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 in | Chemical science (Cambridge) Vol. 15; no. 15; pp. 5589 - 5595 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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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 |
AuthorAffiliation_xml | – sequence: 0 name: Zhejiang Normal University – sequence: 0 name: Key Laboratory of Rubber-Plastics of the Ministry of Education – sequence: 0 name: Department of Chemistry – sequence: 0 name: State Key Laboratory of Supramolecular Structure and Materials – sequence: 0 name: Key Laboratory of the Ministry of Education for Advanced Catalysis Materials – sequence: 0 name: Institute of Theoretical Chemistry – sequence: 0 name: College of Chemistry Jilin University – sequence: 0 name: Qingdao University of Science and Technology – sequence: 0 name: School of Polymer Science & Engineering |
Author_xml | – sequence: 1 givenname: Mingliang surname: Xie fullname: Xie, Mingliang – sequence: 2 givenname: Yannan surname: Zhou fullname: Zhou, Yannan – sequence: 3 givenname: Huayi surname: Zhou fullname: Zhou, Huayi – sequence: 4 givenname: Chengling surname: Ma fullname: Ma, Chengling – sequence: 5 givenname: Qikun surname: Sun fullname: Sun, Qikun – sequence: 6 givenname: Shi-Tong surname: Zhang fullname: Zhang, Shi-Tong – sequence: 7 givenname: Yujian surname: Zhang fullname: Zhang, Yujian – sequence: 8 givenname: Wenjun surname: Yang fullname: Yang, Wenjun – sequence: 9 givenname: Shanfeng surname: Xue fullname: Xue, Shanfeng |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38638218$$D View this record in MEDLINE/PubMed |
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diodes publication-title: NATURE REVIEWS MATERIALS doi: 10.1038/natrevmats.2018.20 |
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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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