We have compared and contrasted magnetic, magnetocaloric and magnetoresistive properties of Gd and Dy members of the rare-earth (R) series RFe5Al7, crystallizing in ThMn12 structure, known to order antiferromagnetically. Among other observations, we
would like to emphasize on the following novel findings: (i) There are multiple sign-crossovers in the temperature (T) dependence of isothermal entropy change (DeltaS) in the case of Dy compound; in addition to nil DeltaS at the magnetic compensation point known for two-magnetic-sublattice systems, there is an additional sign-crossover at low temperatures, as though there is a re-entrant inverse magnetocaloric phenomenon. Corresponding sign reversals could also be observed in the magnetoresistance data. (ii) The plots of magnetoresistance versus magnetic field are found to be highly asymmetric with the reversal of the direction of magnetic-field (H) well below TN for both compounds, similar to that known for an antiferromagnetic tunnel junctions. We attribute these to subtle changes in spin orientations of R and Fe moments induced by T and H.
We have recently reported that the Haldane spin-chain system, Er2BaNiO5, undergoing antiferromagnetic order below 32 K, is characterized by the onset of ferroelectricity near 60K due to magnetoelectric coupling induced by short-range magnetic-order w
ithin spin-chains. We have carried out additional magnetic and dielectric studies to understand the properties well below antiferromagnetic ordering temperature. We emphasize here on the following: (i) A strong frequency dependent behaviors of ac magnetic susceptibility and complex dielectric properties have been observed at much lower temperatures (below 8 K), that is, reentrant multiglass-like phenomenon, naturally suggesting the existence of an additional transition well below Neel temperature; ii) Magnetoelectric phase coexistence is observed at very low temperature (e.g., T =2K), where the high-field magnetoelectric phase is partially arrested on returning to zero magnetic field after a cycling through metamagnetic transition.
We have investigated the magnetic, dielectric and magnetodielectric (MDE) behavior of a geometrically frustrated spin-chain system, Ca3Co1.4Rh0.6O6, in the single crystalline form for different orientations. The results bring out that the magnetic be
havior of this compound is by itself interesting in the sense that this compound exhibits an anisotropic glassy-like magnetic behavior with a huge frequency dependence of ac susceptibility peak for an orientation along the spin-chain in the range 30-60 K; this behavior is robust to applications of large external magnetic fields (H) unlike in canonical spin-glasses. The temperature dependence of dielectric constant also shows strong frequency dependence with similar robustness to H. The isothermal H-dependent dielectric results at low temperatures establishes anisotropic MDE coupling. It is intriguing to note that there is a step roughly at one-third of saturation values as in the case of isothermal magnetization curves for same temperatures (for orientation along spin-chain), a correlation hitherto unrealized for geometrically frustrated systems.
We report that the spin-chain compound Dy2BaNiO5 recently proven to exhibit magnetoelectric coupling below its Neel temperature (T_N) of 58 K, exhibits strong frequency-dependent behavior in ac magnetic susceptibility and complex dielectric propertie
s at low temperatures (<10K), mimicking reentrant multiglass phenomenon. Such a behavior is not known among undoped compounds. A new finding in the field of multiferroics is that the characteristic magnetic feature at such low temperatures moves towards higher temperatures in the presence of a magnetic-field (H), whereas the corresponding dielectric feature shifts towards lower temperatures with H, unlike the situation near T_N. This observation indicates that the alignment of spins by external magnetic fields tends to inhibit glassy-like slow electric-dipole dynamics, at least in this system, possibly arising from peculiarities in the magnetic structure.
We present magnetic characterization of a binary rare-earth intermetallic compound Er5Si3, crystallizing in Mn5Si3-type hexagonal structure, through magnetization, heat-capacity, electrical resistivity, and magnetoresistance measurements. Our investi
gations confirm that the compound exhibits two magnetic transitions with decreasing temperature, first one at 35 K and the second one at 15 K. The present results reveal that the second magnetic transition is a disorder-broadened first-order transition, as shown by thermal hysteresis in the measured data. Another important finding is that, below 15 K, there is a magnetic-field-induced transition with a hysteretic effect with the electrical resistance getting unusually enhanced at this transition and the magnetorsistance (MR) is found to exhibit intriguing magnetic-field dependence indicating novel magnetic phase-co-existence phenomenon. It thus appears that this compound is characterized by interesting magnetic anomalies in the temperature-magnetic-field phase diagram.
Despite intense research in the field of strongly correlated electron behavior for the past few decades, there has been very little effort to understand this phenomenon in nano particles of the Kondo lattices. In this article, we review the results o
f our investigation on the fine particles (less than 1 micron) of some of the alloys obtained by high-energy ball-milling to bring out that this synthetic method paves a way to study strong electron correlations in nanocrystals of such alloys. We primarily focus on the alloys of the series, CeRu(2-x)Rh(x)Si2, lying at different positions in Doniachs magnetic phase diagram. While CeRu2Si2, a bulk paramagnet, appears to become magnetic (of a glassy type) below about 8 K in fine particle form, in CeRh2Si2, an antiferromagnet (T_N= 36 K) in bulk form, magnetism is destroyed (at least down to 0.5 K) in fine particles. In the alloy, CeRu(0.8)Rh(1.2)Si2, at the quantum critical point, no long range magnetic ordering is found
