压电
材料科学
无定形固体
退火(玻璃)
复合材料
聚合物
偶极子
热的
衍射
数码产品
工作(物理)
体积分数
极化(电化学)
纳米技术
柔性电子器件
共聚物
热分析
热稳定性
导电体
作者
Ziwen Yang,Liwei Zhang,Liqiang Peng,Zhiwen Zhu,Yanfei Huang
出处
期刊:Macromolecules
[American Chemical Society]
日期:2025-12-05
卷期号:59 (1): 361-368
被引量:1
标识
DOI:10.1021/acs.macromol.5c02217
摘要
Piezoelectric polymers like poly(vinylidene fluoride-trifluoroethylene) [P(VDF-TrFE)] copolymers are ideal for flexible electronics but suffer from low piezoelectric coefficients (| d 33 | < 30 pC/N). While intrinsic structural regulation offers enhancement potential, uncertainty persists regarding the primary piezoelectric contributor (crystal/amorphous/interface). We recently identified the oriented amorphous fraction (OAF) at crystalline–amorphous interfaces as critical for high piezoelectricity. However, the OAF induction requires extreme processing (>600 MV/m poling), presenting a great challenge for further manipulating the OAF structure. Here, we demonstrate for the first time thermal annealing as an effective OAF control strategy in stretched P(VDF-TrFE) 55/45 mol % films. When annealed at 130 °C, OAF content reaches 0.37, which contributes to a breakthrough d 33 of −54 pC/N, far surpassing the −17 pC/N of commercial PVDF piezoelectric films and most PVDF-based polymers (| d 33 | < 30 pC/N). This exceptional d 33 enhancement originates from the increased concentration of mechanically reorientable dipoles and the elevated polarization enabled by increased OAF content. This work presents a novel strategy for improving piezoelectric polymers by manipulating the structure of OAF through thermal annealing.
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