Do you want to publish a course? Click here

Wustite: Electric, thermodynamic and optical properties of FeO

162   0   0.0 ( 0 )
 Added by Florian Schrettle
 Publication date 2012
  fields Physics
and research's language is English




Ask ChatGPT about the research

We report on a systematic optical investigation of wustite. In addition, the sample under consideration, Fe0.93O, has been characterized in detail by electrical transport, dielectric, magnetic and thermodynamic measurements. From infrared reflectivity experiments, phonon properties, Drude-like conductivity contributions and electronic transitions have been systematically investigated. The phonon modes reveal a clear splitting below the antiferromagnetic ordering temperature, similar to observations in other transition-metal monoxides and in spinel compounds which have been explained in terms of a spin-driven Jahn-Teller effect. The electronic transitions can best be described assuming a crystal-field parameter Dq = 750 cm-1 and a spin-orbit coupling constant lambda = 95 cm-1. A well defined crystal field excitation at low temperatures reveals significant broadening on increasing temperature with an overall transfer of optical weight into dc conductivity contributions. This fact seems to indicate a melting of the on-site excitation into a Drude behavior of delocalized charge carriers. The optical band gap in wustite is close to 1.0 eV at room temperature. With decreasing temperatures and passing the magnetic phase transition we have detected a strong blue shift of the correlation-induced band edge, which amounts more than 15% and has been rarely observed in antiferromagnets.

rate research

Read More

179 - S. Widmann , A. Gunther , E. Ruff 2016
The lacunar spinel GeV4S8 undergoes orbital and ferroelectric ordering at the Jahn-Teller transition around 30 K and exhibits antiferromagnetic order below about 14 K. In addition to this orbitally driven ferroelectricity, lacunar spinels are an interesting material class, as the vanadium ions form V4 clusters representing stable molecular entities with a common electron distribution and a well-defined level scheme of molecular states resulting in a unique spin state per V4 molecule. Here we report detailed x-ray, magnetic susceptibility, electrical resistivity, heat capacity, thermal expansion, and dielectric results to characterize the structural, electric, dielectric, magnetic, and thermodynamic properties of this interesting material, which also exhibits strong electronic correlations. From the magnetic susceptibility, we determine a negative Curie-Weiss temperature, indicative for antiferromagnetic exchange and a paramagnetic moment close to a spin S = 1 of the V4 molecular clusters. The low-temperature heat capacity provides experimental evidence for gapped magnon excitations. From the entropy release, we conclude about strong correlations between magnetic order and lattice distortions. In addition, the observed anomalies at the phase transitions also indicate strong coupling between structural and electronic degrees of freedom. Utilizing dielectric spectroscopy, we find the onset of significant dispersion effects at the polar Jahn-Teller transition. The dispersion becomes fully suppressed again with the onset of spin order. In addition, the temperature dependencies of dielectric constant and specific heat possibly indicate a sequential appearance of orbital and polar order.
We present the results of the magnetic and specific heat measurements on V4 tetrahedral-cluster compound GaV4S8 between 2 to 300K. We find two transitions related to a structural change at 42K followed by ferromagnetic order at 12K on cooling. Remarkably similar properties were previously reported for the cluster compounds of Mo4. These compounds show an extremely high density of low energy excitations in their electronic properties. We explain this behavior in a cluster compound as due to the reduction of coulomb repulsion among electrons that occupy highly degenerate orbits of different clusters.
Effects of bond randomness and site dilution are systematically investigated for the Kitaev model describing a quantum spin liquid with fractional excitations of itinerant Majorana fermions and localized fluxes. We find that, in the high-temperature region where the itinerant Majorana fermions release their entropy, both types of disorders suppress the longitudinal thermal conductivity while keeping the specific heat almost unchanged. This suggests that both disorders reduce the mean-free path of the Majorana fermions. On the other hand, in the low-temperature region, the other specific heat peak associated with the entropy release from the localized fluxes is suppressed for both cases, but it is broadened and shifted to the lower-temperature side by the bond randomness, while the position and the width are almost unchanged against the site dilution. Contrasting behavior is also found in the thermal Hall effect under a magnetic field; the half quantization of the thermal Hall conductivity is fragile against the site dilution, while it remains for the bond randomness despite the reduced onset temperature. We discuss the contrasting behavior from the stability of the topological nature by calculating flux condensation and Majorana excitation gap.
We present an extensive study of the structural, magnetic and thermodynamic properties of high-quality monocrystals of the two heterometallic oxyborates from the ludwigite family: Cu$_2$GaBO$_5$ and Cu$_2$AlBO$_5$ in the temperature range above 2 K. The distinctive feature of the investigated structures is the selective distribution of Cu and Ga/Al cations. The unit cell of Cu$_2$GaBO$_5$ and Cu$_2$AlBO$_5$ contains four nonequivalent crystallographic sites of metal ions. Two sites in the structure from four nonequivalent crystallographic sites of metal ions of Cu$_2$GaBO$_5$ are fully occupied by Cu atoms which form the quasi one-dimensional chains along the a-axis. For Cu$_2$AlBO$_5$ all sites are partially occupied by Al and Cu atoms. The joint analysis of low-temperature data on magnetic susceptibility and magnetic contribution to the specific heat showed that Cu$_2$AlBO$_5$ and Cu$_2$GaBO$_5$ exhibit an antiferromagnetic transition at $T_{rm N} approx 3$ and 4 K, respectively. The magnetic contributions to the specific heat for both compounds were obtained after subtracting the phonon contribution. It is shown that the external magnetic field above 2.5 T leads to a broadening of the magnetic phase transition indicating suppression of the long-range antiferromagnetic order.
296 - H.T. Lu , Y.H. Su , L.Q. Sun 2004
Thermodynamic properties of a tetrameric bond-alternating Heisenberg spin chain with ferromagnetic-ferromagnetic-antiferromagnetic-antiferromagnetic exchange interactions are studied using the transfer-matrix renormalization group and compared to experimental measurements. The temperature dependence of the uniform susceptibility exhibits typical ferrimagnetic features. Both the uniform and staggered magnetic susceptibilities diverge in the limit $Tto 0$, indicating that the ground state has both ferromagnetic and antiferromagnetic long-range orders. A double-peak structure appears in the temperature dependence of the specific heat. Our numerical calculation gives a good account for the temperature and field dependence of the susceptibility, the magnetization, and the specific heat for Cu(3-Clpy)$_{2}$(N$_{3}$)$_{2}$ (3-Clpy=3-Chloroyridine).
comments
Fetching comments Fetching comments
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا