arXiv subjects

G. Monaco

Publications and source records attributed to G. Monaco.

At least 37 records · Page 2Linked to original sources

arXiv2015

Evidence of quantum dimer excitations in Sr$_3$Ir$_2$O$_7$

The magnetic excitation spectrum in the bilayer iridate Sr$_3$Ir$_2$O$_7$ has been investigated using high-resolution resonant inelastic x-ray scattering (RIXS) performed at the iridium L$_3$ edge and theoretical techniques. A study of the systematic dependence of the RIXS spectrum on the orientation of the wavevector transfer, $\mathbf{Q}$, with respect to the iridium-oxide bilayer has revealed that the magnon dispersion is comprised of two branches well separated in energy and gapped across the entire Brillouin zone. Our results contrast with those of an earlier study which reported the existence of a single dominant branch. While these earlier results were interpreted as two overlapping modes within a spin-wave model of weakly coupled iridium-oxide planes, our results are more reminiscent of those expected for a system of weakly coupled dimers. In this latter approach the lower and higher energy modes find a natural explanation as those corresponding to transverse and longitudinal fluctuations, respectively. We have therefore developed a bond-operator theory which describes the magnetic dispersion in Sr$_3$Ir$_2$O$_7$ in terms of quantum dimer excitations. In our model dimerisation is produced by the leading Heisenberg exchange, $J_c$, which couples iridium ions in adjacent planes of the bilayer. The Hamiltonian also includes in plane exchange, $J$, as well as further neighbour couplings and relevant anisotropies. The bond-operator theory provides an excellent account of the dispersion of both modes, while the measured $\mathbf{Q}$ dependence of the RIXS intensities is in reasonable qualitative accord with the spin-spin correlation function calculated from the theory. We discuss our results in the context of the quantum criticality of bilayer dimer systems in the presence of anisotropic interactions derived from strong spin-orbit coupling.

cond-mat.str-el↗

arXiv2015

Temperature dependence of iron local magnetic moment in phase-separated superconducting chalcogenide

We have studied local magnetic moment and electronic phase separation in superconducting K$_{x}$Fe$_{2-y}$Se$_2$ by x-ray emission and absorption spectroscopy. Detailed temperature dependent measurements at the Fe K-edge have revealed coexisting electronic phases and their correlation with the transport properties. By cooling down, the local magnetic moment of Fe shows a sharp drop across the superconducting transition temperature (T$_c$) and the coexisting phases exchange spectral weights with the low spin state gaining intensity at the expense of the higher spin state. After annealing the sample across the iron-vacancy order temperature, the system does not recover the initial state and the spectral weight anomaly at T$_c$ as well as superconductivity disappear. The results clearly underline that the coexistence of the low spin and high spin phases and the transitions between them provide unusual magnetic fluctuations and have a fundamental role in the superconducting mechanism of electronically inhomogeneous K$_{x}$Fe$_{2-y}$Se$_2$ system.

cond-mat.supr-con↗

arXiv2014

Crystal field splitting in Sr$_{n+1}$Ir$_n$O$_{3n+1}$ ($n$ = 1, 2) iridates probed by x-ray Raman spectroscopy

Non-resonant Raman spectroscopy in the hard X-ray regime has been used to explore the electronic structure of the first two members of the Ruddlesden-Popper series Sr$_{n+1}$Ir$_n$O$_{3n+1}$ of iridates. By tuning the photon energy transfer around 530 eV we have been able to explore the oxygen K near edge structure with bulk sensitivity. The angular dependence of the spectra has been exploited to assign features in the 528-535 eV energy range to specific transitions involving the Ir 5d orbitals. This has allowed us to extract reliable values for both the t2g-eg splitting arising from the cubic component of the crystal field (10Dq), in addition to the splitting of the eg orbitals due to tetragonal distortions. The values we obtain are (3.8, 1.6) eV and (3.55, 1.9) eV for Sr$_2$IrO$_4$ and Sr$_3$Ir$_2$O$_7$, respectively.

