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Journal of Luminescence

Q-switching of phonon amplification in ruby by pulsed inhomogeneous magnetic fields

Peter A. Fokker, Richard S. Meltzer, J. I. Dijkhuis, H. W. de Wijn

Published Jul 1, 1992• 0 citations
Publisher
DOI
10.1016/0022-2313(92)90101-e

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Diffusion of bottlenecked 29- cm−1 phonons in optically excited ruby

J. I. Dijkhuis, H. W. de Wijn

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 ${R}_{2}$ 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 ${\mathrm{Cr}}^{3+}$ populations in the two-level scheme ($2\overline{A}$,$\overline{E}$) 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.

Physical review. B, Condensed matter•Sep 1, 1979•27 citations
Avalanches of phonons are generated following population inversion of the Zeeman-split E‾(2E)\overline{E}(^{2}E)E(2E) Kramers doublet in a single crystal of dilute ruby (Al2O3:Cr3+)({\mathrm{Al}}_{2}{\mathrm{O}}_{3}:{\mathrm{Cr}}^{3+})(Al2​O3​:Cr3+) at 1.4K1.4\phantom{\rule{0.3em}{0ex}}\mathrm{K}1.4K. The inversion is achieved in a narrow zone of limited extent by selective pulsed optical pumping, and the phonons are detected via luminescence. The associated acoustic wave emanating from the zone propagates through the crystal, reverberates in the acoustic cavity formed by the crystalline end faces, and engages in further amplification each time it passes through the zone until the inversion becomes exhausted. The systems thus acts as a saser (sound amplification by stimulated emission of radiation). The avalanche is adequately described by coherent Bloch equations governing the acoustic wave and the interacting spin polarization, the losses being due to surface scattering and divergence. This conclusion holds good upon reducing the resonance length of the zone by a gradient magnetic field. Finally, the frequency and angular distributions of the avalanche are measured by using two disjunct zones located at opposite ends of the crystal, one serving as generator and the other as detector, in conjunction with a gradient field and lateral displacement. The frequency spread is found to be compatible with the inhomogeneously broadened transition within E‾(2E)\overline{E}(^{2}E)E(2E), while the angular divergence is determined by the geometry of the zone.
It is demonstrated that a magnetic-field gradient can suppress amplified stimulated emission of phonons taking place within the Zeeman-split E-bar(2{(}^{2}(2E) doublet of Cr3+{\mathrm{Cr}}^{3+}Cr3+ in 700 ppm ruby. The doublet is initially inverted by selective pulsed optical pumping. The field gradient produces a gradient in the transition frequency, thereby reducing the gain of the amplifying medium. The experiments are described with rate equations in which the gain is accounted for by the interaction length over which the phonons remain at resonance.
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∗{N}^{*}N∗ up to ${N}^{*}\ensuremath{\sim}3\ifmmode\times\else\texttimes\fi{}{10}^{17}/{\mathrm{cm}}^{3}$. At higher N∗{N}^{*}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{R}_{2}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∗{N}^{*}N∗ and ground-state concentration. Rate equations governing the Cr3+{\mathrm{Cr}}^{3+}Cr3+ populations in the two-level scheme (2A‾2\overline{A}2A,E‾\overline{E}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 RRR 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.