Abstract
A new type of spin-current filter is proposed, which consists of a single-molecule magnet (SMM) coupled to two normal metal electrodes. It is shown that this tunneling junction can generate a highly spin-polarized current, whose spin polarization can be switched by the magnetic field and gate voltage applied to the SMM. Such a spin switching in the SMM tunnel junction arises from the spin-selected single electron resonant tunneling via the lowest unoccupied molecular orbit of the SMM. And the electron current spectrum in absences of external magnetic field is still spin-polarized, which can help us to judge if the molecule’s spin state has reach to the ground-state doublet |±S). This device can be realized with current technologies and may have practical use in spintronics and quantum information.PACS numbers: 72.25.-b, 75.50.Xx, 85.75.-d
A dichlorido-bridged
dinuclear dysprosium(III) single-molecule magnet [Dy<sub>2</sub>L<sub>2</sub>(<i>µ</i>-Cl)<sub>2</sub>(THF)<sub>2</sub>] has been made using a diamine-bis(phenolate)
ligand, H<sub>2</sub>L. Magnetic studies show an energy barrier for
magnetization reversal (<i>U</i><sub>eff</sub>)
around 1000 K. Exchange-biasing effect is clearly seen in magnetic hysteresis with steps up to 4 K. <i>Ab</i> initio calculations exclude the
possibility of pure dipolar origin of this effect leading to the conclusion
that super-exchange <i>via</i> the chloride bridging ligands is important.
We report a six coordinate DyIII single-molecule magnet<br>(SMM) with an energy barrier of 1110 K for thermal relaxation of<br>magnetization. The sample shows no retention of magnetization<br>even at 2 K and this led us to find a good correlation between the<br>blocking temperature and the Raman relaxation regime for SMMs.<br>The key parameter is the relaxation time (𝜏<sub>switch</sub>) at the point where<br>the Raman relaxation mechanism becomes more important than<br>Orbach.
Dinuclear [M(H3L1,2,4)]2 (M = Dy, Dy2; M = Ho, Ho2) complexes were isolated from an heptadentate aminophenol ligand. The crystal structures of Dy2·2THF, and the pyridine adducts Dy2·2Py and Ho2·2Py,...