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Charge Mobility Enhancement for Conjugated DPP-Selenophene Polymer by Simply Replacing One Bulky Branching Alkyl Chain with Linear One at Each DPP Unit
Author(s) -
Zhijie Wang,
Zitong Liu,
Ning Lü,
Mingfei Xiao,
Yuanping Yi,
Zhengxu Cai,
Aditya Sadhanala,
Guanxin Zhang,
Wei Chen,
Henning Sirringhaus,
Deqing Zhang
Publication year - 2018
Publication title -
chemistry of materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.741
H-Index - 375
eISSN - 1520-5002
pISSN - 0897-4756
DOI - 10.1021/acs.chemmater.8b01007
Subject(s) - branching (polymer chemistry) , conjugated system , alkyl , ambipolar diffusion , materials science , side chain , steric effects , polymer , crystallinity , semiconductor , polymer chemistry , chemistry , crystallography , stereochemistry , organic chemistry , electron , optoelectronics , physics , quantum mechanics
We demonstrate a simple, but efficient, approach for improving the semiconducting performances of DPP-based conjugated D-A polymers. This approach involves the replacement of one bulky branching alkyl chain with the linear one at each DPP unit in regular polymer PDPPSe-10 and PDPPSe-12. The UV–vis absorption, Raman spectra, PDS data, and theoretical calculations support that the replacement of bulky branching chains with linear ones can weaken the steric hindrance, and accordingly conjugated backbones become more planar and rigid. GIWAXS data show that the incorporation of linear alkyl chains as in PDPPSe-10 and PDPPSe-12 is beneficial for side-chain interdigitation and interchain dense packing, leading to improvement of interchain packing order and thin film crystallinity by comparing with PDPPSe, which contains branching alkyl chains. On the basis of field-effect transistor (FET) studies, charge mobilities of PDPPSe-10 and PDPPSe-12 are remarkably enhanced. Hole mobilities of PDPPSe-10 and PDPPSe-12 in ...

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