Abstract
The ultrafast excited-state dynamics of endohedral fullerenes are crucial in their photophysical and photochemical processes when they are employed as photovoltaic devices, photocatalytic devices, and single-molecule devices. In this study, by employing the ab initio non-adiabatic molecular dynamics simulations based on the time-dependent Kohn-Sham (TD-KS) method, we theoretically studied the size effect on ultrafast excited-state decay dynamics of the photoexcited 7Be electron in endohedral fullerenes 7Be@C2n (2n = 60, 70, and 80). These excited-state decay dynamics, which involve the charge-transfer process, occur in an ultrafast time scale of about 3 ps. The larger fullerene cage delays the excited-state decay process because the presence of significant energy gaps and phonon modes in large endohedral fullerenes slows the non-radiative electron transitions among energy levels. Those findings not only provide physical insights into the excited-state decay dynamics of confined atoms but also stimulate further research to develop efficient endohedral-fullerene-based photoelectric and photocatalytic devices.
| Original language | English |
|---|---|
| Pages (from-to) | 1206-1212 |
| Number of pages | 7 |
| Journal | Journal of Physical Chemistry Letters |
| Volume | 16 |
| Issue number | 5 |
| DOIs | |
| State | Published - 6 Feb 2025 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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