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Vanadium dioxide (VO2) has drawn significant attention for its near room temperature insulator to metal transition and associated structural phase transition. The underlying Physics behind the temperature induced insulator to metal and concomitant structural phase transition in VO2 is yet to be fully understood. We have investigated the kinetics of the above phase transition behaviors of VO2 with the help of resistivity measurements and Raman spectroscopy. Resistance thermal hysteresis scaling and relaxation measurements across the temperature induced insulator to metal transition reveal the unusual behaviour of this first-order phase transition, whereas Raman relaxation measurements show that the temperature induced structural phase transition in VO2 follows usual behaviour and is consistent with mean field prediction. At higher temperature sweeping rates decoupling of insulator to metal transition and structural phase transition have been confirmed. The observed anomalous first order phase transition behavior in VO2 is attributed to the unconventional quasi particle dynamics, i.e. significantly lowered electronic thermal conductivity across insulator to metal transition, which is confirmed by ultrafast optical pump-probe time domain thermoreflectance measurements., Comment: 25 pages, 8 figures

We report experimental evidence of emergent broken symmetry Fermi liquid state in an isolated single crystalline nanorod of $\rm Pr_2 Ir_2 O_7$. We find clear signature of the onset of the Fermi liquid behavior at low temperature marked by the sign inversion of magnetoresistance from negative at high temperature, characteristic of incoherent Kondo scattering, to positive as well as a $\rm T^2$ dependence of resistivity at low temperature. A resistive anomaly is observed, which is accompanied by thermal hysteresis in the presence of magnetic field, suggesting itinerant metamagnetism. The observed high field negative magnetoresistance with quadratic field dependence at low temperature, which is most likely due to suppression of itinerant spin fluctuation, and the irreversibility of the magneto-resistive properties in the Fermi liquid regime suggest existence of an unusual state with broken spin rotation and time reversal symmetry, hallmark of `hastatic' order. The major features of such temperature dependence of resistivity and magnetoresistance can be explained in a phenomenological model incorporating two distinct hybridization channels, which is physically consistent with the possibility of the formation of the `hastatic' Fermi liquid phase., Comment: 10 pages with appendix

The thermodynamic stability of the premartensite (PM) phase has been a topic of extensive investigation in shape memory alloys as it affects the main martensite phase transition and the related physical properties. In general, the PM phase is stable over a rather narrow temperature-composition range. We present here evidence for chemical pressure induced suppression of the main martensite transition and stabilization of the PM phase over a very wide temperature range from 300 K to around 5 K in a magnetic shape memory alloy (MSMA) Ni50Mn34In16 using magnetic susceptibility, synchrotron X-ray powder diffraction (SXRPD) studies and first-principles calculations. The ac-susceptibility studies show a highly skewed and smeared peak around 300 K without any further transition up to the lowest temperature of our measurement (5 K) for around 5% Al substitution. The temperature evolution of the SXRPD patterns confirms the appearance of the PM phase related satellite peaks at and below 300 K without any splitting of the main austenite (220) peak showing preserved cubic symmetry. This is in marked contrast to the temperature evolution of the SXRPD patterns of the martensite phase of the Al free as well as around 3% Al substituted compositions where the austenite (220) peak shows a clear splitting due to Bain distortion/symmetry breaking transition. Our theoretical calculations support the experimental findings and reveal that the substitution at the In site by a smaller size atom, like Al, can stabilize the PM phase with preserved cubic symmetry. Our results demonstrate that Al-substituted Ni-Mn-In MSMAs provide an ideal platform for investigating the physics of various phenomena related to the PM state.

