2020
DOI: 10.1039/d0tc01637c
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Realization of deep-blue TADF in sterically controlled naphthyridines for vacuum- and solution-processed OLEDs

Abstract:

Efficient deep-blue naphthyridine-based TADF emitters featuring narrow-band-emission with low roll-off were designed by using the H-bonding and sterically controlled charge-transfer interactions.

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Cited by 37 publications
(16 citation statements)
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“…As illustrated in Figurer 5f , to our best knowledge, the EQE value of 27.13% for BD‐F based device is at a record high for solution‐processed OLEDs devices. [ 44 , 45 , 46 , 47 , 48 , 49 , 50 , 51 , 52 , 53 , 54 , 55 , 56 , 57 , 58 , 59 , 60 ] It also should be noted that the solution‐processable emitters with deep‐blue or near‐infrared color still obviously lag behind others, and thus we need to pay more concentration on promoting their luminescence efficiency through elaborate molecular designing and structural regulation depicted in our work.…”
Section: Resultsmentioning
confidence: 99%
“…As illustrated in Figurer 5f , to our best knowledge, the EQE value of 27.13% for BD‐F based device is at a record high for solution‐processed OLEDs devices. [ 44 , 45 , 46 , 47 , 48 , 49 , 50 , 51 , 52 , 53 , 54 , 55 , 56 , 57 , 58 , 59 , 60 ] It also should be noted that the solution‐processable emitters with deep‐blue or near‐infrared color still obviously lag behind others, and thus we need to pay more concentration on promoting their luminescence efficiency through elaborate molecular designing and structural regulation depicted in our work.…”
Section: Resultsmentioning
confidence: 99%
“…Such a high k r for tCN-ND was in line with the rapid PF decay and high oscillator strength of the S 0 → S 1 transition. 27 However, the rapid k r with values exceeding 10 7 , 1 order of magnitude larger than the accurate ones, could be derived if the overestimated Φ PF was used. In this case, k r ranged from 22.7 ( ACRPyr ) to the remarkable 135 × 10 6 s –1 for tCz-ND .…”
Section: Resultsmentioning
confidence: 99%
“…Serving as the smallest alkyl group, the methyl group demonstrates a weak hyperconjugation effect and a steric hindrance effect when linked to an aromatic ring. 4 The methyl group plays an important role in the design of TADF materials where three types of methyl effects can be concluded. 5–10 Type 1: the introduction of methyl groups can effectively improve the luminescence performance of TADF materials.…”
Section: Introductionmentioning
confidence: 99%