Abstract
The identification of the third-nearest-neighbor monoclinic (Cs) site comprised of a Sm2+-K+ vacancy pair with the vacancy at the (2,1,1) lattice point in KCl has been made through a high-resolution Zeeman anisotropy fluorescence spectroscopic investigation of several prominent transitions between the D5 and F7 multiplets. The establishment of the dominant presence of the Cs site in KCl:M2+, which constitutes an important feature of the Maxwell-Boltzmann distribution of the M2+K+ vacancy pairs, is of fundamental importance in the understanding of numerous phenomena in polar crystals.