Spin canting in a Dy-based Single-Chain Magnet with dominant next-nearest neighbor antiferromagnetic interactions
arXiv:0901.4409 · doi:10.1103/PhysRevB.79.134419
Abstract
We investigate theoretically and experimentally the static magnetic properties of single crystals of the molecular-based Single-Chain Magnet (SCM) of formula [Dy(hfac)NIT(CHOPh)] comprising alternating Dy and organic radicals. A peculiar inversion between maxima and minima in the angular dependence of the magnetic molar susceptibility occurs on increasing temperature. Using information regarding the monomeric building block as well as an {\it ab initio} estimation of the magnetic anisotropy of the Dy ion, this anisotropy-inversion phenomenon can be assigned to weak one-dimensional ferromagnetism along the chain axis. This indicates that antiferromagnetic next-nearest-neighbor interactions between Dy ions dominate, despite the large Dy-Dy separation, over the nearest-neighbor interactions between the radicals and the Dy ions. Measurements of the field dependence of the magnetization, both along and perpendicularly to the chain, and of the angular dependence of in a strong magnetic field confirm such an interpretation. Transfer matrix simulations of the experimental measurements are performed using a classical one-dimensional spin model with antiferromagnetic Heisenberg exchange interaction and non-collinear uniaxial single-ion anisotropies favoring a canted antiferromagnetic spin arrangement, with a net magnetic moment along the chain axis. The fine agreement obtained with experimental data provides estimates of the Hamiltonian parameters, essential for further study of the dynamics of rare-earths based molecular chains.
11 pages, 8 figures
References in corpus (4)
Cited by in corpus (5)
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