CS bonds mediated rapid charge transfer in hm-C4N3/CdS heterostructure for efficient photocatalytic CO2 reduction

J Colloid Interface Sci. 2025 Jan 3;684(Pt 1):300-308. doi: 10.1016/j.jcis.2024.12.247. Online ahead of print.

Abstract

The quest for stable and high-performance photocatalysts is pivotal in advancing the field of photocatalytic CO2 reduction. Traditional single-component semiconductors are often impeded by their inability to concurrently achieve a broad light absorption spectrum, efficient separation of photogenerated charge carriers, and enduring stability, thereby constraining their photocatalytic efficacy. In this study, we introduce an innovative hm-C4N3/CdS heterojunction that broadens the light absorption spectrum and significantly enhances the separation efficiency of photogenerated charge carriers. Notably, this type-II heterojunction design effectively curbs the photocorrosion of CdS, and the CS bonds within the structure expedite electron transfer. Under irradiation, the photocatalyst exhibits a marked increase in activity and stability, yielding CO and CH4 at rates of 67.5 μmol g-1 h-1 and 7.4 μmol g-1 h-1, respectively. This work provides valuable insights for promoting efficient and stable photocatalyst for CO2 reduction.

Keywords: CO(2) reduction; Photocatalytic; Type-II heterojunction; hm-C(4)N(3).