Here, we study the electrical transport and specific heat in 4$d$ based ferromagnetic material SrRuO$_3$ and its Ti substituted SrRu$_{1-x}$Ti$_x$O$_3$ series ($x$ $\le$ 0.7). The SrRuO$_3$ is a metal and shows itinerant ferromagnetism with transition temperature $T_c$ $\sim$ 160 K. The nonmagnetic Ti$^{4+}$ (3$d^0$) substitution would not only weaken the active Ru-O-Ru channel but is also expected to tune the electronic density and electron correlation effect. A metal to insulator transition has been observed around $x$ $\sim$ 0.4. The nature of charge transport in paramagnetic-metallic state ($x$ $\leq$ 0.4) and in insulating state ($x$ $>$ 0.4) follows modified Mott's variable range hopping model. In ferromagnetic-metallic state, resistivity shows a $T^2$ dependence below $T_c$ which though modifies to $T^{3/2}$ dependence at low temperature. In Ti substituted samples, temperature range for $T^{3/2}$ dependence extends to higher temperature. Interestingly, this $T^{3/2}$ dependence dominates in whole ferromagnetic regime in presence of magnetic field. This evolution of electronic transport behavior can be explained within the framework of Fermi liquid theory and electron-magnon scattering mechanism. The negative magnetoresistance exhibits a hysteresis and a crossover between negative and positive value with magnetic field which is connected with magnetic behavior in series. The decreasing electronic coefficient of specific heat with $x$ supports the increasing insulating behavior in present series. We calculate a high Kadowaki-Woods ratio ($x$ $\leq$ 0.3) for SrRuO$_3$ which increases with substitution concentration. This signifies an increasing electronic correlation effect with substitution concentration., Comment: 21 pages, 10 figures

We report large magnetoresistance (MR) and Shubnikov-de Haas (SdH) oscillations in single crystals of magnetically (M= Ni and Fe) doped M$_x$Bi$_{0.97-x}$Sb$_{0.03}$ ($x=$ 0, 0.02) topological insulators. The R$\bar{3}$m symmetry and phase have been confirmed by the Rietveld refinement of x-ray diffraction data. Interestingly, a magnetic field induced phase transition from semi-metallic to semi-conducting type is found with the energy gap around 80 meV at 15 Tesla in the $x=$ 0 sample. Moreover, we observe linear behavior of MR up to 15 Tesla in transverse mode and SdH oscillations in longitudinal mode where the field direction is with respect to the current and crystal plane. For the parent sample, we found the coherence length L$_\phi=$ 12.7 nm through the fitting of MR data in transverse mode with modified H-L-N equation. The extracted frequencies of SdH oscillations using the fast Fourier transform method and Landau level (LL) fan diagram are found to be consistent for the parent and Ni doped samples. The determined Fermi surface area is found to be slightly larger in Ni doped as compared to the parent sample possibly due to change in the Fermi energy. The Kohler's plot indicates a single scattering mechanism below 100 K. More importantly, the analysis with the help of LL fan diagram reveals the non-zero Berry phase $\phi_{\rm B}= -$(1$\pm$0.1)$\pi$, which demonstrates the non-trivial topological states near the Dirac point in the parent and Ni doped samples., Comment: submitted, added fig2c, corrected fig4

The nature of the magnetic transition, critical scaling of magnetization, and magnetocaloric effect in Mn$_{1+x}$Fe$_{4-x}$Si$_{3}$ ($ x =$ 0 to 1) are studied in detail. Our measurements show no thermal hysteresis across the magnetic transition for the parent compound which is in contrast with the previous report and corroborate the second order nature of the transition. The magnetic transition could be tuned continuously with Mn substitution at the Fe site. The Mn substitution leads to a linear increase in the unit cell volume and a slight reduction in the effective moment. A detailed critical analysis of the magnetization data for $x = 0.0$ and 0.2 is performed in the critical regime using the modified Arrott plots, Kouvel-Fisher plot, universal curve scaling, and scaling analysis of magnetocaloric effect. The magnetization isotherms follow modified Arrott plots with critical exponent ($\beta \simeq 0.308$, $\gamma \simeq 1.448$, and $\delta \simeq 5.64$) for the parent compound ($x=0.0$) and ($\beta \simeq 0.304$, $\gamma \simeq 1.445$, and $\delta \simeq 5.64$) for $x = 0.2$. The Kouvel-Fisher and universal scaling plots of the magnetization isotherms further confirm the reliability of our critical analysis and values of the exponents. These values of the critical exponents are found to be same for both the parent and doped samples which do not fall under any of the standard universality classes. A reasonable magnetocaloric effect $\Delta S_{\rm m}\simeq-6.67$~J/Kg-K and -5.84~J/Kg-K for $x= 0.0$ and 0.2 compounds, respectively, with a huge relative cooling power ($RCP \sim 700$~J/Kg) for 9~T field change is observed. The universal scaling of magnetocaloric effect further mimics the second order character of the magnetic transition. The obtained critical exponents from the critical analysis of magnetocaloric effect agree with the values deduced from the magnetic isotherm analysis., Comment: 18 pages, 13 figures, 1 table

