arXiv subjects

Wei Tian

Publications and source records attributed to Wei Tian.

At least 91 records · Page 5Linked to original sources

arXiv2017

Mn-induced magnetic symmetry breaking and its correlation with the metal-insulator transition in bilayered Sr3(Ru1-xMnx)2O7

Bilayered Sr3Ru2O7 is an unusual metamagnetic metal with inherently antiferromagnetic (AFM) and ferromagnetic (FM) fluctuations. Partial substitution of Ru by Mn results in the establishment of metal-insulator transition (MIT) at TMIT and AFM ordering at TM in Sr3(Ru1-xMnx)2O7. Using elastic neutron scattering we determined the effect of Mn doping on the magnetic structure and in-plane magnetic correlation lengths in Sr3(Ru1-xMnx)2O7 (x = 0.06 and 0.12). With increasing Mn doping (x) from 0.06 to 0.12 or decreasing temperatures for x=0.12, an evolution from an in-plane short-range to long-range double-stripe AFM ground state occurs. For both compounds, the onset of magnetic correlation with an anisotropic behavior coincides with the sharp rise of the electrical resistivity and the specific heat. Since it does not induce measurable lattice distortion, the double-stripe magnetic order with anisotropic spin texture breaks the symmetry from C4v crystal lattice to C2v magnetic sublattice. These observations shed new light on an age-old question of Slater versus Mott-type MIT.

cond-mat.str-el↗

arXiv2017

Uniaxial pressure effect on the magnetic ordered moment and transition temperatures in BaFe$_{2-x}T_x$As$_2$ ($T=$Co, Ni)

We use neutron diffraction and muon spin relaxation to study the effect of in-plane uniaxial pressure on the antiferromagnetic (AF) orthorhombic phase in BaFe$_2$As$_2$ and its Co- and Ni-substituted members near optimal superconductivity. In the low temperature AF ordered state, uniaxial pressure necessary to detwin the orthorhombic crystals also increases the magnetic ordered moment, reaching an 11$\%$ increase under 40 MPa for BaFe$_{1.9}$Co$_{0.1}$As$_2$, and a 15$\%$ increase for BaFe$_{1.915}$Ni$_{0.085}$As$_2$. We also observe an increase of the AF ordering temperature ($T_N$) of about 0.25 K/MPa in all compounds, consistent with density functional theory calculations that reveal better Fermi surface nesting for itinerant electrons under uniaxial pressure. The doping dependence of the magnetic ordered moment is captured by combining dynamical mean field theory with density functional theory, suggesting that the pressure-induced moment increase near optimal superconductivity is closely related to quantum fluctuations and the nearby electronic nematic phase.

cond-mat.supr-con↗

arXiv2016

A Mott insulator continuously connected to iron pnictide superconductors

Iron-based superconductivity develops near an antiferromagnetic order and out of a bad metal normal state, which has been interpreted as originating from a proximate Mott transition. Whether an actual Mott insulator can be realized in the phase diagram of the iron pnictides remains an open question. Here we use transport, transmission electron microscopy, X-ray absorption spectroscopy, and neutron scattering to demonstrate that NaFe$_{1-x}$Cu$_x$As near $x\approx 0.5$ exhibits real space Fe and Cu ordering, and are antiferromagnetic insulators with the insulating behavior persisting above the Néel temperature, indicative of a Mott insulator. Upon decreasing $x$ from $0.5$, the antiferromagnetic ordered moment continuously decreases, yielding to superconductivity around $x=0.05$. Our discovery of a Mott insulating state in NaFe$_{1-x}$Cu$_x$As thus makes it the only known Fe-based material in which superconductivity can be smoothly connected to the Mott insulating state, highlighting the important role of electron correlations in the high-$T_{\rm c}$ superconductivity.

cond-mat.supr-con↗

arXiv2016

Pressure effects on magnetic ground states in cobalt doped multiferroic Mn$_{1-x}$Co$_{x}$WO$_4$

