期刊
MATERIALS CHEMISTRY FRONTIERS
卷 5, 期 9, 页码 3646-3656出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1qm00105a
关键词
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资金
- National Natural Science Foundation of China [51773164]
- Natural Science Basic Research Plan in Shaanxi Province of China [2019JM030]
- Key Laboratory Construction Program of Xi'an Municipal Bureau of Science and Technology [201805056ZD7CG40]
A novel P(VDF-HFP)/MS composite film with enhanced energy density and discharge efficiency was fabricated through an electrospinning-hot press strategy, exhibiting higher breakdown strength and more uniform electric field distribution.
Poly(vinylidene fluoride) (PVDF) based fluoropolymers possess high permittivity and breakdown strength (E-b), and have been extensively studied because of their dielectric applications. However, their practical applications are greatly hampered by the low energy density (U-e) and efficiency (eta). Herein, using an electrospinning-hot press strategy, a novel P(VDF-HFP)/MS (poly(vinylidene fluoride-hexafluoropropylene)/poly(methyl methacrylate-co-styrene)) composite film with concomitantly enhanced U-e of 20 J cm(-3) and discharge efficiency (eta approximate to 81%) was fabricated. Due to the strong electrostatic force and confining effect during electrospinning, two polymers exhibit substantially enhanced compatibility and form a much more homogeneous microstructure as compared with the blend control, leading to higher E-b and more even electric field distribution as simulated by the finite element analysis. Strikingly, composite films containing 30 wt% MS copolymer exhibit typical relaxor polarization behaviors (and thus improved E-b and U-e), which are 157% and 262% that of the pristine P(VDF-HFP), respectively. Moreover, the eta of composite films can be well retained, even if it is under a high E-b of 550 MV m(-1), and is still greater than previous reported values. This work provides a straightforward and scalable strategy to achieve PVDF-based dielectrics with both high U-e and eta for the applications of energy storage capacitors.
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