The effect of Sr doping in BaTiO3 (BTO) with nominal compositions Ba0.80Sr0.20TiO3 (BSTO) have been explored in its structural, lattice vibration, dielectric, ferroelectric and electrocaloric properties. The temperature dependent dielectric results elucidate the enhancement in dielectric constant and exhibit three frequency independent transitions around 335, 250 and 185 K which are related to different structural transitions. All these transitions occur at lower temperature as compared with pristine BTO, however; remnant electric polarization (P) of BSTO is much higher than in BTO. The value of P is around 5 microC/cm2 at room temperature and the maximum P around 8 microC/cm2 is observed at tetragonal to orthorhombic and orthorhombic to rhombohedral transitions. The electro-caloric effect shows the maximum adiabatic change in temperature deltaT approx 0.24 K at cubic to tetragonal transition. The temperature dependent synchrotron X-ray diffraction and Raman results shows correlations between P, crystal structure and lattice vibrations. Our results demonstrate the enhancement in ferroelectric properties of BTO with Sr doping. The origin of the enhancement in ferroelectric property is also discussed which is related to the appearance of superlattice peak around room temperature due to TiO6 octahedral distortion. These enhanced properties would be useful to design lead free high quality ferroelectric and piezoelectric materials., Comment: 22 pages, 7 figures

We report magneto-dielectric properties of partially B-site ordered monoclinic Tb2CoMnO6 double perovskite thin film epitaxially grown by metalorganic aerosol deposition technique. Transmission electron microscopy and electron energy loss spectroscopy mapping shows the presence and distribution of both Co2+ and Co3+ ions in the film, evidencing a partial B-site disorder, which was further confirmed by the observation of reduced saturation magnetization at low temperatures. The ferromagnetic Curie temperature, TC=110 K, is slightly higher as compared to the bulk value (100 K) probably due to an in plane tensile strain. Remarkably, a short range ordering of spins at T*~190 K>>TC was established and assigned to the B-site disorder in the film. Two different dielectric relaxation peaks have been observed; they merge at the same temperature T* of short range spin correlations. Moreover, an unexpected high temperature dipolar relaxor-glass-like transition at T~T* was observed, at which a coupling to short range magnetic correlations results in a 4% magneto-dielectric coupling., Comment: 19 pages, 6 figures

In RBaCo4O7 (R = Ca, Y and Rare earth) cobaltite family, only CaBaCo4O7 shows 3D long range ferrimagnetic and spin driven electric polarization properties. In the present study, we have investigated the structural, magnetic and electric polarization properties in YBaCo4O7 and DyBaCo4O7 members of this family and the obtained results are compared with the CaBaCo4O7. The compound YBaCo4O7 showed a series of magnetic transitions in agreement with reported literature, additionally, a cluster glass behavior below 5 K is observed. Powder neutron diffraction studies on DyBaCo4O7 cobaltite showed an orthorhombic Pbn21 symmetry and signature of short-range 120 degree magnetic correlations of kagome layer and a spin glass behavior below 65 K. Dielectric measurements on both the samples showed strong frequency dispersion at high temperature and frequency independent behavior at low temperature without dielectric anomaly. Pyroelectric current measurement has showed a broad peak around 50 K in both the samples; however, a careful analysis relates the peak to thermally stimulated depolarization current. This study signifies that the giant structural distortions and cobalt charge ordering at kagome layer are the key factors to drive both long range magnetic ordering and spin driven electric polarization in this cobaltite family., Comment: accepted in EPL

