Trapping of 29-${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$ phonons by optically excited
Cr3+ ions in ruby is studied at phonon occupations of up to order unity. The 29-${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$ phonons are supplied by transient excitation of a metallic point contact and subsequent conversion of the injected phonons to resonance. The growth and the decay of the trapped phonon population are markedly non-single-exponential quantities, particularly at higher phonon populations. A quantitative analysis of these effects is made on the basis of phenomenological rate equations of the ion and phonon populations. These equations make explicit allowance for the line shape of the E\ifmmode\bar\else\textasciimacron\fi{}
(2E)-2A\ifmmode\bar\else\textasciimacron\fi{}
(2E) phonon transition as well as for feeding and loss of resonant phonons by mediation of weakly exchange-coupled
Cr3+ pairs. At the higher phonon occupations, the transition appears to be dynamically broadened by stimulated phonon emission, which reduces the trapping efficiency.
Spatial and, additionally, spectral diffusion of 29-${\mathrm{cm}}^{\ensuremath{-}1}$ phonons trapped in an excited cylindrical region with diameter \ensuremath{\sim}0.1 mm has been investigated under continuous optical pumping of ruby. For 130- and 700-ppm ruby, phonon decay strictly limited by spatial diffusion is reflected in a quadratic dependence of the bottlenecking factor $\ensuremath{\sigma}$ on the excited-state concentration
N∗ up to ${N}^{*}\ensuremath{\sim}3\ifmmode\times\else\texttimes\fi{}{10}^{17}/{\mathrm{cm}}^{3}$. At higher
N∗, attainable in 700- and 2500-ppm ruby, the observed reduction of $\ensuremath{\sigma}$ relative to the second-power dependence, as well as the increased width of the dependence of $\ensuremath{\sigma}$ on magnetic field, reveal that spectral diffusion from inhomogeneous packet to packet is operative. In the spatially diffusive regime, evidence for Zeeman-induced spectral diffusion is found in a characteristic narrowing of the magnetic-field dependence of the
R2 fluorescence upon raising $\ensuremath{\sigma}$. At full separation of the Zeeman transitions $2\overline{A}(^{2}E)\ensuremath{\leftrightarrow}\overline{E}(^{2}E)$, $\ensuremath{\sigma}$ is reduced to 15-40% relative to zero field, depending on
N∗ and ground-state concentration. Rate equations governing the
Cr3+ populations in the two-level scheme (
2A,
E) with inclusion of spatial diffusion and anharmonic decay of the phonons account for the second-power dependence. Diffusive phonon decay turns out to dominate from ${N}^{*}R\ensuremath{\sim}4\ifmmode\times\else\texttimes\fi{}{10}^{13}/{\mathrm{cm}}^{2}$ up to at least ${N}^{*}{R}^{2}\ensuremath{\sim}{10}^{14}/\mathrm{cm}$, with
R the characteristic dimension of the excited region. Spectral diffusion, treated as a perturbation, satisfactorily fits the data at higher $\ensuremath{\sigma}$, yielding a diffusive step of \ensuremath{\sim}2% of the linewidth. At low bottlenecking, the functional form of the magnetic field dependence of $\ensuremath{\sigma}$, including its width and level at full separation, is closely described by use of rate equations, taking the line shape to be Gaussian-type, and assuming the phonons associated with spin flip and those with non spin flip to belong to distinct classes.
We introduce a technique utilizing the evanescent field of an optical waveguide to examine the dynamics of nonequilibrium high-frequency phonons resonant with optically excited centers in zones of submicrometer dimension. The technique is used to create a nearly saturated zone of excited
Cr3+ ions at the surface of a 700-at. ppm ruby crystal at 1.5 K by optical pumping through the broad bands. At the same time, the optical pumping serves to generate resonant 29-${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$ phonons. The decay of the combined spin-phonon system, measured via the
R2 luminescence following interruption of the optical pumping, is explained by elastic spatial diffusion in parallel with spectral wipeout. The time constant for loss by spatial diffusion is derived rigorously from rate equations. Spectral wipeout is treated according to the model developed by Goossens et al. based on one-site inelastic scattering by weakly exchange-coupled
Cr3+ pairs, but modified to include the appreciable elastic diffusion remaining after wipeout under the present extreme conditions. Spectral wipeout turns out to predominate at high excited-state concentration. The optical feeding into 2A\ifmmode\bar\else\textasciimacron\fi{}
(2E) is found to result mainly from excited-state absorption starting from E\ifmmode\bar\else\textasciimacron\fi{}
(2E), despite the low probability of the latter at the light wavelength used (514.5 nm).
