Constructing multifunctional novel noble-metal free NiS/ZnS/g-C3N4 ternary nanocomposites for highly active superior photocatalytic water splitting
Keywords: energy, active sites, H2 production, Co-catalysis, Carrier transfer
Abstract
Ultrasound-assisted wet-impregnation approach and cation-exchange hydrothermal method are employed effectively to develop the ternary nanocomposites NiS/ZnS/g-C3N4 (NZ-CN) with promising photocatalytic hydrogen (H2) generation activity. Several analytical techniques are utilized to characterize the as-synthesized NiS/ZnS/g-C3N4 nanocomposites to study their physical and chemical characteristics. The H2 production activity of the synthesized photocatalysts was tested using a 250 W halogen lamp with Na2S (0.25 M) and Na2SO3 (0.35 M) as sacrificial reagents. The optimized NZ-CN7.5% (3% NiS/ZnS/7.5% g-C3N4) catalyst displayed an exceptional H2 generation rate of 8624 mu mol h-1 g-1, exceeding both, pristine g-C3N4 (by 22.1 times) and 3% NiS/ ZnS (by 3 times). This represents the highest reported rate of H2evolution for a graphitic carbon nitride (g-C3N4) based ternary nanocomposite under simulated solar radiation. By reusing the used NZ-CN7.5% (3% NiS/ZnS/ 7.5% g-C3N4) photocatalyst in four consecutive runs, the stability of the catalyst was investigated, and their individual activity in the H2 production activity was assessed. This study provides valuable insights for designing efficient noble metal-free g-C3N4-based photocatalysts, which can significantly contribute to the transition to solar-driven hydrogen generation. Further, we proposed a plausible mechanism for the photocatalytic H2 generation process over the NiS/ZnS/g-C3N4 photocatalyst.
Más información
| Título según WOS: | Constructing multifunctional novel noble-metal free NiS/ZnS/g-C3N4 ternary nanocomposites for highly active superior photocatalytic water splitting |
| Título de la Revista: | INTERNATIONAL JOURNAL OF HYDROGEN ENERGY |
| Volumen: | 139 |
| Editorial: | PERGAMON-ELSEVIER SCIENCE LTD |
| Fecha de publicación: | 2025 |
| Página de inicio: | 935 |
| Página final: | 945 |
| Idioma: | English |
| DOI: |
10.1016/j.ijhydene.2024.07.090 |
| Notas: | ISI |