Photon echo measurements made at 2 °K on the 3H4 - 1D2 transition in Pr3+:LaF3 show that magnetic dipolar couplings between the Pr and F nuclei account for the 56 kHz homogeneous linewidth of this transition.1 The homogeneous broadening arises from the enhanced 141Pr nuclear moment (I=5/2) interacting with the local field fluctuations of the 19F nuclear moments undergoing mutual spin flip transitions. Such resonant fluctuations should, in the absence of a fluorine spin diffusion barrier, produce a homogeneous linewidth of about 200 kHz which is, in fact, roughly what is observed for the inhomogeneous broadening of the Pr3+ hyperfine levels and is considerably broader than that obtained by the photon echo measurements. Shelby et al2 proposed a simple model analogous to the spin diffusion barriers responsible for narrowing the homogeneous lines in certain electron paramagnetic resonance transitions3. In such systems, the field produced by the electron magnetic dipole moment (2-3 orders of magnitude larger than the enhanced nuclear moment associated with the ground state of Pr3+ in LaF3) de-tunes the nearest neighbors from each other, prohibiting mutual spin flips among them. Thus, the fields produced by the neighboring spins are static and their interaction with the paramagnetic ion contributes to the inhomogeneous linewidth and not to homogeneous broadening. The de-tuned neighbors are referred to as the "frozen core." Application of this picture to the case of Pr3+:LaF3 is supported by the calculation of Devoe et al.4 Their Monte Carlo calculation of the Pr3+ optical dephasing times shows that the observed homogeneous linewidth could be explained by deleting the nearest neighbor F spins from the lattice of rapidly fluctuating fluorine moments, in effect, treating them as part of a frozen core.
Recent optical free-induction-decay (FID) measurements of the impurity ion
Pr3+ in La
F3 at 2 \ifmmode^\circ\else\textdegree\fi{}K reveal optical homogeneous linewidths of only a few kilohertz, considerably narrower than the inhomogeneous broadening due to crystalline strains (5 GHz) or the static local magnetic fields of the
19F nuclei (100 kHz). In this regime, the homogeneous broadening arises from local field fluctuations, as in NMR, and is due to the
19F nuclei which undergo resonant flip-flops and modulate the
Pr3+ optical transition frequency. We treat the optical response of a two-level quantum system to an intense coherent field and to fluctuating perturbations using a Monte Carlo computer routine that assumes (1) the La
F3 crystal structure and (2) a sudden fluorine spin-flip model. This procedure avoids many of the approximations of previous analytic theories of spectral diffusion in magnetic resonance and extends the calculation specifically to optical FID. The decay behavior is obtained by sampling statistically the
Pr3+ phase history as subgroups of
19F spins flip randomly in space and time. These fluctuations modify the Bloch equations where the solutions for the preparative and post-preparative periods are obtained by numerical integration. In spite of the large lattice size assumed (2250 fluorines), only a few
19F spins contribute substantially to the homogeneous width, a result which shows for the first time that spin-flip correlations are not significant. Furthermore, a
Pr3+ ion polarizes and detunes the nearest fluorines forming a frozen core that is incapable of resonant spin flipping with the bulk fluorines. We demonstrate that the core grows radially as the
141Pr(I=25) magnetic moment increases with
Iz, but the Pr optical linewidth changes little, producing essentially one rather than three linewidths. Our calculations utilize no free parameters and predict a Lorentzian line shape of 8.4 kHz half-width at half maximum which compares to the optical FID observation of a 10.1-kHz Lorentzian. The Monte Carlo algorithm is verified further by the static local magnetic broadening of a Pr quadrupole transition which is found to be Gaussian, 82 kHz full width at half maximum, in agreement with a second-moment calculation and current observations.
