Photoluminescence decay of mobile carriers influenced by imperfect quenching at particle surfaces with subdiffusive spread
We recently presented a quantitative model to explain the particle-size dependence of photoluminescence (PL) quantum yields and revealed that exciton quenching is not diffusion controlled, but limited by surface reactions. However, the exciton decay kinetics has not been analyzed yet using our theor...
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Veröffentlicht in: | The Journal of chemical physics 2024-09, Vol.161 (12) |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | We recently presented a quantitative model to explain the particle-size dependence of photoluminescence (PL) quantum yields and revealed that exciton quenching is not diffusion controlled, but limited by surface reactions. However, the exciton decay kinetics has not been analyzed yet using our theoretical model. Here, we study kinetic aspects of the model and show that it should be extended to take into account subdiffusion rather than normal diffusion to maintain consistency with the observed complex decay kinetics; we also show that the PL decay kinetics is nonexponential even when the PL quenching is limited by surface reactions under subdiffusion. Our theoretical analysis of the PL quantum yield and the PL decay kinetics provides a comprehensive picture of mobile charge carriers, immobile polarons, and self-trapped excitons. |
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ISSN: | 0021-9606 1089-7690 1089-7690 |
DOI: | 10.1063/5.0226352 |