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    Publication Date: 2018
    Description: 〈p〉Publication date: March 2019〈/p〉 〈p〉〈b〉Source:〈/b〉 Carbon, Volume 143〈/p〉 〈p〉Author(s): Ke Chu, Jing Wang, Ya-ping Liu, Yuan-bo Li, Cheng-chang Jia, Hu Zhang〈/p〉 〈div xml:lang="en"〉 〈h5〉Abstract〈/h5〉 〈div〉〈p〉In-situ formation of appropriate interfacial carbides by matrix-alloying with carbide-forming elements offers an efficient approach to improve the interfacial bonding of graphene/CuX composites. However, the carbide formation commonly occurs at graphene edge/matrix interface, which is not enough to achieve the sufficient interfacial bonding because the vast majority of graphene/matrix interface is basal-plane/matrix interface rather than edge/matrix interface. To alleviate this limitation, we reported a new design of 〈em〉creating defects on graphene basal-plane〈/em〉 (CDGB) to optimize the interface and mechanical properties of graphene/CuCr composites. Plasma treatment was employed to create the structural defects (∼7 nm nanopores) on graphene basal-plane. When incorporating the plasma-treated graphene into the CuCr matrix, the Cr〈sub〉7〈/sub〉C〈sub〉3〈/sub〉 carbides were found to be in-situ formed at both basal-plane/matrix and edge/matrix interfaces. Ex-situ and in-situ tensile tests both demonstrated that the plasma-treated graphene led to the composite that showed a larger strength enhancement and a higher load transfer capability than untreated counterpart, which was ascribed to the largely improved interfacial bonding contributed by the Cr〈sub〉7〈/sub〉C〈sub〉3〈/sub〉 formed at basal-plane/matrix interface. This study suggests that the CDBG via plasma treatment affords a feasible solution for the interface optimization of graphene/CuX composites with enhanced mechanical properties.〈/p〉〈/div〉 〈/div〉 〈h5〉Graphical abstract〈/h5〉 〈div〉〈p〉〈figure〉〈img src="https://ars.els-cdn.com/content/image/1-s2.0-S0008622318310145-fx1.jpg" width="477" alt="Image 1" title="Image 1"〉〈/figure〉〈/p〉〈/div〉
    Print ISSN: 0008-6223
    Electronic ISSN: 1873-3891
    Topics: Chemistry and Pharmacology , Geosciences
    Published by Elsevier
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