Spin decoupling and line narrowing are observed for the first time in an opticaltransition, 3H4elDZ of Pr3~ in LaF 3 at zOK, using optical FID. The 19F nuclei, when irradiated by an appropriate rf field, undergo forced precession about an effective field at the magic angle in the rotating frame. The fluctuating 19F_19F dipolar interaction is thereby quenched and the optical linewidth drops from -10 to - Z kHz, as predicted in a theory of spin diffusion. In the field of nuclear magnetic resonance (NMR) , there exist several ways of reducing the time-dependent magnetic dipolar interaction between spins. Examples are motional narrowing (l,Z), macroscopic sampIe rotation (3), spontaneous spin flip-flop processes (4), and forced spin precession (5-10). In this article, we report the first observation of this kind in an optical transition of a low temperature solid, LaF 3:Pr 3+, where the dilute nuclear spin (I) is praseodymium and the abundant spin (S) is fluorine. The Pr 3+ ions are coherently prepared by a laser field and thereafter exhibit nonlinear optical free induction decay (FID). The Pr3+ dephasing time, as suggested in earlier work (11), is limited by spin diffusion among the 19F nuclei which undergo resonant flip-flops and impress weak fluctuating fields on the l4lpr nuclei. This action adiabatically modulates the Pr 3+ optical transition frequency through the dipolar I-S interaction and broadens the line. We now show that the half-width half-maximum (HWHM) optical linewidth is reduced from -10 to - Z kHz when the fluorine spin diffusion process is quenched by application of suitable magnetic static snd rf fields, causing the 19F nuclei to precess about an effective magnetic field at the magie angle in the rotating frame. This observation enables us to identify in an unambiguous way that the 19F_19F dipolar interaction is the dominant optical line broadening mechanism and provides the first test of spin diffusion theory' in an optical transition. As we shall see, the behavior at optical and rf frequencies is different. 3+
We have investigated the process of quenching of fluorescence from the
3P0 excited state of
Pr3+ in La
F3 due to cross relaxation among the Pr ions. The fluorescence decay of the ensemble of Pr ions after pulsed excitation is measured as a function of temperature for Pr concentration of 20 mol%. About 12% of the ions are in nonquenching sites and contribute an exponential component to the decay. The remainder of the decay originates from the bulk of the ions in quenching sites. Cross relaxation occurs directly in steps after transfer within the inhomogeneous line. Knowledge of the dynamics occurring within the inhomogeneous line derived from fluorescence line-narrowing experiments is used to analyze the cross-relaxation process from a microscopic viewpoint based on a recent model for fluorescence in the presence of traps. At 2 K the decay is consistent with an electric dipole-dipole transfer mechanism with a nearest-neighbor quenching rate of 8.9 \ifmmode\times\else\texttimes\fi{}
104 ${\mathrm{s}}^{\ensuremath{-}1}$ which is independent of temperature for
T<32 K and which successfully predicts the observed decay rate in Pr
F3. The temperature dependence of the decay for $8\ensuremath{\le}T\ensuremath{\le}32$ K is well described by a hopping model for excitation trapping. For
T>35 K an activation process becomes dominant consistent with the onset of cross relaxation involving the
1D2(5) and
3H6(1) states in which a 190-${\mathrm{cm}}^{\ensuremath{-}1}$ phonon is created.
Optical hole burning has been observed in the 5941-A transition of Pr(3+) in a charge-compensated tetragonal site of CaF(2) . The Pr(3+) ground state is doubly degenerate and shows a large first-order hyperfine splitting, which is clearly resolved because of the very narrow inhomogeneous linewidth of 650 MHz. The hole burning involves a new mechanism, in which optically induced spin flips of neighboring nuclei (here (19)F) shift the optical transition frequency outside its homogeneous linewidth. This mechanism was confirmed by optical rf double resonance.
Flip-flop processes due to magnetic dipole-dipole interaction between neighboring ions in crystals doped by rare-earth ions are one of the mechanisms of relaxation between hyperfine levels. Modeling of this mechanism has so far been macroscopic, characterized by an average rate describing the relaxation of all ions. Here, however, we present a microscopic model of flip-flop interactions between individual nuclear spins of dopant ions. Every ion is situated in a unique local environment in the crystal, where each ion has different distances and a unique orientation relative to its nearest neighbors, as determined by the lattice structure. Thus each ion has a unique flip-flop rate and the collective relaxation dynamics of all ions in a bulk crystal is a sum of many exponential decays, giving rise to a distribution of rates rather than a single average decay rate. We employ this model to calculate flip-flop rates in
Pr3+:
Y2SiO5 and show experimental measurements of population decay of the ground state hyperfine levels at $\ensuremath{\sim}2$ K. We also present a method to measure rates of individual transitions from hole burning spectra that requires significantly fewer fitting parameters in theoretical rate equations compared to earlier work. Furthermore, we measure the effect of external magnetic field on the flip-flop rates and observe that the rates slow down by two orders of magnitude in a field of 5--10 mT.