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Synergistic Photoelectrochemical and Photocatalytic Properties of the Cobalt Nanoparticles-Embedded TiVO(4) Thin Film
[Image: see text] To optimize the semiconductor properties of TiVO(4) thin films and enhance their performance, we incorporated cobalt nanoparticles as an effective co-catalyst consisting of a non-noble metal. Through an investigation into the impact of cobalt loading on spray pyrolyzed TiVO(4) thin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10398684/ https://www.ncbi.nlm.nih.gov/pubmed/37546630 http://dx.doi.org/10.1021/acsomega.3c02089 |
Sumario: | [Image: see text] To optimize the semiconductor properties of TiVO(4) thin films and enhance their performance, we incorporated cobalt nanoparticles as an effective co-catalyst consisting of a non-noble metal. Through an investigation into the impact of cobalt loading on spray pyrolyzed TiVO(4) thin films, we observed a significant enhancement in the photoelectrochemical (PEC) performance. This was accomplished by carefully optimizing the concentrations of Co(2+) (3 mM) to fabricate a composite electrode, resulting in a higher photocurrent density for the TiVO(4):Co photoanode. When an applied potential of 1.23 V (vs RHE) was used, the photocurrent density reached 450 μA/cm(2), approximately 5 times higher than that of bare TiVO(4). We conducted a thorough characterization of the composite structure and optical properties. Additionally, electrochemical impedance spectroscopy analysis indicated that the TiVO(4)/Co thin film exhibited a smaller semicircle, indicating a significant improvement in charge transfer at the interface. In comparison to bare TiVO(4), the TiVO(4)/Co composite exhibited a notable improvement in photocatalytic activity when degrading methylene blue (MB) dye, a widely employed model dye. Under light illumination, a TiVO(4)/Co thin film exhibited a notable dye degradation rate of 97% within a 45 min duration. The scalability of our fabrication method makes it suitable for large-area devices intended for sunlight-driven PEC seawater splitting studies. |
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