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      A near-wearless and extremely long lifetime amorphous carbon film under high vacuum

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          Abstract

          Prolonging wear life of amorphous carbon films under vacuum was an enormous challenge. In this work, we firstly reported that amorphous carbon film as a lubricant layer containing hydrogen, oxygen, fluorine and silicon (a-C:H:O:F:Si) exhibited low friction (~0.1), ultra-low wear rate (9.0 × 10 –13 mm 3 N –1 mm –1) and ultra-long wear life (>2 × 10 6 cycles) under high vacuum. We systematically examined microstructure and composition of transfer film for understanding of the underlying frictional mechanism, which suggested that the extraordinarily excellent tribological properties were attributed to the thermodynamically and structurally stable FeF 2 nanocrystallites corroborated using first-principles calculations, which were induced by the tribochemical reaction.

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          Generalized Gradient Approximation Made Simple.

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            Cross-sectional imaging of individual layers and buried interfaces of graphene-based heterostructures and superlattices

            By stacking various two-dimensional (2D) atomic crystals [1] on top of each other, it is possible to create multilayer heterostructures and devices with designed electronic properties [2-5]. However, various adsorbates become trapped between layers during their assembly, and this not only affects the resulting quality but also prevents the formation of a true artificial layered crystal upheld by van der Waals interaction, creating instead a laminate glued together by contamination. Transmission electron microscopy (TEM) has shown that graphene and boron nitride monolayers, the two best characterized 2D crystals, are densely covered with hydrocarbons (even after thermal annealing in high vacuum) and exhibit only small clean patches suitable for atomic resolution imaging [6-10]. This observation seems detrimental for any realistic prospect of creating van der Waals materials and heterostructures with atomically sharp interfaces. Here we employ cross sectional TEM to take a side view of several graphene-boron nitride heterostructures. We find that the trapped hydrocarbons segregate into isolated pockets, leaving the interfaces atomically clean. Moreover, we observe a clear correlation between interface roughness and the electronic quality of encapsulated graphene. This work proves the concept of heterostructures assembled with atomic layer precision and provides their first TEM images.
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              A near-frictionless and extremely elastic hydrogenated amorphous carbon film with self-assembled dual nanostructure.

              A highly crosslinking network combined with a fullerene-like structure is disclosed in a hydrogenated amorphous carbon film. The very soft carbon film exhibits super-low friction and excellent wear resistance even under a Hertzian contact pressure comparable to its hardness under vacuum, which is an extraordinary tribological behavior in the filed of solid lubrication films or coatings.
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                Author and article information

                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                10 June 2015
                2015
                : 5
                : 11119
                Affiliations
                [1 ]State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Science , Lanzhou 730000, China
                [2 ]University of Chinese Academy of Sciences , Beijing 100039, China
                [3 ]Department of Materials Chemistry, The Ångström Laboratory, Uppsala University , box 538, SE-751 21 Uppsala, Sweden
                Author notes
                Article
                srep11119
                10.1038/srep11119
                4461914
                26059254
                55e4764d-b63d-406a-9069-76739bb0769f
                Copyright © 2015, Macmillan Publishers Limited

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 20 January 2015
                : 15 May 2015
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