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Polyoxothiometalate-Derivatized Silicon Photocathodes for Sunlight-Driven Hydrogen Evolution Reaction
[Image: see text] Silicon photocathodes coated with drop-casted {Mo(3)S(4)}-based polyoxothiometalate assemblies are demonstrated to be effective for sunlight-driven hydrogen evolution reaction (HER) in acid conditions. These photocathodes are catalytically more efficient than that coated with the p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645094/ https://www.ncbi.nlm.nih.gov/pubmed/31458082 http://dx.doi.org/10.1021/acsomega.8b01734 |
Sumario: | [Image: see text] Silicon photocathodes coated with drop-casted {Mo(3)S(4)}-based polyoxothiometalate assemblies are demonstrated to be effective for sunlight-driven hydrogen evolution reaction (HER) in acid conditions. These photocathodes are catalytically more efficient than that coated with the parent thiomolybdate incorporating an organic ligand, as supported by a higher onset potential and a lower overvoltage at 10 mA cm(–2). At pH 7.3, the trend is inversed and the beneficial effect of the polyoxometalate for the HER is not observed. Moreover, the polyoxothiometalate-modified photocathode is found to be also more stable under acid conditions and can be operated at the light-limited catalytic current for more than 40 h. Furthermore, X-ray photoelectron spectroscopy and atomic force microscopy measurements indicate that the cathodic polarization of both photocathodes leads to the release of a large amount of the deposited material into the electrolyte solution concomitantly with the formation of mixed valence species {Mo(IV)(3–x)Mo(III)(x)O(4–n)S(n)}((4–x)+) resulting from the replacement of S(2–) sulfido ligands in the cluster by oxo O(2–) groups; these combined effects are shown to be beneficial for the photoelectrocatalysis. |
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