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Enhanced Vertical Charge Transport of Homo‐ and Blended Semiconducting Polymers by Nanoconfinement
Author(s) -
Ko Jongkuk,
Kim Youngkeol,
Kang Jin Soo,
Berger Rüdiger,
Yoon Hyunsik,
Char Kookheon
Publication year - 2020
Publication title -
advanced materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.707
H-Index - 527
eISSN - 1521-4095
pISSN - 0935-9648
DOI - 10.1002/adma.201908087
Subject(s) - crystallinity , materials science , amorphous solid , polymer , crystallite , conjugated system , nanostructure , nanotechnology , conductive polymer , chemical engineering , chemical physics , composite material , crystallography , chemistry , engineering , metallurgy
The morphology of conjugated polymers has critical influences on electronic and optical properties of optoelectronic devices. Even though lots of techniques and methods are suggested to control the morphology of polymers, very few studies have been performed inducing high charge transport along out‐of‐plane direction. In this study, the self‐assembly of homo‐ and blended conjugated polymers which are confined in nanostructures is utilized. The resulting structures lead to high charge mobility along vertical direction for both homo‐ and blended conjugated polymers. Both semicrystalline and amorphous polymers show highly increased population of face‐on crystallite despite intrinsic crystallinity of polymers. They result in more than two orders of magnitude enhanced charge mobility along vertical direction revealed by nanoscale conductive scanning force microscopy and macroscale IV characteristic measurements. Moreover, blends of semicrystalline and amorphous polymers, which are known to show inferior optical and electrical properties due to their structural incompatibility, are formed into harmonious states by this approach. Assembly of blends of semicrystalline and amorphous polymers under nanoconfinement shows charge mobility in out‐of‐plane direction of 0.73 cm 2 V −1 s −1 with wide range of absorption wavelength from 300 to 750 nm demonstrating the synergistic effects of two different polymers.