arXiv subjects

Thorsten Schmitt

Publications and source records attributed to Thorsten Schmitt.

At least 19 recordsLinked to original sources

arXiv2026

Electronic excitations in the Shastry-Sutherland compound SrCu$_2$(BO$_3$)$_2$

SrCu2(BO3)2 (SCBO) is a paradigmatic realization of the Shastry-Sutherland model, hosting geometrically frustrated spin dimers and a variety of quantum magnetic phases and phenomena. Although its magnetic properties have been extensively studied, the high-energy electronic excitations that determine the crystal-field environment and Cu-O hybridization have remained largely unexplored. Here we combine Cu L3-edge resonant inelastic x-ray scattering (RIXS), broadband optical spectroscopy, and electronic-structure calculations to determine the relevant local and interband excitation energy scales in SCBO. RIXS resolves a well-defined manifold of localized Cu2+ d-d excitations between 1.8 and 2.4 eV, whose energies and polarization dependence are well reproduced by multireference quantum-chemistry calculations. In contrast, optical spectroscopy identifies charge-transfer excitations with an absorption onset near 1.2-1.6 eV and a broader higher-energy structure around 4.5 eV, which are qualitatively captured by DFT+U calculations. Taken together, these results define the characteristic energy scales of d-d and CT excitations, offering quantitative benchmarks for computational frameworks and providing essential input for refining superexchange-based magnetic models of this prototypical frustrated quantum antiferromagnet.

cond-mat.str-el↗

arXiv2026

Coherent spin waves in a maximal entropy phase

In solids, disorder is conventionally regarded as detrimental to coherence. It typically localizes and dampens collective excitations, as exemplified by Anderson localization or the broadening of magnetic modes in systems lacking long-range order. While high-entropy materials are specifically designed to harness disorder and stabilize homogeneous mixed-phase structures that can display unique properties, this same disorder is nonetheless expected to preclude the formation of coherent magnetic excitations. To test the limits of this picture, we selected the antiferromagnetic system YBaCuFeO5, as it features two distinct transition metal atoms with significantly different magnetic moments, rendering its spin dynamics exceptionally sensitive to local atomic ordering. Combining resonant inelastic x-ray scattering and linear spin wave theory, we reveal a surprising paradox: YBaCuFeO5 exhibits an unexpected, entropy-driven mixed phase, in which disorder, rather than reducing the lifetime of the collective excitations, favors coherence. In this mixed phase, the spin waves remain dispersive, markedly distinct from those expected for an ordered ground state, and exhibit well-defined acoustic and optical branches separated by a large optical gap. These results demonstrate that in entropy-stabilized magnets, disorder can favor coherent collective modes previously thought to be exclusive to low-entropy systems.

cond-mat.str-el↗

arXiv2026

Doping evolution of spin excitations in La$_{3-x}$Sr$_{x}$Ni$_2$O$_7$/SrLaAlO$_4$ superconducting thin films

Ambient-pressure superconductivity in compressively strained bilayer nickelate films provides a unique platform to test pairing scenarios, yet the evolution of magnetism with carrier doping remains largely unexplored. Here, we utilize Ni $L_3$-edge resonant inelastic x-ray scattering to systematically track the evolution of spin and electronic excitations in coherently strained La$_{3-x}$Sr$_x$Ni$_2$O$_7$/SrLaAlO$_4$ thin films, spanning the superconducting ($x \le 0.21$) and overdoped non-superconducting ($x = 0.38$) regimes. We reveal that dispersive spin excitations, characterized by double-stripe correlations and nearly doping-independent exchange scales, persist robustly throughout the entire superconducting dome. In stark contrast, upon entering the overdoped non-superconducting state, this coherent magnetic framework undergoes an abrupt collapse, melting into a heavily damped, low-spectral-weight continuum. We show that this magnetic breakdown is fundamentally driven by a selective doping-induced orbital reconstruction. While the invariant $\sim\!1.0$~eV intra-atomic $dd$ peak confirms an intact local octahedral crystal field, the concurrent quenching of the $\sim\!0.4$~eV and $\sim\!1.6$~eV features signifies a severe degradation of the apical-oxygen-mediated $d_{z^2}$--$p_z$--$d_{z^2}$ singlet sector and bilayer charge-transfer coherence. The synchronized demise of coherent spin excitations and macroscopic pairing establishes a direct, doping-controlled link, underscoring that maintaining the localized $d_{z^2}$ magnetic framework and robust apical-oxygen coupling is the fundamental prerequisite for high-$T_c$ superconductivity in bilayer nickelates.

