Efficient near-infrared emission benefits from slowing down the internal conversion process

Organic deep-red (DR) and near-infrared (NIR) emitters with high photoluminescence quantum yield (PLQY) are rare due to the strong non-radiative ( k nr ) decay. Here, we report two DR/NIR emitters with high PLQY, TPANZPyPI and TPANZ3PI . Interestingly, the TPANZPyPI film exhibits 46.5% PLQY at 699 n...

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Published inChemical science (Cambridge) Vol. 15; no. 15; pp. 5589 - 5595
Main Authors Xie, Mingliang, Zhou, Yannan, Zhou, Huayi, Ma, Chengling, Sun, Qikun, Zhang, Shi-Tong, Zhang, Yujian, Yang, Wenjun, Xue, Shanfeng
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 17.04.2024
Royal Society of Chemistry
The Royal Society of Chemistry
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Abstract Organic deep-red (DR) and near-infrared (NIR) emitters with high photoluminescence quantum yield (PLQY) are rare due to the strong non-radiative ( k nr ) decay. Here, we report two DR/NIR emitters with high PLQY, TPANZPyPI and TPANZ3PI . Interestingly, the TPANZPyPI film exhibits 46.5% PLQY at 699 nm. Theoretical calculations indicate that TPANZPyPI can achieve this high PLQY in the near-infrared emission region due to its small S 1 to S 0 internal conversion (IC) rate. Meanwhile, research has found that, compared to TPANZ3PI , TPANZPyPI with a more rigid structure can effectively suppress the T 2 to T 1 IC process, which is conducive to higher exciton utilization efficiency (EUE). TPANZPyPI 's non-doped OLED shows NIR emission with 4.6% @ 684 nm maximum external quantum efficiency (EQE max ). Its doped OLEDs radiate DR with an EQE max of 6.9% @ 666 nm. These EQEs are among the highest values for hybridized local charge transfer state materials emitting more than 640 nm. This work demonstrates for the first time, based on a combination of theory and experiment, that increasing the molecular rigidity can inhibit the excited state IC process in addition to the S 1 to S 0 IC, realizing efficient electroluminescence. This work demonstrates for the first time that emitters with appropriate qualifications can affect the IC from S 1 to S 0 and the IC of the triple excluded state, achieving high-efficiency device performance.
AbstractList Organic deep-red (DR) and near-infrared (NIR) emitters with high photoluminescence quantum yield (PLQY) are rare due to the strong non-radiative ( k nr ) decay. Here, we report two DR/NIR emitters with high PLQY, TPANZPyPI and TPANZ3PI . Interestingly, the TPANZPyPI film exhibits 46.5% PLQY at 699 nm. Theoretical calculations indicate that TPANZPyPI can achieve this high PLQY in the near-infrared emission region due to its small S 1 to S 0 internal conversion (IC) rate. Meanwhile, research has found that, compared to TPANZ3PI , TPANZPyPI with a more rigid structure can effectively suppress the T 2 to T 1 IC process, which is conducive to higher exciton utilization efficiency (EUE). TPANZPyPI 's non-doped OLED shows NIR emission with 4.6% @ 684 nm maximum external quantum efficiency (EQE max ). Its doped OLEDs radiate DR with an EQE max of 6.9% @ 666 nm. These EQEs are among the highest values for hybridized local charge transfer state materials emitting more than 640 nm. This work demonstrates for the first time, based on a combination of theory and experiment, that increasing the molecular rigidity can inhibit the excited state IC process in addition to the S 1 to S 0 IC, realizing efficient electroluminescence. This work demonstrates for the first time that emitters with appropriate qualifications can affect the IC from S 1 to S 0 and the IC of the triple excluded state, achieving high-efficiency device performance.
