arXiv subjects

Chin-Wei Wang

Publications and source records attributed to Chin-Wei Wang.

18 recordsLinked to original sources

arXiv2025

Wombat, the high intensity diffractometer in operation at the Australian Centre for Neutron Scattering

Wombat is the high intensity neutron diffractometer in operation at the Australian Centre for Neutron Scattering. While primarily used as a high-speed powder diffractometer, the high-performance area detector allows both texture characterisation and single-crystal measurements. The instrument can be configured over a large range of operational parameters, which are characterised in this contribution to aid experimental planning. Wombat is particularly optimised for the study of materials in situ and in operando using the wide range of sample environment available at the centre. Over 17 years of operation, Wombat has been used to explore a broad range of materials, including: novel hydrogen-storage materials, negative-thermal-expansion materials, cryogenic minerals, piezoelectrics, high performance battery anodes and cathodes, high strength alloys, multiferroics, superconductors and novel magnetic materials. This paper will highlight the capacity of the instrument, recent comprehensive characterisation measurements, and how the instrument has been utilised by our user community to date.

physics.ins-det↗

arXiv2025

Magnetic structure evolution and magnetoelastic coupling across the spin reorientation transition in TmCrO3

We present a comprehensive study of the magnetic structure evolution across the spin reorientation transition in orthorhombic (Pnma) TmCrO3. Magnetic susceptibility reveals canted antiferromagnetic (CAFM) ordering at T_N = 125 K, two compensation points (T_comp1 and T_comp2), followed by magnetization reversal with a magnetic susceptibility minimum between T_comp1 and T_comp2. Heat capacity shows a sharp lambda-type transition at T_N, associated with the long-range antiferromagnetic ordering of Cr, followed by a broad feature near 9 K. Neutron powder diffraction (NPD) establishes the Pn'm'a (Gamma2) magnetic structure below T_N. A gradual change in magnetic structure occurs during the spin-reorientation (SRO) transition below 30 K, where the magnetic symmetry transforms from Pn'm'a (Gamma2) to Pn'ma' (Gamma4) phase. However, below the SRO, neither Gamma2 nor Gamma4 alone adequately fit the intensity of magnetic reflections. A satisfactory refinement is achieved using the monoclinic subgroup P21'/c', derived from a combination of Gamma2 and Gamma4. The gradual SRO of Tm and Cr moments across the compensation regime is consistent with the magnetic symmetry P21'/c'. Furthermore, the ordered moments of Cr and Tm in TmCrO3 exhibit a complex, non-monotonic temperature dependence, with the Tm sublattice driving the spin-reorientation transition near the compensation point. Anomalies in the lattice parameters reveal strong magnetoelastic coupling, linking structural distortions to the SRO.

cond-mat.str-el↗

arXiv2025

Structural Inhomogeneities and Suppressed Magneto-Structural Coupling in Mn-Substituted GeCo2O4

A comprehensive study of Ge1-xMnxCo2O4 (GMCO) system was conducted using neutron powder diffraction (NPD), x-ray diffraction (XRD), Scanning electron microscopy, magnetometry, and heat capacity measurements. Comparative analysis with GeCo2O4 (GCO) highlights the influence of Mn substitution on the crystal and magnetic structure at low temperature. Surprisingly, phase separation is observed in GMCO with a targeted nominal composition of Ge0.5Mn0.5Co2O4. SEM/EDX analysis reveals that the sample predominantly consists of a Mn-rich primary phase with approximate stoichiometry Mn0.74Ge0.18Co2O4, along with a minor Ge-rich secondary phase of composition Ge0.91Mn0.19Co2O4. Although both GCO and GMCO crystallize in cubic symmetry at room temperature, a substantial difference in low-temperature structural properties has been observed. Magnetic and heat capacity data indicate ferrimagnetic ordering in the Mn-rich phase near TC = 108 K, while the Ge-rich phase exhibits antiferromagnetic order at TN = 22 K in GMCO. Analysis of heat capacity data reveals that the estimated magnetic entropy amounts to only 63% of the theoretical value expected in GMCO. A collinear ferrimagnetic arrangement is observed in the Mn rich phase below the magnetic ordering temperature, characterized by antiparallel spins of the Mn at A site and Co at B site along the c-direction. At 5 K, the refined magnetic moments are 2.31(3) for MnA and 1.82(3) uB for CoB in the Mn rich ferrimagnetic phase. The magnetic structure at 5 K in the Ge rich secondary phase is identical to the antiferromagnetic structure of the parent compound GeCo2O4. The refined value of the CoB moment in this phase at 5 K is 2.53(3) uB.

