Literature DB >> 28429591

High-Performance Furan-Containing Conjugated Polymer for Environmentally Benign Solution Processing.

Sang Myeon Lee1, Hae Rang Lee2, A-Reum Han2, Junghoon Lee1, Joon Hak Oh2, Changduk Yang1.   

Abstract

Developing semiconducting polymers that exhibit both strong charge transport capability via highly ordered structures and good processability in environmentally benign solvents remains a challenge. Given that furan-based materials have better solubility in various solvents than analogous thiophene-based materials, we have synthesized and characterized furanyl-diketopyrrolopyrrole polymer (PFDPPTT-Si) together with its thienyl-diketopyrrolopyrrole-based analogue (PTDPPTT-Si) to understand subtle changes induced by the use of furan instead of thiophene units. PTDPPTT-Si films processed in common chlorinated solvent exhibit a higher hole mobility (3.57 cm2 V-1 s-1) than PFDPPTT-Si films (2.40 cm2 V-1 s-1) under the same conditions; this greater hole mobility is a result of tightly aggregated π-stacking structures in PTDPPTT-Si. By contrast, because of its enhanced solubility, PFDPPTT-Si using chlorine-free solution processing results in a device with higher mobility (as high as 1.87 cm2 V-1 s-1) compared to that of the corresponding device fabricated using PTDPPTT-Si. This mobility of 1.87 cm2 V-1 s-1 represents the highest performances among furan-containing polymers reported to the best of our knowledge for nonchlorinated solvents. Our study demonstrates an important step toward environmentally compatible electronics, and we expect the results of our study to reinvigorate the furan-containing semiconductors field.

Entities:  

Keywords:  diketopyrrolopyrrole; furan-containing conjugated polymers; nonchlorinated solvents; organic field-effect transistors; siloxane-hybrid chains

Year:  2017        PMID: 28429591     DOI: 10.1021/acsami.7b04014

Source DB:  PubMed          Journal:  ACS Appl Mater Interfaces        ISSN: 1944-8244            Impact factor:   9.229


  1 in total

1.  Molecular Tuning in Diaryl-Capped Pyrrolo[2,3-d:5,4-d']bisthiazoles: Effects of Terminal Aryl Unit and Comparison to Dithieno[3,2-b:2',3'-d]pyrrole Analogues.

Authors:  Eric J Uzelac; Irene Badía-Domínguez; Spencer J Gilman; M Carmen Ruiz Delgado; Seth C Rasmussen
Journal:  Molecules       Date:  2022-10-06       Impact factor: 4.927

  1 in total

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