Abstract
Optical absorption, fluorescence, and paramagnetic-resonance experiments on single crystals of β-Ga2 O3 doped with chromium were performed from room temperature down to a few degrees Kelvin. All the important low-lying energy levels have been identified from the optical data. The average positions of the three sets of sharp lines (doublet transitions) are almost identical to those of ruby, whereas the two prominent bands (quartet transitions) are broadened and shifted to the red for Ga2 O3. Comparison of the 77°K absorption data with octahedral crystal-field calculations for the d3 configuration yielded the values B=700 cm1 and DqB=2.35. Fluorescence is observed from the E2 to A24 transition with a room-temperature lifetime of 0.23 msec. At 77°K these emission peaks occur at 6885 and 6956 Å. The fluorescence efficiency of crystals grown from different starting materials varied considerably, but the factors that give rise to this variation are only partly understood. The spin Hamiltonian parameters for the A24 ground state were determined from X-band paramagnetic-resonance measurements and are: D=14.01 kMc/sec, E=+6.14 kMc/sec, gx=1.978, gy=1.978, and gz=1.983 for the z axis along [010]. The zero-field ground-state splitting was observed at a frequency of 35.18 kMc/sec. Calculations for the angular spectrum using this spin Hamiltonian are in excellent agreement with the X-band measurements. The possibility of using Cr3+ in Ga2 O3 as the active material in an optical or microwave maser is briefly discussed.

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