cond-mat.mtrl-sci↗

arXiv2025

Giant Magnetocaloric Effect in Spin Supersolid Candidate Na$_2$BaCo(PO$_4$)$_2$

Supersolid, an exotic quantum state of matter that consists of particles forming an incompressible solid structure while simultaneously showing superfluidity of zero viscosity [1], is one of the long-standing pursuits in fundamental research [2, 3]. Although the initial report of $^4$He supersolid turned out to be an artifact [4], this intriguing quantum matter has inspired enthusiastic investigations into ultracold quantum gases [5-8]. Nevertheless, the realization of supersolidity in condensed matter remains elusive. Here we find evidence for a quantum magnetic analogue of supersolid -- the spin supersolid -- in the recently synthesized triangular-lattice antiferromagnet Na$_2$BaCo(PO$_4$)$_2$ [9]. Notably, a giant magnetocaloric effect related to the spin supersolidity is observed in the demagnetization cooling process, manifesting itself as two prominent valley-like regimes, with the lowest temperature attaining below 100 mK. Not only is there an experimentally determined series of critical fields but the demagnetization cooling profile also shows excellent agreement with the theoretical simulations with an easy-axis Heisenberg model. Neutron diffractions also successfully locate the proposed spin supersolid phases by revealing the coexistence of three-sublattice spin solid order and interlayer incommensurability indicative of the spin superfluidity. Thus, our results indicate a strong entropic effect of the spin supersolid phase in a frustrated quantum magnet and open up a viable and promising avenue for applications in sub-Kelvin refrigeration, especially in the context of persistent concerns about helium shortages [10, 11].

cond-mat.str-el↗

arXiv2025

A double-spiral spin ordering in the helimagnet YBaCuFeO$_{5}$

Materials with a spiral spin ordering always show a rich phase diagram and can be a playground for studying the exotic physical properties associated with spiral magnetism. Using neutron elastic and resonant x-ray scattering on a high-quality single crystal YBaCuFeO$_{5}$, we demonstrate YBaCuFeO$_{5}$ to be a helimagnet consisting of a double-spiral spin ordering. YBaCuFeO$_{5}$ undergoes a commensurate to incommensurate magnetic phase transition at $T_{N2}$$\sim$ 175 K, and the incommensurate phase consists of two spin-ordered components. Both components have different periodicities but with the same propagating direction along the {\it c}-axis below $T_{N2}$. Using resonant x-ray scattering at the Fe and Cu \textit{K}-edges, we further demonstrate that both spiral spin orderings result from the Fe$^{3+}$ and Cu$^{2+}$, respectively, forming a double-spiral spin ordering structure. This can be understood to be caused by the coupling between both sublattices of Fe$^{3+}$ and Cu$^{2+}$ with the atomic lattice.

cond-mat.str-el↗

arXiv2025

Enhanced deep-freezing magneto- and elasto-caloric effects by modifying lattice anharmonicity and electronic structures

