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Register a new userQuadrupolar ordering and exotic magnetocaloric effect in RB4 (R = Dy, Ho)
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The interplay of charge, spin, orbital and lattice degrees of freedom has recently received great interest due to its potential to improve the magnetocaloric effect (MCE) for the purpose of magnetic cooling applications. Here we propose a new mechanism for a giant inverse MCE in rare-earth tetraborides, especially for Ho1-xDyxB4 (x = 0.0, 0.5, and 1.0). For x = 0.0, 0.5, and 1.0, the maximum entropy changes of the giant inverse MCE are found to be 22.7 J/kgK, 19.6 J/kgK, and 19.0 J/kgK with critical fields of 25 kOe, 40 kOe, and 50 kOe, respectively. It is remarkable that such a giant MCE is realized, even when applying a low magnetic field, which enables a field-tuned entropy change and brings about a significant advantage for several applications. For all compounds, we have systematically studied how the entropy changes as a function of the field and temperature and investigated their correlation with consecutive double transitions, i.e., the magnetic dipolar order at T = TN and the quadrupolar order at T = TQ (TQ < TN). We found that the maximum entropy change occurs at T = TQ and the critical field associated with the meta-magnetic transition, which is in good agreement with the experimental data. Thus, we elucidate that this unique behaviour is attributed to the strong coupling between magnetic dipoles and quadrupoles in the presence of strong spin-orbit coupling and geometric frustration. Our work offers new insights into both the academic interest of multipolar degrees of freedom in magnetic materials and the discovery of giant MCE with various applications for magnetic cooling systems.
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X-ray circular magnetic dichroism (XMCD), longitudinal ($chi_{ac}$) and transverse (TS) ac magnetic susceptibility have been measured in several members of the $R$Co$_2$ series ($R$ = Dy, Ho, and Tm) as a function of temperature and applied magnetic field. We show that parimagnetism is a general behavior along the $R$Co$_2$ ferrimagnetic series ($R$ being a heavy rare earth ion). XMCD results evidence the presence of two compensation temperatures, defining two different parimagnetic configurations, which is a fully unexpected result. The inverse $chi_{ac}$ curve exhibits a deviation from Curie-Weiss behavior which is recovered under applied magnetic field. The large excess of polarizability above the critical temperature proves the existence of an enhanced effective moment due to the presence of short range magnetic correlations, which are also observed in TS measurements. The combination of TS and XMCD measurements allows to depict new magnetic phase diagrams for the $R$Co$_2$ series. A new scenario allowing to understand the observed phenomenology as a Griffiths phase-like behavior is proposed, where the amorphous $R$Co$_2$ represents the undiluted system case.
A detailed study on the crystal structure and bulk magnetic properties of Cr substituted Ising type lanthanide gallium garnets $Ln_3text{CrGa}_4text{O}_{12}$ ($Ln$ = Tb, Dy, Ho) has been carried out using room temperature powder X-Ray and neutron diffraction, magnetic susceptibility, isothermal magnetisation and heat capacity measurements. The magnetocaloric effect (MCE) in $Ln_3text{CrGa}_4text{O}_{12}$ is compared to that of $Ln_3text{Ga}_5text{O}_{12}$. In lower magnetic fields attainable by a permanent magnet ($leq$ 2 T), Cr substitution greatly enhances the MCE by 20% for $Ln$ = Dy and 120% for $Ln$ = Ho compared to the unsubstituted $Ln_3text{Ga}_5text{O}_{12}$. This is likely due to changes in the magnetic ground state as Cr substitution also significantly reduces the frustration in the magnetic lattice for the Ising type $Ln_3text{Ga}_5text{O}_{12}$.
The compounds, PrCo9Si4 and NdCo9Si4, have been recently reported to exhibit first-order ferromagnetic transitions near 24 K. We have subjected this compound for further characterization by magnetization, heat-capacity and electrical resistivity measurements at low temperatures in the presence of magnetic fields, particularly to probe magnetocaloric effect and magnetoresistance. The compounds are found to exhibit rather modest magnetocaloric effect at low temperatures peaking at Curie temperature, tracking the behavior of magnetoresistance. The magnetic transition does not appear to be first order in its character.
Recently, a massive magnetocaloric effect near the liquefaction temperature of hydrogen has been reported in the ferromagnetic material HoB$_{2}$. Here we investigate the effects of Dy substitution in the magnetocaloric properties of Ho$_{1-x}$Dy$_{x}$B$_{2}$ alloys ($textit{x}$ = 0, 0.3, 0.5, 0.7, 1.0). We find that the Curie temperature ($textit{T}$$_{C}$) gradually increases upon Dy substitution, while the magnitude of the magnetic entropy change |$Delta textit{S}_{M}$| at $textit{T}$ = $textit{T}_{C}$ decreases from 0.35 to 0.15 J cm$^{-3}$ K$^{-1}$ for a field change of 5 T. Due to the presence of two magnetic transitions in these alloys, despite the change in the peak magnitude of |$Delta textit{S}_{M}$|, the refrigerant capacity ($textit{RC}$) and refrigerant cooling power ($textit{RCP}$) remains almost constant in all doping range, which as large as 5.5 J cm$^{-3}$ and 7.0 J cm$^{-3}$ for a field change of 5 T. These results imply that this series of alloys could be an exciting candidate for magnetic refrigeration in the temperature range between 10-50 K.
$La_{0.7}Ca_{0.3}MnO_3$ samples were prepared in nano- and polycrystalline forms by sol-gel and solid state reaction methods, respectively, and structurally characterized by synchrotron X-ray diffraction. The magnetic properties determined by ac susceptibility and dc magnetization measurements are discussed. The magnetocaloric effect in this nanocrystalline manganite is spread over a broader temperature interval than in the polycrystalline case. The relative cooling power of the poly- and nanocrystalline manganites is used to evaluate a possible application for magnetic cooling below room temperature.
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