Mechanism of Friction Enhancement Induced by Nanoscale Liquid Film: A Brief Review

IF 2 3区 工程技术 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY
Tianyan Gao, Guorui Wang, Xin’an Chen, Zhong Zhang
{"title":"Mechanism of Friction Enhancement Induced by Nanoscale Liquid Film: A Brief Review","authors":"Tianyan Gao,&nbsp;Guorui Wang,&nbsp;Xin’an Chen,&nbsp;Zhong Zhang","doi":"10.1007/s10338-024-00545-w","DOIUrl":null,"url":null,"abstract":"<div><p>Surficial water adsorption and interfacial water condensation as natural phenomena play an essential role in the contact adhesion and friction performances of the solid interface. As the characteristic dimensions downscale to nanometers, the structure and dynamics of the water film at an interface differ significantly from those of its bulk counterpart. In particular, a specific wetting condition termed as the tacky regime has recently sparked great interest in the community, where transient high friction and contact instabilities are observed at the interface that is subjected to the wet-to-dry transition. Unveiling the influence of nanoscale water film on the friction enhancement in the tacky regime will provide theoretical guidance for the friction regulation in the wetting condition. In this article, special emphasis is placed on the development of experimental techniques which allow the visualization of the contact interface (e.g., contact surface deformation, real contact area) and characterization of water film structures (e.g., film thickness, molecular configuration). Building upon the accumulation of recent research activities, we provide an overview of significant advances in understanding the critical mechanisms for friction enhancement, such as vertical capillary force, interfacial shear strength, and ice-like water. Some common design strategies are further given to regulate the friction behavior by tuning the distribution of the water film, surface roughness, and elastic modulus. Finally, we end this review article with a summary of the research status and outlook on areas for future research directions.</p></div>","PeriodicalId":50892,"journal":{"name":"Acta Mechanica Solida Sinica","volume":"38 2","pages":"183 - 194"},"PeriodicalIF":2.0000,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Mechanica Solida Sinica","FirstCategoryId":"5","ListUrlMain":"https://link.springer.com/article/10.1007/s10338-024-00545-w","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Surficial water adsorption and interfacial water condensation as natural phenomena play an essential role in the contact adhesion and friction performances of the solid interface. As the characteristic dimensions downscale to nanometers, the structure and dynamics of the water film at an interface differ significantly from those of its bulk counterpart. In particular, a specific wetting condition termed as the tacky regime has recently sparked great interest in the community, where transient high friction and contact instabilities are observed at the interface that is subjected to the wet-to-dry transition. Unveiling the influence of nanoscale water film on the friction enhancement in the tacky regime will provide theoretical guidance for the friction regulation in the wetting condition. In this article, special emphasis is placed on the development of experimental techniques which allow the visualization of the contact interface (e.g., contact surface deformation, real contact area) and characterization of water film structures (e.g., film thickness, molecular configuration). Building upon the accumulation of recent research activities, we provide an overview of significant advances in understanding the critical mechanisms for friction enhancement, such as vertical capillary force, interfacial shear strength, and ice-like water. Some common design strategies are further given to regulate the friction behavior by tuning the distribution of the water film, surface roughness, and elastic modulus. Finally, we end this review article with a summary of the research status and outlook on areas for future research directions.

纳米级液体膜诱导摩擦增强机理综述
表面水的吸附和界面水的凝结是影响固体界面接触粘附和摩擦性能的重要因素。当特征尺寸缩小到纳米级时,界面上的水膜的结构和动力学与体膜的结构和动力学有很大的不同。特别是,一种特殊的湿润状态,称为粘性状态,最近引起了社区的极大兴趣,在这种状态下,在受湿到干转变的界面上观察到短暂的高摩擦和接触不稳定性。揭示纳米尺度水膜对粘滞状态下摩擦增强的影响,将为润湿状态下的摩擦调节提供理论指导。在这篇文章中,特别强调了实验技术的发展,这些技术允许接触界面的可视化(例如,接触面变形,实际接触面积)和水膜结构的表征(例如,膜厚度,分子构型)。基于最近研究活动的积累,我们概述了在理解摩擦增强的关键机制方面取得的重大进展,例如垂直毛细力、界面剪切强度和冰状水。进一步给出了通过调整水膜分布、表面粗糙度和弹性模量来调节摩擦行为的一些常用设计策略。最后,对本文的研究现状进行了总结,并对未来研究方向进行了展望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Acta Mechanica Solida Sinica
Acta Mechanica Solida Sinica 物理-材料科学:综合
CiteScore
3.80
自引率
9.10%
发文量
1088
审稿时长
9 months
期刊介绍: Acta Mechanica Solida Sinica aims to become the best journal of solid mechanics in China and a worldwide well-known one in the field of mechanics, by providing original, perspective and even breakthrough theories and methods for the research on solid mechanics. The Journal is devoted to the publication of research papers in English in all fields of solid-state mechanics and its related disciplines in science, technology and engineering, with a balanced coverage on analytical, experimental, numerical and applied investigations. Articles, Short Communications, Discussions on previously published papers, and invitation-based Reviews are published bimonthly. The maximum length of an article is 30 pages, including equations, figures and tables
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信