cond-mat.supr-con↗

arXiv2026

Disorder-induced damping of spin excitations in Cr-doped BaFe$_2$As$_2$

In doped Hund's metals, such as the iron-based superconductors, effects like charge doping and chemical pressure are often considered the dominant factors. Partial chemical substitution, however, inevitably introduces disorder. Here, we investigate spin excitations in Ba(Fe$_{1-x}$Cr$_x$)$_2$As$_{2}$ (CrBFA) by high-resolution resonant inelastic x-ray scattering (RIXS) for samples with $x = 0, 0.035,$ and $ 0.085$. In CrBFA, Cr acts as a hole dopant, but also introduces localized spins that compete with Fe-derived magnetic excitations. We found that the Fe-derived magnetic excitations are softened and damped, becoming overdamped for $x = 0.085$. At this doping level, complementary angle-resolved photoemission spectroscopy measurements (ARPES) show increased electronic localization and a suppression of the nematic $d_{xz}/d_{yz}$ band splitting present in the parent compound. We thus propose a localized spin model that explicitly incorporates substitutional disorder and Cr local moments, successfully reproducing our key observations. Our findings reveal a case where disorder dominates over charge doping in the case of a Hund's metal.

cond-mat.supr-con↗

arXiv2025

Persistence of small polarons into the superconducting phase of Ba$_{1-x}$K$_x$BiO$_3$

Bipolaronic superconductivity is an exotic pairing mechanism proposed for materials like Ba$_{1-x}$K$_x$BiO$_3$ (BKBO); however, conclusive experimental evidence for a (bi)polaron metallic state in this material remains elusive. Here, we combine resonant inelastic x-ray and neutron total scattering techniques with advanced modelling to study the local lattice distortions, electronic structure, and electron-phonon coupling ($e$-ph) in BKBO as a function of doping. Data for the parent compound ($x = 0$) indicates that the electronic gap opens in predominantly oxygen-derived states strongly coupled to a long-range ordered breathing distortion of the oxygen sublattice. Upon doping, short-range breathing distortions and sizable ($e$-ph) coupling persist into the superconducting regime ($x = 0.4$). Comparisons with exact diagonalization and determinant quantum Monte Carlo calculations further support this conclusion. Our results provide compelling evidence that BKBO's metallic phase hosts a liquid of small (bi)polarons derived from local breathing distortions of the lattice, with implications for understanding the low-temperature superconducting instability

cond-mat.supr-con↗

arXiv2025

Coexistence of insulator-like paramagnon and metallic spin-orbit exciton modes in SrIrO$_3$

We probe the spectrum of elementary excitations in SrIrO$_3$ by using heterostructured [(SrIrO$_3$)$_m$/(SrTiO$_3$)$_l$] samples to approach the bulk limit. Our resonant inelastic x-ray scattering (RIXS) measurements at the Ir $L_3$-edge reveal a robust low-lying collective magnetic mode with an antiferromagnetic (AF) dispersion similar to the insulators Sr$_2$IrO$_4$ and Sr$_3$Ir$_2$O$_7$, albeit with a large gap and much larger linewidth. At higher energies we find the spin-orbit exciton, also strongly broadened, but with an inverted dispersion and doubled periodicity that are controlled by the charge hopping. These results demonstrate that the AF paramagnon persists, somewhat counterintuitively, far into the metallic regime of the insulator-metal transition driven by the degree of confinement in the heterostructure. We conclude that these two excitations, which are contrasting but coexisting hallmarks of strong AF pseudospin and charge fluctuations in a spin-orbit-coupled Mott-Slater material, are properties intrinsic to the ground state of semimetallic perovskite SrIrO$_3$.

