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Physical review. B, Condensed matter

Photon-echo attenuation in rare-earth-ion-doped crystals

Stefan B. Altner, G. Zumofen, Urs P. Wild, Masaharu Mitsunaga

Published Dec 15, 1996• 22 citations
Publisher

Abstract

We study the optical properties of rare-earth-ion-doped inorganic crystals with an emphasis on the dependence of two-pulse photon echoes on the excitation density in the system. The experimental investigations concentrate on ${\mathrm{Pr}}^{3+}$:${\mathrm{Nd}}^{3+}$:${\mathrm{Eu}}^{3+}$ codoped ${\mathrm{Y}}_{2}$Si${\mathrm{O}}_{5}$ and YAl${\mathrm{O}}_{3}$ crystals at low temperatures. With two pulses of one laser the echo is induced in one ion species and with a third, "scrambler" pulse of a second laser another species is excited. These scrambler excitations lead to a dephasing and thus to an echo attenuation which depends on the strength, frequency, and time of the scrambler pulse. The spectral sensitivity of the echo attenuation is used for a spectroscopic technique: "photon-echo attenuation spectroscopy." As a function of the delay time ${t}_{s}$ between the scrambler pulse and the onset of the two-pulse echo sequence the attenuation shows a very specific behavior dictated by the excitation-induced frequency shifts (EFS's). For ${t}_{s}$ between the two echo-inducing pulses the echo intensity is partially regained by the "dephasing-rephasing balancing" of the reversible EFS's. For the theoretical description a stochastic model is introduced and the dephasing by excitation-induced lattice vibrations and by EFS's are analyzed in detail. The present results are discussed in the light of previous experimental and theoretical investigations.

