ترغب بنشر مسار تعليمي؟ اضغط هنا

Quantum Tunneling of Magnetization in a Large Molecular Nanomagnet -- Approaching the Mesoscale

86   0   0.0 ( 0 )
 نشر من قبل Wernsdorfer Wolfgang
 تاريخ النشر 2003
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

A Mn30 molecular cluster is established to be the largest single-molecule magnet (SMM) discovered to date. Magnetization versus field measurements show coercive fields of about 0.5 T at low temperatures. Magnetization decay experiments reveal an Arrhenius behavior and temperature-independent relaxation below 0.2 K diagnostic of quantum tunneling of magnetization through the anisotropy barrier.The quantum hole digging method is used to establish resonant quantum tunneling. These results demonstrate that large molecular nanomagnets,having a volume of 15 nm^3, with dimensions approaching the mesoscale can still exhibit the quantum physics of the microscale.

قيم البحث

اقرأ أيضاً

247 - O. Parcollet , X. Waintal 2005
We present a complete theory of the spin torque phenomena in a ultrasmall nanomagnet coupled to non-collinear ferromagnetic electrodes through tunnelling junctions. This model system can be described by a simple microscopic model which captures many physical effects characteristic of spintronics: tunneling magneto resistance, intrinsic and transport induced magnetic relaxation, current induced magnetization reversal and spin accumulation. Treating on the same footing the magnetic and transport degrees of freedom, we arrive at a closed equation for the time evolution of the magnetization. This equation is very close to the Landau-Lifshitz-Gilbert equation used in spin valves structures. We discuss how the presence of the Coulomb blockade phenomena and the discretization of the one-body spectrum gives some additional features to the current induced spin torque. Depending on the regime, the dynamic induced by the coupling to electrode can be viewed either as a spin torque or as a relaxation process. In addition to the possibility of stabilizing uniform spin precession states, we find that the system is highly hysteretic: up to three different magnetic states can be simultaneously stable in one region of the parameter space (magnetic field and bias voltage).We also discuss how the magneto-resistance can be used to provide additional information on the non-equilibrium peaks present in the nanomagnet spectroscopy experiments.
We present magnetization measurements on the single molecule magnet Mn6, revealing various tunnel transitions inconsistent with a giant-spin description. We propose a dimeric model of the molecule with two coupled spins S=6, which involves crystal-fi eld anisotropy, symmetric Heisenberg exchange interaction, and antisymmetric Dzyaloshinskii-Moriya exchange interaction. We show that this simplified model of the molecule explains the experimentally observed tunnel transitions and that the antisymmetric exchange interaction between the spins gives rise to tunneling processes between spin states belonging to different spin multiplets.
Time-dependent specific heat experiments on the molecular nanomagnet Fe8 and the isotopic enriched analogue 57Fe8 are presented. The inclusion of the 57Fe nuclear spins leads to a huge enhancement of the specific heat below 1 K, ascribed to a strong increase in the spin-lattice relaxation rate Gamma arising from incoherent, nuclear-spin-mediated magnetic quantum tunneling in the ground-doublet. Since Gamma is found comparable to the expected tunneling rate, the latter process has to be inelastic. A model for the coupling of the tunneling levels to the lattice is presented. Under transverse field, a crossover from nuclear-spin-mediated to phonon-induced tunneling is observed.
The nature of magnetization reversal in an isolated cylindrical nanomagnet has been studied employing time-resolved magnetoresistance measurement. We find that the reversal mode is highly stochastic, occurring either by multimode or single-step switc hing. Intriguingly, the stochasticity was found to depend on the alignment of the driving magnetic field to the long axis of the nanowires, where predominantly multimode switching gives way to single-step switching behavior as the field direction is rotated from parallel to transverse with respect to the nanowire axis.
Below 360 mK, Fe magnetic molecular clusters are in the pure quantum relaxation regime and we show that the predicted square-root time relaxation is obeyed, allowing us to develop a new method for watching the evolution of the distribution of molecul ar spin states in the sample. We measure as a function of applied field H the statistical distribution P(xi_H) of magnetic energy bias xi_H$ acting on the molecules. Tunneling initially causes rapid transitions of molecules, thereby digging a hole in P(xi_H) (around the resonant condition xi_H = 0). For small initial magnetization values, the hole width shows an intrinsic broadening which may be due to nuclear spins.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا