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K. W. Plumb

Publications and source records attributed to K. W. Plumb.

At least 19 recordsLinked to original sources

Stability of the Local Ni$^{2+}$ Electronic Structure to $A$-site Disorder in the Pyrochlore Antiferromagnet NaCaNi$_2$F$_7$

NaCaNi$_2$F$_7$ is a unique example of spin-1 Heisenberg antiferromagnet on the pyrochlore lattice, but the presence of Na$^{1+}$/Ca$^{2+}$ $A$-site disorder complicates the local electronic and magnetic environment of the Ni$^{2+}$ $B$-site. We utilize resonant inelastic X-ray scattering (RIXS) to study the influence of $A$-site disorder on the $B$-site electronic structure of NaCaNi$_2$F$_7$. Ni L-edge RIXS measurements reveal a Ni$^{2+}$ electronic structure in nearly ideal octahedral coordination, with only a small trigonal compression ($δ$ = -200$\;$meV) required to capture all spectral features. Within the $D_{3d}$ symmetry of the Ni local environment, we extract an anisotropic $g$-factor of $g_{\parallel} = 2.26$ and $g_{\perp} = 2.27$, and a corresponding paramagnetic moment of $μ_{\rm{eff}}=3.2\;μ_B$. To simulate disorder, RIXS spectra were calculated with realistic distributions of crystal field parameters; however, these spectra are invariant relative to a disorder-free model, demonstrating the robustness of the Ni$^{2+}$ electronic environment to the $A$-site disorder, within the resolution of our measurement.

cond-mat.str-el

Non-Fermi liquid quasiparticles in strain-tuned Sr2RuO4

Interacting electrons can form metallic states beyond the Fermi liquid paradigm, a conceptual frontier of many-body physics mainly explored via bulk thermodynamics and transport. In contrast, the microscopics of anomalous single-particle excitations underlying non-Fermi liquid properties have largely remained in the dark. Here we spectroscopically map such quantum-critical excitations in Sr$_2$RuO$_4$ under uniaxial pressure, an experimental challenge overcome by technical advances combining focused ion beam micro-milling with laser angle resolved photoemission. We show that quasiparticle excitations acquire a non-Fermi liquid scattering rate near the critical point but remain remarkably robust throughout the transition. These experiments serve as a benchmark for the theory of anomalous metals and settle the long-standing question if quantum-critical systems host quasiparticle excitations.

cond-mat.str-el

Dynamic phase transition into a mixed-CDW state in 1$T$-TaS$_2$ via a thermal quench

Ultrafast light-matter interaction has emerged as a new mechanism to exert control over the macroscopic properties of quantum materials toward novel functionality. To date, technological applications of these non-thermal phases are limited by their ultrashort lifetimes and low-ordering temperatures. Among the most studied photoinduced metastable phases for their technological promise is the hidden metallic charge density wave (H-CDW) in the model correlated CDW compound 1$T$-TaS$_2$. Despite active study and engineering, the nature of the photoinduced H-CDW remains the subject of debate and is only accessible at cryogenic temperatures. Here, we stabilize the H-CDW phase at thermal equilibrium up to near-room temperature by accessing an intermediate mixed CDW order regime via thermal quenching. Using x-ray high dynamic range reciprocal space mapping (HDRM) and scanning tunneling spectroscopy (STS), we reveal the coexistence of commensurate (C) CDW and H-CDW domains below 180 K during cooling and below 210 K during warming. Our findings show that each order parameter breaks basal plane mirror symmetry with different chiral orientations and induces out-of-plane unit cell tripling in the H-CDW phase. Despite metallic domain walls and a finite density of states at zero bias observed via STS, bulk resistance remains insulating due to CDW stacking disorder. This study establishes the H-CDW as a thermally stable phase and introduces a new mechanism for switchable metallic behavior in thin flakes of 1$T$-TaS$_2$ and similar materials with competing order phases.

cond-mat.mtrl-sci

Continuum of magnetic excitations in the Kitaev honeycomb iridate D$_3$LiIr$_2$O$_6$

