Author
Listed:
- Nan Meng
(Queen Mary University of London)
- Xintong Ren
(Queen Mary University of London)
- Giovanni Santagiuliana
(Queen Mary University of London)
- Leonardo Ventura
(Queen Mary University of London)
- Han Zhang
(Queen Mary University of London
Queen Mary University of London)
- Jiyue Wu
(Queen Mary University of London)
- Haixue Yan
(Queen Mary University of London
Queen Mary University of London)
- Michael J Reece
(Queen Mary University of London
Queen Mary University of London)
- Emiliano Bilotti
(Queen Mary University of London
Queen Mary University of London)
Abstract
Poly(vinylidene fluoride)-based dielectric materials are prospective candidates for high power density electric storage applications because of their ferroelectric nature, high dielectric breakdown strength and superior processability. However, obtaining a polar phase with relaxor-like behavior in poly(vinylidene fluoride), as required for high energy storage density, is a major challenge. To date, this has been achieved using complex and expensive synthesis of copolymers and terpolymers or via irradiation with high-energy electron-beam or γ-ray radiations. Herein, a facile process of pressing-and-folding is proposed to produce β-poly(vinylidene fluoride) (β-phase content: ~98%) with relaxor-like behavior observed in poly(vinylidene fluoride) with high molecular weight > 534 kg mol−1, without the need of any hazardous gases, solvents, electrical or chemical treatments. An ultra-high energy density (35 J cm−3) with a high efficiency (74%) is achieved in a pressed-and-folded poly(vinylidene fluoride) (670-700 kg mol−1), which is higher than that of other reported polymer-based dielectric capacitors to the best of our knowledge.
Suggested Citation
Nan Meng & Xintong Ren & Giovanni Santagiuliana & Leonardo Ventura & Han Zhang & Jiyue Wu & Haixue Yan & Michael J Reece & Emiliano Bilotti, 2019.
"Ultrahigh β-phase content poly(vinylidene fluoride) with relaxor-like ferroelectricity for high energy density capacitors,"
Nature Communications, Nature, vol. 10(1), pages 1-9, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-12391-3
DOI: 10.1038/s41467-019-12391-3
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