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1.
Achieving High‐Performance Nondoped OLEDs with Extremely Small Efficiency Roll‐Off by Combining Aggregation‐Induced Emission and Thermally Activated Delayed Fluorescence
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Jingjing Guo Xiang‐Long Li Han Nie Wenwen Luo Shifeng Gan Shimin Hu Rongrong Hu Anjun Qin Zujin Zhao Shi‐Jian Su Ben Zhong Tang 《Advanced functional materials》2017,27(13)
Luminescent materials with thermally activated delayed fluorescence (TADF) can harvest singlet and triplet excitons to afford high electroluminescence (EL) efficiencies for organic light‐emitting diodes (OLEDs). However, TADF emitters generally have to be dispersed into host matrices to suppress emission quenching and/or exciton annihilation, and most doped OLEDs of TADF emitters encounter a thorny problem of swift efficiency roll‐off as luminance increases. To address this issue, in this study, a new tailor‐made luminogen (dibenzothiophene‐benzoyl‐9,9‐dimethyl‐9,10‐dihydroacridine, DBT‐BZ‐DMAC) with an unsymmetrical structure is synthesized and investigated by crystallography, theoretical calculation, spectroscopies, etc. It shows aggregation‐induced emission, prominent TADF, and interesting mechanoluminescence property. Doped OLEDs of DBT‐BZ‐DMAC show high peak current and external quantum efficiencies of up to 51.7 cd A?1 and 17.9%, respectively, but the efficiency roll‐off is large at high luminance. High‐performance nondoped OLED is also achieved with neat film of DBT‐BZ‐DMAC, providing excellent maxima EL efficiencies of 43.3 cd A?1 and 14.2%, negligible current efficiency roll‐off of 0.46%, and external quantum efficiency roll‐off approaching null from peak values to those at 1000 cd m?2. To the best of the authors' knowledge, this is one of the most efficient nondoped TADF OLEDs with small efficiency roll‐off reported so far. 相似文献
2.
OLEDs: Achieving High‐Performance Nondoped OLEDs with Extremely Small Efficiency Roll‐Off by Combining Aggregation‐Induced Emission and Thermally Activated Delayed Fluorescence (Adv. Funct. Mater. 13/2017)
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Jingjing Guo Xiang‐Long Li Han Nie Wenwen Luo Shifeng Gan Shimin Hu Rongrong Hu Anjun Qin Zujin Zhao Shi‐Jian Su Ben Zhong Tang 《Advanced functional materials》2017,27(13)
3.
Novel Blue Bipolar Thermally Activated Delayed Fluorescence Material as Host Emitter for High‐Efficiency Hybrid Warm‐White OLEDs with Stable High Color‐Rendering Index
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Jie Liang Chenglong Li Xuming Zhuang Kaiqi Ye Yu Liu Yue Wang 《Advanced functional materials》2018,28(17)
A novel thermally activated delayed fluorescence (TADF) molecule, PHCz2BP, is synthesized and used to construct high performance organic light‐emitting diodes (OLEDs) in this work. PHCz2BP is not only the neat emitting layer for efficient sky‐blue OLED, with very high peak external quantum efficiency/power efficiency (EQE/PE) values of 4.0%/6.9 lm W?1, but also acts as a host to sensitize high‐luminance and high‐efficiency green, orange, and red electrophosphorescence with the universal high EQEs of >20%. More importantly, two hybrid white OLEDs based on the double‐layer emitting system of PHCz2BP:green phosphor/PHCz2BP:red phosphor are achieved. To the best of the knowledge, this is the first report for three‐color (blue–green–red) white devices that adopt a TADF blue host emitter and two phosphorescent dopants without any other additional host. Such simple emitting systems thus realized the best electroluminescent performance to date for the WOLEDs utilizing the hybrid TADF/phosphor strategy: forward‐viewing EQEs of 25.1/23.6% and PEs of 24.1/22.5 lm W?1 at the luminance of 1000 cd m?2 with the color rendering indexes of 85/87 and warm‐white Commission Internationale de L'Eclairage coordinates of (0.41, 0.46)/(0.42, 0.45), indicating its potential to be used as practical eye‐friendly solid‐state lighting in future. 相似文献
4.
