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S. Nallamuthu

Publications and source records attributed to S. Nallamuthu.

3 recordsLinked to original sources

Quantum Fluctuations in Magnetically Frustrated Gd2GaSbO7 and Gd2InSbO7 Pyrochlores

Gd2GaSbO7 and Gd2InSbO7 pyrochlore compounds exhibit quantum fluctuations in a spin ice-like state. These compounds have not been adequately studied based on the concept of magnetic frustration. Here, we have synthesised and characterised Gd2GaSbO7 and Gd2InSbO7 to investigate their ground-state magnetic properties. We confirmed the cubic pyrochlore structure via X-ray powder diffraction. Magnetic and heat capacity measurements show an absence of magnetic order down to 400 mK. Interestingly, the low-temperature magnetic heat capacity of Gd2GaSbO7 and Gd2InSbO7 exhibits a broad maximum around T_{\text{max}} = 0.9 K and T_{\text{max}} = 1 K, respectively. The low-temperature Cmag data fit with the power-law C_{\text{mag}} \approx T^{\frac{d}{n}} with dependencies of T^{1.71} for Gd2GaSbO7 and T^{1.49} for Gd2InSbO7, suggesting spin fluctuations caused by the disorder of magnetic moments at low temperatures. Both compounds retain residual entropy akin to water ice, resembling the spin ice state. Additionally, we analysed the ratio between nearest-neighbour exchange and dipolar interaction for all reported Gd-based pyrochlores, finding that Gd2InSbO7 has the lowest and weakest exchange interaction among them. This indicates that chemical pressure affects exchange interaction due to the different pathways of mediators between magnetic ions. This study reveals robust quantum fluctuations in the ground state in GGSO and GISO, similar to quantum spin ice compounds such as Pr2Zr2O7, Pr2Sn2O7, and Yb2GaSbO7. Other Gd-pyrochlore compounds exhibit long-range magnetic order, which is in stark contrast to this.

cond-mat.str-el

Ferromagnetism in orthorhombic RAgAl3 (R = Ce and Pr) compounds

We present a detailed study on magnetic, thermodynamic and transport properties of polycrystalline RAgAl3(R = Ce and Pr) compounds. Both compounds crystallize in orthorhombic structure, which is distorted from the tetragonal BaAl4 structure with the space group Cmcm. Heat capacity measurement indicates the bulk magnetic ordering of the compounds. CeAgAl3 and PrAgAl3 order ferromagnetically at TC = 3.8 K and 5.8 K, respectively as it was confirmed from magnetic measurements. CeAgAl3 exhibits heavy Fermion behaviour. The Schottky behaviour in heat capacity data was observed in both compounds. The crystalline electric field (CEF) analysis of the magnetic parts of heat capacity of CeAgAl3 and PrAgAl3 yielded to a CEF level scheme with three doublets and nine singlets and with an overall splitting of 51 K and 180 K, respectively. Fit yielded a magnetic doublet state for CeAgAl3, whereas for PrAgAl3 a pseudo-doublet ground-state with an energy difference of 15 K has been obtained. The resistivity measurements display a low temperature drop at the magnetic ordering temperature of the compounds. Negative magnetoresistance (MR) due to the ferromagnetic ordering has been observed for both Ce and Pr compounds.

cond-mat.str-el

Competing magnetic interactions in the orthorhombic GdNiAl3

Magnetization and heat capacity measurements of ternary rare earth intermetallic compound GdNiAl3 demonstrate para to ferromagnetic transition at Tc=165.5K. In addition multiple short range magnetic transitions observed below Tc are suggestive of competing interactions in this compound. As a result of this a weak Griffiths phase type behaviour is observed in the paramagnetic region. This complex behaviour is rather supported by the random orientation of Ni centered tricapped trigonal prisms with additional Al atoms in the structure. Heat capacity and resistivity data display an interesting peak at 72 K, which is highly unaffected by magnetic fields up to 90KOe.

cond-mat.str-el