Metal-Controlled Magnetoresistance at Room Temperature in Single-Molecule Devices
The appropriate choice of the transition metal complex and metal surface electronic structure opens the possibility to control the spin of the charge carriers through the resulting hybrid molecule/metal spinterface in a single molecule electrical contact at room temperature. The single molecule cond...
| Autores: | , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2017 |
| País: | España |
| Institución: | Universidad de Barcelona |
| Repositorio: | Dipòsit Digital de la UB |
| OAI Identifier: | oai:diposit.ub.edu:2445/154758 |
| Acceso en línea: | https://hdl.handle.net/2445/154758 |
| Access Level: | acceso abierto |
| Palabra clave: | Magnetoresistència Teoria del funcional de densitat Espintrònica Magnetoresistance Density functionals Spintronics |
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Metal-Controlled Magnetoresistance at Room Temperature in Single-Molecule DevicesAragonès, Albert C.Aravena Ponce, Daniel AlejandroValverde-Muñoz, Francisco J.Real, José AntonioSanz Carrasco, FaustoDíez Pérez, IsmaelRuiz Sabín, EliseoMagnetoresistènciaTeoria del funcional de densitatEspintrònicaMagnetoresistanceDensity functionalsSpintronicsThe appropriate choice of the transition metal complex and metal surface electronic structure opens the possibility to control the spin of the charge carriers through the resulting hybrid molecule/metal spinterface in a single molecule electrical contact at room temperature. The single molecule conductance of a Au/molecule/Ni junction can be switched by flipping the magnetization direction of the ferromagnetic electrode. The requirements of the molecule include not just the presence of unpaired electrons: the electronic configuration of the metal center has to provide occupied or empty orbitals that strongly interact with the junction metal electrodes and that are close in energy to their Fermi levels for one of the electronic spins only. The key ingredient for the metal surface is to provide an efficient spin texture induced by the spin orbit coupling in the topological surface states that results in an efficient spin-dependent interaction with the orbitals of the molecule. The strong magnetoresistance effect found in this kind of single-molecule wire opens a new approach for the design of room-temperature nanoscale devices based on spin-polarized currents controlled at molecular level.American Chemical Society2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersionapplication/pdfhttps://hdl.handle.net/2445/154758Articles publicats en revistes (Química Inorgànica i Orgànica)reponame:Dipòsit Digital de la UBinstname:Universidad de BarcelonaInglésVersió postprint del document publicat a: https://doi.org/10.1021/jacs.6b11166Journal of the American Chemical Society, 2017, vol. 139, num. 16, p. 5768-5778https://doi.org/10.1021/jacs.6b11166(c) American Chemical Society , 2017info:eu-repo/semantics/openAccessoai:diposit.ub.edu:2445/1547582026-05-27T06:46:51Z |
| dc.title.none.fl_str_mv |
Metal-Controlled Magnetoresistance at Room Temperature in Single-Molecule Devices |
| title |
Metal-Controlled Magnetoresistance at Room Temperature in Single-Molecule Devices |
| spellingShingle |
Metal-Controlled Magnetoresistance at Room Temperature in Single-Molecule Devices Aragonès, Albert C. Magnetoresistència Teoria del funcional de densitat Espintrònica Magnetoresistance Density functionals Spintronics |
| title_short |
Metal-Controlled Magnetoresistance at Room Temperature in Single-Molecule Devices |
| title_full |
Metal-Controlled Magnetoresistance at Room Temperature in Single-Molecule Devices |
| title_fullStr |
Metal-Controlled Magnetoresistance at Room Temperature in Single-Molecule Devices |
| title_full_unstemmed |
Metal-Controlled Magnetoresistance at Room Temperature in Single-Molecule Devices |
| title_sort |
Metal-Controlled Magnetoresistance at Room Temperature in Single-Molecule Devices |
| dc.creator.none.fl_str_mv |
Aragonès, Albert C. Aravena Ponce, Daniel Alejandro Valverde-Muñoz, Francisco J. Real, José Antonio Sanz Carrasco, Fausto Díez Pérez, Ismael Ruiz Sabín, Eliseo |
| author |
Aragonès, Albert C. |
| author_facet |
Aragonès, Albert C. Aravena Ponce, Daniel Alejandro Valverde-Muñoz, Francisco J. Real, José Antonio Sanz Carrasco, Fausto Díez Pérez, Ismael Ruiz Sabín, Eliseo |
| author_role |
author |
| author2 |
Aravena Ponce, Daniel Alejandro Valverde-Muñoz, Francisco J. Real, José Antonio Sanz Carrasco, Fausto Díez Pérez, Ismael Ruiz Sabín, Eliseo |
| author2_role |
author author author author author author |
| dc.subject.none.fl_str_mv |
Magnetoresistència Teoria del funcional de densitat Espintrònica Magnetoresistance Density functionals Spintronics |
| topic |
Magnetoresistència Teoria del funcional de densitat Espintrònica Magnetoresistance Density functionals Spintronics |
| description |
The appropriate choice of the transition metal complex and metal surface electronic structure opens the possibility to control the spin of the charge carriers through the resulting hybrid molecule/metal spinterface in a single molecule electrical contact at room temperature. The single molecule conductance of a Au/molecule/Ni junction can be switched by flipping the magnetization direction of the ferromagnetic electrode. The requirements of the molecule include not just the presence of unpaired electrons: the electronic configuration of the metal center has to provide occupied or empty orbitals that strongly interact with the junction metal electrodes and that are close in energy to their Fermi levels for one of the electronic spins only. The key ingredient for the metal surface is to provide an efficient spin texture induced by the spin orbit coupling in the topological surface states that results in an efficient spin-dependent interaction with the orbitals of the molecule. The strong magnetoresistance effect found in this kind of single-molecule wire opens a new approach for the design of room-temperature nanoscale devices based on spin-polarized currents controlled at molecular level. |
| publishDate |
2017 |
| dc.date.none.fl_str_mv |
2017 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion |
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article |
| status_str |
acceptedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2445/154758 |
| url |
https://hdl.handle.net/2445/154758 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Versió postprint del document publicat a: https://doi.org/10.1021/jacs.6b11166 Journal of the American Chemical Society, 2017, vol. 139, num. 16, p. 5768-5778 https://doi.org/10.1021/jacs.6b11166 |
| dc.rights.none.fl_str_mv |
(c) American Chemical Society , 2017 info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
(c) American Chemical Society , 2017 |
| eu_rights_str_mv |
openAccess |
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application/pdf |
| dc.publisher.none.fl_str_mv |
American Chemical Society |
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American Chemical Society |
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Articles publicats en revistes (Química Inorgànica i Orgànica) reponame:Dipòsit Digital de la UB instname:Universidad de Barcelona |
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Universidad de Barcelona |
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Dipòsit Digital de la UB |
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Dipòsit Digital de la UB |
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1869405515405066240 |
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15.300724 |