We report here a discovery of electrically driven insulator to metal transition (IMT) and concomitant isostructural volume expansion in the layered cobaltates which otherwise do not exhibit temperature dependent IMT. These findings are demonstrated at macroscopic, microscopic and atomic scales. With application of voltage growth of metallic regions have been observed in the 2D layered La2-xSrxCoO4. Growth of metallic regions is associated with volume increase (strain as high as 0.3%). Non thermal IMT and electro-strain are proposed to be caused by electro-proliferation of the Co3+ high spin states., Comment: 13 pages, 7 figures

Complex magneto structural behaviour of rare rich intermetallic Tb$_3$Co is reported in this study. Below the 84K (T$_N$), it undergoes a first order magnetic transition 72K confirmed from specific heat and magnetization measurements. Detailed study using magnetization, specific heat, neuron diffraction and ac-susceptibility measurements suggests that the compound in the question possesses canted magnetic structure. Neutron diffraction reveals that Tb moments are aligned antiferromagnetically (AFM) in ab plane and ferromagnetically (FM) along c direction. This study focusses on the temperature evolution of magnetic order at low temperatures. Neutron Diffraction clearly shows that magnetic structure remains more or less same up to 70K although low field magnetization exhibits a transition like feature around 30K. Field dependent neutron diffraction suggests that a strong spin-lattice coupling is present at lower temperature region (below 20K) compared to that for T above 40K. This is responsible for the observed drop in ZFC magnetization around 30K and is not due to any change in magnetic structure. Another important but surprising result that observed is the signature of magnetic glass below 72K in frequency dependent ac susceptibility measurements. Real part of ac-susceptibility data shows dispersion with frequency which on detailed analysis provides evidence for spin glass behaviour in the compound riding on top of non-collinear AFM order. Higher order harmonics in ac non-linear) susceptibilities, which are expected to show a well-defined behaviour for pure FM or AFM or spin glass or cluster glass systems, were also measured. However, the non-linear susceptibilities do not exhibit any well-known variation but show complex behaviour thus indicating Tb$_3$Co is neither a pure AFM or FM or spin glass system but provides another evidence for non-collinear magnetic structure., Comment: 10 pages, 15 figures being submited as regular paper

Effect of Ge substitution on first order ferrimagnetic (FRI) - antiferromagnetic (AFM) transition in Mn$_2$Sb has been studied. It shows that transition temperature (T$_t$) can be tuned between 119~K - 271~K by substituting 2.5-10\% Ge at Sb site in Mn$_2$Sb. The variation of density of state at Fermi level N(E$_f$) with Ge substitution shows that dN(E)/dE is positive at E$_f$ in the AFM state. With the application of magnetic field T$_t$ shifts to low temperature, which results in a giant negative magnetoresistance (MR) reaching a value of 70\% for 2.5\% substitution. Our results show that FRI to AFM transformation during cooling stops around 35 K, even though it remains incomplete. It along with non-monotonic variation of lower critical field, open loop in isothermal MR and increasing difference in zero field cooled warming (ZFCW) and field cooled warming (FCW) resistivity with increasing magnetic field shows that FRI to AFM transition is kinetically arrested in the case of 2.5\% Ge substitution.

Multiferroics where at least two primary ferroic orders are present and coupled in a single system constitute an important class of materials. They attracted special consideration as they present both intriguing fundamental physics problems and technological importance for potential multifunctional devices. Here, we present the evidence of multiferroicity and magnetoelectric (ME) coupling in alpha-Mn2O3; a unique binary perovskite. Corresponding to the antiferromagnetic (AFM) ordering around 80K, a clear frequency independent transition is observed in the dielectric permittivity. We showed that electric polarization emerges near AFM regime that can be modulated with magnetic field. The detailed structural analysis using synchrotron radiation X-ray diffraction demonstrates the increase in structural distortion with decreasing temperature, as well as changes in the unit cell parameters and bond lengths across the ferroelectric and magnetic ordering temperatures. This observation of multiferroicity and magnetoelastic coupling in alpha-Mn2O3 provides insights for the exploration of ME coupling in related materials., Comment: Page 20 and 6 figures

