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Thiagarajan Maran

Publications and source records attributed to Thiagarajan Maran.

2 recordsLinked to original sources

Evolution of the electronic and superconducting properties of Re-based quinary high-entropy alloys under chemical and physical pressure

We report a comparative study of chemical- and physical-pressure effects on the electronic and superconducting properties of the Re-based quinary high-entropy alloys (HEAs) [Nb0.67-xRex][TiZrHf]0.33 (x = 0.10, 0.20, and 0.56). Increasing Re concentration suppresses the superconducting transition temperature Tc from 5.4 to 3.9 K while producing positive, composition-dependent cocktail-effect ratios. Field-dependent transport and magnetization establish all three compositions as strongly type-II superconductors and identify x = 0.20 as the most distinctive composition, with the largest upper critical field and Ginzburg-Landau parameter and a Maki parameter close to unity. Most importantly, the pressure coefficient of Tc changes sign across the bcc-hcp structural change: dTc/dP is positive for the bcc x = 0.10 and 0.20 samples, with values of approximately 0.018 and 0.053 K/GPa, respectively, but negative for the hcp x = 0.56 sample, with a value of approximately -0.033 K/GPa. This systematic contrast within a single chemically related alloy series establishes a robust structure-associated superconducting response and identifies crystal structure as a key organizing variable under compression. Metallic transport and superconductivity remain robust up to approximately 8 GPa in all three compositions. These results reveal that chemical substitution and hydrostatic compression are complementary but nonequivalent routes for tuning superconductivity in Re-based HEAs.

cond-mat.supr-con↗

Hydrostatic pressure effect on structural and transport properties of co-existing layered and disordered rock-salt phase of LixCoO2

It is widely believed that the origin of a significant cause for the voltage and capacity fading observed in lithium (Li)-ion batteries is related to structural modifications occurring in the cathode material during the Li-ion insertion/de-insertion process. The Li-ion insertion/de-insertion mechanism and the resulting structural changes are known to exert a severe strain on the lattice, and consequently leading to performance degradation. Here, with a view to shed more light on the effect of such strain on the structural properties of the cathode material, we have systematically investigated the pressure dependence of structural and transport properties of an LixCoO2 single crystal, grown using 5% excess Li in the precursors. Ambient pressure synchrotron diffraction on these crystals reveals that, the excess Li during the growth, has facilitated the stabilization of a layered rhombohedral phase (space group R3m) as well as a disordered rock-salt phase (space group Fm3m). The volume fraction of the rhombohedral and cubic phase is 60:40, respectively, which remains unchanged up to 10.6 GPa. No structural phase transition has been observed up to 10.6 GPa. An increase in resistance with a decrease in temperature has revealed the semi-metallic nature of the sample. Further, the application of hydrostatic pressure up to 2.8 GPa shows the enhancement of semi-metallic nature. The obtained experimental results can be qualitatively explained via density functional theory (DFT) and thermodynamics modelling. The calculated density of states was reduced, and the activation energy was increased by applied pressure. Our investigations indicate a significant phase stability of the mixed phase crystals under externally applied high pressure and thus suggest the possible use of such mixed phase materials as a cathode in lithium-ion batteries.

cond-mat.mtrl-sci↗