Indexed by:
Abstract:
Localized accumulation of carriers frequently induces corrosion on the surfaces of photocatalysts, restricting the efficacy of photocatalytic technology. The development of a strategy that precisely targets and transforms passivated corrosion regions into reactive sites holds significant potential, yet remains technically challenging. Herein, an advanced microscopy study reveals that BiOBr photocatalysts are susceptible to severe photo-corrosion, leading to a continual thickening of Bi2O3 crystalline films as the photo-oxidation products accumulate on the photocatalytic surfaces. Through a metal cation intercalation process, it is demonstrated that the passivated Bi2O3 films are precisely targeted by the accumulated holes and in situ converted to MxBiyOz (M = Co, Mn, Fe, Pb) nanobeads that act as co-catalysts to expedite charge transfer and enhance photostability. This work deepens the understanding of the atomistic photocorrosion mechanism of BiOBr photocatalysts and contributes to a versatile surface-targeted photochemical modification approach to tackle widespread photocorrosion challenges. © 2025 Wiley-VCH GmbH.
Keyword:
Reprint 's Address:
Email:
Source :
Advanced Functional Materials
ISSN: 1616-301X
Year: 2025
1 8 . 5 0 0
JCR@2023
Cited Count:
SCOPUS Cited Count:
ESI Highly Cited Papers on the List: 0 Unfold All
WanFang Cited Count:
Chinese Cited Count:
30 Days PV: 0
Affiliated Colleges: