AI Article Synopsis

  • Heterostructure WO/BiVO photoanodes show promise for solar-driven hydrogen production but face challenges like poor charge separation and photocorrosion.
  • The addition of cocatalysts like NiOOH increases photocurrent density during water splitting but leads to significant degradation over time; however, using TiO passivation layers can significantly improve performance and stability.
  • The study also finds that natural mine wastewater can be effectively used as an electrolyte, allowing for hydrogen generation and recovery of zinc heavy metals during the process.

Article Abstract

The heterostructure WO/BiVO-based photoanodes have garnered significant interest for photoelectrochemical (PEC) solar-driven water splitting to produce hydrogen. However, challenges such as inadequate charge separation and photocorrosion significantly hinder their performance, limiting overall solar-to-hydrogen conversion efficiency. The incorporation of cocatalysts has shown promise in improving charge separation at the photoanode, yet mitigating photocorrosion remains a formidable challenge. Amorphous metal oxide-based passivation layers offer a potential solution to safeguard semiconductor catalysts. We examine the structural, surface morphological, and optical properties of two-step-integrated sputter and spray-coated TiO thin films and their integration onto WO/BiVO, both with and without NiOOH cocatalyst deposition. The - experiments reveal that the NiOOH cocatalyst enhances the photocurrent density of the WO/BiVO photoanode in water splitting reactions from 2.81 to 3.87 mA/cm. However, during prolonged operation, the photocurrent density degrades by 52%. In contrast, integrated sputter and spray-coated TiO passivation layer-coated WO/BiVO/NiOOH samples demonstrate a ∼88% enhancement in photocurrent density (5.3 mA/cm) with minimal degradation, emphasizing the importance of a strategic coating protocol to sustain photocurrent generation. We further explore the feasibility of using natural mine wastewater as an electrolyte feedstock in PEC generation. Two-compartment PEC cells, utilizing both fresh water and metal mine wastewater feedstocks exhibit 66.6 and 74.2 μmol/h cm hydrogen generation, respectively. Intriguingly, the recovery of zinc (Zn) heavy metals on the cathode surface in the mine wastewater electrolyte is confirmed through surface morphology and elemental analysis. This work underscores the significance of passivation layer and cocatalyst coating methodologies in a sequential order to enhance charge separation and protect the photoanode from photocorrosion, contributing to sustainable hydrogen generation. Additionally, it suggests the potential of utilizing wastewater in electrolyzers as an alternative to freshwater resources.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10900524PMC
http://dx.doi.org/10.1021/acssuschemeng.3c06528DOI Listing

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