Linewidth of single photon transitions in Mn-acetate
arXiv:cond-mat/0110658 · doi:10.1103/PhysRevB.64.184426
Abstract
We use time-domain terahertz spectroscopy to measure the position and linewidth of single photon transitions in Mn-acetate. This linewidth is compared to the linewidth measured in tunneling experiments. We conclude that local magnetic fields (due to dipole or hyperfine interactions) cannot be responsible for the observed linewidth, and suggest that the linewidth is due to variations in the anisotropy constants for different clusters. We also calculate a lower limit on the dipole field distribution that would be expected due to random orientations of clusters and find that collective effects must narrow this distribution in tunneling measurements.
5 pages, accepted to Physical Review B
Cited by in corpus (12)
- The origin of second-order transverse magnetic anisotropy in Mn12-acetate
- Detailed single crystal EPR lineshape measurements for the single molecule magnets Fe8Br and Mn12-ac
- Superradiance from crystals of molecular nanomagnets
- Role of dipolar and exchange interactions in the positions and widths of EPR transitions for the single-molecule magnets Fe8 and Mn12
- Crystal lattice desolvation effects on the magnetic quantum tunneling of single-molecule magnets
- Rapid and Precise Determination of Zero-Field Splittings by Terahertz Time-Domain Electron Paramagnetic Resonance Spectroscopy
- Asymmetric Lineshape due to Inhomogeneous Broadening of the Crystal-Field Transitions in Mn12ac Single Crystals
- Pulsed field studies of the magnetization reversal in molecular nanomagnets
- Phonon bottleneck in the low-excitation limit
- On Ground State Tunneling in Mn-Acetate
- Quantum dynamics of crystals of molecular nanomagnets inside a resonant cavity
- More Evidence for a Distribution of Tunnel Splittings in Mn-acetate