Pulsed field studies of the magnetization reversal in molecular nanomagnets
arXiv:cond-mat/0404041 · doi:10.1103/PhysRevB.70.220401
Abstract
We report experimental studies of crystals of Mn12 molecular magnetic clusters in pulsed magnetic fields with sweep rates up to 4x10^3 T/s. The steps in the magnetization curve are observed at fields that are shifted with respect to the resonant field values. The shift systematically increases as the rate of the field sweep goes up. These data are consistent with the theory of the collective dipolar relaxation in molecular magnets.
arXiv comment4 pages, 4 figures
References in corpus (13)
- High frequency EPR spectra of a molecular nanomagnet provide a key to understand Quantum Tunneling of the Magnetization
- The origin of second-order transverse magnetic anisotropy in Mn12-acetate
- Spin-spin cross-relaxation in single-molecule magnets
- Definitive spectroscopic determination of the transverse interactions responsible for the magnetic quantum tunneling in Mn12-acetate
- Spin tunneling via dislocations in Mn-12 acetate crystals
- Dislocation-induced spin tunneling in Mn-12 acetate
- Quantum Coherence in Fe8 Molecular Nanomagnets
- Symmetry of Magnetic Quantum Tunneling in Single Molecule Magnet Mn12-acetate
- Superradiance from crystals of molecular nanomagnets
- A Distribution of Tunnel Splittings in Mn-Acetate
- High frequency resonant experiments in Fe molecular clusters
- Linewidth of single photon transitions in Mn-acetate
- Electromagnetic radiation produced by avalanches in the magnetization reversal of Mn12-Acetate