Designing the high performance magneto or elastocaloric effect in NiMnIn alloys with spin-lattice coupling in a deep freezing temperature range of 200 K to 255 K is challenging due to the limited lattice entropy change and large negative contribution of magnetic entropy change during phase transitions. In this work, we systematically study the first order magneto-structural transition in NiMnIn based alloys by in-situ microstructural characterizations, physical property measurements, and first principles calculations. A multi element alloying strategy involving Cu and Ga co doping is proposed to manipulate the phase transition. The co doping reduces the lattice anharmonicity and thermal expansion coefficient of the martensitic phase, leading to an increase in the unit cell volume change and lattice entropy change. It also modifies the electronic density of states, causing a decrease in the magnetization change .The relief of the lattice mismatch reduces hysteresis losses in the refrigeration cycle. These synergetic effects yield excellent magneto and elastocaloric effects,with the effective magnetocaloric refrigeration capacity reaching up to 182 J/kg under the magnetic field of 5 T or an adiabatic temperature change of -4 K under a low field of 1.5 T and the elastocaloric coefficient of performance to 30 or an adiabatic temperature change of -7 K with the strain of 5% at 230 K, offering a potential solution for solid-state deep-freezing refrigeration.

cond-mat.mtrl-sci↗

arXiv2024

Structural and Magnetic properties of Ge0.5Mn0.5Co2O4 using neutron diffraction

The structural and magnetic properties of Ge0.5Mn0.5Co2O4 (GMCO) have been investigated in detail utilizing neutron powder diffraction (NPD), x-ray diffraction (XRD), DC magnetometry, and heat capacity analysis and compared with GeCo2O4. Despite both compounds exhibiting a cubic structure at room temperature, a substantial difference on low temperature structural properties have been observed for GMCO, indicating the effect of Mn substitution on crystal structure. The magnetic and heat capacity data reveal a ferrimagnetic ordering around 108 K in GMCO. A minor secondary phase is confirmed which undergoes long range AFM ordering at further lower temperatures. This secondary phase remains undetected in XRD due to identical lattice parameters. Furthermore, the analysis of heat capacity data indicates a broadening of the high-temperature transition, attributing to the short-range correlation persisting up to higher temperatures. The estimated magnetic entropy amounts is 63% of the value expected for GMCO. The missing entropy is likely linked with the short-range magnetic correlations persisting well above the transition temperature. Cation distribution at the A and B sites has been estimated in GMCO using NPD. Magnetic structures are also confirmed in the main phase as well as in the secondary phase using NPD analysis. The high-temperature transition corresponds to the ferrimagnetic ordering of A and B site cations in the main phase. A collinear ferrimagnetic arrangement of A and B site spins aligned parallel to c axis is observed. The average values of A and B site moments in the ferrimagnetic phase at 5 K are 2.31(3) and 1.82(3)mB, respectively, with the temperature dependence of moments following the expected power law behavior. The low-temperature ordering is attributed to the antiferromagnetic ordering of B site ions associated with the secondary phase, something similar to GeCo2O4.

cond-mat.str-el↗

arXiv2024

Annealing-tunable charge density wave in the kagome antiferromagnet FeGe

The unprecedented phenomenon that a charge density wave (CDW) emerges inside the antiferromagnetic (AFM) phase indicates an unusual CDW mechanism associated with magnetism in FeGe. Here, we demonstrate that both the CDW and magnetism of FeGe can be effectively tuned through post-growth annealing treatments. Instead of the short-range CDW reported earlier, a long-range CDW order is realized below 110 K in single crystals annealed at \SI{320}{\degreeCelsius} for over 48 h. The CDW and AFM transition temperatures appear to be inversely correlated with each other. The entrance of the CDW phase significantly reduces the critical field of the spin-flop transition, whereas the CDW transition remains stable against minor variations in magnetic orders such as annealing-induced magnetic clusters and spin-canting transitions. Single-crystal x-ray diffraction measurements reveal substantial disorder on the Ge1 site, which is characterized by displacement of the Ge1 atom from Fe$_3$Ge layer along the $c$ axis and can be reversibly modified by the annealing process. The observed annealing-tunable CDW and magnetic orders can be well understood in terms of disorder on the Ge1 site. Our study provides a vital starting point for the exploration of the unconventional CDW mechanism in FeGe and of kagome materials in general.

cond-mat.str-el↗

arXiv2022

Zigzag magnetic order in a novel tellurate compound Na$_{4-δ}$NiTeO$_{6}$ with $\mathit{S}$ = 1 chains

