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Article: Models of charge transport and transfer in molecular switch tunnel junctions of bistable catenanes and rotaxanes

TitleModels of charge transport and transfer in molecular switch tunnel junctions of bistable catenanes and rotaxanes
Authors
KeywordsHopping
Molecular electronics
Molecular machines
Raman spectroscopy
Tunneling
Issue Date2006
Citation
Chemical Physics, 2006, v. 324, n. 1 SPEC. ISS., p. 280-290 How to Cite?
AbstractThe processes by which charge transfer can occur play a foundational role in molecular electronics. Here we consider simplified models of the transfer processes that could be present in bistable molecular switch tunnel junction (MSTJ) devices during one complete cycle of the device from its low- to high- and back to low-conductance state. The bistable molecular switches, which are composed of a monolayer of either switchable catenanes or rotaxanes, exist in either a ground-state co-conformation or a metastable one in which the conduction properties of the two co-conformations, when measured at small biases (+0.1 V), are significantly different irrespective of whether transport is dominated by tunneling or hopping. The voltage-driven generation (±2 V) of molecule-based redox states, which are sufficiently long-lived to allow the relative mechanical movements necessary to switch between the two co-conformations, rely upon unequal charge transfer rates on to and/or off of the molecules. Surface-enhanced Raman spectroscopy has been used to image the ground state of the bistable rotaxane in MSTJ-like devices. Consideration of these models provide new ways of looking at molecular electronic devices that rely, not only on nanoscale charge-transport, but also upon the bustling world of molecular motion in mechanically interlocked bistable molecules. © 2005 Elsevier B.V. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/332667
ISSN
2023 Impact Factor: 2.0
2023 SCImago Journal Rankings: 0.439
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorFlood, Amar H.-
dc.contributor.authorWong, Eric W.-
dc.contributor.authorStoddart, J. Fraser-
dc.date.accessioned2023-10-06T05:13:21Z-
dc.date.available2023-10-06T05:13:21Z-
dc.date.issued2006-
dc.identifier.citationChemical Physics, 2006, v. 324, n. 1 SPEC. ISS., p. 280-290-
dc.identifier.issn0301-0104-
dc.identifier.urihttp://hdl.handle.net/10722/332667-
dc.description.abstractThe processes by which charge transfer can occur play a foundational role in molecular electronics. Here we consider simplified models of the transfer processes that could be present in bistable molecular switch tunnel junction (MSTJ) devices during one complete cycle of the device from its low- to high- and back to low-conductance state. The bistable molecular switches, which are composed of a monolayer of either switchable catenanes or rotaxanes, exist in either a ground-state co-conformation or a metastable one in which the conduction properties of the two co-conformations, when measured at small biases (+0.1 V), are significantly different irrespective of whether transport is dominated by tunneling or hopping. The voltage-driven generation (±2 V) of molecule-based redox states, which are sufficiently long-lived to allow the relative mechanical movements necessary to switch between the two co-conformations, rely upon unequal charge transfer rates on to and/or off of the molecules. Surface-enhanced Raman spectroscopy has been used to image the ground state of the bistable rotaxane in MSTJ-like devices. Consideration of these models provide new ways of looking at molecular electronic devices that rely, not only on nanoscale charge-transport, but also upon the bustling world of molecular motion in mechanically interlocked bistable molecules. © 2005 Elsevier B.V. All rights reserved.-
dc.languageeng-
dc.relation.ispartofChemical Physics-
dc.subjectHopping-
dc.subjectMolecular electronics-
dc.subjectMolecular machines-
dc.subjectRaman spectroscopy-
dc.subjectTunneling-
dc.titleModels of charge transport and transfer in molecular switch tunnel junctions of bistable catenanes and rotaxanes-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.chemphys.2005.12.031-
dc.identifier.scopuseid_2-s2.0-33646267676-
dc.identifier.volume324-
dc.identifier.issue1 SPEC. ISS.-
dc.identifier.spage280-
dc.identifier.epage290-
dc.identifier.isiWOS:000237766300028-

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