illumination. This study reveals that amorphous MoOS clusters can be easily photodeposited at the tips of CdS nanorods (NRs) by in situ photodeposition for the first time. The as-prepared MoOS-decorated CdS samples were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma (ICP) to determine the composition and the possible formation pathways of the amorphous MoOS clusters. The MoOS-tipped CdS samples exhibited better hydrogen evolution performance than pure CdS under visible-light illumination. The enhanced activity is attributed to the formation of intimate interfacial contact between CdS and the amorphous MoOS clusters, which facilitates the charge separation and transfer. Through time-resolved photoluminescence (TRPL) measurements, it was clearly observed that all MoOS-decorated CdS samples with different loadings of MoOS showed a faster PL decay when compared to pure CdS, resulting from the effective trapping of photogenerated electrons by the MoOS clusters. Kelvin probe force microscopy (KPFM) was further used to study the surface potentials of pure CdS NRs and MoOS-decorated CdS NRs. A higher surface potential on MoOS-decorated CdS NRs was observed in the dark, indicating that the loading of MoOS resulted in a lower surface work function compared to pure CdS NRs. This contributed to the effective electron trapping and separation, which was also reflected by the increased photoelectrochemical response. Thus, this study demonstrates the design and facile synthesis of MoOS-tipped CdS NRs photocatalysts for efficient solar hydrogen production.