Inelastic neutron scattering (INS) measurements of powder D$_3(^{7}$Li)($^{193}$Ir)$_2$O$_6$ reveal low energy magnetic excitations with a scattering cross section that is broad in $|Q|$ and consistent with a Kitaev spin-liquid (KSL) state. The magnetic nature of the excitation spectrum is demonstrated by longitudinally polarized neutron studies. The total magnetic moment of 1.7(2)$μ_B$/Ir inferred from the total magnetic scattering cross section is consistent with the effective moment inferred from magnetic susceptibility data and expectations for the $J_{\rm eff}=1/2$ single ion state. The rise in the dynamic correlation function ${\cal S}(Q,ω)$ for $\hbarω<5~$meV can be described by a nearest-neighbor Kitaev model with interaction strength $K\approx-13(5)$~meV. Exchange disorder associated with the mixed D-Li site could play an important role in stabilizing the low $T$ quantum fluctuating state.

cond-mat.str-el

Jahn-Teller driven quadrupolar ordering and spin-orbital dimer formation in GaNb$_{4}$Se$_{8}$

The lacunar spinel GaNb$_4$Se$_8$ is a tetrahedral cluster Mott insulator where spin-orbit coupling on molecular orbitals and Jahn-Teller energy scales are competitive. GaNb$_4$Se$_8$ undergoes a structural and anti-polar ordering transition at T$_Q$ = 50 K that corresponds to a quadrupolar ordering of molecular orbitals on Nb$_4$ clusters. A second transition occurs at T$_M$ = 29 K, where local distortions on the Nb$_4$ clusters rearrange. We present a single crystal x-ray diffraction investigation these phase transitions and solve the crystal structure in the intermediate T$_M$ < T < T$_Q$ and low T < T$_M$ temperature phases. The intermediate phase is a primitive cubic P2$_1$3 structure with a staggered arrangement of Nb4 cluster distortions. A symmetry mode analysis reveals that the transition at TQ is continuous and described by a single Jahn-Teller active amplitude mode. In the low temperature phase, the symmetry of Nb$_4$ clusters is further reduced and the unit cell doubles into an orthorhombic P2$_1$2$_1$2$_1$ space group. Nb$_4$ clusters rearrange through this transition to form a staggered arrangement of intercluster dimers, suggesting a valence bond solid magnetic state.

cond-mat.str-el

Nanoscale electronic inhomogeneities in 1T-TaS$_2$

We report a set of scanning tunneling microscopy (STM) and spectroscopy (STS) experiments studying native defects in CVT grown 1T-TaS$_2$. Six different sample surfaces from four bulk crystals were investigated. Wide area imaging reveals a prevalence of nanometer-scale electronic inhomogeneities due to native defects, with pristine regions interspersed. These inhomogeneities appear in typical as-grown crystals and coexist with a well-formed commensurate charge density wave of 1T-TaS$_2$ at low temperatures. Electronic inhomogeneities show up both as variations in the apparent height in STM and in the local density of states in STS; the bands can shift by 60 meV and the gap varies by more than 100 meV across inhomogeneities. These inhomogeneities are present in similar concentration across large-scale areas of all samples studied, but do not influence the charge density wave formation on local or global scales. The commensurate charge density wave exhibits long-range order and remains locally intact in the presence of these inhomogeneities.

cond-mat.mes-hall

Dimensionality dependent electronic structure of the exfoliated van der Waals antiferromagnet NiPS$_3$

Resonant Inelastic X-ray Scattering (RIXS) was used to measure the local electronic structure in few-layer exfoliated flakes of the van der Waals antiferromagnet NiPS$_3$. The resulting spectra show a systematic softening and broadening of $NiS_6$ multiplet excitations with decreasing layer count from the bulk to three atomic layers (3L). These trends are driven by a decrease in the transition metal-ligand and ligand-ligand hopping integrals, and in the charge-transfer energy: $Δ$ = 0.60 eV in the bulk and 0.22 eV in 3L NiPS$_3$. Relevant intralayer magnetic exchange integrals computed from the electronic parameters exhibit a systematic decrease in the average interaction strength with thickness and place 2D NiPS$_3$ close to the phase boundary between stripy and spiral antiferromagnetic order, which may explain the apparent vanishing of long-range order in the 2D limit. This study explicitly demonstrates the influence of $inter$layer electronic interactions on $intra$layer ones in insulating magnets. As a consequence, the magnetic Hamiltonian in few-layer insulating magnets can be significantly different from that in the bulk.

cond-mat.str-el

Momentum-independent magnetic excitation continuum in the honeycomb iridate H$_3$LiIr$_2$O$_6$