We investigate the temperature evolution of the structural parameters of potential ferrotoroidic LiFeSi2O6 compound across structural and magnetic phase transitions. The structural transition (TS)is around 220K and the paramagnetic to antiferromagnetic transition (TN) is around 18K. The lattice parameters exhibit unusual temperature dependence and based on its behaviour, the exper- imental results can be divided into 3 regions.In region I (300K to 240K), the cell parameters are mainly governed by mere thermal effect. As the compound enters region II (below 240K to 50K), the lattice parameters show non linear behaviour. In this region, the exchange pathways that lead to the magnetic interactions within and between the Fe-Fe chains do not show significant response.The region III (below 50K) is dominated by the magnetic contribution where we observe setting up of intra and inter-chain magnetic interaction. This behaviour is unlike other low dimensional com- pounds like Ca3Co2O6, Sr3NiRhO6, MnTiO3 etc. thereby suggesting the magnetism in LiFeSi2O6 is of three dimensional nature. The present results will be helpful in understanding the evolution of the spin rings that give rise to net toroidal moment and hence its multiferroic behaviour., Comment: 6 pages, 7 figures

Superconducting transition temperature $T_C$ of some of the cubic $\beta$-phase Mo$_{1-x}$Re$_x$ alloys with x > 0.10 is an order of magnitude higher than that in the elements Mo and Re. We investigate this rather enigmatic issue of the enhanced superconductivity with the help of experimental studies of the temperature dependent electrical resistivity ($\rho$(T)) and heat capacity (C$_P$(T)), as well as the theoretical estimation of electronic density of states (DOS) using band structure calculations. The $\rho$(T) in the normal state of the Mo$_{1-x}$Re$_x$ alloys with x > 0.15 is distinctly different from that of Mo and the alloys with x < 0.10. We have also observed that the Sommerfeld coefficient of electronic heat capacity $\gamma$, superconducting transition temperature $T_C$ and the DOS at the Fermi level show an abrupt change above x > 0.10. The analysis of these results indicates that the value of electron-phonon coupling constant {\lambda}ep required to explain the $T_C$ of the alloys with x > 0.10 is much higher than that estimated from $\gamma$. On the other hand the analysis of the results of the $\rho$(T) reveals the presence of phonon assisted inter-band s-d scattering in this composition range. We argue that a strong electron-phonon coupling arising due to the multiband effects is responsible for the enhanced $T_C$ in the $\beta$-phase Mo$_{1-x}$Re$_x$ alloys with x > 0.10.

A wide variation in the disorder strength, as inferred from an order of magnitude variation in the longitudinal resistivity of Co2FeSi (CFS) Huesler alloy thin films of fixed (50 nm) thickness, has been achieved by growing these films on Si(111) substrates at substrate temperatures ranging from room temperature (RT) to 600 C. An in-depth study of the influence of disorder on anomalous Hall resistivity,longitudinal resistivity(LR) and magnetoresistance, enabled by this approach, reveals the following. The side-jump mechanism gives a dominant contribution to anomalous Hall resistivity (AHR) in the CFS thin films, regardless of the degree of disorder present. A new and novel contribution to both LR and AHR characterized by the logarithmic temperature dependence at temperatures below the minimum, exclusive to the amorphous CFS films, originates from the scattering of conduction electrons from the diffusive hydrodynamic modes associated with the longitudinal component of magnetization, called diffusons. In these amorphous CFS films, the electron-diffuson, e d, scattering and weak localization (WL) mechanisms compete with that arising from the inelastic electron magnon, e m, scattering to produce the minimum in longitudinal resistivity, whereas the minimum in AHR is caused by the competing contributions from the e d and e m scattering, as WL does not make any contribution to AHR. In sharp contrast, in crystalline films, enhanced electron electron Coulomb interaction (EEI), which is basically responsible for the resistivity minimum, makes no contribution to AHR with the result that AHR does not exhibit a minimum., Comment: 7 pages, 7 figures

We have performed an experimental study on the temperature dependence of electrical resistivity $\rho$($T$) and heat capacity $C$($T$) of the Mo$_{1-x}$Re$_x$ $(x = 0.20, 0.25)$ alloy superconductors in different magnetic fields. In the presence of applied magnetic field, the electrical resistivity of these alloys go to zero at a temperature well above the bulk superconducting transition temperature obtained with the help of heat capacity measurements in the same magnetic field. Our study indicates the presence of surface superconducting state in these alloys, where the flux lines are pinned in the surface sheath of the superconductor. The configuration of the flux-lines (2d pancake-like) in the surface sheath is understood in the realm of the flux-spot model. Experimental evidence in support of the surface mixed-state state or "Kulik vortex-state" and the occurrence of a vortex-liquid to vortex-glass transition is presented., Comment: 15 pages, 9 figures

