4.8 Article

Charge Transport in Twisted Organic Semiconductor Crystals of Modulated Pitch

Journal

ADVANCED MATERIALS
Volume 34, Issue 38, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202203842

Keywords

charge transport; crystallite organization; organic semiconductors; twisting morphology

Funding

  1. National Science Foundation [DMR-2003968]
  2. New York University Materials Research Science and Engineering Center (MRSEC) program of the National Science Foundation [DMR-1420073]
  3. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  4. Belgian National Fund for Scientific Research (FNRS) [2.4565.11, T.0058.14, T.0072.18, 30489208, U.G001.19]
  5. Federation Wallonie-Bruxelles [ARC No 20061]

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Many molecular crystals grow as twisted, helicoidal ribbons from the melt, and this twisting enhances the charge mobility. The effect of twisting on charge mobility is analyzed for a monocomponent organic semiconductor, and it is found that smaller pitches (more twisted) result in significantly higher carrier mobilities. X-ray scattering and Mueller matrix polarimetry are used to analyze the microscale organization of the polycrystalline films. The greater number of tightly packed twisted fibers in the film allows for better charge transport.
Many molecular crystals (approximately one third) grow as twisted, helicoidal ribbons from the melt, and this preponderance is even higher in restricted classes of materials, for instance, charge-transfer complexes. Previously, twisted crystallites of such complexes present an increase in carrier mobilities. Here, the effect of twisting on charge mobility is better analyzed for a monocomponent organic semiconductor, 2,5-bis(3-dodecyl-2-thienyl)-thiazolo[5,4-d]thiazole (BDT), that forms twisted crystals with varied helicoidal pitches and makes possible a correlation of twist strength with carrier mobility. Films are analyzed by X-ray scattering and Mueller matrix polarimetry to characterize the microscale organization of the polycrystalline ensembles. Carrier mobilities of organic field-effect transistors are five times higher when the crystals are grown with the smallest pitches (most twisted), compared to those with the largest pitches, along the fiber elongation direction. A tenfold increase is observed along the perpendicular direction. Simulation of electrical potential based on scanning electron microscopy images and density functional theory suggests that the twisting-enhanced mobility is mainly controlled by the fiber organization in the film. A greater number of tightly packed twisted fibers separated by numerous smaller gaps permit better charge transport over the film surface compared to fewer big crystallites separated by larger gaps.

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