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Sagar Ghorai

Publications and source records attributed to Sagar Ghorai.

8 recordsLinked to original sources

Design of thermal hysteresis in nonstoichiometric alloys with giant magnetocaloric effect

The non-stoichiometric Fe$_2$P-type (FeMnP$_{0.5}$Si$_{0.5}$)$_{1-x}$(FeV)$_{x}$ alloys ( $x=0, 0.01$, $0.02$, and $0.03$) have been investigated as potential candidates for magnetic refrigeration near room temperature. The magnetic ordering temperature decreases with increasing FeV concentration, $x$, which can be ascribed to decreased ferromagnetic coupling strength between the magnetic atoms. The strong magnetoelastic coupling in these alloys results in large values of the isothermal entropy change ($ΔS_M$); $15.7$ J/kgK, at $2$ T magnetic field for the $x = 0$ alloy. $ΔS_M$ decreases with increasing $x$. Results from M{ö}ssbauer spectroscopy reveal that the average hyperfine field (in the ferromagnetic state) and average center shift (in the paramagnetic state) have the same decreasing trend as $ΔS_M$. The thermal hysteresis ($ΔT_{hyst}$) of the magnetic phase transition decreases with increasing $x$, while the mechanical stability of the alloys improves due to the reduced lattice volume change across the magnetoelastic phase transition. The adiabatic temperature change $ΔT_{ad}$, which highly depends on $ΔT_{hyst}$, is $1.7$ K at $1.9$ T applied field for the $x = 0.02$ alloy.

cond-mat.mtrl-sci

Giant magnetocaloric effect in the (Mn,Fe)NiSi-system

The search for energy-efficient and environmentally friendly cooling technologies is a key driver for the development of magnetic refrigeration based on the magnetocaloric effect (MCE). This phenomenon arises from the interplay between magnetic and lattice degrees of freedom that is strong in certain materials, leading to a change in temperature upon application or removal of a magnetic field. Here we report on a new material, Mn$_{1-x}$Fe$_x$NiSi$_{0.95}$Al$_{0.05}$, with an exceptionally large isothermal entropy at room temperature. By combining experimental and theoretical methods we outline the microscopic mechanism behind the large MCE in this material. It is demonstrated that the competition between the Ni$_2$In-type hexagonal phase and the MnNiSi-type orthorhombic phase, that coexist in this system, combined with the distinctly different magnetic properties of these phases, is a key parameter for the functionality of this material for magnetic cooling.

cond-mat.mtrl-sci

A setup for direct measurement of the adiabatic temperature change in magnetocaloric materials

In order to find a highly efficient, environment-friendly magnetic refrigerant, direct measurements of the adiabatic temperature change $ΔT_{adb}$ is required. Here, in this work, a simple setup for the $ΔT_{adb}$ measurement is presented. Using a permanent magnet Halbach array with a maximum magnetic field of $1.8$ T and a rate of magnetic field change of $5$ T/s, accurate determination of $ΔT_{adb}$ is possible in this system. The operating temperature range of the system is from $100$ K to $400$ K, designed for the characterization of materials with potential for room temperature magnetic refrigeration applications. Using the setup, the $ΔT_{adb}$ of a first-order and a second-order compound have been studied. Results from the direct measurement for the first-order compound have been compared with $ΔT_{adb}$ calculated from the temperature and magnetic field dependent specific heat data. By comparing results from direct and indirect measurements, it is concluded that for a reliable characterization of the magnetocaloric effect, direct measurement of $ΔT_{adb}$ should be adopted.

cond-mat.mtrl-sci

Site-specific atomic substitution in a giant magnetocaloric Fe$_2$P-type system

Giant magnetocaloric (GMC) materials constitute a requirement for near room temperature magnetic refrigeration. (Fe,Mn)$_2$(P,Si) is a GMC compound with strong magnetoelastic coupling. The main hindrance towards application of this material is a comparably large temperature hysteresis, which can be reduced by metal site substitution with a nonmagnetic element. However, the (Fe,Mn)$_2$(P,Si) compound has two equally populated metal sites, the tetrahedrally coordinated $3f$ and the pyramidally coordinated $3g$ sites. The magnetic and magnetocaloric properties of such compounds are highly sensitive to the site specific occupancy of the magnetic atoms. Here we have attempted to study separately the effect of $3f$ and $3g$ site substitution with equal amounts of vanadium. Using formation energy calculations, the site preference of vanadium and its influence on the magnetic phase formation are described. A large difference in the isothermal entropy change (as high as 44\%) with substitution in the $3f$ and $3g$ sites is observed. The role of the lattice parameter change with temperature and the strength of the magnetoelastic coupling on the magnetic properties are highlighted.

cond-mat.mtrl-sci

Effect of small cation occupancy and anomalous Griffiths phase disorder in nonstoichiometric magnetic perovskites

