SearcharxivSearch

arXiv subjects

Thomas M. Linker

Publications and source records attributed to Thomas M. Linker.

8 recordsLinked to original sources

Posterior Inference of Hamiltonian Parameters from RIXS Spectroscopy

We present the first application of simulation-based inference to resonant inelastic X-ray scattering spectroscopy. Using truncated marginal neural ratio estimation to efficiently restrict the prior and conditional flow matching as the joint density estimator, we infer full posteriors with a modest simulation budget for two Ni$^{2+}$ compounds---NiPS$_3$ as a representative covalent case and K$_2$NiF$_4$ as a more atomic one. We demonstrate that a vision transformer encoder whose tokenization matches the physical layout of the RIXS map yields better-covered and sharper posteriors than generic image encoders. Applying the validated method to experimental NiPS$_3$ and K$_2$NiF$_4$ data, we recover a joint posterior that reveals parameter correlations invisible to point estimators, and a posterior predictive distribution that closely matches the observed spectrum. The amortized posterior unlocks a class of analyses not previously available to the field such as nuisance-marginalized uncertainty quantification, multi-measurement posterior fusion and active experimental design.

cond-mat.str-el

Generation of high-fluence and high-intensity hard x-ray attosecond pulses at European XFEL

By combining hard x-ray attosecond pulses from the European XFEL with total-reflection focusing x-ray optics, we generated nanofocused hard x-ray attosecond pulses with intensities and fluences comparable to the highest values attained in the hard x-ray regime. A peak intensity on the order of 10$^{20}$ W/cm$^2$ is confirmed through the observation of saturation in amplified spontaneous emission from copper atoms. These x-ray pulses enable new scientific opportunities, including the exploration of higher-order nonlinear light--matter interactions, damage-free structure determination, and coherent control of atoms and molecules.

physics.optics

X-ray Coherent Attosecond Pulse Pair Spectroscopy

X-ray free electron laser (XFEL) experiments using self-amplified spontaneous emission (SASE) pulses typically achieve temporal resolutions of order several femtoseconds, as the pulse duration puts a practical limit to pump-probe or probe-probe schemes. Even with the emerging capabilities to generate pulses with attosecond durations with new single-spike SASE schemes, direct access to attosecond electron dynamics remains an experimental challenge. Here we show how X-ray coherent attosecond pulse-pair spectroscopy (X-CAPPS) provides a powerful new approach to access the ultrashort time-delay window. Coherent attosecond pulse pairs with time delays varying from ~500 as to ~5 fs are generated with Cu K$\alpha_1$ stimulated X-ray emission from a gain medium pumped by intense SASE XFEL pulses. These pulse pairs are analyzed with two subsequent Bragg crystal spectrometers, and the resulting interference spectrum is captured on two sequential 2D image detectors encoding their time separation, relative amplitudes, and phases with high precision. X-CAPPS requires no split-and-delay X-ray optics, nor XFEL pulse modifications, making it broadly implementable across existing facilities. This technique enables the investigation of attosecond processes with $\mathring{A}$ngstr\"{o}m resolution, providing a new tool for probing ultrafast dynamics across a wide range of atomic, molecular, and solid systems.

physics.optics

Observation of Multiplet Lines in Seeded Stimulated Mn Kα1 X-ray Emission

We report the successful resolution of the multiplet structure of the Kα1 x-ray emission in manganese (Mn) complexes through seeded stimulated X-ray emission spectroscopy (seeded S-XES). By employing a femtosecond pump pulse above the Mn K edge to generate simultaneous 1s core-holes, and a second-color tunable seed pulse to initiate the stimulated emission process, we were able to enhance individual lines within the Kα1 emission. This approach allows to resolve the fine multiplet features that are obscured by the life-time broadening in conventional Mn Kα XES. The work builds on our previous observation that S-XES from Mn(II) and Mn(VII) complexes pumped at high intensities can exhibit stimulated emission without sacrificing the chemical sensitivity to oxidation states. This technique opens the door to controlled high-resolution electronic structure spectroscopy in transition metal complexes beyond core hole life time broadening with potential applications in catalysis, inorganic chemistry, and materials science.

