We investigated the electronic structure and lattice dynamics of double perovskite NdBaMn2O6 single crystals through spectroscopic ellipsometry and Raman scattering spectroscopy. The optical absorption band centered at approximately 0.88 eV was assigned to on-site d–d transitions in Mn, whereas the optical feature at approximately 4.10 eV was assigned to charge-transfer transitions between the 2p state of O and 3d state of Mn. Analysis of the temperature dependence of the d-d transition indicated anomalies at 290 and 235 K. The activated phonon mode, which appeared at approximately 440 cm−1 alongside with the enhancement of the 270 cm−1 phonon mode, coupled strongly to the metal–insulator transition at 290 K, which was associated with a charge/orbital ordering. Moreover, the MnO6 octahedral breathing mode at 610 cm−1 exhibited softening at a temperature lower than 235 K (temperature of the antiferromagnetic phase transition), which revealed the strong coupling between the lattice and magnetic degrees of freedom. The spin–phonon coupling constant obtained was λ = 2.5 cm−1. These findings highlight the importance of charge–orbital–spin interactions in establishing NdBaMn2O6 phases with novel properties.
CuB 2 O 4 has attracted considerable attention because of its unique chemical and physical properties and potential practical applications. In this paper, we investigated the optical properties of CuB 2 O 4 single crystals through spectroscopic ellipsometry and Raman scattering spectroscopy. The optical absorption spectrum at room temperature revealed a direct band gap at approximately 3.88 ± 0.01 eV and two bands near 4.49 and 5.90 eV. The observed bands were related to charge transfer of electrons from the 2p states of the oxygen ions to the 3d states of the copper ions. The band gap exhibited unusual redshift with a decrease in temperature. Upon cooling across 21 K, which is the canted antiferromagnetic ordering temperature, the band gap, peak energy, and normalized intensity of charge-transfer bands presented anomalies. Furthermore, 38 phonon modes were identified in the room-temperature Raman scattering spectrum of CuB 2 O 4 . The phonon modes at approximately 335, 393, 403, 445, 473, 598, 706, 787, and 900 cm −1 exhibited softening below 21 K. The spin−phonon coupling constants were estimated to be 0.02−0.03 cm −1 . These findings highlight a complex nature of spin− charge−lattice interactions in CuB 2 O 4 .
The double perovskite YBaMn 2 O 6 exhibited complex structural, magnetic, and charge/orbital ordering phase transitions. In this paper, we investigated the correlation between the temperature-dependent optical response and complex phase transitions of YBaMn 2 O 6 single crystals through spectroscopic ellipsometry and Raman scattering spectroscopy. The room temperature optical absorption spectrum of YBaMn 2 O 6 revealed three bands of approximately 1.50, 4.05, and 5.49 eV. The lowest optical absorption band was assigned to on-site d–d transitions in Mn ions, whereas the other two optical features were assigned to charge-transfer transitions between the 2p states of O and 3d states of Mn. The room temperature Raman scattering spectrum revealed 25 phonon modes. Notably, the MnO 6 octahedral tilting and bending modes between 360 and 440 cm –1 increased in intensity at temperatures <200 K. Furthermore, several new phonon peaks appeared at temperatures <200 K, which were associated with charge ordering. Additionally, the magnetic order-induced changes were observed in the breathing modes, with reduced intensity of the 620 cm –1 and a substantial enhancement of the 644 cm –1 phonon peaks. The Jahn–Teller mode at approximately 496 cm –1 exhibited strong hardening at temperatures <200 K, which indicated a linear correlation with the square of the magnetic susceptibility and thus revealed the occurrence of spin–phonon coupling. Anomalies in the phonon frequency, line width, and intensity observed near the phase transition temperatures highlighted the importance of lattice–charge–spin interactions in YBaMn 2 O 6 .
Copper metaborate had a unique crystal structure and exhibited noteworthy magnetic phase transitions at 21 and 10 K.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.