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Quantum Electronics

Excited-state absorption spectroscopy of Nd3+:SrF2crystals in the 1280 — 1320 nm spectral wavelength range

B. K. Sevast’yanov, А. Г. Охримчук, В. В. Набатов, Yu. N. Martyshev, Tasoltan T. Basiev, Maxim E. Doroshenko, Vyacheslav V Osiko, A.G. Papashvili

Published Feb 28, 1999• 2 citations
Publisher

Abstract

The excited-state absorption (ESA) in Nd 3+ :SrF 2 crystals was investigated in the 1280 — 1320 nm spectral wavelength range by selective laser excitation. It was found that, on excitation at wavelengths of 743 and 800.5 nm, there is no ESA in the ranges 1304 — 1309 and 1295 — 1297 nm. Weak ESA bands are observed in the 1297 — 1304 and 1309 — 1320 nm ranges and the differential ESA cross section does not exceed 0.3 × 10 -21 cm 2 . The results indicate that the ESA does not preclude the use of an Nd 3+ :SrF 2 crystal as the amplifying medium in the wavelength range 1280 — 1320 nm.

DOI
10.1070/qe1999v029n02abeh001428

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Journal of Applied Physics•Apr 15, 1996•21 citations
The excited-state absorption (ESA) in Nd 3+ :SrF 2 crystals was investigated in the 1280 — 1320 nm spectral wavelength range by selective laser excitation. It was found that, on excitation at wavelengths of 743 and 800.5 nm, there is no ESA in the ranges 1304 — 1309 and 1295 — 1297 nm. Weak ESA bands are observed in the 1297 — 1304 and 1309 — 1320 nm ranges and the differential ESA cross section does not exceed 0.3 × 10 -21 cm 2 . The results indicate that the ESA does not preclude the use of an Nd 3+ :SrF 2 crystal as the amplifying medium in the wavelength range 1280 — 1320 nm.
The polarised two-photon (IR) and one-photon (visible) luminescence excitation spectra of Nd 3+ nanoclusters in CaF 2 and SrF 2 crystals are measured at 10 K using a :LiF colour centre laser tunable in spectral ranges 1090 — 1230 nm and 545 — 615 nm with an emission linewidth of ~0.02 — 0.03 cm -1 , an average output power of ~55 mW, and a pulse repetition rate of 10 Hz. The two-photon excitation spectra at the 4 I 9/2 → 4 G 5/2 transition reveal the structure, which is absent upon one-photon excitation, which can be explained by different selection rules for some Stark — Stark transitions upon one- and two-photon absorption.
The optical-absorption transitions originating from the lowest 4f5d excited state of Pr3+{\mathrm{Pr}}^{3+}Pr3+ in Y3{\mathrm{Y}}_{3}Y3​Al5{\mathrm{Al}}_{5}Al5​O12{\mathrm{O}}_{12}O12​ have been studied. The experimental arrangement uses a 7-ns 266-nm light pulse to populate the lowest 4f5d state, and a spatially overlapped, time-sequenced pulse from a frequency-tunable dye laser to induce transitions from that excited state. The excited-state-absorption (ESA) spectrum covering the 900--300-nm probe wavelength range is characterized by two broad peaks centered at 700 and 350 nm on a slowly rising background. The peak ESA cross section at 355 nm is (1\ifmmode\pm\else\textpm\fi{}0.1)\ifmmode\times\else\texttimes\fi{}${10}^{\mathrm{\ensuremath{-}}17}$ cm2{\mathrm{cm}}^{2}cm2. The position, shape, and strength of the spectrum suggest that the terminal states of the ESA transitions are the second 4f5d state of Pr3+{\mathrm{Pr}}^{3+}Pr3+ and the conduction band of the host lattice. The ESA measurements have been extended to transitions from the 3^{3}3P0{\mathit{P}}_{0}P0​ and 1^{1}1D2{\mathit{D}}_{2}D2​ excited states of the 4f2{\mathit{f}}^{2}f2 configuration of Pr3+{\mathrm{Pr}}^{3+}Pr3+ as well. The ESA cross sections at a probe wavelength of 532 nm are (8\ifmmode\pm\else\textpm\fi{}1)\ifmmode\times\else\texttimes\fi{}${10}^{\mathrm{\ensuremath{-}}19}$ cm2{\mathrm{cm}}^{2}cm2 and (5.7\ifmmode\pm\else\textpm\fi{}0.6)\ifmmode\times\else\texttimes\fi{}${10}^{\mathrm{\ensuremath{-}}19}$ cm2{\mathrm{cm}}^{2}cm2 for transitions from the 3^{3}3P0{\mathit{P}}_{0}P0​ and 1^{1}1D2{\mathit{D}}_{2}D2​ excited states, respectively. The terminal state of ESA transitions from these two levels is the lowest 4f5d state. The strong ESA completely inhibits the potential laser action based on emission from these states in this crystal.
We have measured the pump-probe spectrum for CaF2:Sm2+ over a wide (360–1020 nm) spectral range. We observed gain throughout most of the 730-nm emission band, although there is some evidence of excited-state absorption (ESA) in this region. A much stronger ESA was observed near 500 nm. The temperature dependence of the ESA signal clearly indicates that the absorption is associated with divalent samarium. Because of the width and strength of this transition, we assign the ESA to a 4f55d → conduction band transition. We calculated the oscillator strength for this ESA band to be 0.10 and rationalized its magnitude based on an intensity-borrowing mechanism that involves the transition from the valence band to the conduction band.