Accurate Singlet–Triplet Excited States Energy Gap Can Be Mastered by Time-Dependent Density Functional Theory Calculations Based on a Dielectric-Screened Range-Separated Hybrid Functional

The energy gap between the lowest singlet and lowest triplet excited states of molecular emitters is a key property affecting their thermally activated delayed fluorescence (TADF) functionality. In cases in which these states are marked by internal charge transfer, the molecular environment of the emitter significantly stabilizes these states. To address this challenging relationship, a recently developed density functional theory (DFT) framework that alleviates the fundamental orbital gap in the gas phase can be employed, offering a highly effective and predictive description of these states. These modern functionals, range-separated hybrid functionals, are based on a generalized Kohn–Sham exchange functional expression where electronic interactions are separated into long and short ranges. For representing the significant condensed phase effects, especially in the case of charge transfer states, dielectric screening can be affected by functional expression. Dielectric-screened range-separated functionals that are invoked within a polarizable continuum model were shown to properly address the orbital gap challenge in the condensed phase and consequently benchmark well in calculating triplet and charge transfer excited states. We address the excited singlet–triplet state energy gap using such a screened range-separated functional and find that the calculated gaps tend to fall within 0.1 eV of the measured energies for a widely addressed benchmark set. Here, we emphasize the success of the dielectric-screened DFT framework in calculating these important energy gaps, reproducing well the benchmark values and therefore alleviating concerns about the applicability of existing functionals. We posit that dielectric-screened calculations will bear increasing impact on the design of organic materials aiming to enhance optoelectronic applications and in particular of realized TADF efficiencies.

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Publication Details

Journal
The Journal of Physical Chemistry C
Published
2024-12-18
DOI
https://doi.org/10.1021/acs.jpcc.4c04178
Citations
11
Primary Topic
Organic Light-Emitting Diodes Research
Type
article
Field-Weighted Citation Impact
2.30

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article

Accurate Singlet–Triplet Excited States Energy Gap Can Be Mastered by Time-Dependent Density Functional Theory Calculations Based on a Dielectric-Screened Range-Separated Hybrid Functional

Barry D. Dunietz, R. Khatri
11 citations
The Journal of Physical Chemistry C
Organic Light-Emitting Diodes Research
2.30
article

Accurate Singlet–Triplet Excited States Energy Gap Can Be Mastered by Time-Dependent Density Functional Theory Calculations Based on a Dielectric-Screened Range-Separated Hybrid Functional

Barry D. Dunietz, R. Khatri
article en
11 citations

Abstract

The energy gap between the lowest singlet and lowest triplet excited states of molecular emitters is a key property affecting their thermally activated delayed fluorescence (TADF) functionality. In cases in which these states are marked by internal charge transfer, the molecular environment of the emitter significantly stabilizes these states. To address this challenging relationship, a recently developed density functional theory (DFT) framework that alleviates the fundamental orbital gap in the gas phase can be employed, offering a highly effective and predictive description of these states. These modern functionals, range-separated hybrid functionals, are based on a generalized Kohn–Sham exchange functional expression where electronic interactions are separated into long and short ranges. For representing the significant condensed phase effects, especially in the case of charge transfer states, dielectric screening can be affected by functional expression. Dielectric-screened range-separated functionals that are invoked within a polarizable continuum model were shown to properly address the orbital gap challenge in the condensed phase and consequently benchmark well in calculating triplet and charge transfer excited states. We address the excited singlet–triplet state energy gap using such a screened range-separated functional and find that the calculated gaps tend to fall within 0.1 eV of the measured energies for a widely addressed benchmark set. Here, we emphasize the success of the dielectric-screened DFT framework in calculating these important energy gaps, reproducing well the benchmark values and therefore alleviating concerns about the applicability of existing functionals. We posit that dielectric-screened calculations will bear increasing impact on the design of organic materials aiming to enhance optoelectronic applications and in particular of realized TADF efficiencies.

The Journal of Physical Chemistry CVol. 129(1)
Kent State University (US)
Basic Energy Sciences
Affordable and clean energy
Openalex Percentile: Top 11%
Organic Light-Emitting Diodes Research
2.30
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