cond-mat.str-el↗

arXiv2014

CaIrO3: a Spin-Orbit Mott Insulator Beyond the jeff = 1/2 Ground State

In CaIrO3 electronic correlation, spin-orbit coupling, and tetragonal crystal field splitting are predicted to be of comparable strength. However, the nature of its ground state is still object of debate, with contradictory experimental and theoretical results. We probe the ground state of CaIrO3 and assess the effective tetragonal crystal field splitting and spin-orbit coupling at play in this system by means of resonant inelastic x-ray scattering. We conclude that insulating CaIrO3 is not a jeff = 1/2 iridate and discuss the consequences of our finding to the interpretation of previous experiments. In particular, we clarify how the Mott insulating state in iridates can be readily extended beyond the jeff = 1/2 ground state.

cond-mat.str-el↗

arXiv2013

Orbital occupancies and the putative jeff = 1/2 groundstate in Ba2IrO4: a combined oxygen K edge XAS and RIXS study

The nature of the electronic groundstate of Ba2IrO4 has been addressed using soft X-ray absorption and inelastic scattering techniques in the vicinity of the oxygen K edge. From the polarization and angular dependence of XAS we deduce an approximately equal superposition of xy, yz and zx Ir4+ 5d orbitals. By combining the measured orbital occupancies, with the value of the spin-orbit coupling provided by RIXS, we estimate the crystal field splitting associated with the tetragonal distortion of the IrO6 octahedra to be small, Δ=50(50) meV. We thus conclude definitively that Ba2IrO4 is a close realization of a spin-orbit Mott insulator with a jeff = 1/2 groundstate, thereby overcoming ambiguities in this assignment associated with the interpretation of X-ray resonant scattering experiments.

cond-mat.str-el↗

arXiv2013

Resonant X-ray scattering and the $j_{\mathrm{eff}}=1/2$ electronic ground state in iridate perovskites

The resonant X-ray scattering (magnetic elastic, RXMS, and inelastic, RIXS) of Ir$^{4+}$ at the L$_{2,3}$ edges relevant to spin-orbit Mott insulators A$_{n+1}$Ir$_{n}$O$_{3n+1}$ (A=Sr, Ba, etc.) are calculated using a single-ion model which treats the spin-orbit and tetragonal crystal-field terms on an equal footing. Both RXMS and RIXS in the spin-flip channel are found to display a non-trivial dependence on the direction of the magnetic moment, $\boldsymbolμ$. Crucially, we show that for $\boldsymbolμ$ in the \emph{ab}-plane, RXMS at the L$_2$ edge is zero \emph{irrespective} of the tetragonal crystal-field; spin-flip RIXS, relevant to measurements of magnons, behaves reciprocally being zero at L$_2$ when $\boldsymbolμ$ is perpendicular to the \emph{ab}-plane. Our results provide important insights into the interpretation of X-ray data from the iridates, including that a $j_{\mathrm{eff}}=1/2$ ground state cannot be assigned on the basis of L$_2$/L$_3$ intensity ratio alone.

cond-mat.str-el↗

arXiv2013

Compressed correlation functions and fast aging dynamics in metallic glasses

We present x-ray photon correlation spectroscopy measurements of the atomic dynamics in a Zr67Ni33 metallic glass, well below its glass transition temperature. We find that the decay of the density fluctuations can be well described by compressed, thus faster than exponential, correlation functions which can be modeled by the well-known Kohlrausch-Williams-Watts function with a shape exponent β larger than one. This parameter is furthermore found to be independent of both waiting time and wave-vector, leading to the possibility to rescale all the correlation functions to a single master curve. The dynamics in the glassy state is additionally characterized by different aging regimes which persist in the deep glassy state. These features seem to be universal in metallic glasses and suggest a non diffusive nature of the dynamics. This universality is supported by the possibility of describing the fast increase of the structural relaxation time with waiting time using a unique model function, independently of the microscopic details of the system.

cond-mat.soft↗

arXiv2012

Atomic-scale relaxation dynamics and aging in a metallic glass probed by X-ray photon correlation spectroscopy

We use X-Ray Photon Correlation Spectroscopy to investigate the structural relaxation process in a metallic glass on the atomic length scale. We report evidence for a dynamical crossover between the supercooled liquid phase and the metastable glassy state, suggesting different origins of the relaxation process across the transition. Furthermore, using different cooling rates we observe a complex hierarchy of dynamic processes characterized by distinct aging regimes. Strong analogies with the aging dynamics of soft glassy materials, such as gels and concentrated colloidal suspensions, point at stress relaxation as a universal mechanism driving the relaxation dynamics of out-of-equilibrium systems.