Using ambient pressure x-ray and high pressure neutron diffraction, we studied the pressure effect on structural and magnetic properties of multiferroic Mn$_{1-x}$Co$_x$WO$_4$ single crystals ($x=0, 0.05, 0.135$ and $0.17$), and compared it with the effects of doping. Both Co doping and pressure stretch the Mn-Mn chain along the $c$~direction. At high doping level ($x=0.135$ and $0.17$), pressure and Co doping drive the system in a similar way and induce a spin-flop transition for the $x=0.135$ compound. In contrast, magnetic ground states at lower doping level ($x=0$ and $0.05$) are robust against pressure but experience a pronounced change upon Co substitution. As Co introduces both chemical pressure and magnetic anisotropy into the frustrated magnetic system, our results suggest the magnetic anisotropy is the main driving force for the Co induced phase transitions at low doping level, and chemical pressure plays a more significant role at higher Co concentrations.

cond-mat.str-el↗

arXiv2016

Coexistence of superconductivity and antiferromagnetism in Ca$_{0.74(1)}$La$_{0.26(1)}$(Fe$_{1-x}$Co$_{x}$)As$_{2}$ single crystals

We report the transport, thermodynamic, $μ$SR and neutron study of the Ca$_{0.74(1)}$La$_{0.26(1)}$(Fe$_{1-x}$Co$_{x}$)As$_{2}$ single crystals, mapping out the temperature-doping level phase diagram. Upon Co substitution on the Fe site, the structural/magnetic phase transitions in this 112 compound are suppressed and superconductivity up to 20 K occurs. Our measurements of the superconducting and magnetic volume fractions show that these two phases coexist microscopically in the underdoped region, in contrast to the related 10-3-8 Ca$_{10}$(Pt$_{3}$As$_{8}$)((Fe$_{1-x}$Pt$_x$)$_{2}$As$_{2}$)$_{5}$ compound, where coexistence is absent. Supported by model calculations, we discuss the differences in the phase diagrams of the 112 and 10-3-8 compounds in terms of the FeAs interlayer coupling, whose strength is affected by the character of the spacer layer, which is metallic in the 112 and insulating in the 10-3-8.

cond-mat.supr-con↗

arXiv2016

Structural and magnetic phase transitions in Ca$_{0.73}$La$_{0.27}$FeAs$_2$ with electron overdoped FeAs layers

We report a study of the Ca$_{0.73}$La$_{0.27}$FeAs$_2$ single crystals. We unravel a monoclinic to triclinic phase transition at 58 K, and a paramagnetic to stripe antiferromagnetic (AFM) phase transition at 54 K, below which spins order 45$^\circ$ away from the stripe direction. Furthermore, we demonstrate this material is substantially structurally untwinned at ambient pressure with the formation of spin rotation walls (S-walls). Finally, in addition to the central-hole and corner-electron Fermi pockets usually appearing in Fe pnictide superconductors, angle-resolved photoemission (ARPES) measurements resolve a Fermiology where an extra electron pocket of mainly As chain character exists at the Brillouin zone edge.

cond-mat.supr-con↗

arXiv2016

Structure and magnetic properties of {\it Ln}MnSbO ({\it Ln} = La and Ce) and CeMnAsO

Neutron powder diffraction (NPD) study of \textit{Ln}MnSbO (\textit{Ln }$=$ La or Ce) reveals differences between the magnetic ground state of the two compounds due to the strong Ce-Mn coupling compared to La-Mn. The two compounds adopt the \textit{P4/nmm} space group down to 2 K and whereas magnetization measurements do not show obvious anomaly at high temperatures, NPD reveals a C-type antiferromagnetic (AFM) order below $T_{\mathrm{N}} = 255 $ K for LaMnSbO and 240 K for CeMnSbO. While the magnetic structure of LaMnSbO is preserved to base temperature, a sharp transition at $T_{\mathrm{SR}} = 4.5 $K is observed in CeMnSbO due to a spin-reorientation (SR) transition of the Mn$^{\mathrm{2+}}$ magnetic moments from pointing along the $c$-axis to the \textit{ab}-plane. The SR transition in CeMnSbO is accompanied by a simultaneous long-range AFM ordering of the Ce moments which indicates that the Mn SR transition is driven by the Ce-Mn coupling. The ordered moments are found to be somewhat smaller than those expected for Mn$^{\mathrm{2+}}$ ($S = 5/2$) in insulators, but large enough to suggest that these compounds belong to the class of local-moment antiferromagnets. The lower $T_{\mathrm{N\thinspace }}$ found in these two compounds compared to the As-based counterparts ($T_{\mathrm{N}} = 317$ for LaMnAsO, $T_{\mathrm{N}} = 347$ K for CeMnAsO) indicates that the Mn-$Pn$ ($Pn=$ As or Sb) hybridization that mediates the superexchange Mn-$Pn$-Mn coupling is weaker for the Sb-based compounds.

