2008
DOI: 10.1016/j.cplett.2007.12.049
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The unoccupied electronic structure of the semi-conducting room temperature molecular magnet V(TCNE)2

Abstract: The unoccupied electronic structure of the semi-conducting room temperature molecular magnet V(TCNE) 2 , 2008, Chemical Physics Letters, (452) AbstractThe unoccupied electronic structure of the organic-based magnet V(TCNE) x (TCNE = tetracyanoethylene, x~2) has been studied with near edge x-ray absorption fine structure (NEXAFS) and with photoelectron spectroscopy (PES). By studying V(TCNE) x upon sodiumdoping, the electron-accepting state, i.e. the lowest unoccupied molecular orbital (LUMO) of V(TCNE) x was … Show more

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Cited by 11 publications
(11 citation statements)
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“…3(a)) has its absorption onset located at 284 eV, originating from a transition to the LUMO of V(TCNE) x [9,18]. When Ni is deposited on V(TCNE) x , the absorption onset decreases in intensity.…”
Section: Ni/v(tcne) X Interfacementioning
confidence: 99%
See 1 more Smart Citation
“…3(a)) has its absorption onset located at 284 eV, originating from a transition to the LUMO of V(TCNE) x [9,18]. When Ni is deposited on V(TCNE) x , the absorption onset decreases in intensity.…”
Section: Ni/v(tcne) X Interfacementioning
confidence: 99%
“…Vanadium tetracyanoethylene, V(TCNE) x , x~2, is one of very few room temperature organic-based magnets [5]. It is however extremely air sensitive, but recently we have reported on a new preparation method leading to improved air stability [6], which should make device fabrication less complex.The highest occupied molecular orbital (HOMO) of V(TCNE) x is mainly localized on V(3d) and characterized by strong hybridization between V(3d) and TCNE - [7,8], while the lowest unoccupied molecular orbital (LUMO) is localized on TCNE - [9]. The coupling between V 2+ and the two TCNE -is antiferromagnetic, yielding a ferrimagnetic state and hence a net spin of 1/2 for V(TCNE) x [10].…”
mentioning
confidence: 98%
“…In order to discuss the electronic effects of chlorine substitution, it is useful to first build a simple molecular orbital model of the V II -acceptor •− bonding in these systems. Carlegrim et al examined analogous V[TCNE] 2 systems by near-edge x-ray absorption fine structure and photoelectron spectroscopies [28]. Their results suggest that the π* singly occupied molecular orbital (SOMO) of the TCNE •− radical anion is very close in energy to the partially occupied t 2g orbitals (POMO) of V II in a pseudo-octahedral ligand field, which facilitates strong covalent bonding and consequent strong ferrimagnetic communication (large magnetic exchange coupling).…”
Section: Discussionmentioning
confidence: 99%
“…The lack of solvent molecules cause increased structural order, and hence, improved magnetic characteristics. 14 However, the CVD-prepared magnets still contain reacted oxygen and, generally, also residual by-products 13,15 and degrade after only a few minutes or hours in air depending on the precursor used. 9,10 Recently, an ultrahigh vacuum ͑UHV͒ compatible CVD-based preparation method was presented, 12 enabling both preparation and characterization of completely oxygen-free V͑TCNE͒ x thin films.…”
mentioning
confidence: 99%
“…8 A main problem of V͑TCNE͒ x , however, is its extreme air sensitivity 2,[9][10][11]13 and that residual solvent molecules and/or precursor-based by-products negatively affect magnetic properties 11,14 as well as introduce electron trap states. 15 Here, we present a in situ preparation method based on physical vapor deposition ͑PVD͒ resulting in films free from residual solvent molecules and precursor-based byproducts. Our first result shows that PVD-prepared V͑TCNE͒ x films can retain their magnetic properties ͑at least͒ for several weeks in air, which is a necessary step toward development of practical applications.…”
mentioning
confidence: 99%