Organic deep-red (DR) and near-infrared (NIR) emitters with high photoluminescence quantum yield (PLQY) are rare due to the strong non-radiative (knr) decay. Here, we report two DR/NIR emitters with high PLQY, TPANZPyPI and TPANZ3PI. Interestingly, the TPANZPyPI film exhibits 46.5% PLQY at 699 nm. Theoretical calculations indicate that TPANZPyPI can achieve this high PLQY in the near-infrared emission region due to its small S1 to S0 internal conversion (IC) rate. Meanwhile, research has found that, compared to TPANZ3PI, TPANZPyPI with a more rigid structure can effectively suppress the T2 to T1 IC process, which is conducive to higher exciton utilization efficiency (EUE). TPANZPyPI's non-doped OLED shows NIR emission with 4.6% @ 684 nm maximum external quantum efficiency (EQEmax). Its doped OLEDs radiate DR with an EQEmax of 6.9% @ 666 nm. These EQEs are among the highest values for hybridized local charge transfer state materials emitting more than 640 nm. This work demonstrates for the first time, based on a combination of theory and experiment, that increasing the molecular rigidity can inhibit the excited state IC process in addition to the S1 to S0 IC, realizing efficient electroluminescence.Organic deep-red (DR) and near-infrared (NIR) emitters with high photoluminescence quantum yield (PLQY) are rare due to the strong non-radiative (knr) decay. Here, we report two DR/NIR emitters with high PLQY, TPANZPyPI and TPANZ3PI. Interestingly, the TPANZPyPI film exhibits 46.5% PLQY at 699 nm. Theoretical calculations indicate that TPANZPyPI can achieve this high PLQY in the near-infrared emission region due to its small S1 to S0 internal conversion (IC) rate. Meanwhile, research has found that, compared to TPANZ3PI, TPANZPyPI with a more rigid structure can effectively suppress the T2 to T1 IC process, which is conducive to higher exciton utilization efficiency (EUE). TPANZPyPI's non-doped OLED shows NIR emission with 4.6% @ 684 nm maximum external quantum efficiency (EQEmax). Its doped OLEDs radiate DR with an EQEmax of 6.9% @ 666 nm. These EQEs are among the highest values for hybridized local charge transfer state materials emitting more than 640 nm. This work demonstrates for the first time, based on a combination of theory and experiment, that increasing the molecular rigidity can inhibit the excited state IC process in addition to the S1 to S0 IC, realizing efficient electroluminescence.
Organic deep-red (DR) and near-infrared (NIR) emitters with high photoluminescence quantum yield (PLQY) are rare due to the strong non-radiative (knr) decay. Here, we report two DR/NIR emitters with high PLQY, TPANZPyPI and TPANZ3PI. Interestingly, the TPANZPyPI film exhibits 46.5% PLQY at 699 nm. Theoretical calculations indicate that TPANZPyPI can achieve this high PLQY in the near-infrared emission region due to its small S1 to S0 internal conversion (IC) rate. Meanwhile, research has found that, compared to TPANZ3PI, TPANZPyPI with a more rigid structure can effectively suppress the T2 to T1 IC process, which is conducive to higher exciton utilization efficiency (EUE). TPANZPyPI's non-doped OLED shows NIR emission with 4.6% @ 684 nm maximum external quantum efficiency (EQEmax). Its doped OLEDs radiate DR with an EQEmax of 6.9% @ 666 nm. These EQEs are among the highest values for hybridized local charge transfer state materials emitting more than 640 nm. This work demonstrates for the first time, based on a combination of theory and experiment, that increasing the molecular rigidity can inhibit the excited state IC process in addition to the S1 to S0 IC, realizing efficient electroluminescence. This work demonstrates for the first time that emitters with appropriate qualifications can affect the IC from S1 to S0 and the IC of the triple excluded state, achieving high-efficiency device performance.
Organic deep-red (DR) and near-infrared (NIR) emitters with high photoluminescence quantum yield (PLQY) are rare due to the strong non-radiative ( k nr ) decay. Here, we report two DR/NIR emitters with high PLQY, TPANZPyPI and TPANZ3PI. Interestingly, the TPANZPyPI film exhibits 46.5% PLQY at 699 nm. Theoretical calculations indicate that TPANZPyPI can achieve this high PLQY in the near-infrared emission region due to its small S 1 to S 0 internal conversion (IC) rate. Meanwhile, research has found that, compared to TPANZ3PI, TPANZPyPI with a more rigid structure can effectively suppress the T 2 to T 1 IC process, which is conducive to higher exciton utilization efficiency (EUE). TPANZPyPI's non-doped OLED shows NIR emission with 4.6% @ 684 nm maximum external quantum efficiency (EQE max ). Its doped OLEDs radiate DR with an EQE max of 6.9% @ 666 nm. These EQEs are among the highest values for hybridized local charge transfer state materials emitting more than 640 nm. This work demonstrates for the first time, based on a combination of theory and experiment, that increasing the molecular rigidity can inhibit the excited state IC process in addition to the S 1 to S 0 IC, realizing efficient electroluminescence. This work demonstrates for the first time that emitters with appropriate qualifications can affect the IC from S 1 to S 0 and the IC of the triple excluded state, achieving high-efficiency device performance.
Organic deep-red (DR) and near-infrared (NIR) emitters with high photoluminescence quantum yield (PLQY) are rare due to the strong non-radiative ( ) decay. Here, we report two DR/NIR emitters with high PLQY, TPANZPyPI and TPANZ3PI. Interestingly, the TPANZPyPI film exhibits 46.5% PLQY at 699 nm. Theoretical calculations indicate that TPANZPyPI can achieve this high PLQY in the near-infrared emission region due to its small S to S internal conversion (IC) rate. Meanwhile, research has found that, compared to TPANZ3PI, TPANZPyPI with a more rigid structure can effectively suppress the T to T IC process, which is conducive to higher exciton utilization efficiency (EUE). TPANZPyPI's non-doped OLED shows NIR emission with 4.6% @ 684 nm maximum external quantum efficiency (EQE ). Its doped OLEDs radiate DR with an EQE of 6.9% @ 666 nm. These EQEs are among the highest values for hybridized local charge transfer state materials emitting more than 640 nm. This work demonstrates for the first time, based on a combination of theory and experiment, that increasing the molecular rigidity can inhibit the excited state IC process in addition to the S to S IC, realizing efficient electroluminescence.