cond-mat.soft↗

arXiv2012

Coexistence of different electronic phases in the K0.8Fe1.6Se2 superconductor: a bulk-sensitive hard x-rays spectroscopy study

We have studied electronic and magnetic properties of the K0.8Fe1.6Se2 superconductor by x-ray absorption and emission spectroscopy. Detailed temperature dependent measurements alongwith a direct comparison with the binary FeSe system have revealed coexisting electronic phases: a majority phase with high spin 3+Fe state and a minority phase with intermediate spin 2+Fe state. The effect of high temperature annealing suggests that the compressed phase with lower spin 2+Fe state is directly related with the high Tc superconductivity in the title system. The results clearly underline glassy nature of superconductivity in the electronically inhomogeneous K0.8Fe1.6Se2, similar to the superconductivity in granular phases.

cond-mat.supr-con↗

arXiv2011

Plasmons in Sodium under Pressure: Increasing Departure from Nearly-Free-Electron Behavior

We have measured plasmon energies in Na under high pressure up to 43 GPa using inelastic x-ray scattering (IXS). The momentum-resolved results show clear deviations, growing with increasing pressure, from the predictions for a nearly-free electron metal. Plasmon energy calculations based on first-principles electronic band structures and a quasi-classical plasmon model allow us to identify a pressure-induced increase in the electron-ion interaction and associated changes in the electronic band structure as the origin of these deviations, rather than effects of exchange and correlation. Additional IXS results obtained for K and Rb are addressed briefly.

cond-mat.mtrl-sci↗

arXiv2008

Effect of Polymerization on the Boson Peak, from the Liquid to Glassy Phase

Raman scattering measurements are used to follow the modification of the vibrational density of states in a reactive epoxy{amine mixture during isothermal polymerization. Combining with Brillouin light and inelastic x-ray scattering measurements, we analyze the variations of the boson peak and of the Debye level while the system passes from the uid to a glassy phase upon increasing the number of covalent bonds among the constituent molecules. We find that the shift and the intensity decrease of the boson peak are fully explained by the modification of the elastic medium throughout the reaction. Surprisingly, bond-induced modifications of the structure do not affect the relative excess of states over the Debye level.

cond-mat.soft↗

arXiv2005

Adiabatic and isothermal sound waves: the case of supercritical nitrogen

The acoustic sound dispersion of nitrogen in its liquid and supercritical phases has been studied by Inelastic X-Ray Scattering. Approaching supercritical conditions, the gradual disappearance of the positive sound dispersion, characteristic of the low temperature liquid, is observed. In the supercritical state, evidence for a crossover between adiabatic and isothermal sound propagation regimes is inferred by an analysis of the dynamic structure factor based on generalized hydrodynamics.

cond-mat.dis-nn↗

arXiv2005

Acoustic damping in Li$_2$O-2B$_2$O$_3$ glass observed by inelastic x-ray and optical Brillouin scattering

The dynamic structure factor of lithium-diborate glass has been measured at several values of the momentum transfer $Q$ using high resolution inelastic x-ray scattering. Much attention has been devoted to the low $Q$-range, below the observed Ioffe-Regel crossover \qco{}$\simeq$ 2.1 nm$^{-1}$. We find that below \qco{}, the linewidth of longitudinal acoustic waves increases with a high power of either $Q$, or of the frequency $Ω$, up to the crossover frequency \OMco{} $\simeq$ 9 meV that nearly coincides with the center of the boson peak. This new finding strongly supports the view that resonance and hybridization of acoustic waves with a distribution of rather local low frequency modes forming the boson peak is responsible for the end of acoustic branches in strong glasses. Further, we present high resolution Brillouin light-scattering data obtained at much lower frequencies on the same sample. These clearly rule out a simple $Ω^2$-dependence of the acoustic damping over the entire frequency range.

cond-mat.dis-nn↗

arXiv2005

Glass-specific behavior in the damping of acoustic-like vibrations

High frequency sound is observed in lithium diborate glass, Li$_2$O--2B$_2$O$_3$, using Brillouin scattering of light and x-rays. The sound attenuation exhibits a non-trivial dependence on the wavevector, with a remarkably rapid increase towards a Ioffe-Regel crossover as the frequency approaches the boson peak from below. An analysis of literature results reveals the near coincidence of the boson-peak frequency with a Ioffe-Regel limit for sound in {\em all} sufficiently strong glasses. We conjecture that this behavior, specific to glassy materials, must be quite universal among them.

