arXiv subjects

Vasudeva Siruguri

Publications and source records attributed to Vasudeva Siruguri.

5 recordsLinked to original sources

arXiv2021

Short range magnetic correlation, metamagnetism and coincident dielectric anomaly in Na$_5$Co$_{15.5}$Te$_6$O$_{36}$

Here we explore the structural, magnetic and dielectric properties of Co based compound Na$_5$Co$_{15.5}$Te$_6$O$_{36}$ as a candidate of short-range magnetic correlations driven development of dielectric anomaly above N$\acute{e}$el temperature of ($T_N$=) 50 K. Low temperature neutron powder diffraction (NPD) in zero applied magnetic field clearly indicates that the canted spin structure is responsible for the antiferromagnetic transition and partially occupied Co form short range magnetic correlation with other Co, which further facilitates the structural distortion and consequent development of dielectric anomaly above antiferromagnetic transition. Additionally, the temperature dependent magnetic heat capacity and electron spin resonance measurements reveal the presence of short-range magnetic correlations which coincides with an anomaly in the dielectric constant vs temperature curve. Moreover, significant changes in the lattice parameters are also observed around the same temperature, indicating presence of noticeable spin-lattice coupling. Further, sharp jump in the magnetic field dependent magnetization clearly indicates the presence of metamagnetic transition and magnetic field dependent NPD confirms that rotations of Co spins with applied magnetic field are responsible for this metamagnetic phase transition. As a result, this transition causes the magnetocaloric effect to be developed in the system, which is suitable for the application in low temperature refrigeration.

cond-mat.mtrl-sci↗

arXiv2015

Giant magnetocaloric effect from reverse martensitic transformation in Ni-Mn-Ga-Cu ferromagnetic shape memory alloys

In an effort to produce Giant Magnetocaloric effect (GMCE) near room temperature, in a first ever such study, the austenite transformation temperature (As) was fine tuned to ferromagnetic Curie temperature (TC) in Ferromagnetic Shape Memory Alloys (FSMA) and a large GMCE of delta-SM = - 81.75 J/Kg-K was achieved in Ni50Mn18.5Cu6.5Ga25 alloy during reverse martensitic transformation (heating cycle) for a magnetic field change of 9 T at 302.5 K. Fine tuning of As with TC was achieved by Cu substitution in Ni50Mn25-xCuxGa25 (0< x < 7.0)-based FSMAs. Characterizations of these alloys were carried out using Optical and Scanning Electron Microscopy, X-ray Diffraction (XRD), Differential Scanning Calorimetry (DSC) and DC magnetization measurements. Addition of Cu to stoichiometric Heusler type Ni2MnGa increases the martensitic transformation temperatures and decreases TC. Concurrently, DSM increases with Cu addition and peaks at 6.5 at. % Cu for which there is a virtual overlap between TC and As. Maximum Refrigerant Capacity (RCP) of 327.01 J/Kg was also achieved in the heating cycle for 9 T field change at 302.5 K. Corresponding values for the cooling cycle measurements (measured during forward transformation) were 30.4 J/Kg-K and 123.52 J/Kg respectively for the same 6.5 at. % Cu sample and same thermo-magnetic conditions.

cond-mat.mtrl-sci↗

arXiv2015

Spin-orbital liquid state assisted by singlet-triplet excitation in $J~=~0$ ground state of Ba$_3$ZnIr$_2$O$_9$

Strong spin-orbit coupling (SOC) effects of heavy $d$-orbital elements have long been neglected in describing the ground states of their compounds thereby overlooking a variety of fascinating and yet unexplored magnetic and electronic states, until recently. The spin-orbit entangled electrons in such compounds can get stabilized into unusual spin-orbit multiplet $J$-states which warrants severe investigations. Here we show using detailed magnetic and thermodynamic studies and theoretical calculations the ground state of Ba$_3$ZnIr$_2$O$_9$, a 6$H$ hexagonal perovskite is a close realisation of the elusive $J$~=~0 state. However, we find that local Ir moments are spontaneously generated due to the comparable energy scales of the singlet-triplet splitting driven by SOC and the superexchange interaction mediated by strong intra-dimer hopping. While the Ir ions within the structural Ir$_2$O$_9$ dimer prefers to form a spin-orbit singlet state (SOS) with no resultant moment, substantial interdimer exchange interactions from a frustrated lattice ensure quantum fluctuations till the lowest measured temperatures and stabilize a spin-orbital liquid phase.

cond-mat.str-el↗

arXiv2011

Atomic scale chemical fluctuation in LaSrVMoO6: A proposed halfmetallic antiferromagnet

Half metallic antiferromagnets (HMAFM) have been proposed theoretically long ago but have not been realized experimentally yet. Recently, a double perovskite compound, LaSrVMoO6, has been claimed to be an almost real HMAFM system. Here, we report detailed experimental and theoretical studies on this compound. Our results reveal that the compound is neither a half metal nor an ordered antiferromagnet. Most importantly, an unusual chemical fluctuation is observed locally, which finally accounts for all the electronic and magnetic properties of this compound.

cond-mat.mtrl-sci↗

arXiv2004

High Pressure X-Ray Diffraction Study of UMn2Ge2

Uranium manganese germanide, UMn2Ge2, crystallizes in body-centered tetragonal ThCr2Si2 structure with space group I4/mmm, a = 3.993A and c = 10.809A under ambient conditions. Energy dispersive X-ray diffraction was used to study the compression behaviour of UMn2Ge2 in a diamond anvil cell. The sample was studied up to static pressure of 26 GPa and a reversible structural phase transition was observed at a pressure of ~ 16.1 GPa. Unit cell parameters were determined up to 12.4 GPa and the calculated cell volumes were found to be well reproduced by a Murnaghan equation of state with K0 = 73.5 GPa and K' = 11.4. The structure of the high pressure phase above 16.0 GPa is quite complicated with very broad lines and could not be unambiguously determined with the available instrument resolution.

cond-mat.mtrl-sci↗