...
首页> 外文期刊>Nanoscale >A 3D molecular cantilever based on interfacial self-assembly and the cobra-like actuation of long-chain imidazolium ionic liquids
【24h】

A 3D molecular cantilever based on interfacial self-assembly and the cobra-like actuation of long-chain imidazolium ionic liquids

机译:基于界面的三维分子悬臂自组装和眼镜蛇式驱动的长链imidazolium离子液体

获取原文
获取原文并翻译 | 示例

摘要

Cantilever structures usually function as a key building block in the construction of supramolecular systems. In this work, based on the controllable interfacial self-assembly of monolayer long-chain imidazolium ionic liquids (ILs) on multi-walled carbon nanotubes, we design a 3D molecular cantilever with advantages including facile assembly, multi-mechanism actuation and high scalability. Molecular dynamics simulations predict that the lifting of the cation alkyl chain as a cantilever possesses a cobra-like actuation mechanism, including structure-induced and environmental response effects, which is further verified via experimental observations. On one hand, regulating the internal alkyl chain units results in the regular variation of the cantilever tilt angle with respect to the surface; on the other hand, applying external electric fields with various strengths/directions can also drive the cantilever to rise or fall. As expected, the interfacial self-assembly structure of the molecular cantilever directionally induces a change in the phase transition behaviour, delivering significantly enhanced thermal stability for immobilized ILs compared with the bulk state.
机译:悬臂结构通常作为一个关键的函数在建设的构建块超分子体系。控制界面的自组装单层长链imidazolium离子液体多壁碳纳米管(ILs),我们的设计一个3 d分子悬臂与优势包括简单组装机理驱动和高可伸缩性。动态模拟预测的提升作为一个悬臂具有阳离子烷基链眼镜蛇式驱动机制,包括structure-induced和环境响应影响,进一步验证通过实验观察。规范内部烷基链单元的结果在常规悬臂倾斜的变化角的表面;一方面,运用外部电场各种优势/方向也可以驱动悬臂上升或下降。界面的自组装结构分子悬臂定向诱导相变行为的变化,提供显著提高热稳定固定ILs相比大部分国家。

著录项

相似文献

  • 外文文献
  • 中文文献
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