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Towards Prediction of Non-Radiative Decay Pathways in Organic Compounds I: The Case of Naphthalene Quantum Yields
preprintsubmitted on 07.02.2019, 17:35 and posted on 08.02.2019, 16:34 by Alexander Kohn, Zhou Lin, Troy Van Voorhis
Many emerging technologies depend on human’s ability to control and manipulate the excited-state properties of molecular systems. These technologies include fluorescent
labeling in biomedical imaging, light harvesting in photovoltaics, and electroluminescence in light-emitting devices. All of these systems suffer from non-radiative loss pathways that dissipate electronic energy as heat, which causes the overall system efficiency to be directly linked to quantum yield (Φ) of the molecular excited state. Unfortunately, Φ is very difficult to predict from first principles because the description of a slow non-radiative decay mechanism requires an accurate description of long-timescale excited-state quantum dynamics. In the present study, we introduce an efficient semiempirical method of calculating the fluorescence quantum yield (Φfl) for molecular chromophores, which, based on machine learning, converts simple electronic energies computed using time-dependent density functional theory (TDDFT) into an estimate of Φfl. As with all machine learning strategies, the algorithm needs to be trained on fluorescent dyes for which Φfl’s are known, so as to provide a black-box method which can later predict Φfl’s for chemically similar chromophores that have not been studied experimentally. As a first illustration of how our proposed algorithm can be trained, we examine a family of 25 naphthalene derivatives. The simplest application of the energy gap law is found to be inadequate to explain the rates of internal conversion (IC) or intersystem crossing (ISC) – the electronic properties of at least one higher-lying electronic state (Sn or Tn) or one far-from-equilibrium geometry are typically needed to obtain accurate results. Indeed, the key descriptors turn out to be the transition state between the Franck–Condon minimum a distorted local minimum near an S0/S1 conical intersection (which governs IC) and the magnitude of the spin–orbit coupling (which governs ISC). The resulting Φfl’s are predicted with reasonable accuracy (±22%), making our approach a promising ingredient for high-throughput screening and rational design of the molecular excited states with desired Φ’s. We thus conclude that our model, while semi-empirical in nature, does in fact extract sound physical insight into the challenge of describing non-radiative relaxations.
Bimolecular Interactions in Organic Semiconductors: Hot Charge, Hot Excitons, Efficiency Droop, and Instability
Basic Energy SciencesFind out more...
Email Address of Submitting Authorzhoulin@berkeley.edu
InstitutionUniversity of California, Berkeley
ORCID For Submitting Author0000-0003-3271-5345
Declaration of Conflict of InterestNo conflict of interest
Read the published paper
in The Journal of Physical Chemistry C