Probing the role of thermal vibrational disorder in the SPT of VO[Formula: see text] by Raman spectroscopy.

Phase competition in transition metal oxides has attracted remarkable interest for fundamental aspects and technological applications. Here, we report a concurrent study of the phase transitions in undoped and Cr-doped VO[Formula: see text] thin films. The structural, morphological and electrical properties of our films are examined and the microstructural effect on the metal-insulator transition (MIT) are highlighted. We further present a distinctive approach for analyzing the Raman data of undoped and Cr-doped VO[Formula: see text] thin films as a function of temperature, which are quantitatively correlated to the electrical measurements of VO[Formula: see text] films to give an insight into the coupling between the structural phase transition (SPT) and the MIT. These data are also combined with reported EXAFS measurements and a connection between the Raman intensities and the mean Debye-Waller factors [Formula: see text] is established. We found that the temperature dependence of the [Formula: see text] as calculated from the Raman intensity retraces the temperature profile of the [Formula: see text] as obtained from the EXAFS data analysis. Our findings provide an evidence on the critical role of the thermal vibrational disorder in the VO[Formula: see text] phase transitions. Our study demonstrates that correlating Raman data with EXAFS analysis, the lattice and electronic structural dynamics can be probed.

A comparative Raman study between PrMnO 3, NdMnO 3, TbMnO 3 and DyMnO 3.

In this paper, we present a detailed Raman study of the non-multiferroic compounds PrMnO 3 and NdMnO 3 and the multiferroic compounds TbMnO 3 and DyMnO 3 as a function of temperature and magnetic field. All studied systems show anomalous phonon shifts close to the Néel transition T N . In PrMnO 3 and NdMnO 3, the frequency softenings are partly attributed to an orbital-spin-phonon coupling whereas in TbMnO 3 and DyMnO 3, the relatively weak frequency shifts are rather attributed to an expansion of the Mn-O bond lengths. On the other hand, the frequencies of TbMnO 3 phonons are shifted as a function of magnetic field, while those of PrMnO 3 remain unaffected. These frequency shifts are interpreted in terms of local oxygen rearrangements under magnetic field that could play an important role in the multiferroicity of TbMnO 3 and DyMnO 3.