Abstract
We report on the spectroscopic characteristics and upconversion emission in Er 3+ doped Yttria (Y 2 O 3 ) transparent ceramics prepared by a modified two-step sintering method. The near-infrared (1.5 μm) emission properties were evaluated as a function of Er 3+ concentration. Judd-Ofelt intensity parameters, radiative rates, branching ratios, and emission lifetimes were calculated and compared with results reported for Er 3+ doped Y 2 O 3 single crystal and nanocrystals. Following pumping at 1.532 μm, weak blue (~0.41 μm, 2 H 9/2 → 4 I 15/2 ), strong green (~0.56 μm, 2 H 11/2 , 4 S 3/2 → 4 I 15/2 ) and red (~0.67 μm, 4 F 9/2 → 4 I 15/2 ) emission bands were observed as well as weak near-infrared emissions at 0.8 μm ( 4 I 9/2 → 4 I 15/2 ) and 0.85 μm ( 4 S 3/2 → 4 I 13/2 ) at room temperature. The upconversion emission properties under ~1.5 μm pumping were further investigated through pump power dependence and decay time studies. Sequential two-photon absorption leads to the 4 I 9/2 upconversion emission while energy transfer upconversion is responsible for the emission from the higher excited states 2 H 9/2 , 2 H 11/2 , 4 S 3/2 , and 4 F 9/2 . The enhanced red emission with increasing Er 3+ concentration most likely occurred via the cross-relaxation process between ( 4 F 7/2 → 4 F 9/2 ) and ( 4 I 11/2 → 4 F 9/2 ) transitions, which increased the population of the 4 F 9/2 level.
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