cond-mat.str-el↗

arXiv2015

Energy dependence of the spin excitation anisotropy in uniaxial-strained BaFe1.9Ni0.1As2

We use inelastic neutron scattering to study the temperature and energy dependence of the spin excitation anisotropy in uniaxial-strained electron-doped iron pnictide BaFe$_{1.9}$Ni$_{0.1}$As$_2$ near optimal superconductivity ($T_c=20$ K). Our work has been motivated by the observation of in-plane resistivity anisotropy in the paramagnetic tetragonal phase of electron-underdoped iron pnictides under uniaxial pressure, which has been attributed to a spin-driven Ising-nematic state or orbital ordering. Here we show that the spin excitation anisotropy, a signature of the spin-driven Ising-nematic phase, exists for energies below $\sim$60 meV in uniaxial-strained BaFe$_{1.9}$Ni$_{0.1}$As$_2$. Since this energy scale is considerably larger than the energy splitting of the $d_{xz}$ and $d_{yz}$ bands of uniaxial-strained Ba(Fe$_{1-x}$Co$_x$)$_2$As$_2$ near optimal superconductivity, spin Ising-nematic correlations is likely the driving force for the resistivity anisotropy and associated electronic nematic correlations.

cond-mat.supr-con↗

arXiv2015

Elucidating the magnetic and superconducting phases in the alkali metal intercalated iron chalcogenides

The complex interdigitated phases have greatly frustrated attempts to document the basic features of the superconductivity in the alkali metal intercalated iron chalcogenides. Here, using elastic neutron scattering, energy-dispersive x-ray spectroscopy, and resistivity measurements, we elucidate the relations of these phases in Rb$_{1-δ}$Fe$_y$Se$_{2-z}$S$_z$. We find: i) the iron content is crucial in stabilizing the stripe antiferromagnetic (AF) phase with rhombic iron vacancy order ($y\approx1.5$), the block AF phase with $\sqrt{5}\times \sqrt{5}$ iron vacancy order ($y\approx1.6$), and the iron vacancy-free phase ($y\approx2$); ii) the superconducting phase ($z=0$) evolves into a metallic phase ($z>1.5$) with sulfur substitution due to the progressive decrease of the electronic correlation strength. Both the stripe AF phase and the block AF phase are Mott insulators. Our data suggest that there are miscibility gaps between these three phases. The existence of the miscibility gaps in the iron content is the key to understanding the relationship between these complicated phases.

cond-mat.supr-con↗

arXiv2015

The influence of electron-doping on the ground state of (Sr{1-x}La{x})2IrO4

The evolution of the electronic properties of electron-doped (Sr{1-x}La{x})2IrO4 is experimentally explored as the doping limit of La is approached. As electrons are introduced, the electronic ground state transitions from a spin-orbit Mott phase into an electronically phase separated state, where long-range magnetic order vanishes beyond x = 0.02 and charge transport remains percolative up to the limit of La substitution (x~0.06). In particular, the electronic ground state remains inhomogeneous even beyond the collapse of the parent state's long-range antiferromagnetic order, while persistent short-range magnetism survives up to the highest La-substitution levels. Furthermore, as electrons are doped into Sr2IrO4, we observe the appearance of a low temperature magnetic glass-like state intermediate to the complete suppression of antiferromagnetic order. Universalities and differences in the electron-doped phase diagrams of single layer and bilayer Ruddlesden-Popper strontium iridates are discussed.