Design Strategy of Blue and Yellow Thermally Activated Delayed Fluorescence Emitters and Their All‐Fluorescence White OLEDs with External Quantum Efficiency beyond 20%
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Yunchuan Li Xiang‐Long Li Dongjun Chen Xinyi Cai Gaozhan Xie Zuozheng He Yuan‐Chun Wu Alan Lien Yong Cao Shi‐Jian Su 《Advanced functional materials》2016,26(38):6904-6912
Two thioxanthone‐derived isomeric series of thermally activated delayed fluorescence (TADF) emitters 1,6‐2TPA‐TX/3,6‐2TPA‐TX and 1,6‐2TPA‐TXO/3,6‐2TPA‐TXO are developed for organic light‐emitting diodes (OLEDs). Blue emission devices based on symmetrical 3,6‐2TPA‐TX with common vertical transition route realize an extremely high external quantum efficiency (EQE) of 23.7%, and an ever highest EQE of 24.3% is achieved for yellow emission devices based on 3,6‐2TPA‐TXO by solely changing the sulfur atom valence state of the thioxanthone core. In contrast, their corresponding asymmetric isomers are affected by intramolecular energy transfer and more severely by a nonradiative deactivation pathway, to give much low EQE values (<5%). By utilizing 3,6‐2TPA‐TX as a blue emitter and 3,6‐2TPA‐TXO as a yellow emitter, an ever highest EQE of 20.4% is achieved for all‐fluorescence white OLEDs. 相似文献
5.
Efficient Bipolar Blue AIEgens for High‐Performance Nondoped Blue OLEDs and Hybrid White OLEDs
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Bin Chen Baiquan Liu Jiajie Zeng Han Nie Yi Xiong Jianhua Zou Honglong Ning Zhiming Wang Zujin Zhao Ben Zhong Tang 《Advanced functional materials》2018,28(40)
Blue organic luminescent materials play a crucial role in full‐color display and white lighting but efficient ones meeting commercial demands are very rare. Herein, the design and synthesis of tailor‐made bipolar blue luminogens with an anthracene core and various functional groups are reported. The thermal stabilities, photophysical properties, electronic structures, electrochemical behaviors, carrier transport abilities, and electroluminescence performances are systematically investigated. The luminogen TPE‐TAPBI containing a tetraphenylethene moiety shows aggregation‐induced emission, while another luminogen TriPE‐TAPBI bearing a triphenylethene unit exhibits light aggregation‐caused quenching. In comparison with TriPE‐TAPBI, TPE‐TAPBI has stronger blue emission in neat film and functions more efficiently in nondoped organic light‐emitting diodes (OLEDs). High maxima current, power, and external quantum efficiencies of 7.21 cd A?1, 6.78 lm W?1, and 5.73%, respectively, are attained by the nondoped blue OLED of TPE‐TAPBI (CIEx,y = 0.15, 0.16). Moreover, efficient two‐color hybrid warm white OLEDs (CIEx,y = 0.457, 0.470) are achieved using TPE‐TAPBI neat film as the blue‐emitting component, which provide total current, power, external quantum efficiencies of up to 70.5 lm W?1, 76.0 cd A?1, and 28% at 1000 cd m?2, respectively. These blue and white OLEDs are among the most efficient devices with similar colors in the literature. 相似文献
6.
Subeesh Madayanad Suresh David Hall David Beljonne Yoann Olivier Eli Zysman‐Colman 《Advanced functional materials》2020,30(33)
Since the first report in 2015, multiresonant thermally activated delayed fluorescent (MR‐TADF) compounds, a subclass of TADF emitters based on a heteroatom‐doped nanographene material, have come to the fore as attractive hosts as well as emitters for organic light‐emitting diodes (OLEDs). MR‐TADF compounds typically show very narrow‐band emission, high photoluminescence quantum yields, and small ΔEST values, typically around 200 meV, coupled with high chemical and thermal stabilities. These materials properties have translated into some of the best reported deep‐blue TADF OLEDs. Here, a detailed review of MR‐TADF compounds and their derivatives reported so far is presented. This review comprehensively documents all MR‐TADF compounds, with a focus on the synthesis, optoelectronic behavior, and OLED performance. In addition, computational approaches are surveyed to accurately model the excited state properties of these compounds. 相似文献
7.
