Abstract
Oxygen vacancy-rich bismuth vanadate (BiVO4−x) photoanodes usually exhibit excellent bulk charge separation efficiency and relatively low onset potential, but the Fermi-level pinning effect leads to a relatively low photovoltage (Vph). Herein, we propose a synergistic strategy of F element doping and in situ deposition of the NiCoBi co-catalyst to amplify the Vph of BiVO4−x. Systematic investigations demonstrate that F doping modifies the electronic structure of BiVO4−x, increases the electron work function, and synergizes with the NiCoBi co-catalyst to repair surface defect states, thereby enhancing the Vph of the F-BiVO4−x/NiCoBi photoanode by 37.78% compared to its unmodified BiVO4−x counterpart. Consequently, both organic oxidation reactions and water oxidation reactions are significantly activated. More importantly, the enhanced Vph can also improve the long-term operational stability of the photoanode. Such improvements in multiple performance metrics can provide a universal strategy for the design of next-generation photoelectrode materials.
| Original language | English |
|---|---|
| Journal | Advanced Energy Materials |
| DOIs | |
| State | Accepted/In press - 2026 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- bismuth vanadate
- electrode–electrolyte interface
- photoanode
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