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Triazatruxene: A Rigid Central Donor Unit for a D-A3 Thermally Activated Delayed Fluorescence Material Exhibiting Sub-Microsecond Reverse Intersystem Crossing and Unity Quantum Yield via Multiple Singlet-Triplet State Pairs

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Triazatruxene: A Rigid Central Donor Unit for a D-A3 Thermally Activated Delayed Fluorescence Material Exhibiting Sub-Microsecond Reverse Intersystem Crossing and Unity Quantum Yield via Multiple Singlet-Triplet State Pairs. / Santos, Paloma L. dos; Ward, Jonathan S.; Congrave, Daniel G. et al.
In: Advanced Science, Vol. 5, No. 6, 1700989, 30.06.2018.

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@article{0b02156f307b4f7f9d76e80ff26d72a7,
title = "Triazatruxene: A Rigid Central Donor Unit for a D-A3 Thermally Activated Delayed Fluorescence Material Exhibiting Sub-Microsecond Reverse Intersystem Crossing and Unity Quantum Yield via Multiple Singlet-Triplet State Pairs",
abstract = "By inverting the common structural motif of thermally activated delayed fluorescence materials to a rigid donor core and multiple peripheral acceptors, reverse intersystem crossing (rISC) rates are demonstrated in an organic material that enables utilization of triplet excited states at faster rates than Ir-based phosphorescent materials. A combination of the inverted structure and multiple donor–acceptor interactions yields up to 30 vibronically coupled singlet and triplet states within 0.2 eV that are involved in rISC. This gives a significant enhancement to the rISC rate, leading to delayed fluorescence decay times as low as 103.9 ns. This new material also has an emission quantum yield ≈1 and a very small singlet–triplet gap. This work shows that it is possible to achieve both high photoluminescence quantum yield and fast rISC in the same molecule. Green organic light-emitting diode devices with external quantum efficiency >30% are demonstrated at 76 cd m−2.",
author = "Santos, {Paloma L. dos} and Ward, {Jonathan S.} and Congrave, {Daniel G.} and Batsanov, {Andrei S.} and Julien Eng and Stacey, {Jessica E.} and Penfold, {Thomas J.} and Monkman, {Andrew P.} and Bryce, {Martin R.}",
year = "2018",
month = jun,
day = "30",
doi = "10.1002/advs.201700989",
language = "English",
volume = "5",
journal = "Advanced Science",
issn = "2198-3844",
publisher = "Wiley",
number = "6",

}

RIS

TY - JOUR

T1 - Triazatruxene: A Rigid Central Donor Unit for a D-A3 Thermally Activated Delayed Fluorescence Material Exhibiting Sub-Microsecond Reverse Intersystem Crossing and Unity Quantum Yield via Multiple Singlet-Triplet State Pairs

AU - Santos, Paloma L. dos

AU - Ward, Jonathan S.

AU - Congrave, Daniel G.

AU - Batsanov, Andrei S.

AU - Eng, Julien

AU - Stacey, Jessica E.

AU - Penfold, Thomas J.

AU - Monkman, Andrew P.

AU - Bryce, Martin R.

PY - 2018/6/30

Y1 - 2018/6/30

N2 - By inverting the common structural motif of thermally activated delayed fluorescence materials to a rigid donor core and multiple peripheral acceptors, reverse intersystem crossing (rISC) rates are demonstrated in an organic material that enables utilization of triplet excited states at faster rates than Ir-based phosphorescent materials. A combination of the inverted structure and multiple donor–acceptor interactions yields up to 30 vibronically coupled singlet and triplet states within 0.2 eV that are involved in rISC. This gives a significant enhancement to the rISC rate, leading to delayed fluorescence decay times as low as 103.9 ns. This new material also has an emission quantum yield ≈1 and a very small singlet–triplet gap. This work shows that it is possible to achieve both high photoluminescence quantum yield and fast rISC in the same molecule. Green organic light-emitting diode devices with external quantum efficiency >30% are demonstrated at 76 cd m−2.

AB - By inverting the common structural motif of thermally activated delayed fluorescence materials to a rigid donor core and multiple peripheral acceptors, reverse intersystem crossing (rISC) rates are demonstrated in an organic material that enables utilization of triplet excited states at faster rates than Ir-based phosphorescent materials. A combination of the inverted structure and multiple donor–acceptor interactions yields up to 30 vibronically coupled singlet and triplet states within 0.2 eV that are involved in rISC. This gives a significant enhancement to the rISC rate, leading to delayed fluorescence decay times as low as 103.9 ns. This new material also has an emission quantum yield ≈1 and a very small singlet–triplet gap. This work shows that it is possible to achieve both high photoluminescence quantum yield and fast rISC in the same molecule. Green organic light-emitting diode devices with external quantum efficiency >30% are demonstrated at 76 cd m−2.

U2 - 10.1002/advs.201700989

DO - 10.1002/advs.201700989

M3 - Journal article

VL - 5

JO - Advanced Science

JF - Advanced Science

SN - 2198-3844

IS - 6

M1 - 1700989

ER -