Singlet–Triplet Splitting Energy Management via Acceptor Substitution: Complanation Molecular Design for Deep‐Blue Thermally Activated Delayed Fluorescence Emitters and Organic Light‐Emitting Diodes Application
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Xinyi Cai Bin Gao Xiang‐Long Li Yong Cao Shi‐Jian Su 《Advanced functional materials》2016,26(44):8042-8052
A barely reached balance between weak intramolecular‐charge‐transfer (ICT) and small singlet–triplet splitting energy (ΔEST) for reverse intersystem crossing from non‐emissive triplet state to radiative singlet state impedes the realization of deep‐blue thermally activated delayed fluorescence (TADF) materials. By discarding the twisted‐ICT framework for a flattened molecular backbone and introducing a strong acceptor possessing n–π* transition character, hypsochromic color, a large radiative rate (kF), and small ΔEST are achieved simultaneously. Six molecules with a 9,9‐dimethyl‐10‐phenyl‐9,10‐dihydroacridine (i‐DMAc) donor are synthesized and investigated. Coinciding with time‐dependent density functional theory, the reduced dihedral angles between donor (D) and acceptor (A) weaken ICT from dispersed charge density and enable a large kF from increased frontier molecular orbitals overlap. Despite the separated highest occupied (HOMO) and lowest unoccupied molecular orbital (LUMO) population, the intercalation of phenyl bridges between D–A increases kF but significantly lowers the local triplet excited state, indicating small HOMO and LUMO overlap is not a sufficient, but necessary condition for reduced ΔEST. Integrating short conjugation length and carbonyl or triazine acceptors into the complanation molecules, deep‐blue TADF organic light‐emitting diodes demonstrate maximum external quantum efficiencies of 11.5% and 10.9% with Commission Internationale de l'Eclairage coordinates of (0.16, 0.09) and (0.15, 0.11), respectively, which is quite close to the stringent National Television System Committee blue standard. 相似文献
8.
High‐Performance Dibenzoheteraborin‐Based Thermally Activated Delayed Fluorescence Emitters: Molecular Architectonics for Concurrently Achieving Narrowband Emission and Efficient Triplet–Singlet Spin Conversion
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Thermally activated delayed fluorescence (TADF) materials, which enable the full harvesting of singlet and triplet excited states for light emission, are expected as the third‐generation emitters for organic light‐emitting diodes (OLEDs), superseding the conventional fluorescence and phosphorescence materials. High photoluminescence quantum yield (ΦPL), narrow‐band emission (or high color purity), and short delayed fluorescence lifetime are all strongly desired for practical applications. However, to date, no rational design strategy of TADF emitters is established to fulfill these requirements. Here, an epoch‐making design strategy is proposed for producing high‐performance TADF emitters that concurrently exhibiting high ΦPL values close to 100%, narrow emission bandwidths, and short emission lifetimes of ≈1 µs, with a fast reverse intersystem crossing rate of over 106 s?1. A new family of TADF emitters based on dibenzoheteraborins is introduced, which enable both doped and non‐doped TADF‐OLEDs to achieve markedly high external electroluminescence quantum efficiencies, exceeding 20%, and negligible efficiency roll‐offs at a practical high luminance. Systematic photophysical and theoretical investigations and device evaluations for these dibenzoheteraborin‐based TADF emitters are reported here. 相似文献
9.
High‐Performance Hybrid White Organic Light‐Emitting Diodes with Superior Efficiency/Color Rendering Index/Color Stability and Low Efficiency Roll‐Off Based on a Blue Thermally Activated Delayed Fluorescent Emitter
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Zhongbin Wu Jiajia Luo Ning Sun Liping Zhu Hengda Sun Ling Yu Dezhi Yang Xianfeng Qiao Jiangshan Chen Chuluo Yang Dongge Ma 《Advanced functional materials》2016,26(19):3306-3313
Thermally activated delayed fluorescence (TADF)‐based white organic light‐emitting diodes (WOLEDs) are highly attractive because the TADF emitters provide a promising alternative route to harvest triplet excitons. One of the major challenges is to achieve superior efficiency/color rendering index/color stability and low efficiency roll‐off simultaneously. In this paper, high‐performance hybrid WOLEDs are demonstrated by employing an efficient blue TADF emitter combined with red and green phosphorescent emitters. The resulting WOLED shows the maximum external quantum efficiency, current efficiency, and power efficiency of 23.0%, 51.0 cd A?1, and 51.7 lm W?1, respectively. Moreover, the device exhibits extremely stable electroluminescence spectra with a high color rendering index of 89 and Commission Internationale de L'Eclairage coordinates of (0.438, 0.438) at the practical brightness of 1000 cd m?2. The achievement of these excellent performances is systematically investigated by versatile experimental and theoretical evidences, from which it is concluded that the utilization of a blue‐green‐red cascade energy transfer structure and the precise manipulation of charges and excitons are the key points. It can be anticipated that this work might be a starting point for further research towards high‐performance hybrid WOLEDs. 相似文献
10.
