Long-range ferromagnetism of Mn12 acetate single-molecule magnets under a transverse magnetic field
arXiv:cond-mat/0508627 · doi:10.1103/PhysRevLett.95.227202
Abstract
We use neutron diffraction to probe the magnetization components of a crystal of Mn12 single-molecule magnets. Each of these molecules behaves, at low temperatures, as a nanomagnet with spin S = 10 and strong anisotropy along the crystallographic c axis. Application of a magnetic field perpendicular to c induces quantum tunneling between opposite spin orientations, enabling the spins to attain thermal equilibrium. Below approximately 0.9 K, intermolecular interactions turn this equilibrium state into a ferromagnetically ordered phase. However, long range ferromagnetic correlations nearly disappear for fields larger 5.5 T, possibly suggesting the existence of a quantum critical point.
arXiv comment4 pages, 4 figures
References in corpus (8)
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- High frequency EPR spectra of a molecular nanomagnet provide a key to understand Quantum Tunneling of the Magnetization
- Determination of the magnetic anisotropy axes of single-molecule magnets
- Ordering of dipolar Ising crystals
- Quantum Coherence in Fe8 Molecular Nanomagnets
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- Realization of random-field dipolar Ising ferromagnetism in a molecular magnet
- Magnetic dipolar ordering and relaxation in the high-spin molecular cluster compound Mn6
- Experimental determination of the dipolar field in Mn12-acetate
- Dipolar Ordering and Quantum Dynamics of Domain Walls in Mn-12 Acetate
- Phases of anisotropic dipolar antiferromagnets
- Experimental determination of the Weiss temperature of Mn-ac and Mn-ac-MeOH
- Dipolar-controlled spin tunneling and relaxation in molecular magnets
- Transverse Field Ising Ferromagnetism in Mn-acetate-MeOH
- Dipolar ordering in crystals of Mn12 Ac
- Quantum Fluctuations and Long-Range Order in Molecular Magnets