期刊
CHEMISTRY OF MATERIALS
卷 32, 期 6, 页码 2330-2340出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.9b04425
关键词
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资金
- National Key Research and Development Program of China [2016YFB0401102, 2017YFA0204703]
- National Natural Science Foundation of China [21774134, 51773016, 21673258]
Herein, we report a series of tetrafluoroethylene (TFE)-containing semiconducting polymers PNBDO-FDTEm (m = 90, 80, 70, 60, and 0), in which the TFE segments were first introduced into polymeric main chains as flexible pi-nonconjugated nodes, and its fully conjugated analogue PNBDO-FDTE100. Our results indicate that the TFE segment is quite compatible with the NBDO-alt-FDTE conjugated matrix system. The HOMO/LUMO energy levels (approximately -6.0/-4.0 eV) and optical band gaps (1.28 eV) remain almost the same in the polymers with the TFE content varying from 0% to 40%. The polymers PNBDO-FDTEm (m = 90, 80, 70, and 60) have similar highly ordered molecular packing with close pi-pi stacking in a thin film as PNBDO-FDTE100 does, implying that the TFE segments exert no clear negative influences on the molecular packing of these polymers either. PNBDO-FDTE100 exhibited a much high electron mobility (mu(e)) of 7.43 cm(2) V-1 s(-1), while PNBDO-FDTE90 and PNBDO-FDTE80 also showed impressively high mu(e) values of 7.25 and 6.00 cm(2) V-1 s(-1), respectively. However, PNBDO-FDTEm (m = 70, 60, and 0) afforded a mu(e) as low as 0.182 cm(2) V-1 s(-1). We attributed this to the transition of the carrier transport mode caused by the increase in the number of p-nonconjugated nodes.
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