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DOI 10.1063/5.0238657

Медицинская библиотека · The Journal of chemical physics · 2025

Non-adiabatic quantum electrodynamic effects on electron-nucleus-photon systems: Single photonic mode vs infinite photonic modes.

Shen Chih-En, Tsai Hung-Sheng, Hsu Liang-Yan

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Аннотация

The quantum-electrodynamic non-adiabatic emission (QED-NAE) is a type of radiatively assisted vibronic de-excitation due to electromagnetic vacuum fluctuations on non-adiabatic processes. Building on our previous work [Tsai et al., J. Phys. Chem. Lett. 14, 5924 (2023)], we extend the theory of the QED-NAE rate from a single cavity photonic mode to infinite photonic modes and calculate the QED-NAE rates of 9-cyanoanthracene at the first-principles level. To avoid the confusion, the quantum electrodynamic internal conversion process is renamed as "QED-NAE" in our present work. According to our theory, we identify three key factors influencing the QED-NAE processes: light-matter coupling strength (mode volume), mass-weighted orientation factor, and photonic density of states. The mode volume is the primary factor causing rate differences between the two scenarios. In a single cavity with a small mode volume, strong light-matter coupling strength boosts QED-NAE rates. In contrast, in free space with infinite photonic modes, weak coupling strength significantly reduces these rates. From a single cavity photonic mode to infinite photonic modes, the mass-weighted orientation factor only causes an 8π/3-fold increase in the QED-NAE rate. In free space, the photonic density of state exhibits a flat and quadratic distribution, which slightly reduces the QED-NAE rate. Our study shows that cavities can significantly enhance non-adiabatic QED effects while providing a robust analysis demonstrating that QED vibronic effects can be safely ignored in free space.

Для цитирования: Shen Chih-En, Tsai Hung-Sheng, Hsu Liang-Yan. Non-adiabatic quantum electrodynamic effects on electron-nucleus-photon systems: Single photonic mode vs infinite photonic modes.. The Journal of chemical physics. 2025. DOI: 10.1063/5.0238657.
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