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    Optical Linewidth and Line-Shape Studies of Energy Transfer Mechanisms between Rare-Earth Impurity Ions

    W. M. Yen, R. L. Greene, and W. C. Scott*

    D. L. Huber

    • Department of Physics, Stanford University, Stanford, California

    • Department of Physics, University of Wisconsin, Madison, Wisconsin

    • *NSF predoctoral fellow, 1964-65.
    • Alfred P. Sloan fellow, 1965-67.

    Phys. Rev. 140, A1188 – Published 15 November, 1965

    DOI: https://doi.org/10.1103/PhysRev.140.A1188

    Abstract

    We present optical linewidth and line-shape studies of transitions of 4f impurity ions in doubly doped systems and show that interactions which involve excitation transfer between the impurity systems produce homogeneous broadening and line-shape changes in the optical transitions. In particular, we have studied the behavior of the 5985-Å line of Pr3+ in doubly doped LaF3: Pr3+, Nd3+ as a function of Nd3+ concentration. The 5985-Å Pr3+ transition at 4.2°K involves two long-lived electronic states of the Pr3+ ion; it follows that in the singly doped LaF3: Pr3+ the transition shows a Gaussian shape which is characteristic of inhomogeneous strain and imperfection broadening. As Nd3+ is added to the system, a broader Lorentzian component begins to appear in the 5985-Å Pr3+ transition and eventually (at Nd3+ concentrations of ∼1% or above) completely dominates the width and shape of the transition. The Lorentzian component of the transition line shape was successfully separated using a Fourier-transform technique and the width of this component was studied as a function of the Nd3+ concentration. The width is found to increase linearly with increasing Nd3+ concentration up to concentrations of 2%; at higher concentrations, the linewidth saturates and approaches an asymptotic value of ∼2 cm1. We construe this homogeneous component to be evidence of a rapid short-range energy transfer mechanism between the Pr3+ and Nd3+ systems at the terminating (H63)1 level of the 5985-Å Pr3+ transition. Various mechanisms are investigated as causes of the energy transfer process; it is concluded that the spin-exchange interaction is the most probable cause for the transfer. Results of other spectroscopic measurements on the doubly doped LaF3: Pr3+, Nd3+ system are also presented.

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