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Register a new userObservation of a multiferroic critical end point
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The study of abrupt increases in magnetization with magnetic field known as metamagnetic transitions has opened a rich vein of new physics in itinerant electron systems, including the discovery of quantum critical end points with a marked propensity to develop new kinds of order. However, the electric analogue of the metamagnetic critical end point, a metaelectric critical end point has not yet been realized. Multiferroic materials wherein magnetism and ferroelectricity are cross-coupled are ideal candidates for the exploration of this novel possibility using magnetic-field (emph{H}) as a tuning parameter. Herein, we report the discovery of a magnetic-field-induced metaelectric transition in multiferroic BiMn$_{2}$O$_{5}$ in which the electric polarization (emph{P}) switches polarity along with a concomitant Mn spin-flop transition at a critical magnetic field emph{H}$_{rm c}$. The simultaneous metaelectric and spin-flop transitions become sharper upon cooling, but remain a continuous crossover even down to 0.5 K. Near the emph{P}=0 line realized at $mu_{0}$emph{H}$_{rm c}$$approx$18 T below 20 K, the dielectric constant ($varepsilon$) increases significantly over wide field- and temperature (emph{T})-ranges. Furthermore, a characteristic power-law behavior is found in the emph{P}(emph{H}) and $varepsilon$(emph{H}) curves at emph{T}=0.66 K. These findings indicate that a magnetic-field-induced metaelectric critical end point is realized in BiMn$_2$O$_5$ near zero temperature.
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The electric polarization and its magnetic origins in multiferroic RMn2O5, where R is rare-earth ion, are still issues under debate. In this work, the temperature-dependent electric polarization of DyMn2O5, the most attractive member of this RMn2O5 family, is investigated using the pyroelectric current method upon varying endpoint temperature of the electric cooling, plus the positive-up-negative-down (PUND) technique. It is revealed that DyMn2O5 at low temperature does exhibit the unusual ferrielectricity rather than ferroelectricity, characterized by two interactive and anti-parallel ferroelectric sublattices which show different temperature-dependences. The two ferroelectric sublattices are believed to be generated from the symmetric exchange-striction mechanisms associated with the Mn-Mn spin interactions and Dy-Mn spin interactions, respectively. The path-dependent electric polarization reflects the first-order magnetic transitions in the low temperature regime. The magnetoelectric effect is mainly attributed to the Dy spin order which is sensitive to magnetic field. The present experiments may be helpful for clarifying the puzzling issues on the multiferroicity in DyMn2O5 and probably other RMn2O5 multiferroics.
The electrocaloric effect (ECE), i.e., the reversible temperature change due to the adiabatic variation of the electric field, is of great interest due to its potential technological applications. Based on entropy arguments, we present a new framework to attain giant ECE. Our findings are fourfold: $i$) we employ the recently-proposed electric Gruneisen parameter $Gamma_E$ to quantify the ECE and discuss its advantages over the existing so-called electrocaloric strength; $ii$) prediction of giant caloric effects $close$ to $any$ critical end point; $iii$) proposal of potential key-ingredients to enhance the ECE; $iv$) demonstration of $Gamma_E$ as a proper parameter to probe quantum ferroelectricity in connection with the celebrated Barretts formula. Our findings enable us to interpret the recently-reported large ECE at room-temperature in oxide multilayer capacitors [Nature 575, 468 (2019)], paving thus the way for new venues in the field.
InMnO$_3$ is a peculiar member of the hexagonal manganites h-RMnO$_3$ (where R is a rare earth metal element), showing crystalline, electronic and magnetic properties at variance with the other compounds of the family. We have studied high quality samples synthesized at high pressure and temperature by powder neutron diffraction. The position of the Mn ions is found to be close to the threshold $it{x}=1/3$ where superexchange Mn-Mn interactions along the $it{c}$ axis compensate. Magnetic long range order occurs below $T_{rm N}$= 120(2) K with a magnetic unit cell doubled along $it{c}$, whereas short range two dimensional dynamical spin correlations are observed above $T_{rm N}$. We propose that pseudo-dipolar interactions are responsible for the long period magnetic structure.
We examine the electronic properties of newly discovered ferroelectric metal LiOsO$_3$ combining density-functional and dynamical mean-field theories. We show that the material is close to a Mott transition and that electronic correlations can be tuned to engineer a Mott multiferroic state in 1/1 superlattice of LiOsO$_3$ and LiNbO$_3$. We use electronic structure calculations to predict that the (LiOsO$_3$)$_1$/(LiNbO$_3$)$_1$ superlattice is a type-I multiferroic material with a ferrolectric polarization of 41.2~$mu$C cm$^{-2}$, Curie temperature of 927,K, and Neel temperature of 671,K. Our results support a route towards high-temperature multiferroics, emph{i.e.}, driving non-magnetic emph{polar metals} into correlated insulating magnetic states.
Some of the Multiferroics [1] form a rare class of materials that exhibit magnetoelectric coupling arising from the coexistence of ferromagnetism and ferroelectricity, with potential for many technological applications.[2,3] Over the last decade, an active research on multiferroics has resulted in the identification of a few routes that lead to multiferroicity in bulk materials.[4-6] While ferroelectricity in a classic ferroelectric such as BaTiO3 is expected to diminish with the reducing particle size,[7,8] ferromagnetism cannot occur in its bulk form.[9] Here, we use a combination of experiment and first-principles simulations to demonstrate that multiferroic nature emerges in intermediate size nanocrystalline BaTiO3, ferromagnetism arising from the oxygen vacancies at the surface and ferroelectricity from the core. A strong coupling between a surface polar phonon and spin is shown to result in a magnetocapacitance effect observed at room temperature, which can open up possibilities of new electro-magneto-mechanical devices at the nano-scale.
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