The hyperfine structure coupling of the magnetic moment of the nucleus with the magnetic moment of the electronic cloud of a paramagnetic ion gives rise to a Schottky specific heat anomaly at an appropriate temperature. For the cobaltous ion in a single crystal of cobalt ammonium sulfate this temperature is about 0.1^∘{}K. In the region where the specific heat goes as AT² and where the Curie law χ=C/T holds, one can make measurements of A by means of an ac mutual inductance bridge which measures the susceptibility of the paramagnetic salt. The method of measurement consists in superposing a dc magnetic field on the salt already in the ac field of the bridge. This dc field depresses the susceptibility an amount depending on the parameter C/A which is therefore a constant of the material being investigated. If one knows the Curie constant, then one has A immediately. This measured A, however, is made up of two contributions: (a) that arising from the nuclear-electronic coupling and (b) that arising from the dipole interaction of neighboring paramagnetic ions. The (b) contribution is a function of concentration of the ions, so that by making measurements of A at various dilutions and plotting A as a function of dilution, one obtains an intercept by extrapolation to infinite dilution which is the part of A due to nuclear specific heat. The thermodynamic measurements made thus give a nuclear specific heat of CᵥT²=16.1×10^-4R, where R is the gas constant, which is in excellent agreement with CᵥT²=16×10^-4R calculated from microwave data. It is observed that pure cobalt ammonium sulfate has a Curie point at {~}0.125^∘{}K, while the diluted salts do not possess one in the same temperature region.
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Stephen F. Malaker (1951) studied this question.
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