{"title":"水接触层内的密度分布决定了滑移:超出表面润湿性","authors":"Shiyu Lv , Qingwei Gao , Qian Sun , Shuangliang Zhao","doi":"10.1016/j.jcis.2025.138371","DOIUrl":null,"url":null,"abstract":"<div><h3>Hypothesis</h3><div>Both hydrophobic and hydrophilic surfaces have been shown to promote solid-liquid boundary slippage, which leading to a controversy regarding the role of surface wettability in liquid slippage. We hypothesize that liquid slippage is determined by a more fundamental physical mechanism beyond surface wettability effect.</div></div><div><h3>Simulations</h3><div>Through equilibrium (EMD) and non-equilibrium molecular dynamics (NEMD) simulations, we investigate the effect of solid-liquid Lennard-Jones (L-J) interactions, solid lattice constants, surface charges, and roughness on water wetting and slippage on solid surfaces.</div></div><div><h3>Findings</h3><div><em>We</em> demonstrate that the density distribution within the water contact layer on solid surfaces determines water slippage, beyond surface wettability. The new concept of <em>Roughness of Contact Density</em> (<em>RCD</em>) is proposed to quantitatively describe this effect and revealing a power-law relationship between <em>RCD</em> and slip length. The slip length increases as the <em>RCD</em> decreases, with significant slippage and a slip length of 10 nm occurring when the <em>RCD</em> equals 0.2. Our work not only clarifies the persistent ambiguous role of surface wettability in liquid slippage but also provides a new physical mechanism for liquid slippage.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"700 ","pages":"Article 138371"},"PeriodicalIF":9.4000,"publicationDate":"2025-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Density distribution within the water contact layer determines slippage: Beyond surface wettability\",\"authors\":\"Shiyu Lv , Qingwei Gao , Qian Sun , Shuangliang Zhao\",\"doi\":\"10.1016/j.jcis.2025.138371\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Hypothesis</h3><div>Both hydrophobic and hydrophilic surfaces have been shown to promote solid-liquid boundary slippage, which leading to a controversy regarding the role of surface wettability in liquid slippage. We hypothesize that liquid slippage is determined by a more fundamental physical mechanism beyond surface wettability effect.</div></div><div><h3>Simulations</h3><div>Through equilibrium (EMD) and non-equilibrium molecular dynamics (NEMD) simulations, we investigate the effect of solid-liquid Lennard-Jones (L-J) interactions, solid lattice constants, surface charges, and roughness on water wetting and slippage on solid surfaces.</div></div><div><h3>Findings</h3><div><em>We</em> demonstrate that the density distribution within the water contact layer on solid surfaces determines water slippage, beyond surface wettability. The new concept of <em>Roughness of Contact Density</em> (<em>RCD</em>) is proposed to quantitatively describe this effect and revealing a power-law relationship between <em>RCD</em> and slip length. The slip length increases as the <em>RCD</em> decreases, with significant slippage and a slip length of 10 nm occurring when the <em>RCD</em> equals 0.2. Our work not only clarifies the persistent ambiguous role of surface wettability in liquid slippage but also provides a new physical mechanism for liquid slippage.</div></div>\",\"PeriodicalId\":351,\"journal\":{\"name\":\"Journal of Colloid and Interface Science\",\"volume\":\"700 \",\"pages\":\"Article 138371\"},\"PeriodicalIF\":9.4000,\"publicationDate\":\"2025-07-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Colloid and Interface Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S002197972501762X\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Colloid and Interface Science","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S002197972501762X","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Density distribution within the water contact layer determines slippage: Beyond surface wettability
Hypothesis
Both hydrophobic and hydrophilic surfaces have been shown to promote solid-liquid boundary slippage, which leading to a controversy regarding the role of surface wettability in liquid slippage. We hypothesize that liquid slippage is determined by a more fundamental physical mechanism beyond surface wettability effect.
Simulations
Through equilibrium (EMD) and non-equilibrium molecular dynamics (NEMD) simulations, we investigate the effect of solid-liquid Lennard-Jones (L-J) interactions, solid lattice constants, surface charges, and roughness on water wetting and slippage on solid surfaces.
Findings
We demonstrate that the density distribution within the water contact layer on solid surfaces determines water slippage, beyond surface wettability. The new concept of Roughness of Contact Density (RCD) is proposed to quantitatively describe this effect and revealing a power-law relationship between RCD and slip length. The slip length increases as the RCD decreases, with significant slippage and a slip length of 10 nm occurring when the RCD equals 0.2. Our work not only clarifies the persistent ambiguous role of surface wettability in liquid slippage but also provides a new physical mechanism for liquid slippage.
期刊介绍:
The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality.
Emphasis:
The journal emphasizes fundamental scientific innovation within the following categories:
A.Colloidal Materials and Nanomaterials
B.Soft Colloidal and Self-Assembly Systems
C.Adsorption, Catalysis, and Electrochemistry
D.Interfacial Processes, Capillarity, and Wetting
E.Biomaterials and Nanomedicine
F.Energy Conversion and Storage, and Environmental Technologies