Relaxation processes in Nd are studied. We find that resonance coupling between Nd and other rare earth ions seems to exist. Nd plus Yb in Na0.5Gd0.5WO4 results in a coupled system in which the Yb may be caused to fluoresce by pumping the Nd. Radiation trapping is found to play only a minor role.
Laser-induced fluorescence line narrowing has been observed for the first time in a nonresonantly excited rare-earth system. Excitation with the 4727-\AA{} A+ line into the 4G211 level of Nd3+ in glass results in narrowing of transitions from the 4F23 to both the 4I29 ground manifold and the 4I211 excited manifold. The concentration dependence of the line narrowing provides information regarding resonant ion-ion energy transfer within the inhomogeneously broadened system.
The dynamics of trapping of optical excitation in a disordered system of ions in a solid is studied using time-resolved fluorescence measurements. In the system PrF3 doped with Nd, the randomly distributed Nd ions act as sinks for the Pr excitation. The transfer to the Nd traps can occur in conjunction with transfer among the Pr ions. In this system the Pr-Pr transfer is strongly temperature dependent while the Pr-Nd transfer is temperature independent at low temperatures. By changing the temperature we can span the range from no Pr-Pr transfer to very (infinitely) fast Pr-Pr transfer in one single system. We have identified these limits. In addition we have placed boundaries on the applicability of the diffusion and hopping models in describing trapping in the intermediate temperature regime where the Pr-Pr and Pr-Nd transfer rates are comparable.
Photon-echo-relaxation measurements made on the 3H4${\mathrm{\ensuremath{-}}}^{3}$P0 transition of 0.01 at. % Pr3+:YAG (where YAG represents yttrium aluminum garnet), 3H4${\mathrm{\ensuremath{-}}}^{1}$D2 transition in 0.1 at. % Pr3+:YAlO3, and 7F0${\mathrm{\ensuremath{-}}}^{5}$D0 transition in 0.25 at. % Eu3+:YAlO3 show that the photon-echo relaxation rate increases when the intensities of the excitation pulses are increased. Although a part of the relaxation-rate increase in Pr3+:YAG may be attributed to an instantaneous spectral diffusion (ISD) in which the presence of excited neighboring Pr3+ ions change the local field and the absorption frequency of the rare-earth ions, our data deviate significantly from the ISD-model predictions. An additional intensity-dependent relaxation mechanism is required to explain the results.