In the search for realizations of Quantum Spin Liquids (QSL), it is essential to understand the interplay between inherent disorder and the correlated fluctuating spin ground state. H$_3$LiIr$_2$O$_6$ is regarded as a spin liquid proximate to the Kitaev-limit (KQSL) in which H zero-point motion and stacking faults are known to be present. Bond disorder has been invoked to account for the existence of unexpected low-energy spin excitations. Controversy remains about the nature of the underlying correlated state and if any KQSL physics survives. Here, we use resonant X-ray spectroscopies to map the collective excitations in H$_3$LiIr$_2$O$_6$ and characterize its magnetic state. We uncover a broad bandwidth and momentum-independent continuum of magnetic excitations at low temperatures that are distinct from the paramagnetic state. The center energy and high-energy tail of the continuum are consistent with expectations for dominant ferromagnetic Kitaev interactions between dynamically fluctuating spins. The absence of a momentum dependence to these excitations indicates a broken translational invariance. Our data support an interpretation of H$_3$LiIr$_2$O$_6$ as a disordered topological spin liquid in close proximity to bond-disordered versions of the KQSL. Our results shed light on how random disorder affects topological magnetic states and have implications for future experimental and theoretical works toward realizing the Kitaev model in condensed matter systems

cond-mat.str-el

On the electronic ground state of two non-magnetic pentavalent honeycomb iridates

We investigate the electronic structure of two Ir$^{5+}$ honeycomb iridates, Sr$_3$CaIr$_2$O$_9$ and NaIrO$_3$, by means of resonant x-ray techniques. We confirm that Sr$_3$CaIr$_2$O$_9$ realizes a large spin-orbit driven non-magnetic $J = 0$ singlet ground state despite sizable tetragonal distortions of Ir coordinating octahedra. On the other hand, the resonant inelastic x-ray spectra of NaIrO$_3$ are drastically different from expectations for a Mott insulator with octahedrally coordinated Ir$^{5+}$. We find that the data for NaIrO$_3$ can be best interpreted as originating from a narrow gap non-magnetic $S = 0$ band insulating ground state. Our results highlight the complex role of the ligand environment in the electronic structure of honeycomb iridates and the essential role of x-ray spectroscopy to characterize electronic ground states of insulating materials.

cond-mat.str-el

Bond Ordering and Molecular Spin-Orbital Fluctuations in the Cluster Mott Insulator GaTa$_4$Se$_8$

For materials where spin-orbit coupling is competitive with electronic correlations, the spatially anisotropic spin-orbital wavefunctions can stabilize degenerate states that lead to many and diverse quantum phases of matter. Here, we find evidence for a dynamical spin-orbital state preceding a T$^*$=50 K order-disorder spin-orbital ordering transition in the $j\!=\!3/2$ lacunar spinel GaTa$_4$Se$_8$. Above T$^*$, GaTa$_4$Se$_8$ has an average cubic crystal structure, but total scattering measurements indicate local non-cubic distortions of Ta$_4$ tetrahedral clusters for all measured temperatures $2 < T < 300$ K. Inelastic neutron scattering measurements reveal the dynamic nature of these local distortions through symmetry forbidden optical phonon modes that modulate $j\!=\!3/2$ molecular orbital occupation as well as intercluster Ta-Se bonds. Spin-orbital ordering at T$^*$ cannot be attributed to a classic Jahn-Teller mechanism and based on our findings, we propose that intercluster interactions acting on the scale of T$^*$ act to break global symmetry. The resulting staggered intercluster dimerization pattern doubles the unit cell, reflecting a spin-orbital valence bond ground state.

