2019
DOI: 10.1021/acs.jpclett.9b00526
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Polycyclic Aromatic Hydrocarbon Derivatives toward Ideal Electron-Transporting Materials for Organic Light-Emitting Diodes

Abstract: One seemingly fundamental issue for electron-transporting materials (ETMs) in organic light-emitting diodes (OLEDs) is the mutual exclusion of a high electron-transporting mobility (μ e) and a large molecular triplet energy for good exciton confinement. Very recently, a trade-off was realized by adopting polycyclic aromatic hydrocarbon (PAH) derivatives as bipolar ETMs. Though the intrinsic low triplet energy of PAH moieties, good exciton confinement abilities are realized by manipulating the peripheral groups… Show more

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Cited by 32 publications
(16 citation statements)
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References 54 publications
(115 reference statements)
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“…Also, the side group greatly influences the charge injection and exciton confinement abilities of such ETMs. In the authors' previous work, it was mentioned that an asymmetric anthracene derivative motif would be an ideal molecular design strategy to balance all the parameters [4]. In the present study, based on such concept, a novel asymmetric anthracene derivative was designed and synthesized to further improve the performances of such compounds as ETMs.…”
Section: Introductionmentioning
confidence: 98%
“…Also, the side group greatly influences the charge injection and exciton confinement abilities of such ETMs. In the authors' previous work, it was mentioned that an asymmetric anthracene derivative motif would be an ideal molecular design strategy to balance all the parameters [4]. In the present study, based on such concept, a novel asymmetric anthracene derivative was designed and synthesized to further improve the performances of such compounds as ETMs.…”
Section: Introductionmentioning
confidence: 98%
“…[ 41,42 ] In our case, a better electron mobility feature in these materials would arise from the peripheral electron‐withdrawing cyano substituent. [ 43 ] Considering that both electron/hole motilities of TPNACN were slightly higher than TPBACN , which likely benefits from its π–π stacking and strongly interacting solid‐state structure, facilitating charge hopping between the adjacent molecules and thus enhanced charge mobility. [ 44 ] Thus, the superior EL performance of TPNACN ‐based OLED could be attributed to a combination of a close to unity solid‐state Φ PL and a good charge transporting ability of the emitter as well as an improved TTA process in the device, in which all these properties are initiated from a distinctive isolated dimeric π‐stacking of anthracene unit of the molecule in solid‐state.…”
Section: Resultsmentioning
confidence: 99%
“…Electron transfer in organic molecules is essential for the functioning of organic electronic devices, such as secondary batteries, [1,2] electrochromic devices, [3] non‐volatile semiconductor memory, and [4–6] organic light‐emitting diodes (OLEDs) [7] . The kinetics and reversibility of electron transfer are key aspects for the optimal performance and sustainability of these systems.…”
Section: Introductionmentioning
confidence: 99%