Enhanced Photoelectrocatalytic H <sub/>2</sub> Evolution over Two-Dimensional MoS <sub/>2</sub> Nanosheets Loaded on Cu-Doped CdS Nanorods

摘要： Transition-metal ion doping and efficient decoration by using a co-catalyst have been proven to effectively inhibit the recombination of photogenerated electron-hole pairs and broaden the visible-light response region. Here, we have constructed MoS2 nanosheets decorated on a copper-doped CdS nanorod composite as a noble-metal-free photoelectrocatalyst. This kind of composite material was constructed through a simple solvothermal method. The morphology, structure, chemical states, photoelectrochemical properties, and other properties were tested by using a diverse range of analytical techniques. Owing to the Cu2 + doping and the excellent electron-capturing ability of MoS2, 5 % MoS2/Cu(cid:0) CdS (with 7 % Cu2 + doping in CdS) exhibits excellent hydrogen evolution reaction with a rate of 10.18 mmol h(cid:0) 1 g(cid:0) 1, which is about 48 times higher than that of pure CdS. A significant increase in the photoelectrochemical performance of the composite catalytic material benefits from the synergistic effect between CdS and MoS2 and fast interfacial charge transfer, owing to the Cu2 + doping. These findings provide a new thought for further research of the ion doping in photoelectrocatalytic field.