cond-mat.str-el↗

arXiv2025

Persistent quantum vibronic dynamics in a $5d^1$ double perovskite oxide

Quantum entanglement between the spin, orbital, and lattice degrees of freedom in condensed matter systems can emerge due to an interplay between spin-orbit and vibronic interactions. Heavy transition metal ions decorated on a face-centered cubic lattice, for example, in $5d^1$ double perovskites, are particularly suited to support these quantum entangled states, but direct evidence has not yet been presented. In this work, we report additional peaks in the low-energy spectra of a $5d^1$ double perovskite, Ba$_2$CaReO$_6$, which cannot be explained by adopting a purely classical description of lattice vibrations. Instead, our theoretical analysis demonstrates that these spectroscopic signatures are characteristic of orbital-lattice entangled states in Ba$_2$CaReO$_6$. Crucially, both theory and experiment demonstrate that these quantum-entangled states persist to low temperatures, despite the onset of multipolar order.

cond-mat.str-el↗

arXiv2025

Impact of static disorder on quasiparticle spectra: Debye-Waller, mean free path and potential fluctuation effects

ARPES is a widely used characterization technique in condensed matter physics, providing direct access to the single-electron spectral function of crystals, including their electronic band structure and Fermi surface. Measuring the band structure of novel quantum materials has been fundamentally important for determining, for example, non-trivial band topology or for identifying new classes of materials. A key challenge with these emerging quantum materials is that their initial crystalline quality is rarely optimized, which directly affects the spectra measured by ARPES. Here, we present a theoretical framework and experimental evidence addressing two common consequences of static disorder in photoemission experiments: the loss of coherent spectral weight and the broadening of spectral features. ARPES spectra can be understood as a sum of coherent and incoherent intensities, with their relative contributions controlled by atomic disorder. Under thermal disorder, the coherent intensity is exponentially suppressed as temperature increases, a phenomenon analogous to the Debye-Waller factor in diffraction, where Bragg peaks diminish in favor of diffuse scattering as disorder increases. In this work, we report a soft X-ray study of the deliberately disordered (via Ar ion sputtering) InAs(110) surface, characterized both by STM and LEED. We introduce a new framework that enables quantification of coherent photoemission intensity loss with increasing disorder, allowing both thermal and static disorder to be treated within a unified approach. Additionally, we identify a second major effect of disorder beyond lifetime broadening: inhomogeneous spectral broadening arising from local potential fluctuations. We show that such fluctuations increase the linewidths of the spectra of localized and delocalized states, and contribute to the suppression of ARPES intensity from states near the Fermi level.

cond-mat.mtrl-sci↗

arXiv2025

Photo-generated charge-transfer excitons in NiO revealed by ultrafast time-resolved resonant inelastic x-ray scattering

Strong electronic correlation can lead to insulating behavior and to the opening of large optical gaps, even in materials with partly filled valence shells. Although the non-equilibrium optical response encodes both local (quasi atomic) and collective (long range) responses, optical spectroscopy is usually more sensitive to the latter. Resonant x-ray techniques are better suited to investigate the quasi-atomic properties of correlated solids. Using time-resolved resonant inelastic x-ray scattering (RIXS), here we study the ultrafast non-equilibrium processes in NiO following photo-excitation by ultraviolet photons with energy exceeding the optical gap. We observe the creation of charge-transfer excitons that decay with a time constant of about 2\,ps, while itinerant photo-doping persists for tens of picoseconds. Following our discovery, which establishes time-resolved high-resolution RIXS as a powerful tool for the study of transient phenomena in condensed matter, the possible presence of charge-transfer excitons will need to be considered when interpreting optical pump-probe experiments on correlated quantum materials.

cond-mat.str-el↗

arXiv2025

Spin correlations in La$_3$Ni$_2$O$_7$ thin films

The discovery of ambient-pressure superconductivity with $T_{c,\text{onset}} > 40$ K in La$_3$Ni$_2$O$_7$ (LNO) thin films grown on the SrLaAlO$_4$ (SLAO) substrate with compressive ($\varepsilon\approx-2\%$) epitaxial strain provides a unique platform for investigating the superconducting mechanism in nickelate superconductors. Here, we use resonant inelastic X-ray scattering (RIXS) to unveil the dispersive spin excitations in the LNO/SLAO thin film and establish the strain dependence of the electronic and spin excitations in LNO thin films with strain ranging from $\varepsilon\approx-2\%$ to $+1.9\%$. Compared with bulk LNO, LNO/SLAO exhibits similar $dd$ excitations and spin dynamics, but with a larger spin-excitation bandwidth, whereas tensile-strained LNO/SrTiO$_3$ exhibits a marked suppression of both the spin excitations and the Ni $3d_{z^2}$-derived $dd$ excitations. This evolution reflects a strain-tuned interlayer exchange interaction $J_z$ and Ni $3d_{z^2}$-O 2$p_z$ hybridization. Our results demonstrate how epitaxial strain modulates the interlayer magnetic coupling and are consistent with scenarios in which the interlayer antiferromagnetic superexchange interaction promotes interlayer pairing in bilayer nickelates.