The structural, magnetic, magnetocaloric and Griffiths phase (GP) disorder of non-stoichiometric perovskite manganites La_(0.8-x) Sr_(0.2-y) Mn_(1+x+y) O_3 are reported here. Determination of valence states and structural phases evidenced that the smaller cations Mn2+ and Mn3+ will not occupy the A-site of a perovskite under atmospheric synthesis conditions. The same analysis also supports that the vacancy in the A-site of a perovskite induces a similar vacancy in the B-site. The La3+ and Sr2+ cation substitutions in the A-site with vacancy influences the magnetic phase transition temperature (TC) inversely, which is explained in terms of the electronic bandwidth change. An anomalous non-linear change of the GP has been observed in the Sr-substituted compounds. The agglomeration of Mn3+-Mn4+ pairs (denoted as dimerons), into small ferromagnetic clusters, has been identified as the reason for the occurrence of the GP. A threshold limit of the dimeron formation explains the observed non-linear behaviour of the GP formation. The Sr-substituted compounds show a relatively large value of isothermal entropy change (maximum 3.27 J/kgK at μ_0 H=2T) owing to its sharp magnetic transition, while the broad change of magnetization in the La-substituted compound enhances the relative cooling power (maximum 98 J/kg at μ_0 H=2T).

cond-mat.mtrl-sci

Effect of reduced local lattice disorder on the magnetic properties of B-site substituted La0.8Sr0.2MnO3

Disorder induced by chemical inhomogeneity and Jahn-Teller (JT) distortions is often observed in mixed valence perovskite manganites. The main reasons for the evolution of this disorder are connected with the cationic size differences and the ratio between JT active and non-JT active ions. The quenched disorder leads to a spin-cluster state above the magnetic transition temperature. The effect of Cu, a B-site substitution in the La0.8Sr0.2MnO3 compound, on the disordered phase has been addressed here. X-ray powder diffraction reveals rhombohedral (R-3c) structures for the two compounds with negligible change of lattice volume. The chemical compositions of the two compounds were verified by ion beam analysis technique. With the change of electronic bandwidth, the magnetic phase transition temperature has been tuned towards room temperature (318 K), an important requirement for room temperature magnetic refrigeration. However, a small decrease of the isothermal entropy was observed with Cu-substitution, related to the decrease of the saturation magnetization.

cond-mat.mtrl-sci

Field induced crossover in critical behaviour and direct measurement of the magnetocaloric properties of La0.4Pr0.3Ca0.1Sr0.2MnO3

La0.4Pr0.3Ca0.1Sr0.2MnO3 has been investigated as a potential candidate for room temperature magnetic refrigeration. Results from X-ray powder diffraction reveal an orthorhombic structure with Pnma space group. The electronic and chemical properties have been confirmed by X-ray photoelectron spectroscopy and ion-beam analysis. A second-order paramagnetic to ferromagnetic transition was observed near room temperature (289 K), with a mean-field like critical behaviour at low field and a tricritical mean-field like behaviour at high field. The field induced crossover in critical behaviour is a consequence of the system being close to a first-order magnetic transition in combination with a magnetic field induced suppression of local lattice distortions. The lattice distortions consist of interconnected and weakly distorted pairs of Mn-ions, where each pair shares an electron and a hole, dispersed by large Jahn-Teller distortions at Mn3+ lattice sites. A comparatively high value of the isothermal entropy-change (3.08 J/kg-K at 2 T) is observed and the direct measurements of the adiabatic temperature change reveal a temperature change of 1.5 K for a magnetic field change of 1.9 T.

cond-mat.mtrl-sci

Evolution of Griffiths Phase and Critical Behaviour of La1-xPbxMnO3+-y Solid Solutions

Polycrystalline La1-xPbxMnO3+-y (x = 0.3, 0.35, 0.4) solid solutions were prepared by solid state reaction method and their magnetic properties have been investigated. Rietveld refinement of X-ray powder diffraction patterns showed that all samples are single phase and crystallized with the rhombohedral structure in the R-3c space group. A second order paramagnetic to ferromagnetic phase transition was observed for all materials. The Griffiths phase (GP), identified from the temperature dependence of the inverse susceptibility, was suppressed by increasing magnetic field and showed a significant dependence on A-site chemical substitution. The critical behaviour of the compounds was investigated near to their Curie temperatures, using intrinsic magnetic field data. The critical exponents (\b{eta}, γ and δ) are close to the mean-field approximation values for all three compounds. The observed mean-field like behaviour is a consequence of the GP and the formation of ferromagnetic clusters. Long-range ferromagnetic order is established as the result of long-range interactions between ferromagnetic clusters. The magnetocaloric effect was studied in terms of the isothermal entropy change. Our study shows that the material with the lowest chemical substitution (x = 0.3) has the highest potential (among the three compounds) as magnetic refrigerant, owing to its higher relative cooling power (258 J/kg at 5 T field) and a magnetic phase transition near room temperature.

cond-mat.mtrl-sci