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Effects of film viscosity on electric field-induced alignment of graphene flakes in B-stage graphene-epoxy composite films

机译:膜粘度对电场诱导B阶石墨烯-环氧树脂复合膜中石墨烯薄片取向的影响

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Due to the excellent properties of graphene such as high electron mobility, high thermal conductivity, and low gas permeability, graphene-polymer composites have been widely studied for several applications. Moreover, due to the high aspect ratio of graphene, aligned graphene-polymer composites have been also studied by using various aligning techniques. Especially, electric field-induced alignment of graphene flakes has been investigated since the orientation can be easily tailored. Because low viscosity polymer matrix is desired for better alignment by an electric field, many researchers demonstrated carbon nanotube and graphene alignment by applying electric field at liquid-like polymer composites. However, this method has disadvantages in terms of postprocessing. On the other hand, it was demonstrated by our research group that aligned B-stage graphene-epoxy composite films were achieved by applying electric field at higher temperature where the viscosity of the composite films could be reduced without curing reaction. It was also shown that the curing reaction prohibits the graphene flake alignment due to the viscosity increase. Since viscosity is one of the most important factors for efficient alignment, and the viscosity varies temperature, the effects of viscosity change on electric-field induced alignment of graphene need to be investigated. In this study, effects of time and temperature on the film viscosity and electric-field induced graphene flake alignment of B-stage graphene-epoxy composite films were investigated. Film viscosity was measured as a function of temperatures, and isothermal viscosity was also measured with times at constant temperature in order to confirm the curing reaction. Electric field was applied at various times and temperatures. The aligned B-stage graphene-epoxy composite films were characterized by cross-sectional morphology and electrical resistivity.
机译:由于石墨烯的优异性能,例如高电子迁移率,高导热性和低气体渗透性,石墨烯-聚合物复合材料已被广泛研究用于多种应用。此外,由于石墨烯的高长宽比,还已经通过使用各种取向技术来研究取向的石墨烯-聚合物复合材料。特别地,由于可以容易地调整取向,因此已经研究了电场诱导的石墨烯薄片的取向。由于需要低粘度的聚合物基体以通过电场更好地进行配向,因此许多研究人员通过在液体状聚合物复合材料上施加电场来证明碳纳米管和石墨烯的配向。但是,该方法在后处理方面具有缺点。另一方面,我们的研究小组证明,通过在较高的温度下施加电场即可获得取向的B级石墨烯-环氧复合膜,从而无需固化反应即可降低复合膜的粘度。还显示出由于粘度增加,固化反应阻止了石墨烯薄片的排列。由于粘度是有效取向的最重要因素之一,并且粘度随温度变化,因此需要研究粘度变化对电场诱导的石墨烯取向的影响。在这项研究中,研究了时间和温度对B-阶段石墨烯-环氧树脂复合薄膜的膜粘度和电场诱导的石墨烯薄片取向的影响。测量膜粘度随温度的变化,并且还在恒温下随时间测量等温粘度以确认固化反应。在不同的时间和温度下施加电场。取向的B-阶段石墨烯-环氧树脂复合膜的特征在于横截面形态和电阻率。

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