arXiv subjects

Craig P. Schwartz

Publications and source records attributed to Craig P. Schwartz.

8 recordsLinked to original sources

arXiv2026

Full Minimal Coupling All-Electron Real-Time TDDFT for X-Ray-Matter Interactions

Standard real-time time-dependent density functional theory (RT-TDDFT) couples light to matter through a spatially uniform (dipole) vector potential, an approximation that breaks down in the X-ray regime, where the photon wavelength approaches interatomic scales. We present an all-electron, numeric-atom-centered-orbital implementation of full minimal coupling in FHI-aims that retains the spatial structure of the vector potential in both the paramagnetic and diamagnetic couplings, implements a reciprocal-space-resolved current diagnostic, and extends the propagation to periodic systems through a perturbative photon-momentum sideband coupling that recovers the density response at the photon wavevector. Four benchmarks ranging in energy from 100 eV to 5 keV validate the implementation and exercise its reach. The retained photon momentum proves physically consequential throughout, from measurable beyond dipole corrections to the enabling of channels forbidden in the dipole limit. On an all-electron footing, the implementation lays the groundwork for a general ab initio treatment of X-ray light-matter interaction across molecules, surfaces, and solids.

cond-mat.mtrl-sci↗

arXiv2026

The Surface Sensitivity of X-ray Second Harmonic Generation as a Function of Energy

The surface sensitivity and probe depth in the x-ray regime of diamond for second harmonic generation (SHG) was investigated both analytically and computationally with velocity gauge real-time time-dependent density functional theory (VG-RT-TDDFT), which includes a full multipole expansion. This was accomplished using two different approaches, by changing the number and location of layers that can generate SHG computationally and by exploiting the symmetry of a crystal, a similar pattern emerged. We find that by 1000 eV, well above the ~285 eV of the C $K$-edge, the SHG of diamond is dominated by the bulk, quadrupole response, in agreement with our analytic calculations. The bulk response continues to grow as the energy is increased, becoming overwhelming by 7000 eV. Near the C $K$-edge the measurement is quite surface sensitive, however, this surface sensitivity reduces as the energy increases such that by 1000 eV (and certainly by 3500 eV) SHG is largely bulk sensitive. Moreover, we find that the specific details of the crystal orientation (i.e., comparing a (001)-terminated and (111)-terminated surface) appear to have significant effects on the surface sensitivity.

cond-mat.mtrl-sci↗

arXiv2025

Isostructural electronic transition in MoS$_2$ probed by solid-state high harmonic generation spectroscopy

Studying materials under extreme pressure in diamond anvil cells (DACs) is key to discovering new states of matter, yet no method currently allows the direct measurement of the electronic structure in this environment. Solid-state high harmonic generation (sHHG) offers a new all-optical window into the electronic structure of materials. We demonstrate sHHG spectroscopy inside a DAC by probing $2H$-MoS$_2$, up to 30 GPa, revealing a pressure-induced crossover of the lowest direct bandgap from the $\textbf{K}$-point to the $Γ$-point. This transition manifests as a sharp minimum in harmonic intensity and a 30° rotation of the sHHG polarization anisotropy, despite the absence of a structural phase change. First-principles simulations attribute these features to interference between competing excitation pathways at distinct points in the Brillouin zone. Our results establish sHHG as a sensitive probe of electronic transitions at high pressure, enabling access to quantum phenomena that evade detection by conventional techniques.

cond-mat.mtrl-sci↗

arXiv2023

Ultra-fast yttrium hydride chemistry at high pressures via non-equilibrium states induced by x-ray free electron laser

Controlling the formation and stoichiometric content of desired phases of materials has become a central interest for the study of a variety of fields, notably high temperature superconductivity under extreme pressures. The further possibility of accessing metastable states by initiating reactions by x-ray triggered mechanisms over ultra-short timescales is enabled with the development of x-ray free electron lasers (XFEL). Utilizing the exceptionally high brilliance x-ray pulses from the EuXFEL, we report the synthesis of a previously unobserved yttrium hydride under high pressure, along with non-stoichiometric changes in hydrogen content as probed at a repetition rate of 4.5\,MHz using time-resolved x-ray diffraction. Exploiting non-equilibrium pathways we synthesize and characterize a hydride with yttrium cations in an \textit{A}15 structure type at 125\,GPa, predicted using crystal structure searches, with a hydrogen content between 4.0--5.75 hydrogens per cation, that is enthalpically metastable on the convex hull. We demonstrate a tailored approach to changing hydrogen content using changes in x-ray fluence that is not accessible using conventional synthesis methods, and reveals a new paradigm in metastable chemical physics.

cond-mat.mtrl-sci↗

arXiv2022

Saturable absorption of free-electron laser radiation by graphite near the carbon K-edge