cond-mat.supr-con↗

arXiv2024

Emergence of interfacial magnetism in strongly-correlated nickelate-titanate superlattices

Strongly-correlated transition-metal oxides are widely known for their various exotic phenomena. This is exemplified by rare-earth nickelates such as LaNiO$_{3}$, which possess intimate interconnections between their electronic, spin, and lattice degrees of freedom. Their properties can be further enhanced by pairing them in hybrid heterostructures, which can lead to hidden phases and emergent phenomena. An important example is the LaNiO$_{3}$/LaTiO$_{3}$ superlattice, where an interlayer electron transfer has been observed from LaTiO$_{3}$ into LaNiO$_{3}$ leading to a high-spin state. However, macroscopic emergence of magnetic order associated with this high-spin state has so far not been observed. Here, by using muon spin rotation, x-ray absorption, and resonant inelastic x-ray scattering, we present direct evidence of an emergent antiferromagnetic order with high magnon energy and exchange interactions at the LaNiO$_{3}$/LaTiO$_{3}$ interface. As the magnetism is purely interfacial, a single LaNiO$_{3}$/LaTiO$_{3}$ interface can essentially behave as an atomically thin strongly-correlated quasi-two-dimensional antiferromagnet, potentially allowing its technological utilisation in advanced spintronic devices. Furthermore, its strong quasi-two-dimensional magnetic correlations, orbitally-polarized planar ligand holes, and layered superlattice design make its electronic, magnetic, and lattice configurations resemble the precursor states of superconducting cuprates and nickelates, but with an $S \rightarrow 1$ spin state instead.

cond-mat.str-el↗

arXiv2024

Spin waves and orbital contribution to ferromagnetism in a topological metal

Special arrangements of atoms with more than one atom per unit cell, including honeycomb or kagome (woven bamboo mat) lattices, can host propagating excitations with non-trivial topology as defined by their evolution along closed paths in momentum space. Excitations on such lattices can also be momentum-independent, meaning that they are localized notwithstanding strong hopping of the underlying disturbances between neighbouring sites. The associated flat bands are interesting because the interactions between the heavy quasiparticles inhabiting them will become much more important than for strong dispersion, resulting in novel quantum solid and liquid states. Different stackings of two-dimensional lattices, for example twisted graphene bilayers, provide routes to further engineer topology and many-body effects. Here, we report the discovery, using circularly polarized x-rays for the unambiguous isolation of magnetic signals, of a nearly flat spin wave band and large (compared to elemental iron) orbital moment for the metallic ferromagnet Fe3Sn2, built from compact AB-stacked kagome bilayers and which has a topologically non-trivial electronic band structure controllable by modest external magnetic fields. As a function of out-of-plane momentum, the nearly flat optical mode and the global rotation symmetry-restoring acoustic mode are out of phase, consistent with a bilayer exchange coupling that is larger than the already large in-plane couplings. The defining units of this topological metal are therefore a triangular lattice of octahedral iron clusters rather than weakly coupled kagome planes. The spin waves are strongly damped when compared to elemental iron, opening the topic of interactions of topological bosons (spin waves) and fermions (electrons) with the very specific target of explaining boson lifetimes.

cond-mat.str-el↗

arXiv2024

Anionic disorder and its impact on the surface electronic structure of oxynitride photoactive semiconductors

