Design, synthesis and processing of PVDF-based dielectric polymers

Due to the appealing piezoelectric, pyroelectric, and ferroelectric (FE) properties, poly(vinylidene fluoride) (PVDF)-based dielectric polymers have been attracting great attention from both the academic and industrial communities. Depending on the molecular structure and the processing method, PVDF...

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Bibliographic Details
Published inIET Nanodielectrics Vol. 1; no. 2; pp. 80 - 91
Main Authors Wang, Shan, Li, Qi
Format Journal Article
LanguageEnglish
Published Beijing The Institution of Engineering and Technology 01.07.2018
John Wiley & Sons, Inc
Wiley
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Summary:Due to the appealing piezoelectric, pyroelectric, and ferroelectric (FE) properties, poly(vinylidene fluoride) (PVDF)-based dielectric polymers have been attracting great attention from both the academic and industrial communities. Depending on the molecular structure and the processing method, PVDF-based dielectric polymers can exhibit rich dielectric polarisation behaviours covering normal FE, relaxor FE, anti-FE-like and linear dielectric responses, which enables a wide spectrum of application fields such as non-volatile memories, piezoelectric and pyroelectric sensors, actuators, electrocaloric refrigeration, and film capacitors. In this study, the authors first briefly introduce the current practical/promising applications of PVDF-based dielectric polymers, and the corresponding optimum dielectric polarisation behaviour and crystal structure are proposed accordingly. The chemical synthesis and modification strategies for obtaining various fluoropolymers beyond PVDF homopolymer are then summarised with an emphasis on the relationship between the molecular structure and the dielectric polarisation behaviour. In addition, the effect of processing methods on the crystal structure and dielectric properties of the PVDF-based polymers is discussed. Finally, some newly developed processing techniques applicable to PVDF-based polymers are described.
ISSN:2514-3255
2514-3255
DOI:10.1049/iet-nde.2018.0003