DOI
10.1103/physrevb.54.17493

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Journal of Nanoscience and Nanotechnology•Mar 1, 2008•1 citation
We study the optical properties of rare-earth-ion-doped inorganic crystals with an emphasis on the dependence of two-pulse photon echoes on the excitation density in the system. The experimental investigations concentrate on Pr3+{\mathrm{Pr}}^{3+}Pr3+:Nd3+{\mathrm{Nd}}^{3+}Nd3+:Eu3+{\mathrm{Eu}}^{3+}Eu3+ codoped Y2{\mathrm{Y}}_{2}Y2​SiO5{\mathrm{O}}_{5}O5​ and YAlO3{\mathrm{O}}_{3}O3​ crystals at low temperatures. With two pulses of one laser the echo is induced in one ion species and with a third, "scrambler" pulse of a second laser another species is excited. These scrambler excitations lead to a dephasing and thus to an echo attenuation which depends on the strength, frequency, and time of the scrambler pulse. The spectral sensitivity of the echo attenuation is used for a spectroscopic technique: "photon-echo attenuation spectroscopy." As a function of the delay time ts{t}_{s}ts​ between the scrambler pulse and the onset of the two-pulse echo sequence the attenuation shows a very specific behavior dictated by the excitation-induced frequency shifts (EFS's). For ts{t}_{s}ts​ between the two echo-inducing pulses the echo intensity is partially regained by the "dephasing-rephasing balancing" of the reversible EFS's. For the theoretical description a stochastic model is introduced and the dephasing by excitation-induced lattice vibrations and by EFS's are analyzed in detail. The present results are discussed in the light of previous experimental and theoretical investigations.
We study the photon-echo attenuation by various dynamical processes in rare-earth-ion-doped crystals. The experimental investigations concentrate on a Pr3+:Eu3+:Nd3+{\mathrm{Pr}}^{3+}:{\mathrm{Eu}}^{3+}:{\mathrm{Nd}}^{3+}Pr3+:Eu3+:Nd3+ codoped Y2SiO5{\mathrm{Y}}_{2}{\mathrm{SiO}}_{5}Y2​SiO5​ crystal at low temperatures. Two-pulse photon-echo intensities are measured as a function of the pulse intensities when either the Pr3+{\mathrm{Pr}}^{3+}Pr3+ or the Eu3+{\mathrm{Eu}}^{3+}Eu3+ ions are excited. For the quantitative interpretation we consider primarily excitation-induced frequency shifts (EFS) by diagonal and off-diagonal interactions and show that for the systems under consideration EFS are dominated by diagonal interactions. The observed echo attenuation by EFS is compared with the predictions calculated from independent Stark-field measurements and reasonable agreement is obtained. The broadening by spin-ion interactions, by nonequilibrium phonons and the dependence of the echo attenuation on the frequency position in the inhomogeneously broadened band are further investigated.
The excitation dephasing in solids resulting from the interaction with neighboring species' excitations is investigated. The frequency shifts due to these interactions are identified by the observation of partial dephasing-rephasing balancing in bichromatic photon-echo experiments applied to rare-earth ion doped crystals. The experimental observations are in good agreement with the predictions obtained from a model which accounts for the disorder in the crystal and for the stochastic nature of the excitations.
Eu-doped yttrium orthosilicate (Eu(3+) : Y2SiO5) had been a subject being investigated for coherent time-domain optical memory and information processing applications since its ultraslow optical dephasing was discovered several years ago. In this crystal the weakly allowed (7)F0 - (5)D0 transition of europium ions exhibits a sufficient long dephasing time and no spectral difli.usion on a time scale of several hours at low temperature, thus an information pattern or data can be stored as a population grating in the ground state hyperfine levels. On the other hand, the study on photon-echo relaxation shows that the dephasing time T2 of Eu (3+) and other rare-earth ions doped YAG, YAlO3 strongly depends on the intensity of the excitation pulses. In Eu (3+) :YAlO3, an exponential decay of photon-echo with T2 = 53 microseconds if the excitation pulses are weak (5 vJ/pulse) was observed. However, when the excitation pulses are strong (80 pJ/pulse) they observed a much shortened T2 with a highly nonexponential decay pattern. The conclusion they derived is that the intensity-dependent dephasing rate effects are quite general, and it depends on how much the excitation intensity varies. In this paper we use transient grating formation technique showing that a temporal lattice distortion may only occur along crystal c axis, caused by EU (3+) excitation. At high excitation level the produced exciton in conduction band may also couple to the dynamical lattice relaxation process, giving rise to an apparently much shortened dephasing time.
When the intensity of photon echo in a two-level system is measured as a function of delay time of the two input pulses, one obtains a simple exponential decay with the characteristic phase relaxation time. When the two levels contain hyperfine structures, the interference among the hyperfine levels gives rise to modulation of the decay envelope. The Fourier transform of the modulation pattern reveals the hyperfine structure of the rare-earth ions. The hyperfine structure, and therefore the modulation pattern, are both sensitively affected by the crystal environment of the ionic site. We extend photon-echo modulation spectroscopy to three-pulse, stimulated photon-echo modulation, and we find that the stimulated echo modulation patterns are quite distinct from the two-pulse, photon-echo case and are affected by a different set of atomic and crystal interaction parameters. The modulation is measured, in several photon-echo transitions of praseodymium ions in lanthanum trifluoride and yttrium aluminum garnet crystals, as functions of delay times between first and second pulses and between first and third pulses. Comparison of the experimental results with density-matrix calculations allows us to determine hyperfine parameters that are not easily observed with two-pulse echo modulation.
A detailed description is presented of photon echo experiments in Nd3+{\mathrm{Nd}}^{3+}Nd3+-doped silica optical fibers at temperatures below 1 K. Dephasing rates ${T}_{2}^{\mathrm{\ensuremath{-}}1}$ have been obtained from two-pulse echo sequences at 0.89 \ensuremath{\mu}m and are found to follow a T1.3{T}^{1.3}T1.3 temperature dependence. An interpretation of this result is presented which invokes the interaction of tunneling systems with the optical ions via a dipole-dipole elastic interaction. The dynamics of the interaction originates in a spectral diffusion process and three pulse stimulated echo experiments confirm this interpretation.
Optical dephasing of Pr3+ and Tm3+ ions doped in transparent oxyfluoride glass ceramics was studied with the two-pulse photon echo technique. It was found that the dephasing time of rare earth ions is dramatically less in nanocrystals embedded in a glass matrix than in bulk crystals. A quasi-linear temperature dependence obtained at low temperatures proved that the long-range interaction of the ions inside the nanocrystals with the two level systems of the glass matrix dominates the optical dephasing. The local thermal effect in glass ceramics containing nanocrystals elevates the local temperature, which results in the reduction of optical dephasing time. For Tm(3+)-doped glass ceramics, the elevation of local temperature induced by the irradiation of excitation laser even quenched the photon echo signals in the experimental study.