Jianan Sun Jing Zhang Qianqian Liang Ying Wei Chunbo Duan Chunmiao Han Hui Xu 《Advanced functional materials》2020,30(9)
Despite the success of thermally activated delayed fluorescence (TADF) emitters in monochromatic organic light‐emitting diodes (OLED), only few efficient full‐TADF white OLEDs (WOLED) are reported because of the challenge in rational exciton allocation between blue and other color emitters. Herein, it is demonstrated that the appropriate exciton delocalization in blue TADF matrixes can simultaneously support the sufficient blue emission and the energy loss–free charge and exciton transfer to yellow TADF emitters. Through introducing steric hindrance–modulated intermolecular hydrogen bond networks, a fluorinated carbazole‐phosphine oxide hybrid realizes the balance of exciton localization and delocalization, giving rise to state‐of‐the‐art external quantum efficiency beyond 20% from its simple trilayer full‐TADF WOLEDs, accompanied by excellent spectral stability. The correlation between the efficiencies of the blue TADF matrixes and their intermolecular interactions reveals that the exciton delocalization is crucial for the exciton allocation optimization in multicomponent emission systems. 相似文献
11.
Over 10% EQE Near‐Infrared Electroluminescence Based on a Thermally Activated Delayed Fluorescence Emitter
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Yi Yuan Yun Hu Ye‐Xin Zhang Jiu‐Dong Lin Ya‐Kun Wang Zuo‐Quan Jiang Liang‐Sheng Liao Shuit‐Tong Lee 《Advanced functional materials》2017,27(26)
Significant effort has been made to develop novel material systems to improve the efficiency of near‐infrared organic light‐emitting diodes (NIR OLEDs). Of those, fluorescent chromophores are mostly studied because of their advantages in cost and tunability. However, it is still rare for fluorescent NIR emitters to present good color purities in the NIR range and to have high external quantum efficiency (EQE). Here, a wedge‐shaped D‐π‐A‐π‐D emitter APDC‐DTPA with thermally activated delayed fluorescence property and a small single‐triplet splitting (ΔEst) of 0.14 eV is presented. The non‐doped NIR device exhibits excellent performance with a maximum EQE of 2.19% and a peak wavelength of 777 nm. Remarkably, when 10 wt% of APDC‐DTPA is doped in 1,3,5‐tris(1‐phenyl‐1H‐benzimidazol‐2‐yl)benzene host, an extremely high EQE of 10.19% with an emission peak of 693 nm is achieved. All these values represent the best result for NIR OLEDs based on a pure organic fluorescent emitter with similar device structure and color gamut. 相似文献
12.
Hyung Jong Kim Hyunchul Kang Ji-Eun Jeong Su Hong Park Chang Woo Koh Chai Won Kim Han Young Woo Min Ju Cho Sungnam Park Dong Hoon Choi 《Advanced functional materials》2021,31(33):2102588
Ultra-deep-blue aggregation-induced delayed fluorescence (AIDF) emitters (TB-tCz and TB-tPCz) bearing organoboron-based cores as acceptors and 3,6-substituted carbazoles as donors are presented. The thermally activated delayed fluorescence (TADF) properties of the two emitters are confirmed by theoretical calculations and time-resolved photoluminescence experiments. TB-tCz and TB-tPCz exhibit fast reverse intersystem crossing rate constants owing to efficient spin–orbit coupling between the singlet and triplet states. When applied in solution-processed organic light-emitting diodes (OLEDs), the TB-tCz- and TB-tPCz-based nondoped devices exhibit ultra-deep-blue emissions of 416–428 nm and high color purity owing to their narrow bandwidths of 42.2–44.4 nm, corresponding to the Commission International de l´Eclairage color coordinates of (x = 0.16–0.17, y = 0.05–0.06). They show a maximum external quantum efficiency (EQEmax) of 8.21% and 15.8%, respectively, exhibiting an unprecedented high performance in solution-processed deep-blue TADF-OLEDs. Furthermore, both emitters exhibit excellent device performances (EQEmax = 14.1–15.9%) and color purity in solution-processed doped OLEDs. The current study provides an AIDF emitter design strategy to implement high-efficiency deep-blue OLEDs in the future. 相似文献
13.
