Understanding quantum yields in naphthalenes and boron-dipyrromethenes: Towards a prediction of non-radiative decay pathways in organic optoelectronic materials

Lin, Zhou

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https://hdl.handle.net/2142/100738 Copy

Description

Title

Understanding quantum yields in naphthalenes and boron-dipyrromethenes: Towards a prediction of non-radiative decay pathways in organic optoelectronic materials

Author(s)

Lin, Zhou

Contributor(s)

• Van Voorhis, Troy
• Kohn, Alexander W.

Issue Date

2018-06-19

Keyword(s)

Mini-symposium: New Ways of Understanding Molecular Spectra

Abstract

In recent years, organic optoelectronic materials have attracted considerable attention due to their ease of production and fabrication and great potentials in industrial applications. However, their efficiencies can be strongly limited by non-radiative decay pathways in which the excited energies are lost in the form of thermal energy. In the present study, we focused on two families of organic optoelectronic materials, the derivatives of naphthalene and those of borondipyrromethene (BODIPY), and characterized their efficiencies using the fluorescence quantum yield (φfl) – the probability that a photoexcited molecule fluoresces a photon rather than undergoing a non-radiative decay. To predict these φfl’s, we developed inexpensive, accurate and transferable semi-empirical methods based on time-dependent density functional theory (TDDFT) and its multiple variants, and examined two non-radiative decay mechanisms – internal conversion (IC) and intersystem crossing (ISC). We managed to predict radiative rates (kfl), IC rates (kIC), and ISC rates (kISC), and controlled the mean absolute error (MAE) within 0.4 orders of magnitude. These results, in combination, allowed us to reproduce φfl’s with an MAE of 0.2 for organic optoelectronic materials in question. During this process, we discovered two novel IC pathways through low-energy distorted transition states and intermediates, and indicated that the energy gap law is inadequate to estimate the activation energy (Ea) and account for kIC and kISC. The present study paves the way for the rational design of organic optoelectronic devices by high-throughput computations.

Publisher

International Symposium on Molecular Spectroscopy

Type of Resource

text

Language

eng

Permalink

http://hdl.handle.net/2142/100738

DOI

10.15278/isms.2018.TB08

Copyright and License Information

Copyright 2018 Zhou Lin

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