EPR and optical-absorption studies of Cmsup3+ inYPO4andLuPO4single crystals

Abstract
Cm3+244 has been incorporated as a dilute impurity in single crystals of the tetragonal-symmetry lanthanide orthophosphate hosts, LuPO4 and YPO4. EPR spectroscopic observations were made of all of the excited doublets in the ground S7/28 multiplet of Cm3+ in both host crystals. Excited-state resonances were observed at both 77 and 4.2 K by use of X-band frequencies. The observed axial g values were used to compute the admixed wave functions for all four doublet levels in the ground manifold of Cm3+ and to calculate the g value expected for the lowest-lying doublet that could not be observed by EPR spectroscopy. Optical-absorption and Zeeman-effect investigations were carried out for the case of Cm3+ in YPO4, and a ground-state g value was obtained for the lowest-lying doublet in the ground-state manifold that was in excellent agreement with the value predicted by use of EPR results for the three excited-doublet levels. The Mohr-circle construction was used to obtain additional information regarding the nature of the crystal-field interaction for Cm3+ in the two crystal systems. In particular, the tetragonal crystal-field interaction was found to be stronger in the YPO4 host than in LuPO4. Additionally, the crystal-field-induced admixtures were found to be smaller at 77 K than at 4.2 K for both hosts, and the signs of the Steven’s parameters were determined to be positive for b40 and negative for b20.