Abstract
The intensity of the dielectric absorption arising from the rotation of divalent ion-vacancy pairs in alkali crystals has been measured over a range of concentrations in the crystals NaCl:Ca2+, NaCl:Mn2+, KCl:Sr2+ and LiF:Mg2+ and found to agree with the value calculated from simple theory. In NaCl:Mn2+ (and in some other systems) the absorption is slightly broader than a Debye curve. This is discussed in terms of the relative occupancy by vacancies of nearest neighbour and next nearest neighbour sites to the impurity ions.