Stimulated-emission cross-sections of trivalent erbium ions in the cubic sesquioxides Y2O3, Lu2O3, and Sc2O3

Abstract

We report on a detailed revision of the spectroscopic properties of Er3+ ions in the cubic sesquioxide host crystals R2O3 (R = Y, Lu and Sc). The 4f-4f transition probabilities are calculated by applying a modified Judd-Ofelt theory accounting for configuration interaction based on the measured absorption spectra. The stimulated-emission cross-sections for the 4I11/2 → 4I13/2 (at ∼2.8 µm) and 4I13/2 → 4I15/2 (at ∼1.6 µm) transitions of Er3+ ions are determined and the luminescence dynamics from the 4I11/2 and 4I13/2 manifolds are studied at different temperatures. It is found that the luminescence lifetime of the 4I11/2 state strongly depends on the host-forming R3+ cation even at low temperatures due to a non-negligible non-radiative multiphonon decay channel. Er:Y2O3 exhibits the lowest phonon energies and consequently the longest 4I11/2 luminescence lifetimes. A disagreement between the absorption and emission probabilities for the 4I15/2 ↔ 4I11/2 transition of Er3+ ions is observed at room temperature and explained considering the distribution of Er3+ ions over two non-equivalent crystallographic sites, C2 and C3i.