Na$_{4-δ}$NiTeO$_{6}$ is a rare example in the transition-metal tellurate family of realizing an $S$ = 1 spin-chain structure. By performing neutron powder diffraction measurements, the ground-state magnetic structure of Na$_{4-δ}$NiTeO$_{6}$ is determined. These measurements reveal that below $T\rm_{N}$ ${\sim}$ 6.8(2) K, the Ni$^{2+}$ moments form a screwed ferromagnetic (FM) spin-chain structure running along the crystallographic $a$ axis but these FM spin chains are coupled antiferromagnetically along the $b$ and $c$ directions, giving rise to a magnetic propagation vector of $k$ = (0, 1/2, 1/2). This zigzag magnetic order is well supported by first-principles calculations. The moment size of Ni$^{2+}$ spins is determined to be 2.1(1) $μ$$\rm_{B}$ at 3 K, suggesting a significant quenching of the orbital moment due to the crystalline electric field (CEF) effect. The previously reported metamagnetic transition near $H\rm_{C}$ ${\sim}$ 0.1 T can be understood as a field-induced spin-flip transition. The relatively easy tunability of the dimensionality of its magnetism by external parameters makes Na$_{4-δ}$NiTeO$_{6}$ a promising candidate for further exploring various types of novel spin-chain physics.

cond-mat.str-el↗

arXiv2022

Structural and magnetic properties of the quasicrystal approximant Au$_{65}$Ga$_{21}$Tb$_{14}$

Magnetic properties of the quasicrystal approximant Au$_{65}$Ga$_{21}$Tb$_{14}$ were investigated by the magnetization and the neutron diffraction experiments. The temperature dependences of the magnetic susceptibility and the magnetization curve indicate dominant ferromagnetic interactions, while the whirling antiferromagnetic order was found from the neutron diffraction experiments. In the antiferromagnetic phase, the magnetic moments are aligned almost perpendicular to a pseudo five-fold symmetry axis, which should correspond to the easy-axis direction of a Tb atom. The magnetic properties similar to those of Au$_{72}$Al$_{14}$Tb$_{14}$ in spite of the difference in the electron-per-atom ratio suggest the robustness of the easy-axis anisotropy against the chemical substitution of the nonmagnetic atoms.

cond-mat.str-el↗

arXiv2022

Neutron-diffraction and linear {Grüneisen} parameter studies of magnetism in NdFe$_2$Ga$_8$

We study the magnetism in NdFe$_2$Ga$_8$ by the neutron-diffraction and temperature-modulated linear {Grüneisen} parameter measurements. Previous thermodynamical measurements have demonstrated that there are two magnetic transitions at 10 and 14.5 K, respectively. Neutron-diffraction measurements confirm that the lower one is an antiferromagnetic (AFM) transition with a commensurate magnetic structure. Both the commensurate and the incommensurate (IC) magnetic peaks are found below the higher transition but their intensities only gradually increase with decreasing temperature. Below 10 K, the commensurate peak intensity increases quickly with decreasing temperature, signaling the AFM transition, while the IC peak intensity disappears below 5 K. The linear {Grüneisen} parameter along the $c$ axis, $Γ_c$, shows a hysteresis behavior that is different from the hysteresis behavior for the magnetization $M$. We give a discussion of the origin of the magnetism in NdFe$_2$Ga$_8$.

cond-mat.str-el↗

arXiv2022

Evolution from helical to collinear ferromagnetic order of the Eu$^{2+}$ spins in RbEu(Fe$_{1-x}$Ni$_{x}$)$_{4}$As$_{4}$

