Measurement of the intrinsic strength of crystalline and polycrystalline graphene

The mechanical properties of materials depend strongly on crystal structure and defect configuration. Here we measure the strength of suspended single-crystal and bicrystal graphene membranes prepared by chemical vapour deposition. Membranes of interest are first characterized by transmission electr...

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Bibliographic Details
Published inNature communications Vol. 4; no. 1; p. 2811
Main Authors Rasool, Haider I., Ophus, Colin, Klug, William S., Zettl, A., Gimzewski, James K.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 19.11.2013
Nature Publishing Group
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Summary:The mechanical properties of materials depend strongly on crystal structure and defect configuration. Here we measure the strength of suspended single-crystal and bicrystal graphene membranes prepared by chemical vapour deposition. Membranes of interest are first characterized by transmission electron microscopy and subsequently tested using atomic force microscopy. Single-crystal membranes prepared by chemical vapour deposition show strengths comparable to previous results of single-crystal membranes prepared by mechanical exfoliation. Grain boundaries with large mismatch angles in polycrystalline specimens have higher strengths than their low angle counterparts. Remarkably, these large angle grain boundaries show strength comparable to that of single-crystal graphene. To investigate this enhanced strength, we employ aberration-corrected high-resolution transmission electron microscopy to explicitly map the atomic-scale strain fields in suspended graphene. The high strength is attributed to the presence of low atomic-scale strain in the carbon–carbon bonds at the boundary. The two-dimensional structure of graphene is known to impart high strength, but can be hard to synthesize without grain boundaries. Here, the authors find that strength increases with grain boundary mismatch, which results from low atomic-scale strain in the carbon–carbon bonds at the boundary.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms3811