The metal-insulator transition temperature Tc in VO2 is experimentally shown to be almost the same as a magnetic transition temperature Tm characterized by an abrupt decrease in susceptibility, suggesting the evidence of the same underlying origin for both transitions. The measurement of susceptibility shows that it weakly increases on cooling for temperature range of T > Tm, sharply decreases near Tm and then unusually increases on further cooling. A theoretical approach for such unusual observations in susceptibility near Tm or below is performed by modeling electrons from each two adjacent V4+ ions distributed along V-chains as a two-electron system, which indicates that the spin exchange between electrons could cause a level splitting into a singlet (S = 0) level of lower energy and a triplet (S = 1) level of higher energy. The observed abrupt decrease in susceptibility near Tm is explained to be due to that the sample enters the singlet state in which two electrons from adjacent V4+ ions are paired into dimers in spin antiparallel. By considering paramagnetic contribution of unpaired electrons created by the thermal activation from singlet to triplet levels, an expression for susceptibility is proposed to quantitatively explain the unusual temperature-dependent susceptibility observed at low temperatures. Based on the approach to magnetic features, the observed metal-insulator transition is explained to be due to a transition from high-temperature Pauli paramagnetic metallic state of V4+ions to low-temperature dimerized state of strong electronic localization.
Experiments for vanadium dioxide show a magnetic transition characterized by a sharp variation in susceptibility associated with the metal-insulator transition at the temperature Tc. The sample is shown to be of Pauli paramagnetism above Tc but of anomalous paramagnetism below Tc. Considering co-contributions of Pauli paramagnetism of residual V4+ ions and Curie-like paramagnetism of V-V dimers, we propose a phenomenological expression for the temperature-dependent susceptibility below Tc, which yields an excellent agreement with the experimental data. The unusual temperature dependence of Curie-like susceptibility below Tc is explained to be due to the fact that every dimer is formed by spin paring at an angle θ close to 180° and hence has an effective spin expressed as Seff=cos(θ/2) which decreases with lowering temperature. The observed metal-insulator and magnetic transitions are argued to be due to a transition from the high-temperature Pauli paramagnetic state of V4+ ions to the low-temperature dimerized state.
Obtaining tunable magnetic states in geometrically frustrated multiferroic compound CoCr2O4 by tuning the sublattice magnetic coupling is indeed of high interest from the fundamental and applied points of view.
Polycrystalline Ni(Cr1−xMnx)2O4 (0.1 ≤ x ≤ 0.325) ceramic samples were studied through different protocols of dc magnetization measurements. The samples exhibit 2 kinds of magnetic compensation effects below the ferrimagnetic transition temperature TC. Remarkable magnetization reversal is observed between the 2 compensation temperatures Tcomp1 and Tcomp2, which is regarded as arising from the negative exchange coupling between the 2 magnetic sublattices at different crystallographic sites. The magnetization is reversed at TSR due to spin‐reorientation caused by magnetostructural coupling. The spin‐reorientation is supported by Mn substitution and TSR is increased to 96 K when x reaches 0.325. However, it is suppressed due to the strong ionic site preference and thus the magnetization is slightly increased in the negative direction of the magnetic field. Near the 2 compensation temperatures, tunable magnetic switching effects can be obtained just by changing the magnitude of the applied magnetic field. Moreover, both normal and inverse magnetocaloric effects were also demonstrated.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.