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Optical Materials

On the possibility of laser cooling of Cr3+ ions doped crystals

S.P. Feofilov, A.B. Kulinkin

Published Nov 21, 2017• 10 citations
Publisher
DOI
10.1016/j.optmat.2017.11.002

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Optically pump-induced athermal and nonresonant refractive index changes in the reference Cr-doped laser materials: Cr:GSGG and ruby

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The refractive index of most ion-doped materials increases with the excited state population. This effect was studied in many laser materials, particularly those doped with Cr3+ and rare earth ions, using several techniques, such as interferometry, wave mixing, and Z-scans. This refractive index variation is athermal (has an electronic origin) and is associated with the difference in the polarizabilites of the Cr3+ ion in its excited and ground states, Δαp. The Cr3+ optical transitions in the visible domain are electric-dipole forbidden, and they have low oscillator strengths. Therefore, the major contribution to Δαp has been assigned to allowed transitions to charge transfer bands (CTBs) in the UV with strengths ∼3 orders of magnitude higher. Although this CTB model qualitatively explains the main observations, it was never quantitatively tested. In order to further investigate the physical origin of Δαp in Cr3+-doped crystals, excited state absorption (ESA) and Z-scan measurements were thus performed in Cr:Al2O3 (ruby) and Cr:GSGG. Cr:GSGG was selected because of the proximity of its E2 and T24 emitting levels, and thus the possibility to explore the role of the spin selection rule in the ESA spectra and the resulting variations in polarizability by comparing low and room temperature data, which were never reported before. On the other hand, Cr:Al2O3 (ruby) was selected because it is the only crystal for which it is possible to obtain CTB absorption data from both ground and excited states, and thus for which it is possible to check the CTB model more accurately. Thanks to these more accurate and more complete data, we came to the first conclusion that the spin selection rule does not play any significant role in the variation of the polarizability with the E2–T24 energy mismatch. We also discovered that using the CTB model in the case of ruby would lead to a negative Δαp value, which is contrary to all refractive index variation (including Z-scan) measurements.

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Laser-induced grating measurements were made as a function of laser power and write beam crossing angle for various temperatures between 10 and 300 K on Cr3+ ions in Gd3Ga5O12 (GGG), Gd3Sc2Ga3O12 (GSGG), and GGG mixed with Ca, Mg, and Zr ions. Population gratings were produced in the Cr3+ ions, and the diffusion coefficient describing energy migration among the Cr3+ ions was determined from the grating decay rate. The energy migration was found to increase as the temperature was raised for GGG and to decrease with decreasing temperature for GSGG. This difference is attributed to the differences in the crystal field splittings of the excited states in the two hosts. Enhanced energy diffusion was observed in the multiply doped GGG sample. Contributions to the laser-induced gratings from absorption and dispersion changes were determined, and this was used to provide information on radiationless relaxation and excited state absorption processes. For long writing times, long-lived changes in the refractive index were observed and attributed to optically induced color centers.

Annual Meeting Optical Society of America•Jan 1, 1988•0 citations
The refractive index of most ion-doped materials increases with the excited state population. This effect was studied in many laser materials, particularly those doped with Cr3+ and rare earth ions, using several techniques, such as interferometry, wave mixing, and Z-scans. This refractive index variation is athermal (has an electronic origin) and is associated with the difference in the polarizabilites of the Cr3+ ion in its excited and ground states, Δαp. The Cr3+ optical transitions in the visible domain are electric-dipole forbidden, and they have low oscillator strengths. Therefore, the major contribution to Δαp has been assigned to allowed transitions to charge transfer bands (CTBs) in the UV with strengths ∼3 orders of magnitude higher. Although this CTB model qualitatively explains the main observations, it was never quantitatively tested. In order to further investigate the physical origin of Δαp in Cr3+-doped crystals, excited state absorption (ESA) and Z-scan measurements were thus performed in Cr:Al2O3 (ruby) and Cr:GSGG. Cr:GSGG was selected because of the proximity of its E2 and T24 emitting levels, and thus the possibility to explore the role of the spin selection rule in the ESA spectra and the resulting variations in polarizability by comparing low and room temperature data, which were never reported before. On the other hand, Cr:Al2O3 (ruby) was selected because it is the only crystal for which it is possible to obtain CTB absorption data from both ground and excited states, and thus for which it is possible to check the CTB model more accurately. Thanks to these more accurate and more complete data, we came to the first conclusion that the spin selection rule does not play any significant role in the variation of the polarizability with the E2–T24 energy mismatch. We also discovered that using the CTB model in the case of ruby would lead to a negative Δαp value, which is contrary to all refractive index variation (including Z-scan) measurements.
Laser-induced grating measurements were made as a function of laser power and write beam crossing angle for various temperatures between 10 and 300 K on Cr3+ ions in Gd3Ga5O12 (GGG), Gd3Sc2Ga3O12 (GSGG), and GGG mixed with Ca, Mg, and Zr ions. Population gratings were produced in the Cr3+ ions, and the diffusion coefficient describing energy migration among the Cr3+ ions was determined from the grating decay rate. The energy migration was found to increase as the temperature was raised for GGG and to decrease with decreasing temperature for GSGG. This difference is attributed to the differences in the crystal field splittings of the excited states in the two hosts. Enhanced energy diffusion was observed in the multiply doped GGG sample. Contributions to the laser-induced gratings from absorption and dispersion changes were determined, and this was used to provide information on radiationless relaxation and excited state absorption processes. For long writing times, long-lived changes in the refractive index were observed and attributed to optically induced color centers.