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Engineering the singlet–triplet energy splitting in a TADF molecule

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Engineering the singlet–triplet energy splitting in a TADF molecule. / Santos, Paloma L.; Ward, Jonathan S.; Data, Przemyslaw et al.
In: Journal of Materials Chemistry C, Vol. 4, No. 17, 07.05.2016, p. 3815-3824.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Santos, PL, Ward, JS, Data, P, Batsanov, AS, Bryce, MR, Dias, FB & Monkman, AP 2016, 'Engineering the singlet–triplet energy splitting in a TADF molecule', Journal of Materials Chemistry C, vol. 4, no. 17, pp. 3815-3824. https://doi.org/10.1039/c5tc03849a

APA

Santos, P. L., Ward, J. S., Data, P., Batsanov, A. S., Bryce, M. R., Dias, F. B., & Monkman, A. P. (2016). Engineering the singlet–triplet energy splitting in a TADF molecule. Journal of Materials Chemistry C, 4(17), 3815-3824. https://doi.org/10.1039/c5tc03849a

Vancouver

Santos PL, Ward JS, Data P, Batsanov AS, Bryce MR, Dias FB et al. Engineering the singlet–triplet energy splitting in a TADF molecule. Journal of Materials Chemistry C. 2016 May 7;4(17):3815-3824. Epub 2016 Jan 11. doi: 10.1039/c5tc03849a

Author

Santos, Paloma L. ; Ward, Jonathan S. ; Data, Przemyslaw et al. / Engineering the singlet–triplet energy splitting in a TADF molecule. In: Journal of Materials Chemistry C. 2016 ; Vol. 4, No. 17. pp. 3815-3824.

Bibtex

@article{0407060e291f4717bdfae77d30202fb7,
title = "Engineering the singlet–triplet energy splitting in a TADF molecule",
abstract = "The key to engineering an efficient TADF emitter is to achieve a small energy splitting between a pair of molecular singlet and triplet states. This work makes important contributions towards achieving this goal. By studying the new TADF emitter 2,7-bis(phenoxazin-10-yl)-9,9-dimethylthioxanthene-S,S-dioxide (DPO-TXO2) and the donor and acceptor units separately, the available radiative and non-radiative pathways of DPO-TXO2 have been identified. The energy splitting between singlet and triplet states was clearly identified in four different environments, in solutions and solid state. The results show that DPO-TXO2 is a promising TADF emitter, having ΔEST = 0.01 eV in zeonex matrix. We further show how the environment plays a key role in the fine tuning of the energy levels of the 1CT state with respect to the donor 3LED triplet state, which can then be used to control the ΔEST energy value. We elucidate the TADF mechanism dynamics when the 1CT state is located below the 3LE triplet state which it spin orbit couples to, and we also discuss the OLED device performance with this new emitter, which shows maximum external quantum efficiency (E.Q.E.) of 13.5% at 166 cd m−2.",
author = "Santos, {Paloma L.} and Ward, {Jonathan S.} and Przemyslaw Data and Batsanov, {Andrei S.} and Bryce, {Martin R.} and Dias, {Fernando B.} and Monkman, {Andrew P.}",
year = "2016",
month = may,
day = "7",
doi = "10.1039/c5tc03849a",
language = "English",
volume = "4",
pages = "3815--3824",
journal = "Journal of Materials Chemistry C",
issn = "2050-7526",
publisher = "Royal Society of Chemistry",
number = "17",

}

RIS

TY - JOUR

T1 - Engineering the singlet–triplet energy splitting in a TADF molecule

AU - Santos, Paloma L.

AU - Ward, Jonathan S.

AU - Data, Przemyslaw

AU - Batsanov, Andrei S.

AU - Bryce, Martin R.

AU - Dias, Fernando B.

AU - Monkman, Andrew P.

PY - 2016/5/7

Y1 - 2016/5/7

N2 - The key to engineering an efficient TADF emitter is to achieve a small energy splitting between a pair of molecular singlet and triplet states. This work makes important contributions towards achieving this goal. By studying the new TADF emitter 2,7-bis(phenoxazin-10-yl)-9,9-dimethylthioxanthene-S,S-dioxide (DPO-TXO2) and the donor and acceptor units separately, the available radiative and non-radiative pathways of DPO-TXO2 have been identified. The energy splitting between singlet and triplet states was clearly identified in four different environments, in solutions and solid state. The results show that DPO-TXO2 is a promising TADF emitter, having ΔEST = 0.01 eV in zeonex matrix. We further show how the environment plays a key role in the fine tuning of the energy levels of the 1CT state with respect to the donor 3LED triplet state, which can then be used to control the ΔEST energy value. We elucidate the TADF mechanism dynamics when the 1CT state is located below the 3LE triplet state which it spin orbit couples to, and we also discuss the OLED device performance with this new emitter, which shows maximum external quantum efficiency (E.Q.E.) of 13.5% at 166 cd m−2.

AB - The key to engineering an efficient TADF emitter is to achieve a small energy splitting between a pair of molecular singlet and triplet states. This work makes important contributions towards achieving this goal. By studying the new TADF emitter 2,7-bis(phenoxazin-10-yl)-9,9-dimethylthioxanthene-S,S-dioxide (DPO-TXO2) and the donor and acceptor units separately, the available radiative and non-radiative pathways of DPO-TXO2 have been identified. The energy splitting between singlet and triplet states was clearly identified in four different environments, in solutions and solid state. The results show that DPO-TXO2 is a promising TADF emitter, having ΔEST = 0.01 eV in zeonex matrix. We further show how the environment plays a key role in the fine tuning of the energy levels of the 1CT state with respect to the donor 3LED triplet state, which can then be used to control the ΔEST energy value. We elucidate the TADF mechanism dynamics when the 1CT state is located below the 3LE triplet state which it spin orbit couples to, and we also discuss the OLED device performance with this new emitter, which shows maximum external quantum efficiency (E.Q.E.) of 13.5% at 166 cd m−2.

U2 - 10.1039/c5tc03849a

DO - 10.1039/c5tc03849a

M3 - Journal article

VL - 4

SP - 3815

EP - 3824

JO - Journal of Materials Chemistry C

JF - Journal of Materials Chemistry C

SN - 2050-7526

IS - 17

ER -