Abstract
Nonradiative relaxation by multiple-phonon emission was investigated for excited electronic states of rare-earth ions in YAlO3. Ions studied included Nd3+, Eu3+, Ho3+, Er3+, and Tm3+. Rates of multiphonon emission were determined from the difference of measured excited-state lifetimes and calculated radiative lifetimes. Electric dipole transition probabilities were computed using Judd-Ofelt intensity parameters for rare earths in YAlO3. Multiphonon decay rates, measured for seventeen different levels with energies to the next-lower level ranging from 1400 to 4700 cm1, exhibited an approximately exponential dependence on energy gap ΔE given by W(0)eαΔE, where W(0)=5×109 sec1 and α=4.6×103 cm. Exceptions to the exponential law occur only when selection rules severely restrict the number of terms in the ion-lattice interaction active in inducing transitions. The phonon frequency distribution and ion-phonon coupling in YAlO3 were examined from infrared, Raman, and vibronic spectra. Although phonon energies range up to 750 cm1, measurements of the temperature dependence of multiphonon emission indicate that phonons of energies 550600 cm1 make the dominant contribution to the relaxation at temperatures 77-700 °K.