The ground-state magnetic structures of the Eu$^{2+}$ spins in recently discovered RbEu(Fe$_{1-x}$Ni$_{x}$)$_{4}$As$_{4}$ superconductors have been investigated by neutron powder diffraction measurements. It is found that as the superconductivity gets suppressed with the increase of Ni doping, the magnetic propagation vector of the Eu sublattice diminishes, corresponding to the decrease of the rotation angle between the moments in neighboring Eu layers. The ferromagnetic Eu layers are helically modulated along the $\mathit{c}$ axis with an incommensurate magnetic propagation vector in both the ferromagnetic superconductor RbEu(Fe$_{0.95}$Ni$_{0.05}$)$_{4}$As$_{4}$ and the superconducting ferromagnet RbEu(Fe$_{0.93}$Ni$_{0.07}$)$_{4}$As$_{4}$. Such a helical structure transforms into a purely collinear ferromagnetic structure for non-superconducting RbEu(Fe$_{0.91}$Ni$_{0.09}$)$_{4}$As$_{4}$, with all the Eu$^{2+}$ spins lying along the tetragonal (1 1 0) direction. The evolution from helical to collinear ferromagnetic order of the Eu$^{2+}$ spins with increasing Ni doping is supported by first-principles calculations. The variation of the rotation angle between adjacent Eu$^{2+}$ layers can be well explained by considering the change of magnetic exchange couplings mediated by the indirect Ruderman-Kittel-Kasuya-Yosida (RKKY) interaction.

cond-mat.str-el↗

arXiv2021

Striping of orbital-order with charge-disorder in optimally doped manganites

The phase diagrams of LaMnO$_3$ perovskites have been intensely studied due to the colossal magnetoresistance (CMR) exhibited by compositions around the $\frac{3}{8}^{th}$ doping level. However, phase segregation between ferromagnetic (FM) metallic and antiferromagnetic (AFM) insulating states, which itself is believed to be responsible for the colossal change in resistance under applied magnetic field, has prevented an atomistic-level understanding of the orbital ordered (OO) state at this doping level. Here, through the detailed crystallographic analysis of the phase diagram of a prototype system (AMn$_3^{A'}$Mn$_4^B$O$_{12}$), we show that the superposition of two distinct lattice modes gives rise to a striping of OO Jahn-Teller active Mn$^{3+}$ and charge disordered (CD) Mn$^{3.5+}$ layers in a 1:3 ratio. This superposition only gives a cancellation of the Jahn-Teller-like displacements at the critical doping level. This striping of CD Mn$^{3.5+}$ with Mn$^{3+}$ provides a natural mechanism though which long range OO can melt, giving way to a conducting state.

cond-mat.str-el↗

arXiv2020

Magnetic phase diagram of Cu$_{4-x}$Zn$_x$(OH)$_6$FBr studied by neutron-diffraction and $μ$SR techniques

We have systematically studied the magnetic properties of Cu$_{4-x}$Zn$_x$(OH)$_6$FBr by the neutron diffraction and muon spin rotation and relaxation ($μ$SR) techniques. Neutron-diffraction measurements suggest that the long-range magnetic order and the orthorhombic nuclear structure in the $x$ = 0 sample can persist up to $x$ = 0.23 and 0.43, respectively. The temperature dependence of the zero-field (ZF) $μ$SR spectra provide two characteristic temperatures, $T_{A0}$ and $T_λ$. Comparison between $T_{A0}$ and $T_M$ from previously reported magnetic-susceptibility measurements suggest that the former comes from the short-range interlayer-spin clusters that persist up to $x$ = 0.82. On the other hand, the doping level where $T_λ$ becomes zero is about 0.66, which is much higher than threshold of the long-range order, i.e., $\sim$ 0.4. Our results suggest that the change in the nuclear structure may alter the spin dynamics of the kagome layers and a gapped quantum-spin-liquid state may exist above $x$ = 0.66 with the perfect kagome planes.

cond-mat.str-el↗

arXiv2020

Magnetic ordering and spin dynamics in $S=5/2$ staggered triangular lattice antiferromagnet Ba$_2$MnTeO$_6$

