引用本文:
Bei Li, Zhaoke Zheng. In situ monitoring of the spatial distribution of oxygen vacancies at the single-particle level[J]. Chinese Journal of Structural Chemistry,
2024, 43(10): 100331.
doi:
10.1016/j.cjsc.2024.100331
Citation: Bei Li, Zhaoke Zheng. In situ monitoring of the spatial distribution of oxygen vacancies at the single-particle level[J]. Chinese Journal of Structural Chemistry, 2024, 43(10): 100331. doi: 10.1016/j.cjsc.2024.100331
Citation: Bei Li, Zhaoke Zheng. In situ monitoring of the spatial distribution of oxygen vacancies at the single-particle level[J]. Chinese Journal of Structural Chemistry, 2024, 43(10): 100331. doi: 10.1016/j.cjsc.2024.100331
In situ monitoring of the spatial distribution of oxygen vacancies at the single-particle level
摘要:
In summary, this work establishes a correlation between OVs and bound exciton luminescence by single-particle spectroscopy. It confirms that the PL emission of m-BiVO4 originates from the defect state. Additionally, the study achieves visual imaging of the spatial distribution of oxygen defects by PL lifetime imaging maps. Furthermore, single-particle spectroscopy can be used to monitor charge transfer during photocatalysis in situ, indicating that the generation of OVs at specific crystal facets facilitates efficient charge transfer between electrons and reactants. This work provides an imaging technique to accurately monitor the spatial distribution of defects in single-crystal materials, and a method for spatial high-resolution real-time monitoring of multiphase catalytic reactions, aiming to provide an in-depth understanding of the relationship between the structure-activity of materials.
English
In situ monitoring of the spatial distribution of oxygen vacancies at the single-particle level
Abstract:
In summary, this work establishes a correlation between OVs and bound exciton luminescence by single-particle spectroscopy. It confirms that the PL emission of m-BiVO4 originates from the defect state. Additionally, the study achieves visual imaging of the spatial distribution of oxygen defects by PL lifetime imaging maps. Furthermore, single-particle spectroscopy can be used to monitor charge transfer during photocatalysis in situ, indicating that the generation of OVs at specific crystal facets facilitates efficient charge transfer between electrons and reactants. This work provides an imaging technique to accurately monitor the spatial distribution of defects in single-crystal materials, and a method for spatial high-resolution real-time monitoring of multiphase catalytic reactions, aiming to provide an in-depth understanding of the relationship between the structure-activity of materials.
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