Browsing by Author "Wu, H. C."
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Item type:Item, Anisotropic spin-flip-induced multiferroic behavior in kagome Cu3Bi(SeO3)(2)O2Cl(2017-03-15) ;Wu, H. C. ;Chandrasekhar, K. Devi ;Yuan, J. K. ;Huang, J. R.Lin, J. -Y.Compared to the previous report on Cu3Bi(SeO3)(2)O2X (X = Cl, Br) [V. Gnezdilov et al., (arXiv: 1604.04249)], where no dielectric anomaly was observed without magnetic field near T-N similar to 25.6K, we further present the dielectric behaviors without and with magnetic field in Cu3Bi(SeO3)(2)O2Cl. At zero field H = 0, an antiferromagnetic transition from magnetization and specific heat measurements is clearly established at T-N, while no dielectric anomaly was observed. Those results are similar to the previous report [V. Gnezdilov et al., (arXiv: 1604.04249)]. Above the critical field H-c similar to 0.8 T, a metamagnetic spin-flip transition from antiferromagnetic to ferrimagnetic order at T similar to T-N is induced anisotropically only for H broken vertical bar broken vertical bar c. Meanwhile, a ferroelectric behavior from dielectric and pyroelectric current measurements is observed below T similar to T-N; then a corresponding type-II multiferroics emerges above H-c. The key mechanism of the anisotropic spin-flip-induced multiferroicity in Cu3Bi(SeO3)(2)O2Cl can be ascribed to the breaking of magnetic twofold symmetry in the bc plane above H-c.Item type:Item, Antiferroelectric antiferromagnetic type-I multiferroic Cu9O2(SeO3)(4)Cl-6(2019-12-11) ;Wu, H. C. ;Denisova, K. N. ;Menzel, D. ;Kakarla, D. ChandrasekharMaximova, O. V.We report that Cu9O2(SeO3)(4)Cl-6 is a new multiferroic compound. Comprehensive studies of this compound have been carried out on single crystals as well as polycrystalline samples. Magnetic susceptibility chi and specific heat C with H parallel to c axis both reveal an anomaly at T-N = 37 K associated with the long-range antiferromagnetic order. However, no signature of this phase transition is seen with the H parallel to b axis, providing evidence of the anisotropic nature of its magnetic properties. The results of chi measurements are consistent with the temperature evolution of the intensity of magnetic reflections from the neutron diffraction experiments. The magnetic structure derived from neutron scattering measurements shows that half of the Cu(5) ions carry no moments. Furthermore, an anomaly in the dielectric constant near T-N and observable magnetoelectric coupling below T-N are found. At high temperatures, a dielectric peak at T-E = 267 K is identified with no measurable spontaneous polarization below T-E, thereby suggesting an antiferroelectric order. A steplike anomaly seen in chi(T) at T-E hints the weak spin-lattice coupling. Concomitantly, high-resolution temperature-dependent synchrotron x-ray diffraction experiments elucidate a local structural distortion at T-E.Item type:Item, Antisite disorder driven spontaneous exchange bias effect in La2-xSrxCoMnO6 (0 <= x <= 1)(2016-03-02) ;Murthy, J. Krishna ;Chandrasekhar, K. D. ;Wu, H. C. ;Yang, H. D.Lin, J. Y.Doping at the rare-earth site by divalent alkaline-earth ions in perovskite lattice has witnessed a variety of magnetic and electronic orders with spatially correlated charge, spin and orbital degrees of freedom. Here, we report an antisite disorder driven spontaneous exchange bias effect as a result of hole carrier (Sr2+) doping in La2-xSrxCoMnO6 (0 < x < 1) double perovskites. X-ray diffraction and Raman spectroscopy have evidenced an increase in disorder with the increase of Sr content up to x = 0.5 and thereby a decrease from x = 0.5 to 1. X-ray absorption spectroscopy has revealed that only Co is present in the mixed valence of Co2+ and Co3+ states with Sr doping to compensate the charge neutrality. Magnetotransport is strongly correlated with the increase of antisite disorder. The antisite disorder at the B-site interrupts the long-range ferromagnetic order by introducing various magnetic interactions and instigates reentrant glassy dynamics, phase separation and canted type antiferromagnetic behavior with the decrease of temperature. This leads to a novel magnetic microstructure with unidirectional anisotropy that causes a spontaneous exchange bias effect that can be tuned with the amount of antisite disorder.Item type:Item, Magnetostructural coupling and multiferroic properties in the spin-frustrated system Ni1-xZnxCr2O4(2016-11-28) ;Chandrasekhar, K. Devi ;Murthy, J. Krishna ;Lin, J. -Y. ;Wu, H. C.Tseng, W. J.The magnetic phase diagram of Ni1-xZnxCr2O4 demonstrates complex magnetic transitions for x = 0.05 with two long-range magnetic- order transitions at T-C1 = 41K and T-C2 = 17 K. A glasslike feature emerges between TC1 and TC2 with the application of a direct current (dc) magnetic field in alternating current (ac) susceptibility measurements. Dielectric measurements show a change from the conventional dielectric to a quantum-paraelectric-like behavior without anomalies near the magnetic ordering temperature in the range 0.05 <= x <= 1. The strong correlation among magnetic, dielectric, and ferroelectric properties near the structural