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Hydration layer structure modulates superlubrication by trivalent La <sup>3+</sup> electrolytes

Tianyi HanFaculty of Pharmacy, Université de Montréal, Montreal, Québec H3C 3J7, CanadaWei CaoDepartment of Physical Chemistry, School of Chemistry, The Raymond and Beverly Sackler Faculty of Exact Sciences and The Sackler Center for Computational Molecular and Materials Science, Tel Aviv University, Tel Aviv 6997801, IsraelZhi XuState Key Laboratory of Tribology in Advanced Equipment, Tsinghua University, Beijing 100084, ChinaVahid AdibniaFaculty of Pharmacy, Université de Montréal, Montreal, Québec H3C 3J7, CanadaMatteo OlgiatiInstitute of Applied Physics, Vienna University of Technology, Vienna A-1040, AustriaMarkus ValtinerInstitute of Applied Physics, Vienna University of Technology, Vienna A-1040, AustriaLiran MaState Key Laboratory of Tribology in Advanced Equipment, Tsinghua University, Beijing 100084, ChinaChenhui ZhangState Key Laboratory of Tribology in Advanced Equipment, Tsinghua University, Beijing 100084, ChinaMing MaCenter for Nano and Micro Mechanics, Tsinghua University, Beijing 100084, ChinaJianbin LuoState Key Laboratory of Tribology in Advanced Equipment, Tsinghua University, Beijing 100084, ChinaXavier BanquyDepartment of Chemistry, Faculty of Art and Science, Université de Montréal, Montreal, Québec H3C 3J7, Canada
2023en
ABI

Аннотация

Water-based lubricants provide lubrication of rubbing surfaces in many technical, biological, and physiological applications. The structure of hydrated ion layers adsorbed on solid surfaces that determine the lubricating properties of aqueous lubricants is thought to be invariable in hydration lubrication. However, we prove that the ion surface coverage dictates the roughness of the hydration layer and its lubricating properties, especially under subnanometer confinement. We characterize different hydration layer structures on surfaces lubricated by aqueous trivalent electrolytes. Two superlubrication regimes are observed with friction coefficients of 10 −4 and 10 −3 , depending on the structure and thickness of the hydration layer. Each regime exhibits a distinct energy dissipation pathway and a different dependence to the hydration layer structure. Our analysis supports the idea of an intimate relationship between the dynamic structure of a boundary lubricant film and its tribological properties and offers a framework to study such relationship at the molecular level.

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