The conversion of solar energy into chemical energy, stored in the form of hydrogen, bears enormous potential as a sustainable fuel for powering emerging technologies. Photoactive oxynitrides are promising materials for splitting water into molecular oxygen and hydrogen. However, one of the issues limiting widespread commercial use of oxynitrides is the degradation during operation. While recent studies have shown the loss of nitrogen, its relation to the reduced efficiency has not been directly and systematically addressed with experiments. In this study, we demonstrate the impact of the anionic stoichiometry of BaTaO$_x$N$_y$ on its electronic structure and functional properties. Through experimental ion scattering, electron microscopy, and photoelectron spectroscopy investigations, we determine the anionic composition ranging from the bulk towards the surface of BaTaO$_x$N$_y$ thin films. This further serves as input for band structure computations modeling the substitutional disorder of the anion sites. Combining our experimental and computational approaches, we reveal the depth-dependent elemental composition of oxynitride films, resulting in downward band bending and the loss of semiconducting character towards the surface. Extending beyond idealized systems, we demonstrate the relation between the electronic properties of real oxynitride photoanodes and their performance, providing guidelines for engineering highly efficient photoelectrodes and photocatalysts for clean hydrogen production.

cond-mat.mtrl-sci↗

arXiv2024

Dynamic Jahn-Teller effect in the strong spin-orbit coupling regime

Exotic quantum phases, arising from a complex interplay of charge, spin, lattice and orbital degrees of freedom, are of immense interest to a wide research community. A well-known example of such an entangled behavior is the Jahn-Teller effect, where the lifting of orbital degeneracy proceeds through lattice distortions, often accompanied by ordering of spins and metal-insulator transitions. Static distortions, including cooperative behavior, have been associated with colossal magneto-resistance, multiferroicity, high-$T_\mathrm{C}$ superconductivity and other correlated phenomena. Realizations of the dynamic Jahn-Teller effect, on the other hand, are scarce since the preservation of vibronic symmetries requires subtle tuning of the local environment. Here we demonstrate that a highly-symmetrical 5d$^1$ double perovskite Ba$_2$MgReO$_6$, comprising of a 3D array of isolated ReO$_6$ octahedra, fulfils these requirements, resulting in a unique case of a dynamic Jahn-Teller system with strong spin-orbit coupling. Thermodynamic and resonant inelastic x-ray scattering experiments undoubtedly show that the Jahn-Teller instability leads to a ground-state doublet, invoking a paradigm shift for this family of compounds. The restoration of vibronic degrees of freedom arises from a quantum-mechanical zero-point motion, as revealed by detailed quantum chemistry calculations. The dynamic state of ReO$_6$ octahedra persists down to the lowest temperatures, where a multipolar order sets in, allowing for investigations of the interplay between a dynamic JT effect and strongly correlated electron behavior.

cond-mat.str-el↗

arXiv2024

Spin-orbital excitations encoding the magnetic phase transition in the van der Waals antiferromagnet FePS$_{3}$

In the rich phases of van der Waals (vdW) materials featuring intertwined electronic order and collective phenomena, characterizing elementary dynamics that entail the low-energy Hamiltonian and electronic degrees of freedom is of paramount importance. Here we performed resonant inelastic X-ray scattering (RIXS) to elaborate the spin-orbital ground and excited states of the vdW antiferromagnetic insulator FePS$_{3}$, as well as their relation to magnetism. We observed the spectral enhancement of spin-orbital multiplet transitions about $\sim$ 100 and $\sim$ 220 meV, as well as quasielastic response, when entering the zig-zag antiferromagnetic phase, where the spectral changes develop an order-parameter-like evolution with temperature. By comparing with ligand field theory calculations, we discovered the essential role of trigonal lattice distortion and negative metal-ligand charge-transfer to account for these emergent excitations. Such spectral profiles are further examined upon confinement by mechanical exfoliation. We reveal their spectral robustness down to the few atomic layer limit, in accordance with the persistent antiferromagnetic state previously reported in optical measurements. Our study demonstrates the versatile RIXS capability that resolves magneto-crystalline anisotropy and charge-transfer energetics. These provide the crucial insight to understand how the spontaneous magnetic symmetry-breaking stabilizes in the quasi-two-dimensional limit for the vdW magnet FePS$_{3}$.

cond-mat.str-el↗

arXiv2024

Unraveling the Mn $L_3$-edge RIXS spectrum of lightly manganese doped Sr$_{3}$Ru$_{2}$O$_{7}$