cond-mat.str-el

Electronic structure of the frustrated diamond lattice magnet NiRh$_2$O$_4$

The $A$-site spinel NiRh$_2$O$_4$ is the only known realization of a spin-1 diamond lattice magnet and is predicted to host unconventional magnetic phenomena driven by frustrated nearest and next-nearest neighbor exchange as well as orbital degeneracy. Previous works found no sign of magnetic order but found a gapped dispersive magnetic excitation indicating a possible valence bond magnetic ground state. However, the presence of many competing low energy degrees of freedom and limited empirical microscopic constraints complicates further analysis. Here, we carry out resonant inelastic x-ray scattering (RIXS) and x-ray absorption spectroscopy (XAS) to characterize the local electronic structure of NiRh$_2$O$_4$. The RIXS data can be partly described by a single-ion model for tetrahedrally coordinated Ni$^{2+}$ and indicates a tetragonal distortion $Δt_2\!=\!70$ meV that splits the $t_2$ orbitals into a high energy orbital singlet and lower energy orbital doublet. We identify features of the RIXS spectra that are consistent with a Rh-Ni two-site excitation indicating strong metal-metal hybridization mediated by oxygen in NiRh$_2$O$_4$. We also identify signatures of electron-phonon coupling through the appearance of phonon sidebands that dress crystal field excitations. These results establish the key energy scales relevant to the magnetism in NiRh$_2$O$_4$ and further demonstrate that covalency and lattice dynamics play essential roles in controlling the magnetic ground states of $A$-site spinels.

cond-mat.str-el

Nearly itinerant electronic groundstate in the intercalated honeycomb iridate Ag$_3$LiIr$_2$O$_6$

We use x-ray spectroscopy at Ir L$_3$/L$_2$ absorption edge to study powder samples of the intercalated honeycomb magnet Ag$_3$LiIr$_2$O$_6$. Based on x-ray absorption and resonant inelastic x-ray scattering measurements, and exact diagonalization calculations including next-neighbour Ir-Ir electron hoping integrals, we argue that the intercalation of Ag atoms results in a nearly itinerant electronic structure with enhanced Ir-O hybridization. As a result of the departure from the local relativistic $j_{\rm eff}\! = \!1/2$ state, we find that the relative orbital contribution to the magnetic moment is increased, and the magnetization density is spatially extended and asymmetric. Our results confirm the importance of metal - ligand hybridazation in the magnetism of transition metal oxides and provide empirical guidance for understanding the collective magnetism in intercalated honeycomb iridates.

cond-mat.str-el

From mean-field localized magnetism to itinerant spin fluctuations in the "Non-metallic metal" - FeCrAs

FeCrAs displays an unusual electrical response that is neither metallic in character nor divergent at low temperatures, as expected for an insulating response, and therefore it has been termed a "nonmetal-metal". We carried out neutron scattering experiments on powder and single crystal samples to study the magnetic dynamics and critical fluctuations in FeCrAs. Magnetic neutron diffraction measurements find Cr3+ magnetic order setting in at 115 K with the mean-field critical exponent. Neutron spectroscopy, however, observes gapless stiff magnetic fluctuations emanating from magnetic positions with propagation wave vector q_0=(1/3,1/3), which persists up to at least 80 meV. The magnetism in FeCrAs therefore displays a response which resembles that of itinerant magnets at high energy transfers, such as chromium alloys. We suggest that the presence of stiff high-energy spin fluctuations is the origin of the unusual temperature dependence of the resistivity.

cond-mat.str-el

Continuum of quantum fluctuations in a three-dimensional $S\!=\!1$ Heisenberg magnet

Conventional crystalline magnets are characterized by symmetry breaking and normal modes of excitation called magnons with quantized angular momentum $\hbar$. Neutron scattering correspondingly features extra magnetic Bragg diffraction at low temperatures and dispersive inelastic scattering associated with single magnon creation and annihilation. Exceptions are anticipated in so-called quantum spin liquids as exemplified by the one-dimensional spin-1/2 chain which has no magnetic order and where magnons accordingly fractionalize into spinons with angular momentum $\hbar/2$. This is spectacularly revealed by a continuum of inelastic neutron scattering associated with two-spinon processes and the absence of magnetic Bragg diffraction. Here, we report evidence for these same key features of a quantum spin liquid in the three-dimensional Heisenberg antiferromagnet NaCaNi$_2$F$_7$. Through specific heat and neutron scattering measurements, Monte Carlo simulations, and analytic approximations to the equal time correlations, we show that NaCaNi$_2$F$_7$ is an almost ideal realization of the spin-1 antiferromagnetic Heisenberg model on a pyrochlore lattice with weak connectivity and frustrated interactions. Magnetic Bragg diffraction is absent and 90\% of the spectral weight forms a continuum of magnetic scattering not dissimilar to that of the spin-1/2 chain but with low energy pinch points indicating NaCaNi$_2$F$_7$ is in a Coulomb phase. The residual entropy and diffuse elastic scattering points to an exotic state of matter driven by frustration, quantum fluctuations and weak exchange disorder.