cond-mat.str-el↗

arXiv2015

Spin reorientation and Ce-Mn coupling in antiferromagnetic oxypnictide CeMnAsO

Structure and magnetic properties of high-quality polycrystlline CeMnAsO, a parent compound of the "1111"-type oxypnictides, have been investigated using neutron powder diffraction and magnetization measurements. We find that CeMnAsO undergoes a C-type antiferromagnetic order with Mn$^{2+}$ ($S=5/2$) moments pointing along the \textit{c}-axis below a relatively high Néel temperature of $T_{\rm N} = 345$ K. Below $T_{\rm SR} = 35$ K, two instantaneous transitions occur where the Mn moments reorient from the $c$-axis to the \textit{ab}-plane preserving the C-type magnetic order, and Ce moments undergo long-range AFM ordering with antiparallel moments pointing in the \textit{ab}-plane. Another transition to a noncollinear magnetic structure occurs below 7 K. The ordered moments of Mn and Ce at 2 K are 3.32(4) $μ_{B}$ and 0.81(4)$μ_{B}$, respectively. We find that CeMnAsO primarily falls into the category of a local-moment antiferromagnetic insulator in which the nearest-neighbor interaction ($J_{1}$) is dominant with $J_{2}<J_{1}/2$ in the context of $J_{1}-J_{2}-J_{c}$ model. The spin reorientation transition driven by the coupling between rare earth Ce and transition metal seems to be common to Mn, Fe and Cr ions, but not to Co and Ni ions in the iso-structural oxypnictides. A schematic illustration of magnetic structures in Mn and Ce sublattices in CeMnAsO is proposed.

cond-mat.str-el↗

arXiv2014

Two spatially separated phases in semiconducting Rb$_{0.8}$Fe$_{1.5}$S$_2$

We report neutron scattering and transport measurements on semiconducting Rb$_{0.8}$Fe$_{1.5}$S$_2$, a compound isostructural and isoelectronic to the well-studied $A_{0.8}$Fe$_{y}$Se$_2 (A=$ K, Rb, Cs, Tl/K) superconducting systems. Both resistivity and DC susceptibility measurements reveal a magnetic phase transition at $T=275$ K. Neutron diffraction studies show that the 275 K transition originates from a phase with rhombic iron vacancy order which exhibits an in-plane stripe antiferromagnetic ordering below 275 K. In addition, interdigitated mesoscopically with the rhombic phase is an ubiquitous phase with $\sqrt{5}\times\sqrt{5}$ iron vacancy order. This phase has a magnetic transition at $T_N=425$ K and an iron vacancy order-disorder transition at $T_{S}=600$ K. These two different structural phases are closely similar to those observed in the isomorphous Se materials. Based on the close similarities of the in-plane antiferromagnetic structures, moments sizes, and ordering temperatures in semiconducting Rb$_{0.8}$Fe$_{1.5}$S$_2$ and K$_{0.81}$Fe$_{1.58}$Se$_2$, we argue that the in-plane antiferromagnetic order arises from strong coupling between local moments. Superconductivity, previously observed in the $A_{0.8}$Fe$_{y}$Se$_{2-z}$S$_z$ system, is absent in Rb$_{0.8}$Fe$_{1.5}$S$_2$, which has a semiconducting ground state. The implied relationship between stripe/block antiferromagnetism and superconductivity in these materials as well as a strategy for further investigation is discussed in this paper.

cond-mat.supr-con↗

arXiv2014

Carrier localization and electronic phase separation in a doped spin-orbit driven Mott phase in Sr3(Ir1-xRux)2O7

Interest in many strongly spin-orbit coupled 5d-transition metal oxide insulators stems from mapping their electronic structures to a J=1/2 Mott phase. One of the hopes is to establish their Mott parent states and explore these systems' potential of realizing novel electronic states upon carrier doping. However, once doped, little is understood regarding the role of their reduced Coulomb interaction U relative to their strongly correlated 3d-electron cousins. Here we show that, upon hole-doping a candidate J=1/2 Mott insulator, carriers remain localized within a nanoscale phase separated ground state. A percolative metal-insulator transition occurs with interplay between localized and itinerant regions, stabilizing an antiferromagnetic metallic phase beyond the critical region. Our results demonstrate a surprising parallel between doped 5d- and 3d-electron Mott systems and suggest either through the near degeneracy of nearby electronic phases or direct carrier localization that U is essential to the carrier response of this doped spin-orbit Mott insulator.

cond-mat.str-el↗

arXiv2014

Glass-like phonon scattering from a spontaneous nanostructure in AgSbTe2

Materials with very low thermal conductivity are of high interest for both thermoelectric and optical phase-change applications. Synthetic nanostructuring is most promising to suppress thermal conductivity by scattering phonons, but challenges remain in producing bulk samples. We show that in crystalline AgSbTe$_2$, a spontaneously-forming nanostructure leads to a suppression of thermal conductivity to a glass-like level. Our mapping of the phonon mean-free-paths provides a novel bottom-up microscopic account of thermal conductivity, and also reveals intrinsic anisotropies associated with the nanostructure. Ground-state degeneracy in AgSbTe$_2$ leads to the natural formation of nanoscale domains with different orderings on the cation sublattice, and correlated atomic displacements, which efficiently scatter phonons. This mechanism is general and points to a new avenue in nano-scale engineering of materials, to achieve low thermal conductivities for efficient thermoelectric converters and phase-change memory devices.

