Abstract
Electron beam irradiated poly(vinylidene fluoride–trifluoroethylene) [P(VDF–TrFE)] copolymers have been recently shown to exhibit “giant” electrostrictive stains. In this work, 19 F nuclear magnetic resonance (NMR) spectroscopy was used to probe structure of P(VDF–TrFE) copolymers before and after irradiation in order to elucidate the chemistry associated with the development of outstanding electroactive properties. The two-dimensional solution-state 19 F NMR of as-synthesized copolymers reveals strong (∼300 Hz) geminal indirect coupling ( 2J ) and the resulting assignments have some differences from the previous literature. The most frequently occurring sequence containing TrFE is CH 2CF 2CHFCF 2CH 2, followed by CF 2CH 2CHFCF 2CF 2. This reveals a strong preference for the TrFE units to be isolated and a slight preference for the head-to-tail addition. Both sequences contain VDF polymerized in the same direction around the central TrFE monomer unit. Resolution of bonding environments in the insoluble irradiated P(VDF–TrFE) required the use of fast (25 kHz) magic angle spinning (MAS) solid-state 19 F NMR at elevated temperature. Of the resolved peaks formed by irradiation, the side group CF 3CH<, was present in the highest concentration. Such CF 3 pendant groups are likely to reduce crystallinity and thus impact electroactive properties. Also observed was significant formation of CF 3CF 2, which can be either a pendant group or a side group. Several types of CF 3 end groups were observed: CF 3CHF, CF 3CH 2, and CF 3CH. The latter, indicates the formation of some unsaturated bonds upon irradiation. Small concentrations of CHF 2 and CF 2H were also found. Cross-linking is indirectly evidenced by broadening of the NMR spectra of the irradiated material. In the unirradiated copolymer, two conformation; of sequence CH 2CF 2CHFCF 2CH 2 are observed in the solid-state. In the solution-state in the post-irradiated solid-state, only one of these conformations exists.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.