The crucial role of non-conjugated functional groups in the triplet manipulation of heterocycle aromaticity hot exciton materials

Hot exciton materials have gained widespread attention in the field of organic light-emitting diodes (OLEDs) on the strength of the effective triplet exciton utilization via rapid high-lying excited state reverse intersystem crossing (hRISC) processes. However, the development of hot exciton materia...

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Published inJournal of materials chemistry. C, Materials for optical and electronic devices Vol. 11; no. 37; pp. 12511 - 12516
Main Authors Guo, Shaoting, Wang, Long, Tian, Xiangbin, Zhao, Zhenxiang, Wang, Hua
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 28.09.2023
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ISSN2050-7526
2050-7534
DOI10.1039/d3tc02831c

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Abstract Hot exciton materials have gained widespread attention in the field of organic light-emitting diodes (OLEDs) on the strength of the effective triplet exciton utilization via rapid high-lying excited state reverse intersystem crossing (hRISC) processes. However, the development of hot exciton materials is subject to the lack of a practicable molecular design strategy as well as guidelines, and current material design and screening often have to rely on an experimental trial-and-error process. Taking the proposed heterocycle aromaticity design strategy as a foundation, we systematically investigated the role of non-conjugated functional groups on the fluorescence behavior and exciton dynamics based on a series of pyrazoline hot exciton materials using both theoretical and experimental evidence. Results show that beyond the steric resistance effect, as envisioned, these non-conjugated functional groups also play a crucial role in triplet manipulation via enriching the hRISC channels. A series of new blue-emitting hot exciton materials were successfully fabricated with a high luminous efficiency in the solid state (up to 87%). These findings not only provide an important supplement to the proposed heterocycle aromaticity strategy but also offer some insights into rational excited state manipulation, which could be used to design and develop new luminescent materials for OLED applications. Beyond steric effect, non-conjugated functional groups play a crucial role in triplet manipulation of heterocylce aromaticity hot exciton material. A series of new blue-emitting molecules were successfully fabricated with high luminous efficiency.
AbstractList Hot exciton materials have gained widespread attention in the field of organic light-emitting diodes (OLEDs) on the strength of the effective triplet exciton utilization via rapid high-lying excited state reverse intersystem crossing (hRISC) processes. However, the development of hot exciton materials is subject to the lack of a practicable molecular design strategy as well as guidelines, and current material design and screening often have to rely on an experimental trial-and-error process. Taking the proposed heterocycle aromaticity design strategy as a foundation, we systematically investigated the role of non-conjugated functional groups on the fluorescence behavior and exciton dynamics based on a series of pyrazoline hot exciton materials using both theoretical and experimental evidence. Results show that beyond the steric resistance effect, as envisioned, these non-conjugated functional groups also play a crucial role in triplet manipulation via enriching the hRISC channels. A series of new blue-emitting hot exciton materials were successfully fabricated with a high luminous efficiency in the solid state (up to 87%). These findings not only provide an important supplement to the proposed heterocycle aromaticity strategy but also offer some insights into rational excited state manipulation, which could be used to design and develop new luminescent materials for OLED applications. Beyond steric effect, non-conjugated functional groups play a crucial role in triplet manipulation of heterocylce aromaticity hot exciton material. A series of new blue-emitting molecules were successfully fabricated with high luminous efficiency.
Hot exciton materials have gained widespread attention in the field of organic light-emitting diodes (OLEDs) on the strength of the effective triplet exciton utilization via rapid high-lying excited state reverse intersystem crossing (hRISC) processes. However, the development of hot exciton materials is subject to the lack of a practicable molecular design strategy as well as guidelines, and current material design and screening often have to rely on an experimental trial-and-error process. Taking the proposed heterocycle aromaticity design strategy as a foundation, we systematically investigated the role of non-conjugated functional groups on the fluorescence behavior and exciton dynamics based on a series of pyrazoline hot exciton materials using both theoretical and experimental evidence. Results show that beyond the steric resistance effect, as envisioned, these non-conjugated functional groups also play a crucial role in triplet manipulation via enriching the hRISC channels. A series of new blue-emitting hot exciton materials were successfully fabricated with a high luminous efficiency in the solid state (up to 87%). These findings not only provide an important supplement to the proposed heterocycle aromaticity strategy but also offer some insights into rational excited state manipulation, which could be used to design and develop new luminescent materials for OLED applications.
Hot exciton materials have gained widespread attention in the field of organic light-emitting diodes (OLEDs) on the strength of the effective triplet exciton utilization via rapid high-lying excited state reverse intersystem crossing (hRISC) processes. However, the development of hot exciton materials is subject to the lack of a practicable molecular design strategy as well as guidelines, and current material design and screening often have to rely on an experimental trial-and-error process. Taking the proposed heterocycle aromaticity design strategy as a foundation, we systematically investigated the role of non-conjugated functional groups on the fluorescence behavior and exciton dynamics based on a series of pyrazoline hot exciton materials using both theoretical and experimental evidence. Results show that beyond the steric resistance effect, as envisioned, these non-conjugated functional groups also play a crucial role in triplet manipulation via enriching the hRISC channels. A series of new blue-emitting hot exciton materials were successfully fabricated with a high luminous efficiency in the solid state (up to 87%). These findings not only provide an important supplement to the proposed heterocycle aromaticity strategy but also offer some insights into rational excited state manipulation, which could be used to design and develop new luminescent materials for OLED applications.
Author Wang, Long
Tian, Xiangbin
Zhao, Zhenxiang
Wang, Hua
Guo, Shaoting
AuthorAffiliation Ministry of Education
Taiyuan University of Technology
Key Laboratory of Interface Science and Engineering in Advanced Materials
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SubjectTerms Aromaticity
Excitation
Excitons
Functional groups
Luminous efficacy
Organic light emitting diodes
Title The crucial role of non-conjugated functional groups in the triplet manipulation of heterocycle aromaticity hot exciton materials
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