A Cu(InGa)Se2 film was modified with CdS/ZnO for application to solar water splitting. Platinum was electrodeposited on the ZnO layer as a hydrogen evolution catalyst. The effects of the electroplating time and acidity level of the electrolyte on the photocurrent density were studied. The highest photocurrent density of -32.5 mA/cm(2) under 1.5 AM illumination was achieved with an electroplating time of 30 min at a pH of 9. This photocurrent density is higher than those reported in previous studies. The markedly high performance of the CIGS/CdS/ZnO photocathode was rationalized in terms of its type II cascade structure that facilitated efficient charge separation at the interface junction.
BiVO4 is ubiquitously known for its potential use as photoanode for PEC-WS due to its well-suited band structure; nevertheless, it suffers from the major drawback of a slow electron hole separation and transportation. We have demonstrated the one-pot synthesis of BiVO4/Ag/rGO hybrid photoanodes on a fluorine-doped tin oxide (FTO)-coated glass substrate using a facile and cost-effective hydrothermal method. The structural, morphological, and optical properties were extensively examined, confirming the formation of hybrid heterostructures. Ternary BiVO4/Ag/rGO hybrid photoanode electrode showed enhanced PEC performance with photocurrent densities (J
ph) of ~2.25 and 5 mA/cm2 for the water and sulfate oxidation, respectively. In addition, the BiVO4/Ag/rGO hybrid photoanode can convert up to 3.5% of the illuminating light into photocurrent, and exhibits a 0.9% solar-to-hydrogen conversion efficiency. Similarly, the photocatalytic methylene blue (MB) degradation afforded the highest degradation rate constant value (k = 1.03 × 10−2 min−1) for the BiVO4/Ag/rGO hybrid sample. It is noteworthy that the PEC/photocatalytic performance of BiVO4/Ag/rGO hybrid architectures is markedly more significant than that of the pristine BiVO4 sample. The enhanced PEC/photocatalytic performance of the synthesized BiVO4/Ag/rGO hybrid sample can be attributed to the combined effects of strong visible light absorption, improved charge separation-transportation and excellent surface properties.
We demonstrate, for the first time, electrostatically sprayed bismuth vanadate (BiVO4) thin films for photoelectrochemical water splitting. Characterization of these films by X-ray diffraction, Raman scattering, and high-resolution scanning electron microscopy analyses revealed the formation of nanotextured pillar-like structures of highly photoactive monoclinic scheelite BiVO4. Electrosprayed BiVO4 nanostructured films yielded a photocurrent density of 1.30 and 1.95 mA/cm(2) for water and sulfite oxidation, respectively, under 100 mW/cm(2) illumination. The optimal film thickness was 3 μm, with an optimal postannealing temperature of 550 °C. The enhanced photocurrent is facilitated by formation of pillar-like structures in the deposit. We show through modeling that these structures result from the electrically-driven motion of submicron particles in the direction parallel to the substrate, as they approach the substrate, along with Brownian diffusion. At the same time, opposing thermophoretic forces slow their approach to the surface. The model of these processes proposed here is in good agreement with the experimental observations.
We demonstrate that the addition of a tungsten oxide (WO3) layer beneath a bismuth vanadate (BiVO4) photocatalyst layer with a nanotextured pillar morphology significantly increases the photocurrent density in photoelectrochemical water splitting. The WO3-BiVO4 bilayer films produced a photocurrent of up to 3.3 mA/cm2 under illumination at 100 mW/cm2 (AM1.5 spectrum). The bilayer film was characterized by scanning electron microscopy, X-ray diffraction, and photoelectrochemical methods, which confirmed the superiority of the bilayer film in terms of its morphology and charge separation and transport ability. Both WO3 and BiVO4 were deposited by electrostatic spraying under open-air conditions, which resulted in nanotextured pillars of BiVO4 atop a smooth WO3 film. The optimal coating conditions are also reported.
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