SCHEDULED MAINTENANCE
In-depth understanding of interfacial crystallization via Flash DSC and enhanced energy storage density in ferroelectric P(VDF-CTFE)/Au NRs nanocomposites for capacitor application†
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Qun-Dong
Shen
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Abstract
High-capacity or high-power-density capacitors are being actively investigated for portable electronics, electric vehicles, and electric power systems. We describe the filler system in dielectric nanocomposites with a small loading of Au nanorods [NRs] to elucidate the mechanism of interfacial crystallization behavior including the crystallization kinetics, and crystalline morphology and structure, and to investigate the intrinsic causes for concurrent great improvements in the dielectric constant and energy density in the nanocomposite system. Remarkly, at high crystallization temperature, the addition of Au NRs, which are used as heterogeneous nucleators, can reduce the nucleation barrier, resulting in accelerating the crystallization rate. However, the crystallization rate slows down at low temperatures because the addition of Au NRs limited the mobility of poly(vinylidene fluoride-chlorotrifluoroethylene) [P(VDF-CTFE)] chains, and thus enhanced the diffusion barrier. Furthermore, the addition of NRs has a huge impact on the crystalline morphology and structure which changes from large paraelectric α-phase spherulites with TGTG′ conformations into minor ferroelectric γ-phase spherulites with T3GT3G′ conformations, and also produces more exogenous interfaces between the lamellar crystals and amorphous regions, resulting in a higher dielectric constant and higher electric energy density in P(VDF-CTFE)/Au NRs nanocomposites. Our approach provides a facile and straightforward way to design or understand PVDF-based polymers for their practical applications in high-energy-density capacitors.
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