Asymmetric Lineshape due to Inhomogeneous Broadening of the Crystal-Field Transitions in Mn12ac Single Crystals
arXiv:cond-mat/0307164 · doi:10.1103/PhysRevB.69.104410
Abstract
The lineshape of crystal-field transitions in single crystals of Mn12ac molecular magnets is determined by the magnetic history. The absorption lines are symmetric and Gaussian for the non-magnetized state obtained by zero-field cooling (zfc). In the magnetized state which is reached when the sample is cooled in a magnetic field (fc), however, they are asymmetric even in the absence of an external magnetic field. These observations are quantitatively explained by inhomogeneous symmetrical (Gaussian) broadening of the crystal-field transitions combined with a contribution of off-diagonal components of the magnetic susceptibility to the effective magnetic permeability.
arXiv comment4 pages, 3 figures
References in corpus (13)
- High frequency EPR spectra of a molecular nanomagnet provide a key to understand Quantum Tunneling of the Magnetization
- Low-Temperature Quantum Relaxation in a System of Magnetic Nanomolecules
- Low energy magnetic excitations of the Mn_{12}-acetate spin cluster observed by neutron scattering
- Observation of the distribution of molecular spin states by resonant quantum tunneling of the magnetization
- The origin of second-order transverse magnetic anisotropy in Mn12-acetate
- Effects of D-strain, g-strain, and dipolar interactions on EPR linewidths of the molecular magnets Fe8 and Mn12
- Nuclear spin driven resonant tunnelling of magnetisation in Mn12 acetate
- Detailed single crystal EPR lineshape measurements for the single molecule magnets Fe8Br and Mn12-ac
- 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
- Linewidth of single photon transitions in Mn-acetate
- Electron Paramagnetic Resonance Linewidths and Lineshapes for the Molecular Magnets Fe8 and Mn12