Selection rules for Single-Chain-Magnet behavior in non-collinear Ising systems
arXiv:0811.2118 · doi:10.1088/0953-8984/21/23/236007
Abstract
The magnetic behavior of molecular Single-Chain Magnets is investigated in the framework of a one-dimensional Ising model with single spin-flip Glauber dynamics. Opportune modifications to the original theory are required in order to account for reciprocal non-collinearity of local anisotropy axes and the crystallographic (laboratory) frame. The extension of Glauber's theory to the case of a collinear Ising ferrimagnetic chain is also discussed. Within this formalism, both the dynamics of magnetization reversal in zero field and the response of the system to a weak magnetic field, oscillating in time, are studied. Depending on the geometry, selection rules are found for the occurrence of slow relaxation of the magnetization at low temperatures, as well as for resonant behavior of the a.c. susceptibility as a function of temperature at low frequencies. The present theory applies successfully to some real systems, namely Mn-, Dy-, and Co-based molecular magnetic chains, showing that Single-Chain-Magnet behavior is not only a feature of collinear ferro- and ferrimagnetic, but also of canted antiferromagnetic chains.
15 pages, 6 figures
References in corpus (5)
- Spin Chirality in a Molecular Dysprosium Triangle: the Archetype of the Non-Collinear Ising Model
- Glauber dynamics in a single-chain magnet: From theory to real systems
- Glauber slow dynamics of the magnetization in a molecular Ising chain
- Spin canting in a Dy-based Single-Chain Magnet with dominant next-nearest neighbor antiferromagnetic interactions
- Effect of antiferromagnetic exchange interactions on the Glauber dynamics of one-dimensional Ising models
Cited by in corpus (3)
- Static and dynamic properties of Single-Chain Magnets with sharp and broad domain walls
- Finite-size effects on the dynamic susceptibility of CoPhOMe single-chain molecular magnets in presence of a static magnetic field
- A combined first-principles and thermodynamic approach to M-Nitronyl Nitroxide (M=Co, Mn) spin helices