We report the structure, magnetic property and spin polarization of CoFeMnGe equiatomic quaternary Heusler alloy. The alloy was found to exist in the L21 structure with considerable amount of DO3 disorder. Thermal analysis result indicated the Curie
temperature is about 711K without any other phase transformation up to melting temperature. The magnetization value was close to that predicted by the Slater-Pauling curve. Current spin polarization of P = 0.70 {plus/minus}0.1 was deduced using point contact Andreev reflection (PCAR) measurements. Half-metallic trend in the resistivity has also been observed in the temperature range of 5 K to 300 K. Considering the high spin polarization and Curie temperature, this material appears to be promising for spintronic applications.
The fascinating phenomenon of destabilization of charge/orbital order in Nd0.5Sr0.5MnO3 with the reduction of grain size is critically investigated. Based on our magnetic and transport experiments followed by a theoretical analysis, we analyze variou
s possible mechanisms and try to delineate a universal scenario behind this phenomenon. We, revisit this issue and discuss the overwhelming evidence from experiments on nano and bulk manganites as well as the absence of correlation between size reduction and pressure effects on manganites. We propose a phenomenological understanding on the basis of enhanced surface disorder to explain the appearance of weak ferromagnetism and metallicity in nanoparticles of Nd0.5Sr0.5MnO3. We also provide supportive evidence from an ab-initio electron structure calculation and a recent numerical simulation and argue that the mechanism is universal in all nanosize charge ordered manganites.
The effect of Co on the structural, magnetic and magnetocaloric effect (MCE) of Ni50-xCoxMn38Sb12 (x=0,2,3,4,5) Heusler alloys was studied. Using x-ray diffraction, we show the evolution of the martensitic phase from the austenite phase. The martensi
tic transition temperature is found to decrease monotonically with Co concentration. Remarkable enhancement of MCE is observed near room temperature upon Co substitution. The maximum magnetic entropy change of 34 Jkg-1K-1 was achieved in x=5 at 262 K in a field of 50 kOe and a value of 29 Jkg-1K-1 found near room temperature. The significant increase in the magnetization associated with the reverse martensitic transition is responsible for the giant MCE in these compounds.
We report the observation of large exchange bias in Ni50-xCoxMn38Sb12 Heusler alloys with x=0, 2, 3, 4, 5, which is attributed to the coexistence of ferromagnetic and antiferromagnetic phases in the martensitic phase. The phase coexistence is possibl
y due to the supercooling of the high temperature ferromagnetic phase and the predominant antiferromagnetic component in the martensitic phase. The presence of exchange bias is well supported by the observation of training effect. The exchange bias field increases with Co concentration. The maximum value of 480 Oe at T=3K is observed in x=5 after field cooling in 50 kOe, which is almost double the highest value reported so far in any Heusler alloy system. Increase in the antiferromagnetic coupling after Co substitution is found to be responsible for the increase in the exchange bias.
We present the results of the magnetic and specific heat measurements on V4 tetrahedral-cluster compound GaV4S8 between 2 to 300K. We find two transitions related to a structural change at 42K followed by ferromagnetic order at 12K on cooling. Remark
ably similar properties were previously reported for the cluster compounds of Mo4. These compounds show an extremely high density of low energy excitations in their electronic properties. We explain this behavior in a cluster compound as due to the reduction of coulomb repulsion among electrons that occupy highly degenerate orbits of different clusters.
