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Register a new userLow temperature magnetic and dielectric properties of LnBaCuFeO5 (Ln = Nd, Eu, Gd, Ho and Yb)
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The layered perovskite compounds are interesting due to their intriguing physical properties. In this article we report the structural, magnetic and dielectric properties of LnBaCuFeO5 (Ln=Nd, Eu, Gd, Ho and Yb). The structural parameters decrease from Nd to Yb due to the decrease in the ionic radii of the rare earth ions. An antiferromagnetic transition is observed for EuBaCuFeO5 near 120 K along with the glassy dynamics of the electric dipoles below 100 K. The magnetic transition is absent in other compounds, which may be due to the dominance of the magnetic moment of the rare earth ions. The dielectric constant does not show any anomaly, except in the case of HoBaCuFeO5 where it shows a weak frequency dependence around 54 K. These compounds show a significant enhancement of dielectric constant at high temperatures which have been attributed to Maxwell-Wagner effect. However, no significant magneto-dielectric coupling has been observed in these layered perovskites.
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The lanthanide orthoborates, $Ln$BO$_3$, $Ln$ = Gd, Tb, Dy, Ho, Er, Yb crystallise in a monoclinic structure with the magnetic $Ln^{3+}$ forming an edge-sharing triangular lattice. The triangles are scalene, however all deviations from the ideal equilateral geometry are less than 1.5%. The bulk magnetic properties are studied using magnetic susceptibility, specific heat and isothermal magnetisation measurements. Heat capacity measurements show ordering features at $T leq$ 2 K for $Ln$ = Gd, Tb, Dy, Er. No ordering is observed for YbBO$_3$ at $T geq$ 0.4 K and HoBO$_3$ is proposed to have a non-magnetic singlet state. Isothermal magnetisation measurements indicate isotropic Gd$^{3+}$ spins and strong single-ion anisotropy for the other $Ln^{3+}$. The change in magnetic entropy has been evaluated to determine the magnetocaloric effect in these materials. GdBO$_3$ and DyBO$_3$ are found to be competitive magnetocaloric materials in the liquid helium temperature regime.
The bulk magnetic properties of the lanthanide metaborates, $Ln$(BO$_2$)$_3$, $Ln$ = Pr, Nd, Gd, Tb are studied using magnetic susceptibility, heat capacity and isothermal magnetisation measurements. They crystallise in a monoclinic structure containing chains of magnetic $Ln^{3+}$ and could therefore exhibit features of low-dimensional magnetism and frustration. Pr(BO$_2$)$_3$ is found to have a non-magnetic singlet ground state. No magnetic ordering is observed down to 0.4 K for Nd(BO$_2$)$_3$. Gd(BO$_2$)$_3$ exhibits a sharp magnetic transition at 1.1 K, corresponding to three-dimensional magnetic ordering. Tb(BO$_2$)$_3$ shows two magnetic ordering features at 1.05 K and 1.95 K. A magnetisation plateau at a third of the saturation magnetisation is seen at 2 K for both Nd(BO$_2$)$_3$ and Tb(BO$_2$)$_3$ which persists in an applied field of 14 T. This is proposed to be a signature of quasi one-dimensional behaviour in Nd(BO$_2$)$_3$ and Tb(BO$_2$)$_3$.
Investigation of the oxygen-deficient 112-type ordered oxides of the type LnBaCoMnO5+delta (Ln = Nd, Eu) evidences certain unusual magnetic behavior at low temperatures, compared to the LnBaCo2O5+delta cobaltites. One observes that the substitution of manganese for cobalt suppresses the ferromagnetic state and induces strong antiferromagnetic interactions. Importantly, NdBaCoMnO5.9 depicts a clear paramagnetic to antiferromagnetic type transition around 220 K, whereas for EuBaCoMnO5.7 one observes an unusual magnetic behavior below 177 K which consists of ferromagnetic regions embedded in an antiferromagnetic matrix. The existence of two sorts of crystallographic sites for Co/Mn and their mixed valence states favor the ferromagnetic interaction whereas antiferromagnetism originates from the Co3+-O-Co3+ and Mn4+-O-Mn4+ interactions. Unlike the parent compounds, the present Mn-substituted phases do not exhibit prominent magnetoresistance effects in the temperature range 75-400K.
In this work, we report on the synthesis and magnetic properties of a series of double perovskites Ln$_2$ZnIrO$_6$ with Ln = Nd, Sm, Eu & Gd. These compounds present new examples of the rare case of double perovskites (general formula A$_2$BBO$_6$) with a magnetic 4f -ion on the A-site in combination with the strongly spin-orbit coupled 5d-transition metal ion Ir$^{4+}$ on the B-sublattice. We discuss the impact of different rare earths on the macroscopic magnetic properties. Gd$_2$ZnIrO$_6$ and Eu$_2$ZnIrO$_6$ show weak canted antiferromagnetic order below T$_N$ = 23 K and T$_N$ = 12 K, respectively. Sm$_2$ZnIrO$_6$ orders antiferromagnetically at T$_N$ = 13 K. Nd$_2$ZnIrO$_6$ exhibits complex magnetic properties with strong field dependence ranging from a two-step behavior at H = 0.01 T to an antiferromagnetic ground state at intermediate external fields and a spin-flop phase at H$geq$4 T, which suggests complex interplay between Nd$^{3+}$ and Ir$^{4+}$ . To further shed light on this magnetic interaction, the magnetic structure of Nd$_2$ZnIrO$_6$s ground state is examined via neutron powder diffraction.
Rare-earth (RE) based frustrated magnets as typical systems of combining strong spin-orbit coupling, geometric frustration and anisotropic exchange interactions, can give rise to diverse exotic magnetic ground states such as quantum spin liquid (QSL). The discovery of new RE-based frustrated materials is crucial for exploring the exotic magnetic phases. Herein, we report the synthesis, structure and magnetic properties of a family of melilite-type RE2Be2GeO7 (RE = Pr, Nd, Gd-Yb) compounds crystallized in a tetragonal structure, where magnetic RE3+ ions lay out on Shastry-Sutherland lattice (SSL) within ab-plane and are well separated by nonmagnetic GeBe2O7 polyhedrons along c-axis. Temperature-dependent susceptibilities and isothermal magnetization M(H) measurements reveal that most RE2Be2GeO7 compounds except RE=Tb show no magnetic ordering down to 2 K despite the dominant antiferromagnetic (AFM) interactions, where Tb2Be2GeO7 undergoes AFM transition with Neel temperature TN~ 2.5 K and field-induced spin flop behaviors (T< TN). In addition, the calculated magnetic entropy change from the isothermal M(H) curves reveal a viable magnetocaloric effect (MCE) for RE2Be2GeO7 (RE =Gd, Dy) in liquid helium temperature regimes, Gd2Be2GeO7 shows maximum Sm up to 54.8 J K-1 Kg-1 at H= 7 T and Dy2Be2GeO7 has largest value Sm=16.1 J K-1 kg-1 at H= 2 T in this family. More excitingly, rich diversity of RE ions in this family enables an archetype for exploring exotic quantum magnetic phenomena with large variability of spin located on SSL lattice.
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