TY - JOUR
T1 - Anti-Stokes Emission Utilizing Reverse Intersystem Crossing
AU - Kohata, Shintaro
AU - Nakanotani, Hajime
AU - Hosokai, Takuya
AU - Yasuda, Takuma
AU - Tsuchiya, Youichi
AU - Adachi, Chihaya
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2025/2/10
Y1 - 2025/2/10
N2 - Photon-upconversion (PUC) processes in organic molecular systems, such as triplet-triplet upconversion and hot-band absorption, are promising technologies for future energy harvesting. Although these processes can generate high-energy excitons compared to excitation energy, a PUC process with a high yield and no energy loss has not been established and, therefore, is highly desired. Here, we propose an alternative PUC mechanism that uses reverse intersystem crossing on thermally activated delayed fluorescence (TADF) molecules. This process combines a triplet sensitizer and a TADF molecule, generating a triplet in the former and transferring it to the latter. Specifically, the triplet energy transfer from Ir(ppy)3 (sensitizer) to CzBSe (TADF) results in anti-Stokes emission with an anti-Stokes energy of 0.18 eV. We found that the triplet energy transfer rate strongly depends on the triplet radiative decay rate of TADF molecules and the difference in Gibbs energy between the energy acceptor and donor. Our findings will contribute to understanding triplet energy transfer dynamics in organic energy donor-acceptor systems and will lead to various applications, such as future optical cooling systems.
AB - Photon-upconversion (PUC) processes in organic molecular systems, such as triplet-triplet upconversion and hot-band absorption, are promising technologies for future energy harvesting. Although these processes can generate high-energy excitons compared to excitation energy, a PUC process with a high yield and no energy loss has not been established and, therefore, is highly desired. Here, we propose an alternative PUC mechanism that uses reverse intersystem crossing on thermally activated delayed fluorescence (TADF) molecules. This process combines a triplet sensitizer and a TADF molecule, generating a triplet in the former and transferring it to the latter. Specifically, the triplet energy transfer from Ir(ppy)3 (sensitizer) to CzBSe (TADF) results in anti-Stokes emission with an anti-Stokes energy of 0.18 eV. We found that the triplet energy transfer rate strongly depends on the triplet radiative decay rate of TADF molecules and the difference in Gibbs energy between the energy acceptor and donor. Our findings will contribute to understanding triplet energy transfer dynamics in organic energy donor-acceptor systems and will lead to various applications, such as future optical cooling systems.
KW - Anti-Stokes emission
KW - Dexter-type energy transfer
KW - Förster-type energy transfer
KW - Photon-upconversion
KW - Thermally activated delayed fluorescence
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U2 - 10.1002/anie.202419323
DO - 10.1002/anie.202419323
M3 - Article
AN - SCOPUS:85210378775
SN - 1433-7851
VL - 64
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 7
M1 - e202419323
ER -