Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userCdV2O4: A rare example of a collinear multiferroic spinel
253
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
By studying the dielectric properties of the geometrically frustrated spinel CdV2O4, we observe ferroelectricity developing at the transition into the collinear antiferromagnetic ground state. In this multiferroic spinel, ferroelectricity is driven by local magnetostriction and not by the more common scenario of spiral magnetism. The experimental findings are corroborated by ab-initio calculations of the electric polarization and the underlying spin and orbital order. The results point towards a charge rearrangement due to dimerization, where electronic correlations and the proximity to the insulator-metal transition play an important role.
rate research
Read More
We have determined the physical ground state properties of the compounds CeRuPO and CeOsPO by means of magnetic susceptibility chi(T), specific heat C(T), electrical resistivity rho(T), and thermopower S(T) measurements. chi(T) reveals a trivalent 4f1 cerium state in both compounds. For CeRuPO a pronounced decrease of rho(T) below 50K indicates the onset of coherent Kondo scattering which is confirmed by enhanced S(T). The temperature and magnetic field dependence of chi(T) and C(T) evidence ferromagnetic (FM) order at TC=15K. Thus, CeRuPO seems to be one of the rare example of a FM Kondo lattice. In contrast, CeOsPO shows antiferromagnetic order at TN=4.4K despite only minor changes in lattice parameters and electronic configuration. Additional 31P NMR results support these scenarios. LSDA+U calculations evidence a quasi two dimensional electronic band structure, reflecting a strong covalent bonding within the CeO and RuP layers and a weak ionic like bonding between the layers.
Nuclear magnetic resonance (NMR), neutron diffaction (ND), x-ray diffraction, magnetic susceptibility and specific heat measurements on the frustrated A-site spinel CoAl2O4 compound reveal a collinear antiferromagnetic ordering below Tn = 9.8(2) K. A high quality powder sample characterized by x-ray diffraction that indicates a relatively low Co-Al inversion parameter x = 0.057(20) in (Co1-xAlx)[Al2-xCox]O4, shows a broad maximum around 15 K in magnetic susceptibility and a sharp peak at Tn in heat capacity. The average ordered magnetic moment of Co^2+ (S = 3/2) ions at the A-site is estimated to be 2.4(1) Bohr magneton from NMR and 1.9(5) Bohr magneton from ND which are smaller than the expected value of 3 Bohr magneton for S = 3/2 and g = 2. Antiferromagnetic spin uctuations and correlations in the paramagnetic state are revealed from the magnetic susceptibility, NMR and ND measurements, which are due to spin frustration and site inversion effects in the system. The ND data also show short-range dynamic magnetic ordering that persists to a temperature that is almost twice Tn.
The ground state of the frustrated A-site magnetic spinel CoAl2O4 has been a controversial issue whether it is a collinear antiferromagnetic ordering or a spiral spin - liquid state, as the ratio of the two competing interactions, J2/J1 lies close to the boundary between these two ground states. Here, we address the magnetic ground state in CoAl2O4 with different amount of Co2+/Al3+ site disorder from the study of magnetoelectric effect and Monte Carlo simulations. CoAl2O4 with low site disorder exhibits linear magnetoelectric effect below the magnetic ordering temperature. With increasing disorder, the magnetoelectric effect is suppressed and the sample with 14% disorder exhibits a spin glass behavior without the magnetoelectric effect. Monte Carlo simulations support the experimental findings and suggest that the site disorder suppresses long - range antiferromagnetic order and induces a spin glass state. Since the linear magnetoelectric effect requires a long - range magnetic ordering, we suggest that the ground state of CoAl2O4 with low site disorder is a collinear antiferromagnet.
Non-resonant X-ray magnetic scattering has been used to study the magnetic structure of multiferroic TbMnO3 in its ferroelectric phase. Circularly polarized X-rays were combined with a full polarization analysis of the scattered beam to reveal important new information on the magnetic structure of this canonical multiferroic. An applied electric field is shown to create a magnetic nearly mono-domain state in which the cylcoidal order on the Mn sublattice rotates either clockwise or counter-clockwise depending on the sign of the field. It is demonstrated how this technique provides sensitivity to the absolute sense of rotation of the Mn moments, and to components of the ordering on the Tb sublattice and phase shifts that earlier neutron diffraction experiments could not resolve.
We present a neutron diffraction study of FeV2O4, which is rare in exhibiting spin and orbital degrees of freedom on both cation sublattices of the spinel structure. Our data confirm the existence of three structural phase transitions previously identified with x-ray powder diffraction, and reveal that the lower two transitions are associated with sequential collinear and canted ferrimagnetic transitions involving both cation sites. Through consideration of local crystal and spin symmetry, we further conclude that Fe2+ cations are ferro-orbitally ordered below 135K and V3+ orbitals order at 60K in accordance with predictions for vanadium spinels with large trigonal distortions and strong spin-orbit coupling. Intriguingly, the direction of ordered vanadium spins at low temperatures obey `ice rules more commonly associated with the frustrated rare-earth pyrochlore systems.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