Han Zhang Bing Zhang Yiwen Zhang Zeng Xu Haozhong Wu Ping‐An Yin Zhiming Wang Zujin Zhao Dongge Ma Ben Zhong Tang 《Advanced functional materials》2020,30(35)
Actualizing full singlet exciton yield via a reverse intersystem crossing from the high‐lying triplet state to singlet state, namely, “hot exciton” mechanism, holds great potential for high‐performance fluorescent organic light‐emitting diodes (OLEDs). However, incorporating comprehensive insights into the mechanism and effective molecular design strategies still remains challenging. Herein, three blue emitters (CNNPI, 2TriPE‐CNNPI, and 2CzPh‐CNNPI) with a distinct local excited (LE) state and charge‐transfer (CT) state distributions in excited states are designed and synthesized. They show prominent hybridized local and charge‐transfer (HLCT) states and aggregation‐induced emission enhancement properties. The “hot exciton” mechanism based on these emitters reveals that a balanced LE/CT distribution can simultaneously boost photoluminescence efficiency and exciton utilization. In particular, a nearly 100% exciton utilization is achieved in the electroluminescence (EL) process of 2CzPh‐CNNPI. Moreover, employing 2CzPh‐CNNPI as the emitter, emissive dopant, and sensitizing host, respectively, the EL performances of the corresponding nondoped pure‐blue, doped deep‐blue, and HLCT‐sensitized fluorescent OLEDs are among the most efficient OLEDs with a “hot exciton” mechanism to date. These results could shed light on the design principles for “hot exciton” materials and inspire the development of next‐generation high‐performance OLEDs. 相似文献
14.
Exciton‐Adjustable Interlayers for High Efficiency,Low Efficiency Roll‐Off,and Lifetime Improved Warm White Organic Light‐Emitting Diodes (WOLEDs) Based on a Delayed Fluorescence Assistant Host
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《Advanced functional materials》2018,28(11)
Recently, a new route to achieve 100% internal quantum efficiency white organic light‐emitting diodes (WOLEDs) is proposed by utilizing noble‐metal‐free thermally activated delayed fluorescence (TADF) emitters due to the radiative contributions of triplet excitons by effective reverse intersystem crossing. However, a systematic understanding of their reliability and internal degradation mechanisms is still deficient. Here, it demonstrates high performance and operational stable purely organic fluorescent WOLEDs consisting of a TADF assistant host via a strategic exciton management by multi‐interlayers. By introducing such interlayers, carrier recombination zone could be controlled to suppress the generally unavoidable quenching of long‐range triplet excitons, successfully achieving remarkable external quantum efficiency of 15.1%, maximum power efficiency of 48.9 lm W−1, and extended LT50 lifetime (time to 50% of initial luminance of 1000 cd m−2) exceeding 2000 h. To this knowledge, this is the first pioneering work for realizing high efficiency, low efficiency roll‐off, and operational stable WOLEDs based on a TADF assistant host. The current findings also indicate that broadening the carrier recombination region in both interlayers and yellow emitting layer as well as restraining exciplex quenching at carrier blocking interface make significant roles on reduced efficiency roll‐off and enhanced operational lifetime. 相似文献
15.
Highly Efficient Circularly Polarized Electroluminescence from Aggregation‐Induced Emission Luminogens with Amplified Chirality and Delayed Fluorescence
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Fengyan Song Zeng Xu Qiushuo Zhang Zheng Zhao Haoke Zhang Weijun Zhao Zijie Qiu Chunxuan Qi Han Zhang Herman H. Y. Sung Ian D. Williams Jacky W. Y. Lam Zujin Zhao Anjun Qin Dongge Ma Ben Zhong Tang 《Advanced functional materials》2018,28(17)
Development of highly efficient circularly polarized organic light‐emitting diodes (CPOLEDs) has gained increasing interest as they show improved luminous efficiency and high contract 3D images in OLED displays. In this work, a series of binaphthalene‐containing luminogenic enantiomers with aggregation‐induced emission (AIE) and delayed fluorescence properties is designed and synthesized. These molecules can emit from green to red light depending on the solvent polarity due to the twisted intramolecular charge transfer effect. However, their solid powders show bright light emissions, demonstrating a phenomenon of AIE. All the molecules exhibit Cotton effects and circularly polarized luminescence in toluene solution and films. Multilayer CPOLEDs using the doped and neat films of the molecules as emitting layers are fabricated, which exhibit high external quantum efficiency of up to 9.3% and 3.5% and electroluminescence dissymmetry factor (gEL) of up to +0.026/?0.021 and +0.06/?0.06, respectively. Compared with doped CPOLEDs, the nondoped ones show higher gEL and much smaller current efficiency roll‐off due to the stronger AIE effect. By altering the donor unit, the electroluminescence maximum of the doped film can vary from 493 to 571 nm. As far as it is known, this is the first example of efficient CPOLEDs based on small chiral organic molecules. 相似文献
16.