Organic deep-red (DR) and near-infrared (NIR) emitters with high photoluminescence quantum yield (PLQY) are rare due to the strong non-radiative ( k nr ) decay. Here, we report two DR/NIR emitters with high PLQY, TPANZPyPI and TPANZ3PI. Interestingly, the TPANZPyPI film exhibits 46.5% PLQY at 699 nm. Theoretical calculations indicate that TPANZPyPI can achieve this high PLQY in the near-infrared emission region due to its small S 1 to S 0 internal conversion (IC) rate. Meanwhile, research has found that, compared to TPANZ3PI, TPANZPyPI with a more rigid structure can effectively suppress the T 2 to T 1 IC process, which is conducive to higher exciton utilization efficiency (EUE). TPANZPyPI's non-doped OLED shows NIR emission with 4.6% @ 684 nm maximum external quantum efficiency (EQE max ). Its doped OLEDs radiate DR with an EQE max of 6.9% @ 666 nm. These EQEs are among the highest values for hybridized local charge transfer state materials emitting more than 640 nm. This work demonstrates for the first time, based on a combination of theory and experiment, that increasing the molecular rigidity can inhibit the excited state IC process in addition to the S 1 to S 0 IC, realizing efficient electroluminescence.
Organic deep-red (DR) and near-infrared (NIR) emitters with high photoluminescence quantum yield (PLQY) are rare due to the strong non-radiative (knr) decay. Here, we report two DR/NIR emitters with high PLQY, TPANZPyPI and TPANZ3PI. Interestingly, the TPANZPyPI film exhibits 46.5% PLQY at 699 nm. Theoretical calculations indicate that TPANZPyPI can achieve this high PLQY in the near-infrared emission region due to its small S1 to S0 internal conversion (IC) rate. Meanwhile, research has found that, compared to TPANZ3PI, TPANZPyPI with a more rigid structure can effectively suppress the T2 to T1 IC process, which is conducive to higher exciton utilization efficiency (EUE). TPANZPyPI's non-doped OLED shows NIR emission with 4.6% @ 684 nm maximum external quantum efficiency (EQEmax). Its doped OLEDs radiate DR with an EQEmax of 6.9% @ 666 nm. These EQEs are among the highest values for hybridized local charge transfer state materials emitting more than 640 nm. This work demonstrates for the first time, based on a combination of theory and experiment, that increasing the molecular rigidity can inhibit the excited state IC process in addition to the S1 to S0 IC, realizing efficient electroluminescence.
Author Zhou, Huayi
Xie, Mingliang
Ma, Chengling
Xue, Shanfeng
Sun, Qikun
Zhang, Shi-Tong
Zhou, Yannan
Yang, Wenjun
Zhang, Yujian
AuthorAffiliation Department of Chemistry
School of Polymer Science & Engineering
Qingdao University of Science and Technology
Institute of Theoretical Chemistry
College of Chemistry Jilin University
Key Laboratory of the Ministry of Education for Advanced Catalysis Materials
Zhejiang Normal University
State Key Laboratory of Supramolecular Structure and Materials
Key Laboratory of Rubber-Plastics of the Ministry of Education
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Zhang, HY (WOS:000763036900022) 2022; 60
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Snippet Organic deep-red (DR) and near-infrared (NIR) emitters with high photoluminescence quantum yield (PLQY) are rare due to the strong non-radiative ( k nr )...
Organic deep-red (DR) and near-infrared (NIR) emitters with high photoluminescence quantum yield (PLQY) are rare due to the strong non-radiative (knr) decay....
Organic deep-red (DR) and near-infrared (NIR) emitters with high photoluminescence quantum yield (PLQY) are rare due to the strong non-radiative ( ) decay....
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SubjectTerms Charge materials
Charge transfer
Chemistry
Chemistry, Multidisciplinary
Emitters
Excitons
Internal conversion
Near infrared radiation
Photoluminescence
Physical Sciences
Quantum efficiency
Rigid structures
Science & Technology
Title Efficient near-infrared emission benefits from slowing down the internal conversion process
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https://www.ncbi.nlm.nih.gov/pubmed/38638218
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https://www.proquest.com/docview/3043074593
https://pubmed.ncbi.nlm.nih.gov/PMC11023042
Volume 15
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