Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userWeak ferromagnetism and magnetization reversal in YFe$_{1-x}$Cr$_x$O$_3$
99
0
0.0
(
0
)
Added by
Nagamalleswararao Dasari
Publication date
2015
fields
Physics
and research's language is
English
Ask ChatGPT about the research
No Arabic abstract
We present combined experimental and theoretical studies on the magnetic properties of a solid solution between yttrium orthoferrite and yttrium orthochromite systems, YFe$_{1-x}$Cr$_x$O$_3$ (0 $leq$ x $leq$ 1) where Fe$^{3+}$ and Cr$^{3+}$ ions are distributed randomly at the same crystallographic site (4b). We found that all the compositions exhibit weak ferromagnetism below the Neel temperature that decreases non-linearly with increasing $x$, while certain intermediate compositions ($x = 0.4,0.5$) show a compensation point and magnetization reversal. This unusual behavior is explained based on a simple model comprising the isotropic superexchange and the antisymmetric Dzyaloshinskii-Moriya interactions. This model explains the magnetization behavior in the entire range of doping and temperature including the magnetization reversal which results from an interplay of various DM interactions such as, Fe-O-Fe, Cr-O-Cr and Fe-O-Cr.
rate research
Read More
V2O3 famously features all four combinations of paramagnetic vs antiferromagnetic, and metallic vs insulating states of matter in response to %-level doping, pressure in the GPa range, and temperature below 300 K. Using time-of-flight neutron spectroscopy combined with density functional theory calculations of magnetic interactions, we have mapped and analyzed the inelastic magnetic neutron scattering cross section over a wide range of energy and momentum transfer in the chromium stabilized antiferromagnetic and paramagnetic insulating phases (AFI & PI). Our results reveal an important magnetic frustration and degeneracy of the PI phase which is relieved by the rhombohedral to monoclinic transition at $T_N=185$ K due to a significant magneto-elastic coupling. This leads to the recognition that magnetic frustration is an inherent property of the paramagnetic phase in $rm (V_{1-x}Cr_x)_2O_3$ and plays a key role in suppressing the magnetic long range ordering temperature and exposing a large phase space for the paramagnetic Mott metal-insulator transition to occur.
We report measurements and analyses of resistivity, thermopower, and thermal conductivity of polycrystalline samples of perovskite LaRh$_{1-x}$Ni$_x$O$_3$. The thermopower is found to be large at 800 K (185 $mu$V/K for $x=$0.3), which is ascribed to the high-temperature stability of the low-spin state of Rh$^{3+}$/Rh$^{4+}$ ions. This clearly contrasts with the thermopower of the isostructural oxide LaCoO$_3$, which rapidly decreases above 500 K owing to the spin-state transition. The spin state of the transition-metal ions is one of the most important parameters in oxide thermoelectrics.
We present an investigation of the influence of structural distortions in charge-carrier doped lmco by substituting La$^{3+}$ with alkaline earth metals of strongly different ionic sizes, that is M = Ca$^{2+}$, Sr$^{2+}$, and Ba$^{2+}$, respectively. We find that both, the magnetic properties and the resistivity change non-monotonously as a function of the ionic size of M. Doping lmco with M = Sr$^{2+}$ yields higher transition temperatures to the ferromagnetically ordered states and lower resistivities than doping with either Ca$^{2+}$ or Ba$^{2+}$ having a smaller or larger ionic size than Sr$^{2+}$, respectively. From this observation we conclude that the different transition temperatures and resistivities of lmco for different M (of the same concentration $x$) do not only depend on the varying chemical pressures. The local disorder due to the different ionic sizes of La$^{3+}$ and M$^{2+}$ play an important role, too.
We have investigated the electronic structure of Na$_x$Ca$_{1-x}$Cr$_2$O$_4$ using x-ray absorption spectroscopy together with Anderson impurity model calculations with full multiplets. We show Na$_x$Ca$_{1-x}$Cr$_2$O$_4$ taking a novel mixed-valence electronic state in which the positive charge-transfer (CT) and the negative self-doped states coexist. While CaCr$_2$O$_4$ (one end member) exhibits a typical CT nature with strong covalent character, Na substitution causes a self-doped state with an oxygen hole. In NaCr$_2$O$_4$ (the other end member), positive CT and negative self-doped states coexist with equal weight. This unusual electronic state is in sharp contrast to the conventional mixed-valence description, in which the ground state can be described by the mixture of Cr$^{3+}$ ($3d^3$) and Cr$^{4+}$ ($3d^2$).
Electron-electron (e-e) and electron-hole (e-h) interactions are often associated with many exotic phenomena in correlated electron systems. Here, we report an observation of anomalous excitons at 3.75 , 4.67 and 6.11 eV at 4.2 K in bulk-SrTiO$_3$. Fully supported by ab initio GW Bethe-Salpeter equation calculations, these excitons are due to surprisingly strong e-h and e-e interactions with different characters: 4.67 and 6.11 eV are resonant excitons and 3.75 eV is a bound Wannier-like exciton with an unexpectedly higher level of delocalization. Measurements and calculations on SrTi$_{1-x}$Nb$_x$O$_3$ for 0.0001$leq$x$leq$0.005 further show that energy and spectral-weight of the excitonic peaks vary as a function of electron doping (x) and temperature, which are attributed to screening effects. Our results show the importance of e-h and e-e interactions yielding to anomalous excitons and thus bring out a new fundamental perspective in SrTiO$_3$.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
