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Register a new userField sweep rate dependence of the coercive field of single-molecule magnets: a classical approach with applications to the quantum regime
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Added by
Wolfgang Wernsdorfer
Publication date
2005
fields
Physics
and research's language is
English
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A method, based on the Neel-Brown model of thermally activated magnetization reversal of a magnetic single-domain particle, is proposed to study the field sweep rate dependence of the coercive field of single-molecule magnets (SMMs). The application to Mn12 and Mn84 SMMs allows the determination of the important parameters that characterize the magnetic properties: the energy barrier, the magnetic anisotropy constant, the spin, tau_0, and the crossover temperature from the classical to the quantum regime. The method may be particularly valuable for large SMMs that do not show quantum tunneling steps in the hysteresis loops.
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In this work we study theoretically the coupling of single molecule magnets (SMMs) to a variety of quantum circuits, including microwave resonators with and without constrictions and flux qubits. The main results of this study is that it is possible to achieve strong and ultrastrong coupling regimes between SMM crystals and the superconducting circuit, with strong hints that such a coupling could also be reached for individual molecules close to constrictions. Building on the resulting coupling strengths and the typical coherence times of these molecules (of the order of microseconds), we conclude that SMMs can be used for coherent storage and manipulation of quantum information, either in the context of quantum computing or in quantum simulations. Throughout the work we also discuss in detail the family of molecules that are most suitable for such operations, based not only on the coupling strength, but also on the typical energy gaps and the simplicity with which they can be tuned and oriented. Finally, we also discuss practical advantages of SMMs, such as the possibility to fabricate the SMMs ensembles on the chip through the deposition of small droplets.
We present studies on magnetic nano-structures with 3D architectures, fabricated using electrodeposition in the pores of well-ordered templates prepared by self-assembly of polystyrene latex spheres. The coercive field is found to demonstrate an oscillatory dependence on film thickness reflecting the patterning transverse to the film plane. Our results demonstrate that 3D patterned magnetic materials are prototypes of a new class of geometrical multilayer structures in which the layering is due to local shape effects rather then compositional differences.
We show that the nuclear spin dynamics in the single-molecule magnet Mn12-ac below 1 K is governed by quantum tunneling fluctuations of the cluster spins, combined with intercluster nuclear spin diffusion. We also obtain the first experimental proof that - surprisingly - even deep in the quantum regime the nuclear spins remain in good thermal contact with the lattice phonons. We propose a simple model for how T-independent tunneling fluctuations can relax the nuclear polarization to the lattice, that may serve as a framework for more sophisticated theories.
A Mn4 single-molecule magnet (SMM) is used to show that quantum tunneling of magnetization (QTM) is not suppressed by moderate three dimensional exchange coupling between molecules. Instead, it leads to an exchange bias of the quantum resonances which allows precise measurements of the effective exchange coupling that is mainly due to weak intermolecular hydrogen bounds. The magnetization versus applied field was recorded on single crystals of [Mn4]2 using an array of micro-SQUIDs. The step fine structure was studied via minor hysteresis loops.
Magnetization measurements of a molecular clusters Mn12 with a spin ground state of S = 10 show resonance tunneling at avoided energy level crossings. The observed oscillations of the tunnel probability as a function of the magnetic field applied along the hard anisotropy axis are due to topological quantum phase interference of two tunnel paths of opposite windings. Mn12 is therefore the second molecular clusters presenting quantum phase interference.
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