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This article investigates the physical origins of late-time power laws in fluorescence decays, specifically distinguishing between standard quantum mechanical predictions and alternative mechanisms like nonextensive statistics or energy migration. The study concludes that certain sharp transitions observed in experimental data cannot be replicated by these alternative models, reinforcing the necessity of a quantum-mechanical description for this specific phenomenon.
Late-Time Power Laws in Fluorescence Decays: Quantum Decay or Alternative Mechanisms?
arXiv:2610.00603v1 Announce Type: new Abstract: In quantum mechanics, the properties of an unstable system are closely related to its corresponding energy distribution. One of the predictions of the theory is the emergence of a late-time power law in the survival probability $P(t)$ of the unstable state. However, in complex systems, similar effects may emerge due to other phenomena. This is the case for nonextensive statistical models, for some continuous lifetime distribution models, and also for certain energy-migration models applied to fluorescence. In this work, these alternative interpretations are confronted with data from time-resolved fluorescence spectroscopy experiments with erythrosine B and eosine Y as fluorophores. It turns out that some of the features expected within the quantum-mechanical description, such as the sharp transition from the exponential to the power-law regime, cannot be reproduced by the specific statistical and energy-migration parametrizations fitted in the analysis.
Title:Late-Time Power Laws in Fluorescence Decays: Quantum Decay or Alternative Mechanisms?
Abstract:In quantum mechanics, the properties of an unstable system are closely related to its corresponding energy distribution. One of the predictions of the theory is the emergence of a late-time power law in the survival probability $P(t)$ of the unstable state. However, in complex systems, similar effects may emerge due to other phenomena. This is the case for nonextensive statistical models, for some continuous lifetime distribution models, and also for certain energy-migration models applied to fluorescence. In this work, these alternative interpretations are confronted with data from time-resolved fluorescence spectroscopy experiments with erythrosine B and eosine Y as fluorophores. It turns out that some of the features expected within the quantum-mechanical description, such as the sharp transition from the exponential to the power-law regime, cannot be reproduced by the specific statistical and energy-migration parametrizations fitted in the analysis.
arXiv:2610.00603 [quant-ph]
(or arXiv:2610.00603v1 [quant-ph] for this version)
https://doi.org/10.48550/arXiv.2610.00603 Focus to learn more arXiv-issued DOI via DataCite (pending registration)
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