Hollow cubic CdS@CoS/WS2 dual S-scheme heterojunction superstructure toward optimized photothermal-photocatalytic performance

A hollow polyhedral structure can effectively capture light and facilitate carrier separation, thus enhancing photocatalytic performance. Herein, hollow cubic CdS@CoS/WS2 dual S-scheme heterojunction superstructure photocatalysts are fabricated using a simple sulfidation and hydrothermal method. CdS@CoS/WS2 with a band gap of 1.59 eV and a relatively narrow band gap broadens the photoreaction to the near-infrared region and shows a good photothermal effect, which can promote photocatalytic reactions. It shows a relative specific surface area of 91.58 m(2) g(-1), which provides abundant surface-active sites to enhance the photocatalytic reaction. Under light conditions, the photocatalytic degradation ratios of CdS@CoS/WS2 for tetracycline and bisphenol A are up to 98.9 and 99.1%, and the hydrogen evolution efficiency is also up to 10.62 mmol h(-1) g(-1). The enhanced photothermal-photocatalytic performance could be due to the formation of a dual S-scheme heterojunction superstructure that facilitates space charge separation, a narrow band gap and a mesoporous hollow structure promoting solar light utilization, providing abundant surface-active sites and enhanced mass transfer. This simple strategy provides a new idea for the construction of high-performance hollow superstructure photocatalysts.

Automated summary

In this study, hollow cubic CdS@CoS/WS2 dual S-scheme heterojunction superstructure photocatalysts were successfully fabricated, which showed excellent photocatalytic performance and photothermal effect. The photocatalysts had a broad light absorption range and abundant surface-active sites, enabling efficient degradation of organic pollutants and hydrogen production. This study provides a new avenue for constructing high-performance hollow superstructure photocatalysts.