Suppr超能文献

纳米尺度下柱状阵列表面电润湿的静力学与动力学

Statics and dynamics of electrowetting on pillar-arrayed surfaces at the nanoscale.

作者信息

Zhao Ya-Pu, Yuan Quanzi

机构信息

State Key Laboratory of Nonlinear Mechanics, Institute of Mechanics, Chinese Academy of Sciences, Beijing 100190, People's Republic of China.

出版信息

Nanoscale. 2015 Feb 14;7(6):2561-7. doi: 10.1039/c4nr06759b.

Abstract

The statics and dynamics of electrowetting on pillar-arrayed surfaces at the nanoscale are studied using molecular dynamics simulations. Under a gradually increased electric field, a droplet is pushed by the electromechanical force to spread, and goes through the Cassie state, the Cassie-to-Wenzel wetting transition and the Wenzel state, which can be characterized by the electrowetting number at the microscale ηm. The expansion of the liquid is direction-dependent and influenced by the surface topology. A positive voltage is induced in the bulk droplet, while a negative one is induced in the liquid confined among the pillars, which makes the liquid hard to spread and further polarize. Based on the molecular kinetic theory and the wetting states, theoretical models have been proposed to comprehend the physical mechanisms in the statics and dynamics of electrowetting, and are validated by our simulations. Our findings may help to understand the electrowetting on microtextured surfaces and assist the future design of engineered surfaces in practical applications.

摘要

利用分子动力学模拟研究了纳米尺度下柱状阵列表面的电润湿静态和动态特性。在逐渐增加的电场作用下,液滴受到机电力的推动而展开,并经历了Cassie状态、Cassie到Wenzel的润湿转变以及Wenzel状态,这些状态可以通过微尺度下的电润湿数ηm来表征。液体的扩展具有方向依赖性,并受到表面拓扑结构的影响。在本体液滴中感应出正电压,而在柱状体之间受限的液体中感应出负电压,这使得液体难以展开并进一步极化。基于分子动力学理论和润湿状态,提出了理论模型来理解电润湿静态和动态中的物理机制,并通过我们的模拟进行了验证。我们的研究结果可能有助于理解微纹理表面上的电润湿现象,并为实际应用中工程表面的未来设计提供帮助。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验