2017
DOI: 10.1002/adma.201700907
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Control of Circularly Polarized Electroluminescence in Induced Twist Structure of Conjugate Polymer

Abstract: An extremely high degree of circularly polarized photoluminescence (CPPL) and electroluminescence (CPEL) (dissymmetry factor values: |g | = 0.72 and |g | = 1.13) are generated from twisted stacking of achiral conjugated polymer induced by nonemitting chiral dopant of high helical twisting power for the first time. Using a theoretical analysis incorporating the Stokes parameter, the twisting angle and birefringence of the aligned conjugated polymer, and the degree of linear polarization in the emitted light are… Show more

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Cited by 162 publications
(160 citation statements)
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“…We obtained HTP = 134.4 µm -1 by fitting the data to p ~ 1 / (HTP × c) where p and c are the pitch of the twisted stacking and concentration of the dopant, respectively. This value is very large compared to the HTP of the chiral dopant for the polymer as shown in the previous study and is reasonable results because it has a very small molecular weight as compared with the polymer [13].…”
Section: Resultssupporting
confidence: 84%
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“…We obtained HTP = 134.4 µm -1 by fitting the data to p ~ 1 / (HTP × c) where p and c are the pitch of the twisted stacking and concentration of the dopant, respectively. This value is very large compared to the HTP of the chiral dopant for the polymer as shown in the previous study and is reasonable results because it has a very small molecular weight as compared with the polymer [13].…”
Section: Resultssupporting
confidence: 84%
“…We evaluated the CP property of the twist structure by the Müller matrix calculation using the parameters of the device such as degree of linear polarization, thickness, wavelength of emission, birefringence, twist angle of EML [13]. The degree of linear polarization of the PL was measured in the uniaxially aligned linearly polarized OLED without chiral dopant were 0.85.…”
Section: Figurementioning
confidence: 99%
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“…The crude product was purified through column chromatography (SiO 2 , n-hexane/CH 2 Cl 2 90 : 10) to give 8 (1.17 g, yield 82%) as orange oil. 1 (7). Benzo[1, 2-b:4,5-b']dithiophene-4,8-diol (5) (1.03 g, 4.63 mmol), (S)-1-bromo-3,7-dimethyloctane (2.56 g, 11.6 mmol), K 2 CO 3 (6.40 g, 46.3 mmol), 18-crown-6 (12 mg, 0.045 mmol) and CH 3 CN (100 mL) were mixed together.…”
Section: Experimental Section Synthesismentioning
confidence: 99%
“…Chirality in organic optoelectronic devices is a topic that is rapidly gaining interest . There is at least a two‐fold interest: in the first place it can constitute a means to drive and control the supramolecular order of π‐conjugated molecules constituting the active layers of the devices, and secondly it opens the way to highly specialized applications, such as producing (CP‐OLED), or detecting (CP‐OFET) circularly polarized (CP) light or specifically responding to analyte enantiomers in analytical sensors . Moreover, molecular chirality is a unique way to manipulate electron spins and to construct spin filters .…”
Section: Introductionmentioning
confidence: 99%