Elucidating the Multisite and Multivalence Nature of Mn Ions in Solids and Predicting Their Optical Transition Properties: A Case Study on a Series of Garnet Hosts.

Abstract

The abundant site occupancy and optical transitions of multivalence Mn dopants in luminescent materials have attracted much attention. Here, detailed first-principles calculations based on density functional theory have been carried out to clarify the multisite and multivalence nature of Mn ions in solids and predict their optical transition properties by using garnets as prototype systems. The formation energies of dodecahedral, octahedral, and tetrahedral coordinated Mn dopants are evaluated with chemical potential environments, and the preferable site occupancy and valence state of Mn ions in three garnet systems are clarified. The results show that even in a fixed atmosphere, taking Ca3Al2Ge3O12 in air as an example, not only can the preference of Mn ions switch between dodecahedral and octahedral sites, but also can the valence state change from Mn2+ to Mn3+ and Mn4+. Furthermore, for all of the three garnet systems, the calculation results of the energy-level structure and photoluminescence of Mn ions at different sites in the different valence states provide a reliable interpretation of the available spectroscopic data. The proposed first-principles scheme, with general applicability and encouraging predictive power, provides an effective approach for elucidating and characterizing the site occupancy, valence state, and optical transition of Mn activators in insulators, and will greatly benefit the design and optimization of related materials.