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dc.contributor.authorSader, J. E.en_US
dc.contributor.authorHanay, M. S.en_US
dc.contributor.authorNeumann, A. P.en_US
dc.contributor.authorRoukes, M. L.en_US
dc.date.accessioned2019-02-21T16:02:17Zen_US
dc.date.available2019-02-21T16:02:17Zen_US
dc.date.issued2018en_US
dc.identifier.issn1530-6984en_US
dc.identifier.urihttp://hdl.handle.net/11693/49988en_US
dc.description.abstractThe mass measurement of single molecules, in real time, is performed routinely using resonant nanomechanical devices. This approach models the molecules as point particles. A recent development now allows the spatial extent (and, indeed, image) of the adsorbate to be characterized using multimode measurements (Hanay, M. S., Nature Nanotechnol., 10, 2015, pp.en_US
dc.description.sponsorshipThe authors acknowledge support from an NIH Director’s Pioneer award, the Australian Research Council grants scheme, and the ARC Centre of Excellence in Exciton Science (CE170100026). M.S.H. acknowledges support from FP7 Marie Curie Career Integration Grant. The authors thank Mustafa Kara for useful discussion.en_US
dc.language.isoEnglishen_US
dc.source.titleNano Lettersen_US
dc.relation.isversionofhttps://doi.org/10.1021/acs.nanolett.7b04301en_US
dc.subjectFrequency-shift detectionen_US
dc.subjectInertial imagingen_US
dc.subjectMass spectrometryen_US
dc.subjectNanomechanical systemsen_US
dc.titleMass spectrometry using nanomechanical systems: beyond the point-mass approximationen_US
dc.typeArticleen_US
dc.departmentDepartment of Mechanical Engineeringen_US
dc.departmentNANOTAM - Nanotechnology Research Centeren_US
dc.citation.spage1608en_US
dc.citation.epage1614en_US
dc.citation.volumeNumber18en_US
dc.citation.issueNumber3en_US
dc.relation.projectCE170100026 - NIH Office of the Director, OD - Pioneer Hi-Bred - Australian Research Council, ARCen_US
dc.identifier.doi10.1021/acs.nanolett.7b04301en_US
dc.identifier.doi10.1021/acs.nanolett.7b04301en_US
dc.publisherAmerican Chemical Societyen_US
dc.identifier.eissn1530-6992en_US


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