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Liquid metal interface mechanochemistry disentangles energy density and biaxial stretchability tradeoff in composite capacitor film

Author

Listed:
  • Zilong Xie

    (Sichuan University)

  • Jianan Zhu

    (Sichuan University)

  • Zhengli Dou

    (Sichuan University)

  • Yongzheng Zhang

    (Sichuan University)

  • Ke Wang

    (Sichuan University)

  • Kai Wu

    (Sichuan University
    The University of Texas at Austin)

  • Qiang Fu

    (Sichuan University)

Abstract

Dielectric polymer composites for film capacitors have advanced significantly in recent decades, yet their practical implementation in industrial-scale, thin-film processing faces challenges, particularly due to limited biaxial stretchability. Here, we introduce a mechanochemical solution that applies liquid metal onto rigid dielectric fillers (e.g. boron nitride), dramatically transforming polymer-filler interface characteristics. This approach significantly reduces modulus mismatch and stress concentration at the interface region, enabling polypropylene composites to achieve biaxial stretching ratio up to 450 × 450%. Furthermore, liquid metal integration enhances boron nitride’s dielectric polarization while maintaining inherent insulation, producing high-dielectric-constant, low-loss films. These films, only microns thick yet quasi square meters in area, achieve a 55% increase in energy density over commercial biaxially-oriented polypropylene (from 2.9 to 4.5 J cm−3 at 550 MV/m), keeping 90% discharge efficiency. Coupled with improved thermal conductivity, durability, and device capacitance, this distinctive interface engineering approach makes these composites promising for high-performance film capacitors.

Suggested Citation

  • Zilong Xie & Jianan Zhu & Zhengli Dou & Yongzheng Zhang & Ke Wang & Kai Wu & Qiang Fu, 2024. "Liquid metal interface mechanochemistry disentangles energy density and biaxial stretchability tradeoff in composite capacitor film," Nature Communications, Nature, vol. 15(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-52234-4
    DOI: 10.1038/s41467-024-52234-4
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