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在原子尺度上探究离子界面的水化摩擦。

Probing the hydration friction of ionic interfaces at the atomic scale.

作者信息

Li Zibo, Liu Qian, Zhang Deliang, Wang Yin, Zhang Yuge, Li Qiang, Dong Mingdong

机构信息

Key Laboratory of Colloid and Interface Chemistry of the Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.

Interdisciplinary Nanoscience Center (iNANO), Aarhus University, Aarhus C, DK-8000, Denmark.

出版信息

Nanoscale Horiz. 2022 Mar 28;7(4):368-375. doi: 10.1039/d1nh00564b.

Abstract

Despite the extensive studies conducted in exploring friction in the aqueous environment, the mechanism of hydration friction remains not well understood. Herein, we directly probed hydration friction on mica-electrolyte interfaces with different hydrated alkali cations through a combination of three-dimensional atomic force microscopy and friction force microscopy. The atomic scale imaging of the hydration layers at the mica surface in different electrolyte solutions clearly revealed a correlation between the alkali cations and the structure of the hydration layers. Our detailed analysis showed that the hydration force was much higher at high ionic concentrations than that at low concentrations. The hydration friction coefficient was found to follow the trend K< Na< Li< Cs, which contrasts with the Hofmeister series, indicating that the hydration friction depends not only on the hydration strength of the alkali cations but also on the arrangement of the alkali cations at the interface. The results of this study provide deep insights into the origins of hydration friction, with potential implications for the development of new boundary lubrication in aqueous media.

摘要

尽管在探索水环境中的摩擦方面已经进行了广泛的研究,但水合摩擦的机制仍然没有得到很好的理解。在此,我们通过三维原子力显微镜和摩擦力显微镜相结合的方法,直接探测了不同水合碱金属阳离子在云母 - 电解质界面上的水合摩擦。在不同电解质溶液中云母表面水合层的原子尺度成像清楚地揭示了碱金属阳离子与水合层结构之间的相关性。我们的详细分析表明,高离子浓度下的水合力比低浓度下的水合力高得多。发现水合摩擦系数遵循K<Na<Li<Cs的趋势,这与霍夫迈斯特序列相反,表明水合摩擦不仅取决于碱金属阳离子的水合强度,还取决于碱金属阳离子在界面处的排列。这项研究的结果为水合摩擦的起源提供了深刻的见解,对水性介质中新边界润滑的发展具有潜在的意义。

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