中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
De Novo Design of Excited-State Intramolecular Proton Transfer Emitters via a Thermally Activated Delayed Fluorescence Channel

文献类型:期刊论文

作者Wu, Kailong3,4; Zhang, Tao2; Wang, Zian4; Wang, Lian1; Zhan, Lisi4; Gong, Shaolong4; Zhong, Cheng4; Lu, Zheng-Hong2; Zhang, Song1; Yang, Chuluo3,4
刊名JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
出版日期2018-07-18
卷号140期号:28页码:8877-8886
ISSN号0002-7863
DOI10.1021/jacs.8b04795
英文摘要Developing excited-state intramolecular proton transfer (ESIPT) emitters with high photoluminescence quantum yields (Phi(PL)s) and long fluorescence lifetimes in solid state remains a formidable challenge. In this study, we integrated the molecular design tactics of thermally activated delayed fluorescence (TADF) into ESIPT molecules with the goals of improving their Phi(PL)s and increasing their fluorescence lifetimes. Two proof-of-concept molecules, PXZPDO and DMACP-DO, were developed by adopting symmetric D-pi-A-pi-D molecular architectures (where D and A represent donors and acceptors, respectively) featuring electron donating phenoxazine or a 9,9-dimethyl-9,10-dihydroacridine moiety, an ESIPT core beta-diketone, and phenylene pi-bridges. Both molecules exhibited sole enol-type forms stabilized by intramolecular hydrogen bonds and exhibited a unique and dynamic ESIPT character that was verified by transient absorption analyses. Endowed with distinct TADF features, PXZPDO and DMACPDO showed high Phi(PL)s of 68% and 86% in the film state, coupled with notable delayed fluorescence lifetimes of 1.33 and 1.94 mu s, respectively. Employing these ESIPT emitters successfully achieved maximum external quantum efficiencies (n(ext)s) of 18.8% and 23.9% for yellow and green organic light-emitting diodes (OLEDs), respectively, which represent the state-of-the-art device performances for ESIPT emitters. This study not only opens a new avenue for designing efficient ESIPT emitters with high Phi(PL)s and long fluorescence lifetimes in solid state but also unlocks the huge potential of ESIPT emitters in realizing high-efficiency OLEDs.
WOS关键词LIGHT-EMITTING-DIODES ; EXTERNAL QUANTUM EFFICIENCY ; AGGREGATION-INDUCED EMISSION ; CHARGE-TRANSFER ; RADIATIONLESS PROCESSES ; POWER EFFICIENCY ; ROLL-OFF ; BLUE ; DEVICES ; OLEDS
资助项目National Natural Science Foundation of China[51573141] ; National Natural Science Foundation of China[91433201] ; National Natural Science Foundation of China[11674355] ; National Key R&D Program of China[2016YFB0401002] ; National Basic Research Program of China[2015CB655002] ; Shenzhen Peacock Plan[KQTD20170330110107046] ; Natural Science Foundation for Distinguished Young Scholars of Hubei Province[2017CFA033]
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000439532000037
出版者AMER CHEMICAL SOC
资助机构National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Key R&D Program of China ; National Key R&D Program of China ; National Basic Research Program of China ; National Basic Research Program of China ; Shenzhen Peacock Plan ; Shenzhen Peacock Plan ; Natural Science Foundation for Distinguished Young Scholars of Hubei Province ; Natural Science Foundation for Distinguished Young Scholars of Hubei Province ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Key R&D Program of China ; National Key R&D Program of China ; National Basic Research Program of China ; National Basic Research Program of China ; Shenzhen Peacock Plan ; Shenzhen Peacock Plan ; Natural Science Foundation for Distinguished Young Scholars of Hubei Province ; Natural Science Foundation for Distinguished Young Scholars of Hubei Province ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Key R&D Program of China ; National Key R&D Program of China ; National Basic Research Program of China ; National Basic Research Program of China ; Shenzhen Peacock Plan ; Shenzhen Peacock Plan ; Natural Science Foundation for Distinguished Young Scholars of Hubei Province ; Natural Science Foundation for Distinguished Young Scholars of Hubei Province ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Key R&D Program of China ; National Key R&D Program of China ; National Basic Research Program of China ; National Basic Research Program of China ; Shenzhen Peacock Plan ; Shenzhen Peacock Plan ; Natural Science Foundation for Distinguished Young Scholars of Hubei Province ; Natural Science Foundation for Distinguished Young Scholars of Hubei Province
源URL[http://ir.wipm.ac.cn/handle/112942/21346]  
专题中国科学院武汉物理与数学研究所
通讯作者Gong, Shaolong; Lu, Zheng-Hong; Zhang, Song; Yang, Chuluo
作者单位1.Chinese Acad Sci, Wuhan Inst Phys & Math, State Key Lab Magnet Resonance & Atom & Mol Phys, Wuhan 430071, Hubei, Peoples R China
2.Yunnan Univ, Dept Phys, Yunnan Key Lab Micro Nano Mat & Technol, Kunming 650091, Yunnan, Peoples R China
3.Shenzhen Univ, Coll Mat Sci & Engn, Shenzhen Key Lab Polymer Sci & Technol, Shenzhen 518060, Peoples R China
4.Wuhan Univ, Hubei Key Lab Organ & Polymer Optoelect Mat, Dept Chem, Wuhan 430072, Hubei, Peoples R China
推荐引用方式
GB/T 7714
Wu, Kailong,Zhang, Tao,Wang, Zian,et al. De Novo Design of Excited-State Intramolecular Proton Transfer Emitters via a Thermally Activated Delayed Fluorescence Channel[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,2018,140(28):8877-8886.
APA Wu, Kailong.,Zhang, Tao.,Wang, Zian.,Wang, Lian.,Zhan, Lisi.,...&Yang, Chuluo.(2018).De Novo Design of Excited-State Intramolecular Proton Transfer Emitters via a Thermally Activated Delayed Fluorescence Channel.JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,140(28),8877-8886.
MLA Wu, Kailong,et al."De Novo Design of Excited-State Intramolecular Proton Transfer Emitters via a Thermally Activated Delayed Fluorescence Channel".JOURNAL OF THE AMERICAN CHEMICAL SOCIETY 140.28(2018):8877-8886.

入库方式: OAI收割

来源:武汉物理与数学研究所

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