Journal of Low Temperature Physics

, Volume 140, Issue 1, pp 119–174

Magnetic Quantum Tunneling in the Single-Molecule Magnet Mn12-Acetate

Authors

  • E. del Barco
    • Department of PhysicsNew York University
    • Department of PhysicsUniversity of Central Florida
  • A. D. Kent
    • Department of PhysicsNew York University
    • Department of PhysicsUniversity of Florida
  • J. M. North
    • Department of Chemistry and Biochemistry and National High Magnetic Field LaboratoryFlorida State University
  • N. S. Dalal
    • Department of Chemistry and Biochemistry and National High Magnetic Field LaboratoryFlorida State University
  • E. M. Rumberger
    • Department of Chemistry and BiochemistryUniversity of California San Diego – La Jolla
  • D. N. Hendrickson
    • Department of Chemistry and BiochemistryUniversity of California San Diego – La Jolla
  • N. Chakov
    • Department of ChemistryUniversity of Florida
  • G. Christou
    • Department of ChemistryUniversity of Florida
Article

DOI: 10.1007/s10909-005-6016-3

Cite this article as:
Barco, E.d., Kent, A.D., Hill, S. et al. J Low Temp Phys (2005) 140: 119. doi:10.1007/s10909-005-6016-3

Abstract

The symmetry of magnetic quantum tunneling (MQT) in the single molecule magnet Mn2-acetate has been determined by sensitive low-temperature magnetic measurements in the pure quantum tunneling regime and high frequency EPR spectroscopy in the presence of large transverse magnetic fields. The combined data set definitely establishes the transverse anisotropy terms responsible for the low temperature quantum dynamics. MQT is due to a disorder induced locally varying quadratic transverse anisotropy associated with rhombic distortions in the molecular environment (2nd order in the spin-operators). This is superimposed on a 4th order transverse magnetic anisotropy consistent with the global (average) S4 molecule site symmetry. These forms of the transverse anisotropy are incommensurate, leading to a complex interplay between local and global symmetries, the consequences of which are analyzed in detail. The resulting model explains: (1) the observation of a twofold symmetry of MQT as a function of the angle of the transverse magnetic field when a subset of molecules in a single crystal are studied; (2) the non-monotonic dependence of the tunneling probability on the magnitude of the transverse magnetic field, which is ascribed to an interference (Berry phase)effect; and (3) the angular dependence of EPR absorption peaks, including the fine structure in the peaks, among many other phenomena. This work also establishes the magnitude of the 2nd and 4th order transverse anisotropy terms for Mn12-acetate single crystals and the angle between the hard magnetic anisotropy axes of these terms. EPR as a function of the angle of the field with respect to the easy axes (close to the hard-medium plane) confirms that there are discrete tilts of the molecular magnetic easy axis from the global (average) easy axis of a crystal, also associated with solvent disorder. The latter observation provides a very plausible explanation for the lack of MQT selection rules, which has been a puzzle for many years.

Keywords

single-molecule magnetquantum tunnelingmolecular nanomagnetMn12-AcetateEPRmagnetometry
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Copyright information

© Springer Science+Business Media, Inc. 2005