Crystalline environment of luminescent Tb3+ ions embedded in indium tin oxide thin films: A DFT and crystal field analysis assessment
Resumen
We assess the local symmetry and crystal environment of trivalent terbium ions embedded in an indium tin oxide matrix with bixbyite structure. The Tb3+ ions tend to substitute In3+ ions in two different cationic sites (𝑏 and 𝑑). Density functional theory calculations suggest that the Tb3+ ions are mainly located at 𝐶2 symmetry sites, relaxing selection rules and enabling electric dipole transitions, with the 5 𝐷 4 → 7 𝐹 2 transition being the most intense, providing a red color to the light emission. Photoluminescence emission spectrum under UV excitation at 83 K revealed 30 intra-4𝑓 transitions, which were assigned to the 7 𝐹 𝐽 ground multiplet of the Tb3+ ion. Crystal field analysis shows a strong alignment between calculated and observed energy levels, yielding a standard deviation of 𝜎=15.1cm−1. We believe these results can help to understand the activation mechanisms of Tb3+ luminescent centers in transparent conductive oxides, as well as the potential to modulate Tb3+ emission color through its crystalline environment.
We assess the local symmetry and crystal environment of trivalent terbium ions embedded in an indium tin oxide matrix with bixbyite structure. The Tb3+ ions tend to substitute In3+ ions in two different cationic sites (b and d). Density functional theory calculations suggest that the Tb3+ ions are mainly located at C2 symmetry sites, relaxing selection rules and enabling electric dipole transitions, with the D45→F27 transition being the most intense, providing a red color to the light emission. Photoluminescence emission spectrum under UV excitation at 83 K revealed 30 intra-4f transitions, which were assigned to the FJ7 ground multiplet of the Tb3+ ion. Crystal field analysis shows a strong alignment between calculated and observed energy levels, yielding a standard deviation of σ=15.1cm-1. We believe these results can help to understand the activation mechanisms of Tb3+ luminescent centers in transparent conductive oxides, as well as the potential to modulate Tb3+ emission color through its crystalline environment.
