arXiv subjects

Suja Elizabeth

Publications and source records attributed to Suja Elizabeth.

26 records · Page 2Linked to original sources

arXiv2011

Griffiths phase-like behaviour and spin-phonon coupling in double perovskite Tb$_{2}$NiMnO$_{6}$

The Griffiths phase-like features and the spin-phonon coupling effects observed in Tb$_2$NiMnO$_6$ are reported. The double perovskite compound crystallizes in monoclinic $P2_1/n$ space group and exhibits a magnetic phase transition at $T_c \sim$ 111 K as an abrupt change in magnetization. A negative deviation from ideal Curie-Weiss law exhibited by 1/$χ(T)$ curves and less-than-unity susceptibility exponents from the power-law analysis of inverse susceptibility are reminiscent of Griffiths phase-like features. Arrott plots derived from magnetization isotherms support the inhomogeneous nature of magnetism in this material. The observed effects originate from antiferromagnetic interactions which arise from inherent disorder in the system. Raman scattering experiments display no magnetic-order-induced phonon renormalization below $T_c$ in Tb$_2$NiMnO$_6$ which is different from the results observed in other double perovskites and is correlated to the smaller size of the rare earth. The temperature evolution of full-width-at-half-maximum for the {\it stretching} mode at 645 cm$^{-1}$ presents an anomaly which coincides with the magnetic transition temperature and signals a close connection between magnetism and lattice in this material.

cond-mat.str-el↗

arXiv2011

Magnetic Order of the Hexagonal Rare Earth Manganite Dy(0.5)Y(0.5)MnO3

Hexagonal Dy(0.5)Y(0.5)MnO3, a multiferroic rare-earth manganite with geometrically frustrated antiferromagnetism, has been investigated with single-crystal neutron diffraction measurements. Below 3.4 K magnetic order is observed on both the Mn (antiferromagnetic) and Dy (ferrimagnetic) sublattices that is identical to that of undiluted hexagonal DyMnO3 at low temperature. The Mn moments undergo a spin reorientation transition between 3.4 K and 10 K, with antiferromagnetic order of the Mn sublattice persisting up to 70 K; the antiferromagnetic order in this phase is distinct from that observed in undiluted (h)DyMnO3, yielding a qualitatively new phase diagram not seen in other hexagonal rare-earth manganites. A magnetic field applied parallel to the crystallographic c axis will drive a transition from the antiferromagnetic phase into the low-temperature ferrimagnetic phase with little hysteresis.

cond-mat.str-el↗

arXiv2009

Phase transitions and rare-earth magnetism in hexagonal and orthorhombic DyMnO$_{3}$ single crystals

The floating-zone method with different growth ambiances has been used to selectively obtain hexagonal or orthorhombic DyMnO$_{3}$ single crystals. The crystals were characterized by X-ray powder diffraction of ground specimen and a structure refinement as well as electron diffraction. We report magnetic susceptibility, magnetisation, and specific heat studies of this multiferroic compound in both the hexagonal and the orthorhombic structure. The hexagonal DyMnO$_{3}$ shows magnetic ordering of Mn$^{3+}$ (S =2) spins on a triangular Mn lattice at $T^{\mathrm {Mn}}_{N}$ = 57 K characterized by a cusp in the specific heat. This transition is not apparent in the magnetic susceptibility due to the frustration on the Mn triangular lattice and the dominating paramagnetic susceptibility of the Dy$^{3+}$ (S=9/2) spins. At $T^{\mathrm {Dy}}_{N}$ = 3 K, a partial antiferromagnetic order of Dy moments has been observed. In comparison, the magnetic data for orthorhombic DyMnO$_{3}$ display three transitions. The data broadly agree with results from earlier neutron diffraction experiments, which allows for the following assignment: a transition from an incommensurate antiferromagnetic ordering of Mn$^{3+}$ spins at $T^{\mathrm {Mn}}_N$ = 39 K, a {\textit{lock--in}} transition at $T_{\mathrm {lock-in}}$ = 16 K and a second antiferromagnetic transition at $T^{\mathrm {Dy}}_N$ = 5 K due to the ordering of Dy moments. Both the hexagonal and the orthorhombic crystals show magnetic anisotropy and complex magnetic properties due to 4$f-4f$ and 4$f-3d$ couplings.

cond-mat.str-el↗

arXiv2007

Polaronic state and nanometer-scale phase separation in colossal magnetoresistive manganites

High resolution topographic images obtained by scanning tunneling microscope in the insulating state of Pr0.68Pb0.32MnO3 single crystals showed regular stripe-like or zigzag patterns on a width scale of 0.4 - 0.5 nm confirming a high temperature polaronic state. Spectroscopic studies revealed inhomogeneous maps of zero-bias conductance with small patches of metallic clusters on length scale of 2 - 3 nm only within a narrow temperature range close to the metal-insulator transition. The results give a direct observation of polarons in the insulating state, phase separation of nanometer-scale metallic clusters in the paramagnetic metallic state, and a homogeneous ferromagnetic state.

