| Literature DB >> 35236007 |
Hong-Ji Tan1, Guo-Xi Yang1, Ying-Lan Deng1, Chen Cao2, Ji-Hua Tan2, Ze-Lin Zhu2, Wen-Cheng Chen3, Yuan Xiong2, Jing-Xin Jian1, Chun-Sing Lee2, Qing-Xiao Tong1.
Abstract
To achieve high-efficiency deep-blue electroluminescence satisfying Rec.2020 standard blue gamut, two thermally activated delayed fluorescent (TADF) emitters are developed: 5-(2,12-di-tert-butyl-5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracen-7-yl)-10,10-diphenyl-5,10-dihydrodibenzo[b,e][1,4]azasiline (TDBA-PAS) and 10-(2,12-di-tert-butyl-5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracen-7-yl)-9,9-diphenyl-9,10-dihydroacridine (TDBA-DPAC). Inheriting from their parented organoboron multi-resonance core, both emitters show very promising deep-blue emissions with relatively narrow full width at half-maximum (FWHM, ≈50 nm in solution), high photoluminescence quantum yield (up to 92.3%), and short emission lifetime (≤2.49 µs) with fast reverse intersystem crossing (>106 s-1 ) in doped films. More importantly, replacing the spiro-centered sp3 C atom (TDBA-DPAC) with the larger-radius sp3 Si atom (TDBA-PAS), enhanced conformational heterogeneities in bulky-group-shielded TADF molecules are observed in solution, doped film, and device. Consequently, OLEDs based on TDBA-PAS retain high maximum external quantum efficiencies ≈20% with suppressed efficiency roll-off and color index close to Rec.2020 blue gamut over a wide doping range of 10-50 wt%. This study highlights a new strategy to restrain spectral broadening and redshifting and efficiency roll-off in the design of deep-blue TADF emitters.Entities:
Keywords: deep-blue electroluminescence; doping ratio; dual conformations; organic light-emitting diodes; thermally activated delayed fluorescence
Year: 2022 PMID: 35236007 DOI: 10.1002/adma.202200537
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849