The interaction of intense light with matter gives rise to competing nonlinear responses that can dynamically change material properties. Prominent examples are saturable absorption (SA) and two-photon absorption (TPA), which dynamically increase and decrease the transmission of a sample depending on pulse intensity, respectively. The availability of intense soft X-ray pulses from free-electron lasers (FEL) has led to observations of SA and TPA in separate experiments, leaving open questions about the possible interplay between and relative strength of the two phenomena. Here, we systematically study both phenomena in one experiment by exposing graphite films to soft X-ray FEL pulses of varying intensity, with the FEL energy tuned to match carbon 1s to $π^*$ or 1s to $σ^*$ transitions. It is observed for lower intensities that the nonlinear contribution to the absorption is dominated by SA attributed to ground-state depletion; for larger intensities ($>10^{14}$ W/cm$^2$), TPA becomes more dominant. The relative strengths of the two phenomena depend in turn on the specific transition driven by the X-ray pulse. Both observations are consistent with our real-time electronic structure calculations. Our results reveal the competing contributions of distinct nonlinear material responses to spectroscopic signals measured in the X-ray regime, demonstrating an approach of general utility for interpreting FEL spectroscopies.

physics.optics↗

arXiv2021

Polarization-Resolved Extreme Ultraviolet Second Harmonic Generation from LiNbO$_3$

Second harmonic generation (SHG) spectroscopy ubiquitously enables the investigation of surface chemistry, interfacial chemistry as well as symmetry properties in solids. Polarization-resolved SHG spectroscopy in the visible to infrared regime is regularly used to investigate electronic and magnetic orders through their angular anisotropies within the crystal structure. However, the increasing complexity of novel materials and emerging phenomena hamper the interpretation of experiments solely based on the investigation of hybridized valence states. Here, polarization-resolved SHG in the extreme ultraviolet (XUV-SHG) is demonstrated for the first time, enabling element-resolved angular anisotropy investigations. In non-centrosymmetric LiNbO$_3$, elemental contributions by lithium and niobium are clearly distinguished by energy dependent XUV-SHG measurements. This element-resolved and symmetry-sensitive experiment suggests that the displacement of Li ions in LiNbO$_3$, which is known to lead to ferroelectricity, is accompanied by distortions to the Nb ion environment that breaks the inversion symmetry of the NbO$_{6}$ octahedron as well. Our simulations show that the measured second harmonic spectrum is consistent with Li ion displacements from the centrosymmetric position by $\sim$0.5 Angstrom while the Nb-O bonds are elongated/contracted by displacements of the O atoms by $\sim$0.1 Angstrom. In addition, the polarization-resolved measurement of XUV-SHG shows excellent agreement with numerical predictions based on dipole-induced SHG commonly used in the optical wavelengths. This constitutes the first verification of the dipole-based SHG model in the XUV regime. The findings of this work pave the way for future angle and time-resolved XUV-SHG studies with elemental specificity in condensed matter systems.

cond-mat.mtrl-sci↗

arXiv2020

Ångström-resolved Interfacial Structure in Organic-Inorganic Junctions

Charge transport processes at interfaces which are governed by complex interfacial electronic structure play a crucial role in catalytic reactions, energy storage, photovoltaics, and many biological processes. Here, the first soft X-ray second harmonic generation (SXR-SHG) interfacial spectrum of a buried interface (boron/Parylene-N) is reported. SXR-SHG shows distinct spectral features that are not observed in X-ray absorption spectra, demonstrating its extraordinary interfacial sensitivity. Comparison to electronic structure calculations indicates a boron-organic separation distance of 1.9 Å, wherein changes as small as 0.1 Å result in easily detectable SXR-SHG spectral shifts (ca. 100s of meV). As SXR-SHG is inherently ultrafast and sensitive to individual atomic layers, it creates the possibility to study a variety of interfacial processes, e.g. catalysis, with ultrafast time resolution and bond specificity.

cond-mat.mtrl-sci↗

arXiv2016

Synthesis of a mixed-valent tin nitride and considerations of its possible crystal structures

Recent advances in theoretical structure prediction methods and high-throughput computational techniques are revolutionizing experimental discovery of the thermodynamically stable inorganic materials. Metastable materials represent a new frontier for studies, since even simple binary non ground state compounds of common elements may be awaiting discovery. However, there are significant research challenges related to non-equilibrium thin film synthesis and crystal structure predictions, such as small strained crystals in the experimental samples and energy minimization based theoretical algorithms. Here we report on experimental synthesis and characterization, as well as theoretical first-principles calculations of a previously unreported mixed-valent binary tin nitride. Thin film experiments indicate that this novel material is N-deficient SnN with tin in the mixed II/IV valence state and a small low-symmetry unit cell. Theoretical calculations suggest that the most likely crystal structure has the space group 2 (SG2) related to the distorted delafossite (SG166), which is nearly 0.1 eV/atom above the ground state SnN polymorph. This observation is rationalized by the structural similarity of the SnN distorted delafossite to the chemically related Sn3N4 spinel compound, which provides a fresh scientific insight into the reasons for growth of polymorphs of the metastable material. In addition to reporting on the discovery of the simple binary SnN compound, this paper illustrates a possible way of combining a wide range of advanced characterization techniques with the first-principle property calculation methods, to elucidate the most likely crystal structure of the previously unreported metastable materials.

cond-mat.mtrl-sci↗