Far- and mid-infrared emission and reflectivity of orthorhombic and cubic ErMnO3 : Polarons and bipolarons

Autor: Karsten Holldack, Leire del Campo, Néstor E. Massa, Patrick Echegut, José Antonio Alonso, Vinh Ta Phuoc, Paula Kayser
Rok vydání: 2018
Předmět:
Zdroj: Physical Review B. 98
ISSN: 2469-9969
2469-9950
DOI: 10.1103/physrevb.98.184302
Popis: We report on the high-temperature evolution of far- and mid- infrared reflectivity and emissivity spectra of ambient orthorhombic ErMnO3 from 12 K to sample decomposition above 1800 K. At low temperatures the number of phonons agrees with the predictions for orthorhombic space group D2h16-Pbnm (Z=4) and coexists with a paramagnon spin resonance and rare earth crystal field transitions. Increasing the temperature, a number of vibrational bands undergo profile broadening and softening approaching the orbital disordered phase where the orthorhombic O' lower temperature cooperative phase coexists with cubic-orthorhombic O. O-ErMnO3 undergoes a first order order-disorder transition into the perovskite cubic phase at Tcubic ~1329 K where the three triple degenerate phonons allowed by the space group Pm-3m(Z=1) are identified. At about 800 K, a quantitative small polaron analysis of the orthorhombic mid-infrared real part optical conductivity shows that antisymmetric and symmetric breathing modes sustain the strongest electron-phonon interactions. Above Tcubic the bipolaron fingerprint profile is the mid-infrared dominant and only feature. Its appearance correlates with the localized screening of the highest vibrational mode reststrahlen band. We propose that the longitudinal optical mode macroscopic field screening is consequence of dynamically sharing {\delta} disproportioned eg electrons hovering over the JT distorted octahedral dimer [Mn (QJT)3+{\delta} (Mn(QJT)3-{\delta}))O6/2]2. A thermal driven insulator-metal transition is detected with onset ~1600 K. We also address the occurrence of an inhomogeneity induced THz band result of heating the samples in dry air, triggering Mn3+-Mn4+ double exchange, under the presence of Mn4+ smaller ions stabilizing the orthorhombic lattice.
Databáze: OpenAIRE