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Below 360 mK, Fe8 magnetic molecular clusters are in the pure quantum relaxation regime. We showed recently that the predicted ``square-root time relaxation is obeyed, allowing us to develop a new method for watching the evolution of the distribution of molecular spin states in the sample. We measured the distribution P(H) of molecules which are in resonance at the applied field H. Tunnelling initially causes rapid transitions of molecules, thereby ``digging a hole in P(H). For small initial magnetisation values, the hole width shows an intrinsic broadening which may be due to nuclear spins. We present here hole digging measurements in the thermal activated regime which may allow to study the effect of spin-phonon coupling.
The nuclear spin-mediated quantum relaxation of ensembles of tunneling magnetic molecules causes a hole to appear in the distribution of internal fields in the system. The form of this hole, and its time evolution, are studied using Monte Carlo simul
Reply to the Comment of J.J. Alonso and J.F. Fernandez on the paper Hole-digging in ensembles of tunneling molecular magnets of I.S. Tupitsyn, P.C.E. Stamp and N.V. Prokofev (Phys. Rev. B 69, 132406, (2004)).
Tupitsyn et al. [Phys. Rev. B v69, 132406 (2004)] have recently reported results for the relaxation of crystalline systems of single--molecule magnets, such as Fe_8. They claim that, quite generally, (1) the magnetization and hole widths of field--di
The magnetization of the prototypical molecular magnet Mn12-acetate exhibits a series of sharp steps at low temperatures due to quantum tunneling at specific resonant values of magnetic field applied along the easy c-axis. An abrupt reversal of the m
The reversal of the magnetization of crystals of molecular magnets that have a large spin and high anisotropy barrier generally proceeds below the blocking temperature by quantum tunneling. This is manifested as a series of controlled steps in the hy