cond-mat.str-el↗

arXiv2006

Critical properties in single crystals of Pr1-xPbxMnO3

The critical properties at the ferromagnetic - paramagnetic transition have been analysed from data of static magnetization measurements on single crystals of Pr1-xPbxMnO3, for x = 0.23 and x = 0.30. In Pr1-xPbxMnO3 the ferromagnetic ordering and the metal-insulator transition do not coincide in parts of the phase diagram. The crystal with x = 0.23 is a ferromagnetic insulator with Curie temperature Tc = 173 K, while the crystal with x =0.30 has Tc = 198 K and remains metallic up to a metal-insulator transition temperature Tmi = 235 K. The dc magnetization measurements were carried out in the field range from 0 to 5 T for an interval in the critical temperature range Tc+_10 K corresponding to a reduced temperature interval 0.003 < epsilon < 0.6. The exponents beta for spontaneous magnetization, gamma for the initial susceptibility above Tc and delta for the critical magnetization isotherm at Tc were obtained by static scaling analysis from modified Arrott plots and by the Kouvel Fisher method for the insulating crystal with composition x = 0.23. The data are well described by critical exponents similar to those expected for the Heisenberg universality class relevant for conventional isotropic magnets Systematic deviations from scaling in the data for the metallic crystal with composition x = 0.30 are demonstrated from effective critical exponents near the assumed ordering transition. The unconventional magnetic ordering in this system indicates the presence of frustrated magnetic couplings that suppresses magnetic ordering and lowers the transition temperature.

cond-mat.str-el↗

arXiv2003

Influence of dopant concentration on the structure and physical properties of Nd$_{1-x}$Pb$_{x}$MnO$_{3}$ single crystals

The structure of Nd$_{1-x}$Pb$_{x}$MnO$_{3}$ crystals is determined by single crystal X-ray diffraction. Substitution of Pb at the Nd site results in structural phase change from tetragonal (x = 0.25) to cubic (x = 0.37). These changes are attributed to the progressive removal of inter-octahedral tilting and minimization of the octahedral distortion leading to a higher symmetry as doping concentration increases. While the unit cell volume of tetragonal structure ($\it{P4/mmm}$) is comparable to that of parent NdMnO$_{3}$, the volume of cubic unit cell ($\it{Pm\bar{3}m}$) is doubled. Electron diffraction patterns support these results and rule out the possibility of twinning. Changes in transport properties as a function of temperature at different doping levels are in accordance with the observed structural changes. It is noticed that $\it{T_{c}}$ and $\it{T_{MI}}$ increase with x.

cond-mat.str-el↗

arXiv2003

Critical properties of the double exchange ferromagnet Nd0.4Pb0.4MnO3

Results of a study of dc-magnetization M(T, H), performed on a Nd0.6Pb0.4MnO3 single crystal in the temperature range around T_C (Curie temperature) which embraces the critical region | epsilon | = |T -T_C |/T_C <= 0.05 are reported. The magnetic data analyzed in the critical region using the Kouvel-Fisher method give the values for the T_C =156.47 +/- 0.06 K and the critical exponents, beta = 0.374 +/- 0.006 (from the temperature dependence of magnetization), and gamma = 1.329 +/- 0.003 (from the temperature dependence of initial susceptibility). The critical isotherm M(T_C, H) gives delta = 4.547 +/- 0.1. Thus the scaling law gamma+beta=delta beta is fulfilled. The critical exponents obey the single scaling-equation of state M(H, epsilon) = epsilon^b f_+/- (H/epsilon^(beta + gamma)) where, f_+ for T > T_C and f_- for T< T_C. The exponent values are very close to those expected for the universality class of 3D Heisenberg ferromagnets with short-range interactions.

cond-mat.str-el↗

arXiv1998

The Density of States of hole-doped Manganites: A Scanning Tunneling Microscopy/Spectroscopy study

Variable temperature scanning tunneling microscopy/spectroscopy studies on single crystals and epitaxial thin films of hole-doped manganites, which show colossal magnetoresistance, have been done. We have investigated the variation of the density of states, at and near the Fermi energy ($E_f$), as a function of temperature. Simple calculations have been carried out, to find out the effect of temperature on the tunneling spectra and extract the variation of density of states with temperature, from the observed data. We also report here, atomic resolution images, on the single crystals and larger range images showing the growth patterns on thin films. Our investigation shows unambiguously that there is a rapid variation in density of states for temperatures near the Curie temperature ($T_c$). While for temperatures below $T_c$, a finite DOS is observed at $E_f$, for temperatures near $T_c$ a hard gap opens up in the density of states near $E_f$. For temperatures much higher than $T_c$, this gap most likely gives way to a soft gap. The observed hard gap for temperatures near $T_c$, is somewhat higher than the transport gap for all the materials. For different materials, we find that the magnitude of the hard gap decreases as the $T_c$ of the material increases and eventually, for materials with a $T_c$ close to 400 K, the value of the gap approaches zero.

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