It is a comment on a paper titled "Reversibility of magnetic field driven transition from electronic phase separation state to single-phase state in manganites: A microscopic view" by Liu et al. Phys. Rev. B 96 (2017) 195154., Comment: Comment on Phys. Rev. B 96 (2017) 195154

Co4Nb2O9 (CNO) having {\alpha}-Al2O3 crystal structure with Co chains along c-direction shows gigantic magnetoelelctric coupling below antiferromagnetic ordering temperature of 27 K but above a spin flop field of 1.6 T. We have investigated structural, magnetic and magnetoelectric properties of Fe substituted (10% and 20%) samples and compared with the parent one. In fact magnetic and specific heat measurements have revealed an additional magnetic transition below 10 K and presence of short range magnetic ordering above ~ 50 K in parent as well as in Fe substituted samples. Linear magnetoelelctric and ferroelectric behaviours are evidenced in the Fe substituted samples where an electric field of 5 kV/m is sufficient to align the dipoles and the magnetoelelctric coupling is ensured for magnetic fields as low as 0.25 T, far below the spin flop field., Comment: 13 pages

Single phase polycrystalline sample of perovskite Sr2TiMnO6 (STMO) has been successfully synthesized via solid state reaction route. Its detailed structural and physical properties have been studied using x-ray diffraction, transmission electron microscopy, magnetization, specific heat, and dielectric measurements. Rietveld analysis of the powder XRD data and transmission electron microscopy studies confirm that STMO is not a double perovskite structure with Fm-3m space group. But it is a disordered perovskite structure with Pm-3m space group where Ti4+ and Mn4+ ions are randomly distributed at the 1b site. The dc magnetization (\c{hi}dc-vs-T) measurements in the temperature range 2-300K reveals a single anomaly at ~13K with predominant long range canted antiferromagnetic (AFM) ordering. The frequency invariant maxima at 13K in the ac susceptibility (\c{hi}ac-vs-T) discards the spin-glass behaviour in STMO. Despite the presence of sharp feature in M-T data, the specific heat data (Cp-vs-T) shows only a broad hump around 13K, which has been attributed to the magneto-structural ordering giving rise to canted AFM state in chemically disorder STMO. Matching with the magnetic and specific heat anomaly, the dielectric permittivity also shows a broad anomaly around 14K, indicating the possible magneto-dielectric coupling in STMO., Comment: this paper has been withdrawn due to minor error in the calculation of dielectric constant

A systematic study of thermomagnetic irreversibility CoS$_{1.76}$Se$_{0.24}$ has been carried out. Our study shows that the resistivity at low temperature can be tuned by cooling in different magnetic fields and the critical field required for paramagnetic (PM) to ferromagnetic (FM) transition varies non-monotonically with temperature. The field induced PM to FM transition results in giant positive magnetoresistance (MR) of about 160\% at 5 K. Measurements under CHUF (cooling and heating in unequal magnetic field) protocol show reentrant transition on warming under higher magnetic field (than that applied during cooling). It indicates that the glass like behaviour in this system can be explained in the framework of the kinetic arrest of first order transition. Among the growing list of diverse system showing glass like arrested magnetic states, the present system is the first example where, kinetic arrest is observed for a disordered (here PM) to ordered (here FM) first order transition., Comment: 10 pages, 4 figures, Kinetic arrest, CHUF, Magnetoresistance, Metamagnetism, First order magnetic transition, Di-chalcogenides, Sulphides

Novel thermal effects across the first order antiferromagnetic (AFM) - ferromagnetic (FM) transition in an intermetallic alloy are reported. They show instances of warming when heat is extracted from the sample, and cooling when heat is provided to the sample across AFM-FM transition in Ta doped $HfFe_2$, thus providing indisputable evidence of metastable supercooled AFM and superheated FM states, respectively. Such thermal effects in a magnetic solid prepared from commercially available materials has been reported for the first time. The transition proceeds in multiple steps which is interpreted in the framework of quenched disorder broadening of AFM-FM transition and classical nucleation theory. Measurements in the presence of magnetic field conform to above frame work., Comment: 5 pages, 3 figures and 1 Table