relaxation temperatures 41 and 17 K confirms the emergence of multiferroic behavior in Ni0.95Zn0.05Cr2O4. A significant x-ray magnetic circular dichroism signal at the Ni site and ac susceptibility measurements indicate a spin-canting behavior between TC1 and TC2. The dilute doping of the non-Jahn-Teller Zn ion in the Jahn-Teller Ni site modulate the different magnetic exchange interactions of Ni and Cr, which could invoke spin-canting and multiferroic behaviors.Item type:Item, Metamagnetic behaviour and effect of field cooling on sharp magnetization jumps in multiferroic Y2CoMnO6(2014-10-01) ;Murthy, J. Krishna ;Chandrasekhar, K. D. ;Wu, H. C. ;Yang, H. D.Lin, J. Y.We present sharp magnetization jumps and field-induced irreversibility in magnetization in multiferroic Y2CoMnO6. The appearance of magnetic relaxation and field sweep rate dependence of magnetization jumps resembles the martensite-like scenario and suggests the coexistence of E*-type antiferromagnetic and ferromagnetic phases at low temperatures. In Y2CoMnO6, the critical field required for the sharp jump can be increased or decreased depending on the magnitude and direction of the cooling field; this is remarkably different from manganites or other metamagnetic materials where the critical field increases irrespective of the direction of the applied field cooling. The cooling field dependence on the sharp magnetization jumps has been described by considering exchange pinning mechanism at the interface, like in the exchange bias model. Copyright (C) EPLA, 2014Item type:Item, Metamagnetic transitions and magnetoelectric coupling in acentric and nonpolar Pb2MnO4(2019-05-16) ;Kakarla, D. Chandrasekhar ;Wu, H. C. ;Hsieh, D. J. ;Sun, P. J.Dai, G. J.Acentric and nonpolar Pb2MnO4 was predicted to exhibit unique multipiezo induced magnetoelectric (ME) phenomena. In this paper, we present the results of magnetization as well as dielectric properties as a function of temperature (T), magnetic field (H), pressure (P), and electric field (E) primarily to address the ME coupling and identify the underlying mechanism behind this phenomenon. Magnetization and specific-heat measurements reveal the antiferromagnetic ordering of Mn4+ spins at temperature T-N= 17 K. Metamagnetic transitions at three critical magnetic fields H-c1, H-c2 and H-c3) are observed for T < T-N and H > 3.5 T. Further, the influences of pressure and magnetic field on H-c1 and H-c2 are investigated. The T-N, H-c1, and H(c2)( )all decrease with increasing external pressure. The dielectric anomaly observed at T-N is influenced by applying a magnetic field of H > 3.5 T. However, the electric field has minimal influence on the metamagnetic transition. The scaling between dielectric constant and magnetization meaningfully resolves the existence of magnetic-field-induced higher-order ME coupling in Pb2MnO4 at T < T-N and H > 3.5 T.Item type:Item, Observation of charge-transfer-driven antiferroelectricity in 3d-pyrochlore multiferroic Cu2OCl2(2019-03-01) ;Wu, H. C. ;Yuan, J. K. ;Chandrasekhar, K. D. ;Lee, C. H.Li, W. H.Very recently, multiferroic behavior close to the boiling temperature of liquid nitrogen was reported in oxohalide-based Cu2OCl2. In this study, we have established yet another novel mechanism for the origin of charge ordering in multiferroic Cu2OCl2. The direct current (DC) magnetization, specific heat, and neutron diffraction measurements confirm the antiferromagnetic (AFM) ordering (T-N) of Cu2OCl2 near 70 K. The collinear AFM spin structure in Cu(2)OCl(2)was obtained from neutron powder diffraction experiments based on the fitting to the combination of two irreducible representations-Gamma(1)circle plus Gamma(2). Electrical properties, such as dielectric constant, pyroelectric current, and polarization-electric field hysteresis-loop measurements, together suggest a long-range antiferroelectric ordering near T-E approximate to 75 K. The charge transfer from Cl to O along the c-axis was found to induce antiferroelectricity near TE and is supported from ab initio calculations. This finding largely reduces the possibility of well-known Dzyaloshinskii -Moriya interaction in the observed multiferroic behaviors and provides insight into the various origins of high-T-c multiferroics. (C) 2018 Elsevier Ltd. All rights reserved.Item type:Item, Observation of oscillation like magnetocaloric effect in multiferroic Ni0.95Zn0.05Cr2O4(2019-01-15) ;Chandrasekhar, K. Devi ;Murthy, J. Krishna ;Lin, J-Y ;Wu, H. C.Yang, H. D.In this study, the magnetic and magnetocaloric effects of Ni0.95Zn0.05Cr2O4 have been investigated systematically. The distinct magnetic phases in different temperature zones were identified using a combined analysis of Arrott plots and virgin magnetization curves. The magnetocaloric phenomenon is sensitive to the spin correlation of the nickel and chromium magnetic sublattices within each distinct temperature zone, as is reflected by the modulation of the magnetocaloric sign. This unique oscillatory like magnetocaloric effect within the multiferroic phase may indicate the possibility of a multicaloric effect in Ni0.95Zn0.05Cr2O4. (C) 2018 Elsevier B.V. All rights reserved.