In:
Journal of Materials Chemistry C, Royal Society of Chemistry (RSC), Vol. 10, No. 47 ( 2022), p. 17936-17944
Abstract:
In this study, we design and synthesize three DPP-based dual-acceptor conjugated polymers comprising different proquinoidal heterocyclic acceptors, including benzobisthiadizole (SS), triazolobenzothiadiazole (NS), and benzobistriazole (NN), and investigate their structure–property relationship using a transistor and their conductive states by doping. Owing to the high-spin and proquinoidal characteristics of the NN/NS/SS units, all the prepared polymers possess free radicals. However, a subtle difference in the proquinoidal characteristics among these acceptor units results in varied backbone rigidity and coplanarity of the derived polymers. DPP-NS and DPP-NN are shown to possess better solid-state stacking and crystallinity than DPP-SS, conferred by the alkyl side chains on the triazole unit. Hence, DPP-NS and DPP-NN can deliver enhanced mobilities of 3.0 × 10 −2 and 5.3 × 10 −2 cm 2 V −1 s −1 , respectively, after appropriate thermal annealing whereas the stiff DPP-SS only shows a minor improvement. Furthermore, the intrinsic intense radical characteristic of the NN unit is shown to facilitate the receivability of dopants. At a low doping concentration, DPP-NN delivers the highest conductivity of 23.8 S cm −1 among these polymers. Besides, owing to the higher degree of flexibility in chain packing and associated chain aggregation, DPP-NN displays a superior capability to resist the structural deconstruction in the doping state at a high concentration compared to DPP-NS and DPP-SS. Concisely, our results unravel the non-trivial influence of a proquinoidal acceptor moiety on transistor performance and doping capability of the derived polymers.
Type of Medium:
Online Resource
ISSN:
2050-7526
,
2050-7534
Language:
English
Publisher:
Royal Society of Chemistry (RSC)
Publication Date:
2022
detail.hit.zdb_id:
2702245-6
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