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Open AccessJournal ArticleDOI

Uniaxial Alignment of Conjugated Polymer Films for High‐Performance Organic Field‐Effect Transistors

TLDR
An overview on the processing-structure-property relationships that enable the controlled and uniform alignment of polymer films over large areas with scalable processes is provided with a focus on specific molecular structures, such as planarized backbones with a reduced degree of conformational disorder, solution formulation with controlled aggregation, and deposition techniques inducing suitable directional flow.
Abstract
Polymer semiconductors have been experiencing a remarkable improvement in electronic and optoelectronic properties, which are largely related to the recent development of a vast library of high-performance, donor-acceptor copolymers showing alternation of chemical moieties with different electronic affinities along their backbones. Such steady improvement is making conjugated polymers even more appealing for large-area and flexible electronic applications, from distributed and portable electronics to healthcare devices, where cost-effective manufacturing, light weight, and ease of integration represent key benefits. Recently, a strong boost to charge carrier mobility in polymer-based field-effect transistors, consistently achieving the range from 1.0 to 10 cm2 V-1 s-1 for both holes and electrons, has been given by uniaxial backbone alignment of polymers in thin films, inducing strong transport anisotropy and favoring enhanced transport properties along the alignment direction. Herein, an overview on this topic is provided with a focus on the processing-structure-property relationships that enable the controlled and uniform alignment of polymer films over large areas with scalable processes. The key aspects are specific molecular structures, such as planarized backbones with a reduced degree of conformational disorder, solution formulation with controlled aggregation, and deposition techniques inducing suitable directional flow.

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Recent Progress in High-Mobility Organic Transistors: A Reality Check.

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A general relationship between disorder, aggregation and charge transport in conjugated polymers

TL;DR: A unified model of how charge carriers travel in conjugated polymer films is proposed and it is shown that in high-molecular-weight semiconducting polymers the limiting charge transport step is trapping caused by lattice disorder, and that short-range intermolescular aggregation is sufficient for efficient long-range charge transport.
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Recent Advances in Noncontact External-Field-Assisted Photocatalysis: From Fundamentals to Applications

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Molecular Semiconductors for Logic Operations: Dead-End or Bright Future?

TL;DR: This critical review addresses the community of chemists and materials scientists to share with it a critical analysis of the best performing molecular semiconductors and of the inherent charge transport physics that takes place in them.
References
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Journal ArticleDOI

Light-emitting diodes based on conjugated polymers

TL;DR: In this article, the authors demonstrate that poly(p-phenylene vinylene), prepared by way of a solution-processable precursor, can be used as the active element in a large-area light-emitting diode.
Journal ArticleDOI

Polymer photovoltaic cells : enhanced efficiencies via a network of internal donor-acceptor heterojunctions

TL;DR: In this paper, the carrier collection efficiency and energy conversion efficiency of polymer photovoltaic cells were improved by blending of the semiconducting polymer with C60 or its functionalized derivatives.
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Handbook of conducting polymers

TL;DR: In this paper, the authors presented the theory and properties of conjugated polymers, including transport, optical, and self-assembly properties of poly(3,4-Ethylenedioxythiophene)-polymers.
Journal ArticleDOI

High-efficiency solution processable polymer photovoltaic cells by self-organization of polymer blends

TL;DR: In this article, the authors report highly efficient polymer solar cells based on a bulk heterojunction of polymer poly(3-hexylthiophene) and methanofullerene.
Journal ArticleDOI

Highly efficient organic light-emitting diodes from delayed fluorescence

TL;DR: A class of metal-free organic electroluminescent molecules in which the energy gap between the singlet and triplet excited states is minimized by design, thereby promoting highly efficient spin up-conversion from non-radiative triplet states to radiative singlet states while maintaining high radiative decay rates.
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Trending Questions (1)
How chains in an amorphous conjugated polymer film can be aligned in one direction?

The provided paper does not directly address how chains in an amorphous conjugated polymer film can be aligned in one direction.