Constructing copper Phthalocyanine/Molybdenum disulfide (CuPc/MoS2) S-scheme heterojunction with S-rich vacancies for enhanced Visible-Light photocatalytic CO2 reduction.

A S-scheme heterojunction of CuPc/DR-MoS 2 with abundant sulfur vacancies is proposed, enabling extended visible-light absorption, enhanced charge carrier separation/transfer, and improved efficiency of semiconductors. Additionally, sulfur vacancies play a significant role in enhancing CO 2 adsorption/activation on the photocatalyst surface during photocatalysis. [Display omitted] Constructing a heterojunction by combining two semiconductors with similar band structures is a successful approach to obtaining photocatalysts with high efficiency. Herein, a CuPc/DR-MoS 2 heterojunction involving copper phthalocyanine (CuPc) and molybdenum disulfide with S-rich vacancies (13.66%) is successfully prepared by the facile hydrothermal method. Experimental results and theoretical calculations firmly demonstrated that photoelectrons exhibit an S-scheme charge transfer mechanism in the CuPc/DR-MoS 2 heterojunction. The S-scheme heterojunction system has proven significant advantages in promoting the charge separation and transfer of photogenerated carriers, enhancing visible-light responsiveness, and achieving robust photoredox capability. As a result, the optimized 3CuPc/DR-MoS 2 S-scheme heterojunction exhibits photocatalytic yields of CO and CH 4 at 200 and 111.6 μmol g-1h−1, respectively. These values are four times and 4.5 times greater than the photocatalytic yields of pure DR-MoS 2. This study offers novel perspectives on the advancement of innovative and highly effective heterojunction photocatalysts. [ABSTRACT FROM AUTHOR]