physics.chem-ph

Attosecond Inner-Shell Lasing at Angstrom Wavelengths

Since the invention of the laser nonlinear effects such as filamentation, Rabi-cycling and collective emission have been explored in the optical regime leading to a wide range of scientific and industrial applications. X-ray free electron lasers (XFELs) have led to the extension of many optical techniques to X-rays for their advantages of angstrom scale spatial resolution and elemental specificity. One such example is XFEL driven population inversion of 1s core hole states resulting in inner-shell K$α$ (2p to 1s) X-ray lasing in elements ranging from neon to copper, which has been utilized for nonlinear spectroscopy and development of next generation X-ray laser sources. Here we show that strong lasing effects, similar to those observed in the optical regime, can occur at 1.5 to 2.1 angstrom wavelengths during high intensity (> ${10^{19}}$ W/cm${^{2}}$) XFEL driven inner-shell lasing and superfluorescence of copper and manganese. Depending on the temporal substructure of the XFEL pump pulses(containing ${~10^{6}}$ - ${10^{8}}$ photons) i, the resulting inner-shell X-ray laser pulses can exhibit strong spatial inhomogeneities as well as spectral splitting, inhomogeneities and broadening. Through 3D Maxwell Bloch theory we show that the observed spatial inhomogeneities result from X-ray filamentation, and that the spectral splitting and broadening is driven by Rabi cycling with sub-femtosecond periods. Our simulations indicate that these X-ray pulses can have pulse lengths of less than 100 attoseconds and coherence properties that open the door for quantum X-ray optics applications.

physics.optics

Catalysis in Extreme Field Environments: The Case of Strongly Ionized $SiO_{2}$ Nanoparticle Surfaces

High electric fields can significantly alter catalytic environments and the resultant chemical processes. Such fields arise naturally in biological systems but can also be artificially induced through localized excitations at nanoscale. Recently, strong field excitation of dielectric nanoparticles has emerged as an avenue for studying catalysis in highly ionized environments producing extreme electric fields. While the dynamics of surface ion emission driven by ultrafast laser ionization has been heavily explored, understanding the molecular dynamics leading to fragmentation has remained elusive. To address this, we employed a multiscale approach utilizing non-adiabatic quantum molecular dynamics (NAQMD) simulations on hydrogenated silica surfaces in both bare and wetted environments under field conditions mimicking those of an ionized nanoparticle. Our findings indicate that hole localization drives fragmentation dynamics, leading to surface silanol dissociation within 50 fs and charge transfer-induced water splitting in wetted environments within 150 fs. Further insight into such ultrafast mechanisms is critical for advancement of catalysis on the surface of charged nanosystems.

physics.chem-ph

Tracking Surface Charge Dynamics on Single Nanoparticles

Surface charges play a fundamental role in physics and chemistry, particularly in shaping the catalytic properties of nanomaterials. Tracking nanoscale surface charge dynamics remains challenging due to the involved length and time scales. Here, we demonstrate real-time access to the nanoscale charge dynamics on dielectric nanoparticles employing reaction nanoscopy. We present a four-dimensional visualization of the non-linear charge dynamics on strong-field irradiated single SiO$_2$ nanoparticles with femtosecond-nanometer resolution and reveal how surface charges affect surface molecular bonding with quantum dynamical simulations. We performed semi-classical simulations to uncover the roles of diffusion and charge loss in the surface charge redistribution process. Understanding nanoscale surface charge dynamics and its influence on chemical bonding on a single nanoparticle level unlocks an increased ability to address global needs in renewable energy and advanced healthcare.

cond-mat.mes-hall

Probing the presence and absence of metal-fullerene electron transfer reactions in helium nanodroplets by deflection measurements

Metal-fullerene compounds are characterized by significant electron transfer to the fullerene cage, giving rise to an electric dipole moment. We use the method of electrostatic beam deflection to verify whether such reactions take place within superfluid helium nanodroplets between an embedded C$_{60}$ molecule and either alkali (heliophobic) or rare-earth (heliophilic) atoms. The two cases lead to distinctly different outcomes: C$_{60}$Na$_n$ ($n$=1-4) display no discernible dipole moment, while C$_{60}$Yb is strongly polar. This suggests that the fullerene and small alkali clusters fail to form a charge-transfer bond in the helium matrix despite their strong van der Waals attraction. The C$_{60}$Yb dipole moment, on the other hand, is in agreement with the value expected for an ionic complex.

physics.atm-clus