首页> 外文期刊>RSC Advances >Role of space charges inside a dielectric polymer in the electrohydrodynamic structure formation on a prepatterned polymer (ESF-PP)
【24h】

Role of space charges inside a dielectric polymer in the electrohydrodynamic structure formation on a prepatterned polymer (ESF-PP)

机译:介电聚合物内部在备用聚合物(ESF-PP)上的电介质结构中的空间电荷在电介质结构中的作用

获取原文
获取原文并翻译 | 示例
           

摘要

Electrohydrodynamic structure formation on a prepatterned polymer (ESF-PP) can duplicate structures identical to the initial geometry, but with a higher aspect ratio, under the influence of a spatially modulated electric field. In this process, a voltage is applied between a flat template and a flat substrate, sandwiching a prepatterned polymer and an air gap so as to generate an electrohydrodynamic (EHD) force at the air-polymer interface. Subsequently, the prepatterned polymer can be non-uniformly pulled upwards, causing deformation in its micro/nano-structure. Until now, most of the research into ESF-PP has explored various dielectric polymers, which are all considered to be the perfect dielectrics because of their low electrical conductivity. However, the assumption of a perfect dielectric typically creates discrepancies between theoretical analysis and experimental results in terms of the polymer motion and the final morphology. This phenomenon can be attributed to ignoring the action of the small number of free space charges within dielectric polymer motion (although the electrical conductivity of the dielectric polymer may be even lower than that of deionized water), which emphasizes the importance of the influence of space charges inside the dielectric polymer on deformation. This paper explores the role of free space charges by making a comparison between the perfect dielectric polymer and the leaky dielectric polymer on the progressive development, the surface topography and the aspect ratio from experimental tests and numerical simulations, and a discussion of the effect of the different electrical conductivities. Results show that the free charges inside the dielectric polymer can lead to a larger EHD force because of the additional Coulomb force, even at a low conductivity of 10(-7) S m(-1), thus demonstrating the ability to duplicate a mushroom-like structure with a high aspect ratio, which has wide applications in superhydrophobicity, dry adhesion, nanogenerators, etc.
机译:预先用的聚合物(ESF-PP)上的电液动力学结构形成可以在空间调制电场的影响下重复与初始几何形状相同的结构与初始几何形状相同,但具有较高的纵横比。在该过程中,在平面模板和扁平基板之间施加电压,夹在预先提测的聚合物和气隙之间,以在空气聚合物界面处产生电液动力学(EHD)力。随后,备用聚合物可以不均匀地拉向上,在其微/纳米结构中引起变形。到目前为止,大多数研究ESF-PP都探索了各种介电聚合物,其全部被认为是由于其电导率低而被认为是完美的电介质。然而,完美电介质的假设通常在聚合物运动和最终形态方面产生理论分析和实验结果之间的差异。这种现象可以归因于忽略介电聚合物运动中少量自由空间电荷的动作(尽管介电聚合物的电导率可能甚至低于去离子水的电导率),这强调了空间影响的重要性电介质聚合物内部的变形上的电荷。本文探讨了自由空间收费的作用,通过在逐行发展,表面形貌和实验测试和数值模拟中进行了完美的介电聚合物和泄漏介电聚合物,以及与实验测试和数值模拟的纵横比进行了比较,以及对此的效果不同的电导率。结果表明,由于额外的库仑力,介电聚合物内部的自由电荷可以导致较大的EHD力,即使在低导电率为10(-7)S m(-1),也可以证明重复蘑菇的能力具有高纵横比的结构,其在超疏水性,干粘附,纳米液中具有广泛的应用。

著录项

  • 来源
    《RSC Advances》 |2016年第81期|共9页
  • 作者单位

    Xi An Jiao Tong Univ State Key Lab Mfg Syst Engn Micro &

    Nanotechnol Res Ctr 28 Xianning Rd Xian 710049 Peoples R China;

    Xi An Jiao Tong Univ State Key Lab Mfg Syst Engn Micro &

    Nanotechnol Res Ctr 28 Xianning Rd Xian 710049 Peoples R China;

    Xi An Jiao Tong Univ State Key Lab Mfg Syst Engn Micro &

    Nanotechnol Res Ctr 28 Xianning Rd Xian 710049 Peoples R China;

    Xi An Jiao Tong Univ State Key Lab Mfg Syst Engn Micro &

    Nanotechnol Res Ctr 28 Xianning Rd Xian 710049 Peoples R China;

    Xi An Jiao Tong Univ State Key Lab Mfg Syst Engn Micro &

    Nanotechnol Res Ctr 28 Xianning Rd Xian 710049 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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