1D/1D W 18 O 49 /Cd 0.9 Zn 0.1 S S-scheme heterojunction with spatial charge separation for high-yield photocatalytic H 2 evolution.

Semiconductor photocatalytic water splitting is a green way to convert solar energy into chemical energy, but the recombination of electron and hole pairs and the low utilization of sunlight restrict the development of photocatalytic technology. By comparing the morphologies and hydrogen production properties of different proportions of solid solutions (CdZnS), one-dimensional (1D) CdZnS nanorods (NRs) with the best photocatalytic properties are obtained. In addition, 1D WO nanowires are assembled on the surface of 1D CdZnS NRs to construct a novel 1D/1D step-scheme (S-scheme) WO/CdZnS heterojunction photocatalyst. The WO/CdZnS heterojunction expands the optical absorption capacity of CdZnS NRs to provide more energy for the photoexcitation of electrons. The optimal hydrogen production rate of WO/CdZnS NRs with WO content of 9 wt% is as high as 66.3 mmol·h·g, which is 5.7 times and 1.6 times higher than that of CdZnS NRs and 1 wt% Pt/CdZnS NRs. The apparent quantum efficiency (AQE) of 9 wt% WO/CdZnS reaches 56.0 % and 25.9 % under light wavelength irradiation at 370 and 456 nm, respectively. After the 20 h cycle stability test, the activity of photocatalytic hydrogen evolution does not decrease, due that the severe photo-corrosion of CdZnS NRs is efficiently inhibited. This work not only provides a simple and controllable synthesis method for the preparation of heterojunction structure, but also opens up a new way to improve the hydrogen evolution activity and stability of sulfur compounds.