We have investigated the temperature evolution of magnetism and its interrelation with structural parameters in perovskite-based layered compound Sr$_2$IrO$_4$, which is believed to be a $J_{eff}$ = 1/2 Mott insulator. The structural distortion plays an important role in this material which induces a weak ferromagnetism in otherwise antiferromagnetically ordered magnetic state with transition temperature around 240 K. Interestingly, at low temperature below around 100 K, a change in magnetic moment has been observed. Temperature dependent x-ray diffraction measurements show sudden changes in structural parameters around 100 K are responsible for this. Resistivity measurements show insulating behavior throughout the temperature range across the magnetic phase transition. The electronic transport can be described with Mott's two-dimensional variable range hopping (VRH) mechanism, however, three different temperature ranges are found for VRH, which is a result of varying localization length with temperature. A negative magnetoresistance (MR) has been observed at all temperatures in contrast to positive behavior generally observed in strongly spin-orbit coupled materials. The quadratic field dependence of MR implies a relevance of a quantum interference effect., Comment: 9 pages, 9 figures

We report room temperature giant baro-resistance ($\approx$128\%) in $Fe_{49}(Rh_{0.93}Pd_{0.07})_{51}$. With the application of external pressure and magnetic field the temperature range of giant baro-resistance ($\approx$600\% at 5K and 19.9 kbar and 8 Tesla) and magnetoresistance ($\approx$-85\% at 5K and 8 tesla) can be tuned from 5 K to well above room temperature. As the AFM state is stabilized at room temperature under external pressure, it shows giant room temperature magnetoresistance ($\approx$-55\%) with magnetic field. Due to coupled magnetic and latticel changes, the isothermal change in room temperature resistivity with pressure (in the absence of applied magnetic field) as well as magnetic field (under various constant pressure) can be scaled together to a single curve when plotted as a function of X = T + 12.8*H - 7.2*P.

Large magnetocaloric effect (MCE) and magnetoresistance (MR) together with negligible hysteresis loss has been observed in ErNiSi compound, which undergoes metamagnetic transition at low temperatures. Magnetization, heat capacity and resistivity measurements confirm the metamagnetic transition. The maximum value of isothermal entropy change and MR for a field change of 50 kOe are found to be 19.1 J/kg K and -34 %. Large MCE with negligible magnetic hysteresis loss could make this material promising for low temperature magnetic refrigeration., Comment: 12 pages, 5 figures

Structural phase transition studies employing low-temperature transmission electron microscopy, and low-temperature x-ray diffraction have been carried out on nearly stoichiometric ({\delta}=0.01) and off-stoichiometric ({\delta}=0.12) versions of La0.2Sr0.8MnO3-{\delta} manganite. The nearly stoichiometric La0.2Sr0.8MnO3-{\delta} under goes a cubic to Jahn-Teller distorted C-type antiferromagnetic tetragonal phase-transition at 260K. For off-stoichiometric La0.2Sr0.8MnO3-{\delta} the Jahn-Teller distorted tetragonal phase transition gets totally suppressed and the basic perovskite lattice remains cubic but shows a charge ordered phase. Stabilization of charge ordered phase in the absence of cooperative Jahn-Teller distortion has been attributed to coulomb-repulsion and Hunds coupling energy. The off-stoichiometric sample shows characteristically different physical properties. This has been realized through transport, magnetic and calorimetric measurements. A smooth crossover from variable range hopping transport to power-law dependence of resistivity ({\rho}) on temperature (T) i.e. {\rho}=C.T-{\alpha} has been realized. This has been attributed to multistep inelastic tunneling through channels involving localized states around oxygen vacancy sites., Comment: 26 pages, 5 figures

