Effect of trivalent manganese substitution in α-Al2O3 crystal on the absorption spectra based on first-principles calculations

• Main Authors: Novita, M, Nuvitalia, D, Cholifah, N, Ogasawara, K
• Format: Conference Proceeding
• Language: English
• Subjects: Absorption spectra; Aluminum oxide; Crystals; Electrons; Elongation; First principles; Manganese; Molecular orbitals; Optimization; Physics; Substitutes
• ISSN: 1742-6588; 1742-6596
• DOI: 10.1088/1742-6596/1402/6/066004

The absorption spectra of α-Al2O3: Mn3+ at low-spin (LS) state have been estimated based on first-principles calculations without referring to any experimental parameter. The effect of lattice relaxation due to the Mn3+ substitution was considered under several computational procedures such as the Shannon's crystal radii method and the geometry optimization using Cambridge Serial Total Energy Package (CASTEP) code. Two different sizes of model clusters consisting of 7 and 63 atoms were compared. Next, the molecular orbitals (MO) were estimated using the one-electron calculations discrete variational-Xα (DV-Xα) method while the absorption spectra were estimated using the many-electron calculations discrete variational multi-electron (DVME) method. The results show that the lattice-relaxation ratio is about ca. 104.05-106.43% depending on the computational conditions. Due to the Mn-O bond-length elongation, the crystal field splitting (10Dq) decreased ca. 0.24-0.41 eV. Thus, the peak position originating from 3T1 → 3E transition energy shifted toward the lower energy ca. 0.10-0.26 eV. Both of the larger-cluster size and the lattice-relaxation effect decrease the peak energies.