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Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE

Echo spectroscopy of TLS of multiwell adiabatic potential for Pr3+activator centers in Y 2 SiO 5

Yu. V. Malyukin, R.S. Borysov, P.N. Zhmurin, Alexander N. Lebedenko, Boris V. Grinyov, N. I. Znamenskii, Eduard A. Manykin, Yu. V. Orlov, Evgenii A Petrenko, T. G. Yukina

Published May 30, 2002• 0 citations
Publisher

Abstract

Based on the investigation of the temperature dependence of the two-pulse phonon echo amplitude on the 3H4 3Po resonant optical transition of the Pr3+ doped ions in the Y2SiO5 crystal, unusual for crystals, low-temperature mechanisms of Pr3+ spectral line broadening caused by the interaction of doped ions with TLS have been found. The constants characterizing the interaction of the doped Pr3+ ions with phonons and TLS have been determined.

DOI
10.1117/12.468957

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Physical review. B, Condensed matter•Sep 1, 1998•58 citations
Based on the investigation of the temperature dependence of the two-pulse phonon echo amplitude on the 3H4 3Po resonant optical transition of the Pr3+ doped ions in the Y2SiO5 crystal, unusual for crystals, low-temperature mechanisms of Pr3+ spectral line broadening caused by the interaction of doped ions with TLS have been found. The constants characterizing the interaction of the doped Pr3+ ions with phonons and TLS have been determined.
Experimental results on the investigation of low-temperature optical absorption spectra and temperature dependence of the photon echo (PE) amplitude signal in Y2SiO5:Pr3+ and LaF3:Pr3+ crystals at the transition H43(0)−3P0 of the Pr3+ ion are presented. It is shown that additional relaxation channels exist for PE in addition to the known phonon mechanisms. This is associated in a LaF3:Pr3+ crystal with the temperature variation of dipole moment at the Pr3+ ion transition. In a Y2SiO5:Pr3+ crystal, this is due to the thermally activated transitions for the Pr3+ ion between nonequivalent positions in the crystal lattice.
In a Y2SiO5:Pr3+ crystal characterized by two non-equivalent Pr3+ optical centers, the interaction mechanisms between Pr3+ ions as well as between Pr3+ ions and a crystal lattice have been studied. It has been shown that along with the electron-phonon interaction, the interaction between Pr3+ ions and two-level systems made an additional contribution to the homogeneous linewidth of the 3H4↔3P0 optical transition. Two different mechanisms of the Pr3+ interionic coupling have been found. The first mechanism is associated with a dipole-dipole interaction between non-equivalent Pr3+ optical centers, while the other one is governed by a cooperative cross relaxation of the excitation energy among the same type Pr3+ optical centers.
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.