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Direct Spin-Lattice Relaxation of Divalent Cobalt Ions in Two Hydrated Complexes
Phys. Rev. 152, 403 – Published 2 December, 1966
DOI: https://doi.org/10.1103/PhysRev.152.403
Abstract
Experimental measurements are reported for the allowed and forbidden relaxation rates in the hyperfine structure of divalent cobalt in the site of lanthanum zinc double nitrate and in zinc fluosilicate. The static spin Hamiltonian of the ion is characteristic of a large trigonal distortion, and that for the ion in the fluosilicate is characteristic of an intermediate trigonal distortion. The results are fitted by an extension of a theory used elsewhere to fit similar measurements on cobalt in the site of lanthanum zinc double nitrate. In all three cases, four adjustable constants are allowed by the theory. A good description of all of the many facets of the relaxation is obtained for all three types of sites.
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