cond-mat.dis-nn↗

arXiv2005

High frequency longitudinal and transverse dynamics in water

High-resolution, inelastic x-ray scattering measurements of the dynamic structure factor S(Q,ω) of liquid water have been performed for wave vectors Q between 4 and 30 nm^-1 in distinctly different thermodynamic conditions (T= 263 - 420 K ; at, or close to, ambient pressure and at P = 2 kbar). In agreement with previous inelastic x-ray and neutron studies, the presence of two inelastic contributions (one dispersing with Q and the other almost non-dispersive) is confirmed. The study of their temperature- and Q-dependence provides strong support for a dynamics of liquid water controlled by the structural relaxation process. A viscoelastic analysis of the Q-dispersing mode, associated with the longitudinal dynamics, reveals that the sound velocity undergoes the complete transition from the adiabatic sound velocity (c_0) (viscous limit) to the infinite frequency sound velocity (c_\infinity) (elastic limit). On decreasing Q, as the transition regime is approached from the elastic side, we observe a decrease of the intensity of the second, weakly dispersing feature, which completely disappears when the viscous regime is reached. These findings unambiguously identify the second excitation to be a signature of the transverse dynamics with a longitudinal symmetry component, which becomes visible in the S(Q,ω) as soon as the purely viscous regime is left.

cond-mat.dis-nn↗

arXiv2004

Microscopic dynamics and relaxation processes in liquid Hydrogen Fluoride

Inelastic x-ray scattering and Brillouin light scattering measurements of the dynamic structure factor of liquid hydrogen fluoride have been performed in the temperature range$ T=214÷283 K$. The data, analysed using a viscoelastic model with a two timescale memory function, show a positive dispersion of the sound velocity $c(Q)$ between the low frequency value $c_0(Q)$ and the high frequency value $c_{\infty α}(Q)$. This finding confirms the existence of a structural ($α$) relaxation directly related to the dynamical organization of the hydrogen bonds network of the system. The activation energy $E_a$ of the process has been extracted by the analysis of the temperature behavior of the relaxation time $τ_α(T)$ that follows an Arrhenius law. The obtained value for $E_a$, when compared with that observed in another hydrogen bond liquid as water, suggests that the main parameter governing the $α$-relaxation process is the number of the hydrogen bonds per molecule.

cond-mat.dis-nn↗

arXiv2004

Evidence of anomalous dispersion of the generalized sound velocity in glasses

The dynamic structure factor, S(Q,w), of vitreous silica, has been measured by inelastic X-ray scattering in the exchanged wavevector (Q) region Q=4-16.5 nm-1 and up to energies hw=115 meV in the Stokes side. The unprecedented statistical accuracy in such an extended energy range allows to accurately determine the longitudinal current spectra, and the energies of the vibrational excitations. The simultaneous observation of two excitations in the acoustic region, and the persistence of propagating sound waves up to Q values comparable with the (pseudo-)Brillouin zone edge, allow to observe a positive dispersion in the generalized sound velocity that, around Q=5 nm-1, varies from 6500 to 9000 m/s: this phenomenon was never experimentally observed in a glass.

cond-mat.dis-nn↗

arXiv2004

Collective dynamics in molten potassium: an Inelastic X-ray Scattering study

The high frequency collective dynamics of molten potassium has been investigated by inelastic x-ray scattering, disclosing an energy/momentum transfer region unreachable by previous neutron scattering experiments (INS). We find that a two-step relaxation scenario, similar to that found in other liquid metals, applies to liquid potassium. In particular, we show how the sound velocity determined by INS experiments, exceeding the hydrodynamic value by $\approx 30 %$, is the higher limit of a speed up, located in the momentum region $1<Q<3$ nm$^{-1}$, which marks the departure from the isothermal value. We point out how this phenomenology is the consequence of a microscopic relaxation process that, in turn, can be traced back to the presence of ''instantaneous'' disorder, rather than to the crossover from a liquid to solid-like response.

cond-mat.dis-nn↗