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dc.contributor.authorTa, Huy Quang
dc.contributor.authorYang, Qin Xiao
dc.contributor.authorLiu, Shuyuan
dc.contributor.authorBachmatiuk, Alicja
dc.contributor.authorMendes, Rafael G.
dc.contributor.authorGemming, Thomas
dc.contributor.authorLiu, Yu
dc.contributor.authorLiu, Lijun
dc.contributor.authorTokarska, Klaudia
dc.contributor.authorPatel, Rajen B.
dc.contributor.authorChoi, Jin-Ho
dc.contributor.authorRümmeli, Mark Hermann
dc.date.accessioned2020-07-08T08:49:25Z
dc.date.available2020-07-08T08:49:25Z
dc.date.issued2020
dc.identifier.citationNano Letters. 2020, vol. 20, issue 6, p. 4354-4361.cs
dc.identifier.issn1530-6984
dc.identifier.issn1530-6992
dc.identifier.urihttp://hdl.handle.net/10084/139636
dc.description.abstractCompared to van der Waals two-dimensional (2D) layers with lateral covalent bonds, metallic bonding systems favor close-packed structures, and thus, free-standing 2D metals have remained, for the most part, elusive. However, a number of theoretical studies suggest a number of metals can exist as 2D materials and a few early experiments support this notion. Here we demonstrate free-standing single-atom-thick crystalline chromium (Cr) suspended membranes using aberration-corrected transmission electron microscopy and image simulations. Density functional theory studies confirm the 2D Cr membranes have an antiferromagnetic ground state making them highly attractive for spintronic applications. Moreover, the work also helps consolidate the existence of a new family of 2D metal layers.cs
dc.language.isoencs
dc.publisherAmerican Chemical Societycs
dc.relation.ispartofseriesNano Letterscs
dc.relation.urihttp://doi.org/10.1021/acs.nanolett.0c01082cs
dc.rightsCopyright © 2020, American Chemical Societycs
dc.subjectIn situ TEMcs
dc.subject2D metalscs
dc.subjectsingle-element 2Dcs
dc.subjectchromiumcs
dc.subjectfree-standing single-atom-thick membranecs
dc.subjectantiferromagneticcs
dc.titleIn situ formation of free-standing single-atom-thick antiferromagnetic chromium membranescs
dc.typearticlecs
dc.identifier.doi10.1021/acs.nanolett.0c01082
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume20cs
dc.description.issue6cs
dc.description.lastpage4361cs
dc.description.firstpage4354cs
dc.identifier.wos000541691200038


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