cond-mat.mtrl-sci↗

arXiv2013

Magnetic structures and the Ce-Fe coupling induced Fe spin reorientation in CeFeAsO single crystal

Neutron and synchrotron resonant X-ray magnetic scattering (RXMS) complemented by heat capacity and resistivity measurements reveal the evolution of the magnetic structures of Fe and Ce sublattices in single crystal CeFeAsO. The RXMS of magnetic reflections at the Ce $L_{\rm II}$-edge shows a magnetic transition that is specific to the Ce antiferromagnetic long-range ordering at $T_\texttt{Ce}\approx$ 4 K with short-range Ce ordering above $T_\texttt{Ce}$, whereas neutron diffraction measurements of a few magnetic reflections indicate a transition at $T^{*}\approx$ 12 K with unusual order parameter. Detailed order parameter measurements on several magnetic reflections by neutrons show a weak anomaly at 4 K which we associate with the Ce ordering. The successive transitions at $T_\texttt{Ce}$ and $T^{*}$ can also be clearly identified by two anomalies in heat capacity and resistivity measurements. The higher transition temperature at $T^{*}\approx$ 12 K is mainly ascribed to Fe spin reorientation transition, below which Fe spins rotate uniformly and gradually in the \textit{ab} plane. The Fe spin reorientation transition and short-range Ce ordering above $T_\texttt{Ce}$ reflect the strong Fe-Ce couplings prior to long-range ordering of the Ce. The evolution of the intricate magnetic structures in CeFeAsO going through $T^{*}$ and $T_\texttt{Ce}$ is proposed.

cond-mat.str-el↗

arXiv2013

Avoided quantum criticality and magnetoelastic coupling in BaFe$_{2-x}$Ni$_{x}$As$_{2}$

We study the structural and magnetic orders in electron-doped BaFe2-xNixAs2 by high-resolution synchrotron X-ray and neutron scatterings. Upon Ni-doping x, the nearly simultaneous tetragonal-to-orthorhombic structural T_s and antiferromagnetic (T_N) phase transitions in BaFe2As2 are gradually suppressed and separated, resulting in T_s>T_N with increasing x as was previously observed. However, the temperature separation between T_s and T_N decreases with increasing x for x> 0.065$, tending towards a quantum bi-critical point near optimal superconductivity at x=0.1. The zero-temperature transition is preempted by the formation of a secondary incommensurate magnetic phase in the region 0.088< x < 0.104, resulting in a finite value of T_N \approx T_c+10$ K above the superconducting dome around $x\approx 0.1$. Our results imply an avoided quantum critical point, which is expected to strongly influence the properties of both the normal and superconducting states.

cond-mat.supr-con↗

arXiv2013

Room-temperature multiferroic hexagonal LuFeO$_3$ films

The crystal and magnetic structures of single-crystalline hexagonal LuFeO$_3$ films have been studied using x-ray, electron and neutron diffraction methods. The polar structure of these films are found to persist up to 1050 K; and the switchability of the polar behavior is observed at room temperature, indicating ferroelectricity. An antiferromagnetic order was shown to occur below 440 K, followed by a spin reorientation resulting in a weak ferromagnetic order below 130 K. This observation of coexisting multiple ferroic orders demonstrates that hexagonal LuFeO$_3$ films are room-temperature multiferroics.

cond-mat.mtrl-sci↗

arXiv2013

Persistence of local-moment antiferromagnetic order in Ba(1-x)KxMn2As2

BaMn2As2 is a local-moment antiferromagnetic insulator with a Néel temperature of 625 K and a large ordered moment of 3.9 Bohr magneton per Mn. Remarkably, this compound can be driven metallic by the substitution of as little as 1.6% K for Ba while retaining essentially the same ordered magnetic moment and Néel temperature, as previously reported. Here, using both powder and single crystal neutron diffraction we show that the local moment antiferromagnetic order in Ba(1-x)KxMn2As2 remains robust up to x = 0.4. The ordered moment is nearly independent of x for 0 < x < 0.4 and the Néel transition temperature decreases to 480 K at x = 0.4.

cond-mat.supr-con↗