TY - JOUR
T1 - Charge transport physics of a unique class of rigid-rod conjugated polymers with fused-ring conjugated units linked by double carbon-carbon bonds
AU - Xiao, Mingfei
AU - Carey, Remington L.
AU - Chen, Hu
AU - Jiao, Xuechen
AU - Lemaur, Vincent
AU - Schott, Sam
AU - Nikolka, Mark
AU - Jellett, Cameron
AU - Sadhanala, Aditya
AU - Rogers, Sarah
AU - Senanayak, Satyaprasad P.
AU - Onwubiko, Ada
AU - Han, Sanyang
AU - Zhang, Zhilong
AU - Abdi-Jalebi, Mojtaba
AU - Zhang, Youcheng
AU - Thomas, Tudor H.
AU - Mahmoudi, Najet
AU - Lai, Lianglun
AU - Selezneva, Ekaterina
AU - Ren, Xinglong
AU - Nguyen, Malgorzata
AU - Wang, Qijing
AU - Jacobs, Ian
AU - Yue, Wan
AU - McNeill, Christopher R.
AU - Liu, Guoming
AU - Beljonne, David
AU - McCulloch, Iain
AU - Sirringhaus, Henning
N1 - Publisher Copyright:
Copyright © 2021 The Authors,
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/4/28
Y1 - 2021/4/28
N2 - We investigate the charge transport physics of a previously unidentified class of electron-deficient conjugated polymers that do not contain any single bonds linking monomer units along the backbone but only double-bond linkages. Such polymers would be expected to behave as rigid rods, but little is known about their actual chain conformations and electronic structure. Here, we present a detailed study of the structural and charge transport properties of a family of four such polymers. By adopting a copolymer design, we achieve high electron mobilities up to 0.5 cm2 V−1 s−1. Field-induced electron spin resonance measurements of charge dynamics provide evidence for relatively slow hopping over, however, long distances. Our work provides important insights into the factors that limit charge transport in this unique class of polymers and allows us to identify molecular design strategies for achieving even higher levels of performance.
AB - We investigate the charge transport physics of a previously unidentified class of electron-deficient conjugated polymers that do not contain any single bonds linking monomer units along the backbone but only double-bond linkages. Such polymers would be expected to behave as rigid rods, but little is known about their actual chain conformations and electronic structure. Here, we present a detailed study of the structural and charge transport properties of a family of four such polymers. By adopting a copolymer design, we achieve high electron mobilities up to 0.5 cm2 V−1 s−1. Field-induced electron spin resonance measurements of charge dynamics provide evidence for relatively slow hopping over, however, long distances. Our work provides important insights into the factors that limit charge transport in this unique class of polymers and allows us to identify molecular design strategies for achieving even higher levels of performance.
UR - http://www.scopus.com/inward/record.url?scp=85105097021&partnerID=8YFLogxK
U2 - 10.1126/sciadv.abe5280
DO - 10.1126/sciadv.abe5280
M3 - Article
C2 - 33910909
AN - SCOPUS:85105097021
SN - 2375-2548
VL - 7
JO - Science Advances
JF - Science Advances
IS - 18
M1 - eabe5280
ER -