2020
DOI: 10.1016/j.cej.2020.124694
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Asymmetric anthracene derivatives as multifunctional electronic materials for constructing simplified and efficient non-doped homogeneous deep blue fluorescent OLEDs

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Cited by 39 publications
(7 citation statements)
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“…To further tune the emission color to the deep-blue region, Wang et al proposed an asymmetric bulky periphery enveloping strategy for constructing two bipolar deep-blue TTA emitters (43 and 44) by introducing a relatively weak electron-donating 1,5-diazacarbazole unit. 95 Both compounds 43 and 44 possessed deep-blue emissions at around 420−440 nm, high PLQYs of 93% and 96%, good thermostabilities, and high carrier mobilities. Nondoped homogeneous OLEDs employing these materials as emitters and electron transporting materials (ETM) exhibited high EL performance with narrow fwhms of 50 and 53 nm, CIE coordinates of (0.151, 0.066) and (0.157, 0.071), and maximum EQEs of 6.40% and 4.86%, respectively.…”
Section: And Oledsmentioning
confidence: 99%
See 1 more Smart Citation
“…To further tune the emission color to the deep-blue region, Wang et al proposed an asymmetric bulky periphery enveloping strategy for constructing two bipolar deep-blue TTA emitters (43 and 44) by introducing a relatively weak electron-donating 1,5-diazacarbazole unit. 95 Both compounds 43 and 44 possessed deep-blue emissions at around 420−440 nm, high PLQYs of 93% and 96%, good thermostabilities, and high carrier mobilities. Nondoped homogeneous OLEDs employing these materials as emitters and electron transporting materials (ETM) exhibited high EL performance with narrow fwhms of 50 and 53 nm, CIE coordinates of (0.151, 0.066) and (0.157, 0.071), and maximum EQEs of 6.40% and 4.86%, respectively.…”
Section: And Oledsmentioning
confidence: 99%
“…To further tune the emission color to the deep-blue region, Wang et al proposed an asymmetric bulky periphery enveloping strategy for constructing two bipolar deep-blue TTA emitters ( 43 and 44 ) by introducing a relatively weak electron-donating 1,5-diazacarbazole unit . Both compounds 43 and 44 possessed deep-blue emissions at around 420–440 nm, high PLQYs of 93% and 96%, good thermostabilities, and high carrier mobilities.…”
Section: Triplet–triplet Annihilation Materials and Oledsmentioning
confidence: 99%
“…[27][28][29][30][31] However, there are only a few reports on efficient deep-blue non-doped OLEDs showing an EQE of over 5% and a CIEy coordinate under 0.065. [32][33][34][35][36] As is known, fluorescent/phosphorescent hybrid white OLEDs (WOLEDs) combining stable blue fluorophores with efficient green-red/yellow phosphors have become one of the most promising tools, considering their potential for high efficiency and long lifetime without utilizing unstable blue phosphors. [37][38][39] The triplet state (T 1 ) energy of the blue fluorophore has an important effect on the device structure and EL performance of hybrid WOLEDs.…”
Section: Introductionmentioning
confidence: 99%
“…27–31 However, there are only a few reports on efficient deep-blue non-doped OLEDs showing an EQE of over 5% and a CIEy coordinate under 0.065. 32–36…”
Section: Introductionmentioning
confidence: 99%
“…They can be divided into two categories: conjugated PDs and nonconjugated PDs. Conventional fluorescent conjugated PDs generally contain classic chromophores or extended π-systems, [1,2] inevitably accompanied by the use of additional organic reagents and inherent high toxicities, [5][6][7] which limit further development and application. Interestingly, some of the abundant, nontoxic compounds without π-conjugated chromophores could also emit bright fluorescence, such as natural chitosan, [8] bovine serum albumin, [9] cellulose, [10] poly(amidoamine) dendrimers, [11] hyperbranched poly(amine ester), [12] and polyacrylonitrile.…”
Section: Introductionmentioning
confidence: 99%