The relaxation of resonant 29-${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$ phonons trapped in a laser-excited cylinder of submillimeter diameter is investigated under the conditions of modulated pumping in ruby of 130, 700, and 2500 at. ppm
Cr3+ at 1.5 K. The decay time
Teff of the 2\ifmmode \bar{A}\else \={A}\fi{}
(2E) population, which is a measure of the phonon relaxation time, appears to depend on the metastable population
N∗ and the cylinder diameter L as the product
N∗L only, establishing boundary-limited phonon decay. At
N∗L below 5\ifmmode\times\else\texttimes\fi{}
1015 ${\mathrm{cm}}^{\mathrm{\ensuremath{-}}2}$, pure spatial diffusion prevails.At higher
N∗L, where the measured
Teff levels off at about 1 \ensuremath{\mu}s, dependent on the ground-state concentration, the phonon relaxation is adequately accounted for by the assumption of enhancement by mediation of frequency-shifting Orbach processes at metastable
Cr3+ subject to diagonal exchange with ground-state
Cr3+. Shifts away from resonance to the extent that the phonons escape the zone by ballistic flight are considered active, which predominantly involve distant
Cr3+ neighbors.Furthermore, a random distribution of
Cr3+ is assumed, while the exchange is calibrated with reference to pair spectra. The spin-nonflip transitions of metastable
Cr3+ that are part of the pairs remain at resonance with the phonons because the exchange splittings of \ifmmode \bar{E}\else \={E}\fi{}
(2E) and 2\ifmmode \bar{A}\else \={A}\fi{}
(2E) are comparable. This is borne out by a separate calculation based on a perturbative molecular field. In addition, experiments have been performed as a function of an external magnetic field up to 4 T parallel to the c axis to disclose the effects of successive separation of the spin-flip and spin-nonflip transitions. The resultant complex development of
Teff with field as well as similar data on the
R2 luminescent intensity taken with continuous optical pumping are consistent with exchange-invoked relaxation and, further, yield effective spectral widths of the 29-${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$ transitions of the weakly coupled metastable
Cr3+ of order 1 ${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$.
Fluorescence-line-narrowing and time-resolved studies have been conducted in ruby crystals and powders, in concentrations varying from 0.025 to 0.9 at.%. The resonance fluorescence component of the
R1 line at low temperatures is observed to increase dramatically as the laser is tuned from line center toward the low-energy wing of the inhomogeneously broadened absorption. This is presumed to indicate the presence of weakly coupled pairs in the wings of the line. Intraline and interline (${R}_{1}\ensuremath{\rightarrow}{N}_{1,2}$) energy transfer have also been studied, and an elaboration of earlier work is given. Time-resolved selective-excitation scans have revealed numerous channels in the vicinity of the
R lines by which the different pairs can be directly excited. These are assumed to be Cr ions near enough to a pair to be in a highly perturbed environment. Various experimental results are shown to be consistent with a model of rapid transfer between resonant Cr ions which feeds the pairs via a weak, nonresonant coupling to these perturbed ions. Macroscopic strain broadening is also shown to be favored over microscopic broadening, and the implications for Anderson localization in ruby are discussed.
The first experimental evidence for distinct spectral and spatial energy transfer in ruby via nonradiative coupling is presented. Monochromatic laser excitation of the
R1 line results in a rise of the inhomogeneous background on a millisecond time scale, consistent with a one-phonon---assisted process and contrary to recent theory. However, time-resolved studies of trap fluorescence suggest a rapid, coherent, spatial transfer within the
R1 line which does not shift frequency.