We report studies of the magnetic properties of a staggered stacked triangular lattice Ba$_2$MnTeO$_6$ using magnetic susceptibility, specific heat, neutron powder diffraction and inelastic neutron scattering measurements, as well as first principles density functional theory calculations. Neutron diffraction measurements reveal an antiferromagnetic order with a propagated vector $\textbf{\emph{k}}=(0.5, 0.5, 0)$ and N{é}el transition temperature of $T_\text{N}\approx20$ K. The dominant interaction derived from the Curie-Weiss fitting to the inverse DC susceptibility is antiferromagnetic. Through modelling the INS spectrum with the linear spin wave theory, the magnetic exchange interactions for the nearest intralayer, nearest interlayer, and next nearest interlayer are determined to be $J_1=0.27(3),J_2=0.27(3),$ and $J_3=-0.05(1)$ meV, respectively, and a small value of easy-axis anisotropy of $D_{zz}=-0.01$ meV is introduced. We derive a magnetic phase diagram that reveals that it is the competition between $J_1, J_2$, and $J_3$ that stabilizes the collinear stripe-type antiferromagnetic order.

cond-mat.str-el↗

arXiv2019

Spin dynamics of edge-sharing spin chains in SrCa13Cu24O41

The low-energy magnetic excitation from the highly Ca-doped quasi-one-dimensional magnet SrCa13Cu24O41 was studied in the magnetic ordered state by using inelastic neutron scattering. We observed the gapless spin-wave excitation, dispersive along the a and c axes but nondispersive along the b axis. Such excitations are attributed to the spin wave from the spin-chain sublattice. Model fitting to the experimental data gives the nearest-neighbour interaction Jc as 5.4 meV and the interchain interaction Ja = 4.4 meV. Jc is antiferromagnetic and its value is close to the nearest-neighbour interactions of the similar edge-sharing spin-chain systems such as CuGeO3. Comparing with the hole-doped spin chains in Sr14Cu24O41, which shows a spin gap due to spin dimers formed around Zhang-Rice singlets, the chains in SrCa13Cu24O41 show a gapless excitation in this study. We ascribe such a change from gapped to gapless excitations to holes transferring away from the chain sublattice into the ladder sublattice upon Ca doping.

cond-mat.str-el↗

arXiv2018

Improper Ferroelectric Polarisation in a Perovskite driven by Inter-site Charge Transfer and Ordering

It is of great interest to design and make materials in which ferroelectric polarisation is coupled to other order parameters such as lattice, magnetic and electronic instabilities. Such materials will be invaluable in next-generation data storage devices. Recently, remarkable progress has been made in understanding improper ferroelectric coupling mechanisms that arise from lattice and magnetic instabilities. However, although theoretically predicted, a compact lattice coupling between electronic and ferroelectric (polar) instabilities has yet to be realised. Here we report detailed crystallographic studies of a novel perovskite Hg$^{\textbf{A}}$Mn$^{\textbf{A'}}_{3}$Mn$^{\textbf{B}}_{4}$O$_{12}$ that is found to exhibit a polar ground state on account of such couplings that arise from charge and orbital ordering on both the A' and B-sites, which are themselves driven by a highly unusual Mn$^{A'}$-Mn$^B$ inter-site charge transfer. The inherent coupling of polar, charge, orbital and hence magnetic degrees of freedom, make this a system of great fundamental interest, and demonstrating ferroelectric switching in this and a host of recently reported hybrid improper ferroelectrics remains a substantial challenge.

cond-mat.str-el↗

arXiv2012

Interplay between the magnetic and electric degrees-of-freedom in multiferroic Co3TeO6

Neutron diffraction, magnetic susceptibility, specific heat, and dielectric constant measurements of single crystal Co3TeO6 have been measured to study the interplay between the ferroelectricity and magnetic order. Long range incommensurate magnetic order develops below TM1=26 K, which is followed by three additional zero-field phase transitions at TM2=19.5 K, TM3=18 K, and TM4=16 K where the incommensurate order changes and commensurate order develops. In magnetic fields up to 14 T we find that the magnetic intensities and incommensurate wave vector are dramatically altered as ferroelectricity develops, with a fifth abrupt transition around 10 T. The overall behavior characterizes Co3TeO6 as a type-II multiferroic.

cond-mat.str-el↗