4.2 Article

Carrier transport characteristics of glass-forming chiral liquid crystalline dimers based on oligo(phenylenevinylene) units

Journal

MATERIALS ADVANCES
Volume 3, Issue 23, Pages 8428-8437

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ma00899h

Keywords

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Funding

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT) [15H00753]
  2. Japan Society for the Promotion of Science (JSPS) [15H03797, 21H01904]
  3. Ogasawara Foundation for the Promotion of Science Engineering
  4. SEI Group CSR Foundation
  5. Asahi Glass Foundation
  6. Salt Science Research Foundation [1715]
  7. Iketani Science and Technology Foundation
  8. TEPCO Memorial Foundation
  9. 'Nanotechnology Platform Program' of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan [JPMXP09F19GA0004]

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We synthesized chiral dimeric chiral nematic (N*) liquid crystals with tri(p-phenylene vinylene) units. The mixture of dimeric compounds and monomeric chiral liquid crystals exhibited a glassy N* phase at room temperature, with the reflection band tunable by temperature change. High quality circularly polarized emission with a dissymmetry factor of 1.4 was observed when the reflection band covered the fluorescence peak. Hole mobilities were determined using the TOF method and analyzed using the Gaussian disorder model. The preexponential factors in the N* phase of these compounds were higher than those of amorphous organic semiconductors, attributed to the large pi-conjugated units.
We synthesized chiral dimeric chiral nematic (N*) liquid crystals bearing tri(p-phenylene vinylene) units. The mixture of dimeric compounds and monomeric chiral liquid crystals exhibited a glassy N* phase at room temperature and the reflection band could be tuned by the change of the temperature from which the rapid cooling of the mixture started. When the reflection band covered the fluorescence peak, high quality circularly polarized emission with a dissymmetry factor of 1.4 was observed. Hole mobilities were determined over wide temperature ranges by the TOF method and the hole transport characteristics in the N* phase were analyzed using the Gaussian disorder model. The preexponential factors in the N* phase of these compounds, corresponding to a virtual mobility without energetic and spatial disorders, were one or two order of magnitudes higher than those of amorphous organic semiconductors. This should be attributed to the large pi-conjugated units of these compounds. The energetic and spatial disorders were larger than those of amorphous organic semiconductors in spite of the local uniaxial molecular orientation in the N* phase. This result should be caused by the large anisotropic polarizability of the pi-conjugated units with a large aspect ratio.

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