...
首页> 外文期刊>RSC Advances >Electro-active phase formation in PVDF-BiVO4 flexible nanocomposite films for high energy density storage application
【24h】

Electro-active phase formation in PVDF-BiVO4 flexible nanocomposite films for high energy density storage application

机译:高能量密度存储应用中PVDF-BiVO4柔性纳米复合薄膜中电活性相的形成

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

In this work we report on the preparation of polymer nanocomposite (PNC) films, consisting of poly(vinylidene fluoride) and bismuth vanadium oxide nanoparticles (BiVO4-NPs), and its electroactive phase (beta- and gamma-phase) formation. It was found that BiVO4-NPs can yield up to 98% of the electroactive phases in PVDF. Fourier transform infrared spectroscopy (FTIR) results reveal that electrostatic interactions are present at the interface between surface charges of BiVO4-NPs and -CH2/CF2-molecular dipoles of PVDF favoring and stabilizing the electroactive phases. The electrostatic interaction is further confirmed by X-ray photoelectron spectroscopy (XPS) analysis. Compared to the neat PVDF film, a significantly increased dielectric constant (epsilon similar to 44) and a low loss factor (tan delta similar to 0.02) were observed in the PNC films. In addition, PNC films exhibit a high electrical energy density up to 11 J cm(3) with a breakdown electric field higher than 400 MV m(-1). Furthermore, a dramatic improvement of the toughness (460%) was also noticed for the PNC films. These results underline the high potential of such films for their use as flexible high energy density capacitors and flexible piezoelectric based power sources as well.
机译:在这项工作中,我们报告了由聚偏二氟乙烯和铋钒氧化物纳米粒子(BiVO4-NPs)组成的聚合物纳米复合材料(PNC)膜的制备及其电活性相(β和γ相)的形成。发现BiVO4-NPs可以产生PVDF中高达98%的电活性相。傅立叶变换红外光谱(FTIR)结果表明,BiVO4-NPs和PVDF的-CH2 / CF2分子偶极子的表面电荷之间的界面处存在静电相互作用,有利于并稳定电活性相。通过X射线光电子能谱(XPS)分析进一步证实了静电相互作用。与纯净的PVDF薄膜相比,在PNC薄膜中观察到介电常数(ε类似于44)显着提高,损耗因子较低(tanδ类似于0.02)。此外,PNC薄膜具有高达11 J cm(3)的高电能密度,击穿电场高于400 MV m(-1)。此外,PNC薄膜的韧性也得到了显着提高(460%)。这些结果突显了这种膜用作柔性高能量密度电容器和柔性压电基电源的巨大潜力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号