Tailoring the Surface Termination of BiVO4 Photoanodes Using Ammonium Metavanadate Enhances the Solar Water Oxidation Performance
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Title: | Tailoring the Surface Termination of BiVO4 Photoanodes Using Ammonium Metavanadate Enhances the Solar Water Oxidation Performance |
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Authors: | Wang, Qingjie | Wang, Zeyuan | Liao, Nan | Montilla-Verdú, Salvador | Contreras, Maxime | Guijarro, Nestor | Luo, Jingshan |
Research Group/s: | Grupo de Fotoquímica y Electroquímica de Semiconductores (GFES) |
Center, Department or Service: | Universidad de Alicante. Instituto Universitario de Electroquímica |
Keywords: | Surface termination | BiVO4 photoanodes | Ammonium metavanadate | Solar water oxidation |
Issue Date: | 11-Jun-2024 |
Publisher: | American Chemical Society |
Citation: | ACS Energy Letters. 2024, 9: 3308-3315. https://doi.org/10.1021/acsenergylett.4c01240 |
Abstract: | Altering the surface stoichiometry of semiconductor electrodes is known to affect the photoelectrochemical (PEC) response. To date, several reports have hinted at the influence of the surface Bi:V ratio on the solar water oxidation performance of BiVO4 photoanodes, but only a handful of strategies have been reported to afford tuning of such surface stoichiometry, while a comprehensive understanding at an atomic level of the role of the surface termination remains elusive. Herein, we report a new methodology that modulates the surface Bi:V ratio and maximizes the PEC performance toward the oxygen evolution reaction (OER). The presence of ammonium metavanadate drastically reduces the surface recombination while improving the charge separation. Detailed characterization revealed that this treatment filled the native surface vanadium vacancies, which usually act as recombination centers, while inducing a significant increase in the density of oxygen vacancies, which reinforced the built-in electric field that drives the charge separation. Interestingly, coating with NiFeOx improves, especially, the charge separation in surface V-modified BiVO4. Results suggest that the V-modified surface termination altered the surface energetics of BiVO4, leading to an improved band alignment across the interface. Overall, these results provide a new platform to modulate the surface stoichiometry of BiVO4 thin films while shedding new light on the mechanisms by which the surface termination governs the PEC response. |
Sponsor: | J.L. acknowledges the funding support from the National Key Research and Development Program of China (Grant No. 2020YFA0907300 and 2019YFE0123400), the Excellent Young Scholar Fund from the National Science Foundation of China (22122903), the Tianjin Distinguished Young Scholar Fund (20JCJQJC00260), and the “111” Project (Grant No. B16027). Q.W. acknowledges the funding support from the China Scholarship Council (202206200070). N.G. thanks the Spanish Ministry of Science & Innovation for the “Ramon y Cajal” Program (RYC2018-023888-I) and for support via de project TED2021-132697B-100. This project has also received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (grant agreement No. 948829). |
URI: | http://hdl.handle.net/10045/144618 |
ISSN: | 2380-8195 |
DOI: | 10.1021/acsenergylett.4c01240 |
Language: | eng |
Type: | info:eu-repo/semantics/article |
Rights: | © 2024 American Chemical Society |
Peer Review: | si |
Publisher version: | https://doi.org/10.1021/acsenergylett.4c01240 |
Appears in Collections: | Research funded by the EU INV - GFES - Artículos de Revistas |
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