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原位合成的Fe2O3和Co3O4纳米颗粒对聚偏二氟乙烯薄膜的电活性β相结晶和介电性能的影响。

Effect of in situ synthesized Fe2O3 and Co3O4 nanoparticles on electroactive β phase crystallization and dielectric properties of poly(vinylidene fluoride) thin films.

作者信息

Thakur Pradip, Kool Arpan, Bagchi Biswajoy, Das Sukhen, Nandy Papiya

机构信息

Department of Physics, Jadavpur University, Kolkata-700032, India.

出版信息

Phys Chem Chem Phys. 2015 Jan 14;17(2):1368-78. doi: 10.1039/c4cp04006f. Epub 2014 Nov 26.

Abstract

A simple and low cost in situ process has been developed to synthesize Fe2O3-Co3O4 nanoparticles (NPs) loaded poly(vinylidene fluoride) (PVDF) thin films. The electroactive β phase nucleation mechanism and the dielectric properties of the films have been investigated by X-ray diffraction spectroscopy, Fourier transform infrared spectroscopy, differential scanning calorimetry and using an LCR meter. Results confirmed that the electroactive β phase crystallization in the PVDF matrix is due to the fast nucleating or catalytic effect of the in situ NPs. Homogenous dispersion of in situ Fe2O3-Co3O4 NPs in the polymer matrix leads to strong interfacial interaction between the NPs and the polymer resulting in enhanced β phase nucleation in PVDF and a large dielectric constant of the thin films. The observed variation in the electroactive β phase nucleation by NPs (Fe2O3-Co3O4) and the dielectric properties of the thin films have been explained on the basis of surface charge, size, geometrical shape and extent of agglomeration of the NPs in the polymer matrix.

摘要

已开发出一种简单且低成本的原位工艺来合成负载有Fe2O3-Co3O4纳米颗粒(NPs)的聚偏二氟乙烯(PVDF)薄膜。通过X射线衍射光谱、傅里叶变换红外光谱、差示扫描量热法以及使用LCR测量仪,研究了薄膜的电活性β相成核机理和介电性能。结果证实,PVDF基体中的电活性β相结晶是由于原位NPs的快速成核或催化作用。原位Fe2O3-Co3O4 NPs在聚合物基体中的均匀分散导致NPs与聚合物之间产生强烈的界面相互作用,从而使PVDF中的β相成核增强,并且薄膜具有较大的介电常数。基于NPs(Fe2O3-Co3O4)在聚合物基体中的表面电荷、尺寸、几何形状和团聚程度,对观察到的NPs引起的电活性β相成核变化以及薄膜的介电性能进行了解释。

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