Effect of oxygen off-stoichiometry on the structural and magnetic properties of La0.15Sr0.85MnO3-d (d = 0.02,0.14) has been studied employing low-temperature x-ray diffraction, calorimetry, electrical-transport and magnetization. The nearly stoichiometric composition under goesfirst order phase-transition from cubic to tetragonal P4/mmm at 238 K accompanied by magnetic and electrical phase-transitions. On the contrary the off-stoichiometric composition does not show any transition and remains cubic Pm-3m down to 80 K. Offstoichiometry induced oxygen-vacancy seems to suppress the cooperative JT distortion and possibly stabilize a G-type antiferromagnetic phase with localized cantedspins. Thus we demonstrate that controlling oxygen stoichiometry is a way of structure/property engineering in electron-doped-like manganites., Comment: 17 pages, 5 figures

Present study reveals that the free energy landscape of the La5/8-yPryCa3/8MnO3 (LPCMO) system could be modified by elastic strain interaction in the epitaxial thin films. Epitaxial LPCMO thin films of various thicknesses are grown on LaAlO3 substrate by pulsed laser deposition. With increasing thickness, by virtue of island growth morphology, strain disorder is invoked in thin films during strain relaxation process. The length-scale of phase separation is found to be highly correlated with strain disorder. Magneto-transport measurements demonstrate that coherent strain stabilizes charge ordered insulating phase while strain disorder stabilizes metallic phase. Resistivity under cooling and heating in unequal field (CHUF) protocol exhibits lower value of freezing temperature for strain disordered films compared to bulk system. Raman spectroscopy reveals that the charge ordered insulating and ferromagnetic metallic phases are structurally dissimilar and possess monoclinic and rhombohedral like symmetries respectively. Interfaces between two phases strongly influence low temperature glassy metastable state resulting in different phase separation states in the LPCMO thin films.

We demonstrate interface energy level engineering, exploiting the modification in energy band structure across Verwey phase transition of $Fe_{3}O_{4}$ electrode, in a $Fe_{3}O_{4}$(111)/$Alq_{3}$/Co vertical spin-valve (SV) device. Experimental results on device characteristics I-V) study exhibit a transition in conduction mode from carrier injection to tunneling across Verwey transition temperature ($T_{V}$) of $Fe_{3}O_{4}$ electrode. Both giant magneto-resistance (GMR) and tunneling MR (TMR) have been observed in a single SV device as a function of temperature, below and above $T_{V}$, respectively. Appearance of GMR, accompanied by injection limited natural Schottky-like I-V characteristics, provide evidences of spin injection at electrode/$Alq_{3}$ interface and transport through molecular orbitals in this SV device. Features of TMR exhibit significant differences from that of GMR. This is due to the dominant hyperfine-field interaction in the multi-step tunneling regime. We have achieved room-temperature SV operation in our device. A phenomenological model for device operation has been proposed to explain the transition in the conduction mode and associated MR features across $T_{V}$. We propose that the tuning of charge gap at Fermi level across Verwey transition due to charge ordering on the octahedral iron sites of $Fe_{3}O_{4}$ results in a corresponding tuning of conduction mode causing this unique cross over from GMR to TMR in this ferrite-based organic SV., Comment: GMR to TMR changeover across Verwey transition of the electrode in a single spin-valve device

Low temperature high magnetic field $^{57}Fe$ M$\ddot{o}$ssbauer measurements were carried out on inter-metallic $Hf_{0.77}Ta_{0.23}Fe_2$ compound by following novel paths in H-T space. The ferromagnetic (FM) fraction at 5K and zero magnetic field is shown to depend on cooling field i.e., higher the field higher is the FM fraction. M$\ddot{o}$ssbauer spectra collected in the presence of 4 Tesla magnetic field shows that the antiferromagnetic (AFM) spins cant with respect to the applied magnetic field and hence, contribute to the total bulk magnetization in this compound. The data also show induced magnetic moment even at the 2a site of AFM phase. M$\ddot{o}$ssbauer spectra collected using CHUF (cooling and heating in un-equal magnetic fields) protocol shows re-entrant transition when sample is cooled in zero field and measured during warming in 4 Tesla showing FM state as the equilibrium state. The present work is the first microscopic experimental evidence for the de-vitrification of kinetically arrested magnetic state., Comment: 7 pages, 7 figures and 3 Tables