Light‐Emitting Diodes: Over 10% EQE Near‐Infrared Electroluminescence Based on a Thermally Activated Delayed Fluorescence Emitter (Adv. Funct. Mater. 26/2017)
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Yi Yuan Yun Hu Ye‐Xin Zhang Jiu‐Dong Lin Ya‐Kun Wang Zuo‐Quan Jiang Liang‐Sheng Liao Shuit‐Tong Lee 《Advanced functional materials》2017,27(26)
17.
Tong Yang Zong Cheng Zhiqiang Li Jixiong Liang Yincai Xu Chenglong Li Yue Wang 《Advanced functional materials》2020,30(34)
The development of efficient red thermally activated delayed fluorescence (TADF) emitters with an emission wavelength beyond 600 nm remains a great challenge for organic light‐emitting diodes (OLEDs). Herein, two pairs of isomers are designed and synthesized by attaching electron‐donor 9,9‐diphenyl‐9,10‐dihydroacridine (DPAC) moiety to the different positions of two kinds of highly rigid planar acceptor cores (PDCN and PPDCN). Their TADF efficiencies and emission maxima (599–726 nm) are regulated by molecular isomer manipulation. Interestingly, the photoluminescence quantum yields (ΦPLs) of trans‐isomers T‐DA‐1 and T‐DA‐2 (78% and 89%) are remarkably higher than those of their corresponding cis‐isomers C‐DA‐1 and C‐DA‐2 (12% and 14%). Significantly increased ΦPL values can be explained by single crystal structures and theoretical simulation. As a result, a deep red TADF‐OLED based on T‐DA‐2 displays a maximum external quantum efficiency (EQE) of 26.26% at 640 nm. Notably, at a brightness of 100 cd m?2, the EQE value of T‐DA‐2‐based device still remains at an extremely high level of 23.95%, representing the highest value for reported red TADF‐OLEDs at the same brightness. These results provide a reasonable pathway to optimize optoelectronic properties and thereby construct efficient red TADF emitters through rational isomer engineering. 相似文献
18.
Lucas Frédéric Alaric Desmarchelier Ludovic Favereau Grégory Pieters 《Advanced functional materials》2021,31(20):2010281
The design of fluorophores merging circularly polarized luminescence and thermally activated delayed fluorescence properties has recently emerged as a promising direction for the development of efficient CP-Organic Light-Emitting Diodes (CP-OLEDs). This progress report gives an overview of the molecular designs explored to obtain CP-TADF properties, of their performances as chiral emitters in CP-OLEDs, and discusses future challenges for this burgeoning field of research. 相似文献
19.
Chin‐Yiu Chan Lin‐Song Cui Jong Uk Kim Hajime Nakanotani Chihaya Adachi 《Advanced functional materials》2018,28(11)
By simple modification of the functional groups on the donor unit, the thermally activated delayed fluorescence (TADF) properties of emitters can easily be manipulated. A series of deep blue to blue emissive TADF derivatives is developed, capable of deep‐blue emissions from 403 to 460 nm in toluene. Deep‐blue organic light‐emitting diodes (OLEDs) based on this series of TADF emitters are fabricated, resulting in an electroluminescence peak at 428 nm and a high external quantum efficiency of up to 10.3%. One deep‐blue OLED has achieved the commission internationale de l'eclairage (CIE) coordinates of (0.156, 0.063), which is among the best reported TADF performances for deep‐blue OLEDs with CIEy < 0.07. 相似文献
20.
Luminogens: Efficient Bipolar Blue AIEgens for High‐Performance Nondoped Blue OLEDs and Hybrid White OLEDs (Adv. Funct. Mater. 40/2018)
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Bin Chen Baiquan Liu Jiajie Zeng Han Nie Yi Xiong Jianhua Zou Honglong Ning Zhiming Wang Zujin Zhao Ben Zhong Tang 《Advanced functional materials》2018,28(40)