Resonant inelastic x-ray scattering (RIXS) experiment was performed at the Mn $L_3$ edge. A 10 $\%$ Mn-doped Sr$_{3}$Ru$_{2}$O$_{7}$ compound, where the Mn$^{3+}$ ions are in the 3$d^4$ state, were probed for $dd$ excitations. The dilute doping concentration allows one to treat the dopant Mn$^{3+}$ ions as effectively free in the host ruthenium compound. The local nature of $dd$ RIXS spectroscopy permits one to use a single-site model to simulate the experimental spectra. The simulated spectra reproduces the in-plane [100] experimental RIXS spectrum. We also predict the intensity for the in-plane [110] direction and the out-of-plane spin orientation configuration [001]. Based on our single-ion model we were able to fit the experimental data to obtain the crystal field parameters, the 10Dq value, and the intra-orbital spin-flip energy 2$\mathcal{J}$(or $3J_{H}$, where $J_{H}$ is the Hund's energy) of the Mn$^{3+}$ ion. Utilizing our computed RIXS quantum transition amplitudes between the various $d$ orbitals of the Mn$^{3+}$ ion, the expression for the Kramers-Heisenberg cross section, and a self-consistent fitting procedure we also identify the energy boundaries of the non-spin-flip and spin-flip $dd$ excitations present in the experimental data. From our fitting procedure we obtain $2\mathcal{J} (3J_{H})=2.06$ eV, a value which is in excellent agreement with that computed from the free ion Racah parameters. We also identified the charge transfer boundary. In addition to predicting the microscopic parameters, we find a quantum spin-flip transition in the non-cross ($σ_{in}-σ_{out}$, $π_{in}-π_{out}$) x-ray polarization channels of the $dd$ RIXS spectra. A similar transition, was previously predicted to occur in the $π-π$ channel of the magnon spectrum in the non-collinear non-coplanar Kagome compound composed of Cu$^{2+}$ 3d$^{9}$ ion.

cond-mat.str-el↗

arXiv2024

Collective nature of orbital excitations in layered cuprates in the absence of apical oxygens

We have investigated the 3d orbital excitations in CaCuO2 (CCO), Nd2CuO4 (NCO), and La2CuO4 (LCO) using high-resolution resonant inelastic x-ray scattering. In LCO they behave as well-localized excitations, similarly to several other cuprates. On the contrary, in CCO and NCO the dxy orbital clearly disperse, pointing to a collective character of this excitation (orbiton) in compounds without apical oxygen. We ascribe the origin of the dispersion as stemming from a substantial next-nearest-neighbor (NNN) orbital superexchange. Such an exchange leads to the liberation of orbiton from its coupling to magnons, which is associated with the orbiton hopping between nearest neighbor copper sites. We show that the exceptionally large NNN orbital superexchange can be traced back to the absence of apical oxygens suppressing the charge transfer energy.

cond-mat.str-el↗

arXiv2023

Nematic charge-density-wave correlations in FeSe$_{1-x}$S$_{x}$

The occurrence of charge-density-wave (CDW) order is a common thread in the phase diagram of cuprate high-transition-temperature ($T_c$) superconductors. In iron-based superconductors (FeSCs), nematic order and fluctuations play a decisive role in driving other emergent orders. CDW order has been observed by scanning tunneling microscopy for various FeSCs such as FeSe thin films, uniaxially strained LiFeAs, and tetragonal FeSe$_{0.81}$S$_{0.19}$. However, it remains elusive if the CDW in these materials is a bulk phenomenon as well as if and how it intertwines with the electronic nematicity. Using energy-resolved resonant X-ray scattering at the Fe-L$_3$ edge, we report the discovery of a local-strain-induced incommensurate isotropic CDW order in FeSe$_{0.82}$S$_{0.18}$. A highly anisotropic CDW response under uniaxial strain unambiguously manifests that the CDW is directly coupled to the nematicity. Transforming part of Fe$^{2+}$ to Fe$^{3+}$ on the surface of FeSe$_{1-x}$S$_{x}$ reveals that the same isotropic CDW can be induced, enhanced, and stabilized in the whole nematic regime measured ($x=0-0.19$). As Fe$^{3+}$ can create local lattice distortions on the surface, the CDW could arise from the interaction between the local strain around Fe$^{3+}$ and the nematic electron correlations. Our experimental observation of a local-strain-induced CDW gives vital information for understanding the interplay between electron correlations and the electronic nematicity in FeSCs.

cond-mat.supr-con↗