Controlled Ni doping on a g-C3N4/CuWO4 photocatalyst for improved hydrogen evolution

Phys Chem Chem Phys. 2023 Aug 30;25(34):23033-23046. doi: 10.1039/d3cp03194b.

Abstract

The development of a low-cost, environment-friendly and suitable semiconductor-based heterogeneous photocatalyst poses a great challenge towards extremely competent and substantial hydrogen evolution. A series of environment-friendly and proficient S-scheme Ni-doped CuWO4 nanocrystals supported on g-C3N4 nanocomposites (Ni-CuWO4/g-C3N4) were constructed to ameliorate the photocatalytic efficacy of pure g-C3N4 and Ni-CuWO4 and their activity in H2 generation through photocatalytic water splitting was evaluated. The Ni-CuWO4 nanoparticles were synthesized through doping of Ni2+ on wolframite CuWO4 crystals via the chemical precipitation method. An elevated hydrogen generation rate of 1980 μmol h-1 g-1 was accomplished over the 0.2Ni-CuWO4/g-C3N4 (0.2NCWCN) nanocomposite with an apparent quantum yield (AQY) of 6.49% upon visible light illumination (λ ≥ 420 nm), which is evidently 7.1 and 17.2 fold higher than those produced from pristine g-C3N4 and Ni-CuWO4. The substantial enhancement in the photocatalytic behaviour is primarily because of the large surface area, limited band gap energy of the semiconductor composite and magnified light harvesting capability towards visible light through the inclusion of g-C3N4, thus diminishing the reassembly rate of photoinduced excitons. Further, density functional theory (DFT) calculations were performed to investigate the structural, electronic and optical properties of the composite. Theoretical results confirmed that the Ni-CuWO4/g-C3N4 composite is a potential candidate for visible-light-driven photocatalysts and corroborated with the experimental findings. This research provides a meaningful and appealing perspective on developing cost-effective and very proficient two-dimensional (2D) g-C3N4-based materials for photocatalytic H2 production to accelerate the separation and transmission process of radiative charge carriers.