Ferroelectric polarization, pyroelectric activity and dielectric relaxation in Form IV poly(vinylidene fluoride)

被引:29
作者
Gan, W. C. [1 ]
Abd Majid, W. H. [1 ]
Furukawa, T. [2 ]
机构
[1] Univ Malaya, Fac Sci, Dept Phys, Low Dimens Mat Res Ctr, Kuala Lumpur 50603, Malaysia
[2] Kobayasi Inst Phys Res, Kokubunji, Tokyo 1850022, Japan
关键词
Form IV PVDF; Ferroelectric polarization reversal; Dielectric relaxation; VINYLIDENE FLUORIDE; SWITCHING CHARACTERISTICS; FILMS; PIEZOELECTRICITY; CRYSTALLINE; COPOLYMERS;
D O I
10.1016/j.polymer.2015.11.024
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Ferroelectric, pyroelectric and dielectric properties were investigated for Form IV poly(vinylidene fluoride) (PVDF). We fabricated highly crystalline Form II thin films by spin-casting from acetone or methyl ethyl ketone followed by annealing at 155 degrees C and then converted into Form IV using a high electric field of 500 MV/m. We observed displacement (D) - electric field (E) hysteresis loop and attendant pyroelectric activity that supported ferroelectric polarization reversal in Form IV PVDF. The highly rounded D-E loop with a coercive field of 240 MV/m suggests that reversal of the dipole component perpendicular to TGT (G) over bar chain requires very high field and progresses based on step-by-step switching of respective molecules. We also observed similar crystalline relaxations in Form II and IV suggesting that fluctuations of parallel dipoles in TGT (G) over bar chains were not affected by chain packing. Simultaneous observation of polarization reversal and dielectric relaxation associated with two orthogonal directions (a- and c-axis) of crystallites is interpreted using the tilt angle between of the chain axis and sample surface. Microscopic features are discussed in terms of electric-field-induced and thermally-induced changes in TGT (G) over bar conformational sequences. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:156 / 165
页数:10
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