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Surface Reconstruction and Passivation of BiVO 4 Photoanodes Depending on the "Structure Breaker" Cs
Monoclinic BiVO is one of the most promising photoanode materials for solar water splitting. The photoelectrochemical performance of a BiVO photoanode could be significantly influenced by the noncovalent interactions of redox-inert metal cations at the photoanode-electrolyte interfaces, but this poi...
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Published in: | JACS Au 2023-07, Vol.3 (7), p.1851-1863 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Monoclinic BiVO
is one of the most promising photoanode materials for solar water splitting. The photoelectrochemical performance of a BiVO
photoanode could be significantly influenced by the noncovalent interactions of redox-inert metal cations at the photoanode-electrolyte interfaces, but this point has not been well investigated. In this work, we studied the Cs
-dependent surface reconstruction and passivation of BiVO
photoanodes. Owing to the "structure breaker" nature of Cs
, the Cs
at the BiVO
photoanode-electrolyte interfaces participated in BiVO
surface photocorrosion to form a Cs
-doped bismuth vanadium oxide amorphous thin layer, which inhibited the continuous photocorrosion of BiVO
and promoted surface charge transfer and water oxidation. The resulting cocatalyst-free BiVO
photoanodes achieved 3.3 mA cm
photocurrent for water oxidation. With the modification of FeOOH catalysts, the photocurrent at 1.23 V
reached 5.1 mA cm
, and a steady photocurrent of 3.0 mA cm
at 0.8 V
was maintained for 30 h. This work provides new insights into the understanding of Cs
chemistry and the effects of redox-inert cations at the electrode-electrolyte interfaces. |
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ISSN: | 2691-3704 2691-3704 |
DOI: | 10.1021/jacsau.3c00100 |