cond-mat.str-el

Rearrangement of Van-der-Waals Stacking and Formation of a Singlet State at $T = 90$ K in a Cluster Magnet

Insulating Nb$_3$Cl$_8$ is a layered chloride consisting of two-dimensional triangular layers of $S_{eff}$ = 1/2 Nb$_3$Cl$_{13}$ clusters at room temperature. Magnetic susceptibility measurement show a sharp, hysteretic drop to a temperature independent value below $T = 90$ K. Specific heat measurements show that the transition is first order, with $ΔS \approx 5\ \mathrm{J \cdot K^{-1} \cdot mol\ \mathit{f.u.}^{-1}}$, and a low temperature $T$-linear contribution originating from defect spins. Neutron and X-ray diffraction show a lowering of symmetry from trigonal $P\bar{3}m1$ to monoclinic $C2/m$ symmetry, with a change in layer stacking from -AB-AB- to -AB$^\prime$-BC$^\prime$-CA$^\prime$- and no observed magnetic order. This lowering of symmetry and rearrangement of successive layers evades geometric magnetic frustration to form a singlet ground state. It is the lowest temperature at which a change in stacking sequence is known to occur in a Van-der-Waals solid, occurs in the absence of orbital degeneracies, and suggests that designer 2-D heterostructures may be able to undergo similar phase transitions.

cond-mat.str-el

NaSrMn2F7, NaCaFe2F7, and NaSrFe2F7: novel single crystal pyrochlore antiferromagnets

The crystal structures and magnetic properties of three previously unreported A2B2F7 pyrochlore materials, NaSrMn2F7, NaCaFe2F7, and NaSrFe2F7 are presented. In these compounds, either S=2 Fe2+ or S=5/2 Mn2+ is on the B site, while nonmagnetic Na and Ca (Na and Sr) are disordered on the A site. The materials, which were grown as crystals via the floating zone method, display high effective magnetic moments and large Curie-Weiss thetas. Despite these characteristics, freezing of the magnetic spins, characterized by peaks in the susceptibility or specific heat, is not observed until low temperatures. The empirical frustration index, f=- θcw/Tf, for the materials are 36 (NaSrMn2F7), 27 (NaSrFe2F7), and 19 (NaCaFe2F7). AC susceptibility, DC susceptibility, and heat capacity measurements are used to characterize the observed spin glass behavior. The results suggest that the compounds are frustrated pyrochlore antiferromagnets with weak bond disorder. The magnetic phenomena that these fluoride pyrochlores exhibit, in addition to their availability as relatively large single crystals, make them promising candidates for the study of geometric magnetic frustration.

cond-mat.str-el

Antiferromagnetic and Orbital Ordering on a Diamond Lattice Near Quantum Criticality

We present neutron scattering measurements on powder samples of the spinel FeSc2S4 that reveal a previously unobserved magnetic ordering transition occurring at 11.8(2)~K. Magnetic ordering occurs subsequent to a subtle cubic-to-tetragonal structural transition which distorts Fe coordinating sulfur tetrahedra lifting the orbital degeneracy. The application of 1~GPa hydrostatic pressure appears to destabilize this Néel state, reducing the transition temperature to 8.6(8)~K and redistributing magnetic spectral weight to higher energies. The relative magnitudes of ordered $\langle m \rangle^2\!=\!3.1(2)$ and fluctuating moments $\langle δm \rangle^2\!=\!13(1)$ show that the magnetically ordered ground state of FeSc2S4 is drastically renormalized and in proximity to criticality.

cond-mat.str-el

Quasiparticle-continuum level repulsion in a quantum magnet

When the energy eigenvalues of two coupled quantum states approach each other in a certain parameter space, their energy levels repel each other and level crossing is avoided. Such level repulsion, or avoided level crossing, is commonly used to describe the dispersion relation of quasiparticles in solids. However, little is known about the level repulsion when more than two quasiparticles are present; for example, in an open quantum system where a quasiparticle can spontaneously decay into many particle continuum. Here we show that even in this case level repulsion exists between a long-lived quasiparticle state and a continuum. In our fine resolution neutron spectroscopy study of magnetic quasiparticles in a frustrated quantum magnet BiCu2PO6, we observe a renormalization of quasiparticle dispersion relation due to the presence of the continuum of multi-quasiparticle states. Our results have a broadimplication for understanding open quantum systems described by non-hermitian Hamiltonian.

cond-mat.str-el