Takashima Kenji, Furukawa Yukio
Department of Chemistry and Biochemistry, Graduate School of Advanced Science and Engineering, Waseda University.
Anal Sci. 2017;33(1):59-64. doi: 10.2116/analsci.33.59.
Voltage-induced infrared spectra of annealed spin-cast thin films of ferroelectric poly(vinylidene fluoride-co-trifluoroethylene) (P(VDF-TrFE)) (molar ratio, 3:1) were measured in a stepwise cyclic external electric field. Most of the observed infrared bands originated from the β ferroelectric crystalline phase. The voltage-induced spectral changes were decomposed into zeroth- (original), first-, and second-derivative spectra, and were attributed to the rotational motions of the polymer chains and the vibrational Stark effect. The values of the original spectral absorbance change ratios, ΔA/A, for the 849-cm band (CF symmetric stretching, a) and the 884-cm band (CH rocking, b) of the film exhibited double minimum and maximum peak hysteresis loops, respectively. The intensity of each band increased or decreased suddenly near a coercive field of ±0.6 MV/cm. These sudden intensity changes were attributed to the rotational inversion of the polymer chains that are associated with ferroelectricity.
在逐步循环外部电场中测量了铁电聚偏二氟乙烯-三氟乙烯共聚物(P(VDF-TrFE))(摩尔比3:1)退火旋涂薄膜的电压诱导红外光谱。观察到的大多数红外波段起源于β铁电晶相。电压诱导的光谱变化被分解为零阶(原始)、一阶和二阶导数光谱,并归因于聚合物链的旋转运动和振动斯塔克效应。薄膜在849 cm⁻¹波段(CF对称伸缩振动,a)和884 cm⁻¹波段(CH摇摆振动,b)的原始光谱吸光度变化率ΔA/A值分别呈现双极小值和极大值峰滞后回线。在±0.6 MV/cm的矫顽场附近,每个波段的强度突然增加或减小。这些强度的突然变化归因于与铁电性相关的聚合物链的旋转反转。