Graphite has been conventionally believed to exhibit an inferior lubricating performance with significantly larger friction coefficient and wear rate in a vacuum environment than in ambient air. Dangling bonds at the edge planes of graphite, accounting for the high friction in inert atmosphere are saturated by chemisorbed vapor molecules in air, which contributes to low surface adhesion and low friction. However, there is still a lack of direct experimental evidence whether basal planes of graphite excluding the negative effects of edges or dangling bonds shows intrinsic lubricity when sliding under ultrahigh vacuum (UHV) conditions. By the interlayer friction measurement enabled by graphite flake-wrapped atomic force microscope tips in UHV, we show a record-low friction coefficient of 4 × 10 (slope of friction vs normal force curve) when sliding between graphite layers, which is much lower than that in ambient air. This discrepancy manifests the intrinsic sliding frictional behavior between the graphite basal planes when the tribo-materials and experimental conditions are well-designed and strictly controlled. In addition, the temperature dependence of the kinetic friction between the graphite layers has been investigated under UHV conditions over the temperature range of 125-448 K, which is consistent with the thermally activated process.
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http://dx.doi.org/10.1021/acsami.0c05422 | DOI Listing |
Chemphyschem
January 2025
Chinese Academy of Sciences, Institute of Coal Chemistry, 27 South Taoyuan Road, Taiyuan, Shanxi, P.R.China, 030001, Taiyuan, CHINA.
Electric double layer capacitors (EDLC) require large specific surface area to provide high power density. The generation of pores increases the electrochemical capacitance with more graphitic edge planes exposed to the electrolyte. Conventional theory believes this increasing in capacitance is owed to the increased specific surface area, but our work uncovers another mechanism.
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Helmholtz Institute Ulm (HIU) Electrochemical Energy Storage, Helmholtzstrasse 11, 89081 Ulm, Germany.
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April 2025
College of Physics, Qingdao University, Qingdao 266071, China. Electronic address:
Polyacrylonitrile (PAN)-based composite solid electrolytes (CSEs) hold great promise in the practical deployment of solid lithium batteries (SLBs) owing to their high voltage stability but suffer from poor stability against Li-metal. Herein, a poly(1,3-dioxolane) (PDOL)-graphitic CN (g-CN, i.e.
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Department of Chemistry, Lomonosov Moscow State University, Moscow 119991, Russia.
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Electronic Convergence Division, Korea Institute of Ceramic Engineering & Technology, 101, Soho-Ro, Jinju 52851, Republic of Korea.
Developing thin-film sheets made of oxide-based solid electrolytes is essential for fabricating surface-mounted ultracompact multilayer oxide solid-state batteries. To this end, solid-electrolyte slurry must be optimized for excellent dispersibility. Although oxide-based solid electrolytes for multilayer structures require sintering, high processing temperatures cause problems such as Li-ion volatilization and reactions with graphite anodes.
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