Scholarlink

<p>In this study, the dielectric and ferroelectric responses of P(VDF-TrFE-CFE) terpolymer were systematically investigated under various DC electric fields, frequencies, temperatures, and mechanical strains. The dielectric constant exhibited pronounced decrease at low frequencies under the influence of DC bias. This effect was particularly evident at temperatures where dielectric dispersion was significant. These results indicate that the dynamics of polar nanoregions are of critical importance in both high dielectric tunability (67% at 100 MV/m) and frequency-dependent dielectric behavior. The polarization–electric field hysteresis loops became increasingly slim at elevated temperatures and at high frequencies. These results indicate that the thermal activation and dynamic behavior of polar nanoregions significantly influence the high discharged energy density (3.8&#xa0;J/cm<sup>3</sup> at 200 MV/m) and storage efficiency (65% at 10<sup>2</sup> Hz and 300&#xa0;K). Additionally, the inherent mechanical flexibility of the P(VDF-TrFE-CFE) film leads to highly stable dielectric and ferroelectric properties under compressive/tensile strains and after extensive bending cycles. This work demonstrates that the control of polar nanodomains is a key strategy to enhance the dielectric tunability and energy storage performance of P(VDF-TrFE-CFE) terpolymers for portable and wearable electronics applications.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Frequency, temperature, and strain effects on dielectric tunability and energy storage performance of P(VDF-TrFE-CFE) terpolymer

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年10月13日

查看全文
  • Ying Chieh Hu,
  • Su Min Lee,
  • Kyung Hoon Kim,
  • Hyun Soo Ahn,
  • Jong Hun Kim,
  • Jong Hoon Jung

摘要

In this study, the dielectric and ferroelectric responses of P(VDF-TrFE-CFE) terpolymer were systematically investigated under various DC electric fields, frequencies, temperatures, and mechanical strains. The dielectric constant exhibited pronounced decrease at low frequencies under the influence of DC bias. This effect was particularly evident at temperatures where dielectric dispersion was significant. These results indicate that the dynamics of polar nanoregions are of critical importance in both high dielectric tunability (67% at 100 MV/m) and frequency-dependent dielectric behavior. The polarization–electric field hysteresis loops became increasingly slim at elevated temperatures and at high frequencies. These results indicate that the thermal activation and dynamic behavior of polar nanoregions significantly influence the high discharged energy density (3.8 J/cm3 at 200 MV/m) and storage efficiency (65% at 102 Hz and 300 K). Additionally, the inherent mechanical flexibility of the P(VDF-TrFE-CFE) film leads to highly stable dielectric and ferroelectric properties under compressive/tensile strains and after extensive bending cycles. This work demonstrates that the control of polar nanodomains is a key strategy to enhance the dielectric tunability and energy storage performance of P(VDF-TrFE-CFE) terpolymers for portable and wearable electronics applications.