Realization of random-field dipolar Ising ferromagnetism in a molecular magnet
arXiv:0910.1754 · doi:10.1103/PhysRevB.82.014406
Abstract
The longitudinal magnetic susceptibility of single crystals of the molecular magnet Mn-acetate obeys a Curie-Weiss law, indicating a transition to a ferromagnetic phase due to dipolar interactions. With increasing magnetic field applied transverse to the easy axis, the transition temperature decreases considerably more rapidly than predicted by mean field theory to a T=0 quantum critical point. Our results are consistent with an effective Hamiltonian for a random-field Ising ferromagnet in a transverse field, where the randomness is induced by an external field applied to Mn-acetate crystals that are known to have an intrinsic distribution of locally tilted magnetic easy axes.
arXiv comment4 pages, 4 figures
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Cited by in corpus (12)
- Photon Condensation and Enhanced Magnetism in Cavity QED
- Magnetic dipolar ordering and quantum phase transition in Fe8 molecular magnet
- Field evolution of the magnetic structures in ErTiO through the critical point
- Onset of a Propagating Self-Sustained Spin Reversal Front in a Magnetic System
- Tunneling and inversion symmetry in single-molecule magnets: the case of the Mn12 wheel molecule
- Novel disordering mechanism in ferromagnetic systems with competing interactions
- Experimental determination of the Weiss temperature of Mn-ac and Mn-ac-MeOH
- Transverse Field Ising Ferromagnetism in Mn-acetate-MeOH
- Dipolar-controlled spin tunneling and relaxation in molecular magnets
- Effective realization of random magnetic fields in compounds with large single-ion anisotropy
- Magnetic-field-tuned randomness in inhomogeneous altermagnets
- Quantum Fluctuations and Long-Range Order in Molecular Magnets