Kim Philseok, Doss Natalie M, Tillotson John P, Hotchkiss Peter J, Pan Ming-Jen, Marder Seth R, Li Jiangyu, Calame Jeffery P, Perry Joseph W
School of Chemistry and Biochemistry and Center for Organic Photonics and Electronics, Georgia Institute of Technology, 901 Atlantic Drive, Atlanta, Georgia 30332, USA.
ACS Nano. 2009 Sep 22;3(9):2581-92. doi: 10.1021/nn9006412.
The dielectric permittivity and electric breakdown strength of nanocomposites comprising poly(vinylidene fluoride-co-hexafluoro propylene) and phosphonic acid surface-modified BaTiO(3) nanoparticles have been investigated as a function of the volume fraction of nanoparticles. The mode of binding of pentafluorobenzylphosphonic acid on the BaTiO(3) particles was investigated using infrared and (31)P solid-state nuclear magnetic resonance spectroscopy, and the phosphonic acid was found to form well ordered, tightly bound monolayers. The effective permittivity of nanocomposites with low volume fractions (<50%) was in good agreement with standard theoretical models, with a maximum relative permittivity of 35. However, for nanoparticle volume fractions of greater than 50%, the effective permittivity was observed to decrease with increasing nanoparticle volume fraction, and this was correlated with an increase in porosity of the spin-coated nanocomposite films. The dielectric breakdown strength was also found to decrease with increasing volume fraction of the BaTiO(3) nanoparticles, with an abrupt decrease observed around 10% and a gradual decrease for volume fractions of 20-50%. Comparison of these results with model calculations, using statistical particle packing simulations and effective medium theory for the permittivity and breakdown strength, indicates the important roles of nanoparticle percolation and porosity of the nanocomposites on the dielectric properties. The measured energy density at a field strength of 164 V/mum, well below the breakdown strength, increased to a value of 3.2 J/cm(3) as the nanoparticle volume fraction is increased to 50%, roughly in line with the trend of the permittivity. The calculated maximum energy densities indicate maximal extractable energy (7-8 J/cm(3) at 1 kHz) for two different particle volume fractions, as a result of the interplay of the dependencies of permittivity and breakdown strength on volume fraction.
研究了由聚(偏二氟乙烯 - 共 - 六氟丙烯)和膦酸表面改性的BaTiO₃纳米颗粒组成的纳米复合材料的介电常数和电击穿强度与纳米颗粒体积分数的关系。使用红外光谱和³¹P固体核磁共振光谱研究了五氟苄基膦酸在BaTiO₃颗粒上的结合方式,发现膦酸形成了有序、紧密结合的单分子层。低体积分数(<50%)的纳米复合材料的有效介电常数与标准理论模型吻合良好,最大相对介电常数为35。然而,对于纳米颗粒体积分数大于50%的情况,观察到有效介电常数随纳米颗粒体积分数的增加而降低,这与旋涂纳米复合薄膜孔隙率的增加有关。还发现电击穿强度随BaTiO₃纳米颗粒体积分数的增加而降低,在10%左右观察到突然下降,在20 - 50%的体积分数范围内逐渐下降。将这些结果与模型计算进行比较,使用统计颗粒堆积模拟以及介电常数和击穿强度的有效介质理论,表明纳米颗粒渗流和纳米复合材料孔隙率对介电性能的重要作用。在远低于击穿强度的164 V/μm场强下测得的能量密度,随着纳米颗粒体积分数增加到50%,增加到3.2 J/cm³,大致与介电常数的趋势一致。由于介电常数和击穿强度对体积分数的依赖性相互作用,计算出的最大能量密度表明两种不同颗粒体积分数下的最大可提取能量(在1 kHz时为7 - 8 J/cm³)。