arXiv subjects

Kevin C. Prince

Publications and source records attributed to Kevin C. Prince.

At least 19 recordsLinked to original sources

arXiv2026

Roadmap on Attosecond Science

Twenty-five years have passed since the first experimental demonstration of attosecond pulses, marking the advent of our ability to resolve and control electron motion in real time. What began as a technological breakthrough - generating the shortest flashes ever produced - has evolved into a powerful approach for probing and steering electronic dynamics in atoms, molecules, and solids. This roadmap, authored by leading experts in the field, surveys the recent rapid progress in the generation and characterization of attosecond pulses, emerging attosecond measurement and control techniques, and their expanding range of applications. It reviews current and future developments in attosecond light sources, including novel laser technologies, waveform synthesizers, new schemes for high-order harmonic generation, attosecond pulse generation at free-electron lasers, and structured light. Advances in attosecond measurement methodologies are also discussed, encompassing all-attosecond pump-probe spectroscopy, attosecond four-wave mixing, attosecond microscopy, spectroscopy with light transients, and attosecond interferometry. Furthermore, the roadmap addresses applications of attosecond spectroscopy to reveal electron dynamics in molecules and condensed matter systems from both theoretical and experimental perspectives, and highlights emerging directions at the interface with quantum optics and quantum entanglement. Overall, this work aims to serve as a comprehensive resource for navigating the evolving landscape of attosecond science.

physics.optics↗

arXiv2026

Two-colour coherent control of nuclear and electron dynamics in photoionization of molecular hydrogen with FEL pulses

The extension of coherent $\omega$-$2\omega$ control schemes, recently implemented in free-electron lasers (FELs), to molecular systems offers new opportunities to control chemical dynamics on the electronic timescale, potentially allowing for the steering of reactions along previously inaccessible pathways. We have implemented such a scheme at the seeded FERMI FEL to retrieve the relative phases between one-photon (frequency $2\omega$) and two-photon (frequency $\omega$) ionization paths in the hydrogen molecule as a function of photoelectron energy and emission angle. The narrow bandwidth of the XUV pulses enables selective excitation of vibrational levels of neutral intermediate H$_2$ states in the two-photon ionization path. Here we focus on $\omega$--$2\omega$ ionization of H$_2(X\,^{1}\Sigma_g^{+},\,v=0)$ into the H$_2^{+}(X\,^{2}\Sigma_g^{+},\,v_f)$ ground state involving the H$_2(B\,^{1}\Sigma_u^{+},\,v'=6)$ intermediate state. The relative phases of the $\omega$ and $2\omega$ interfering photoionization amplitudes exhibit a strong dependence on photoelectron energy, i.e.\ on the final vibrational state $v_f$ in the H$_2^{+}$ cation. With the help of accurate theoretical calculations, the observed phase jumps are assigned to the coupled electronic and nuclear dynamics at play in the two-photon process, significantly influenced by H$_2(^{1}\Sigma_g^{+}$ and $^{1}\Pi_g)$ autoionizing states and the mapping of the H$_2(B\,^{1}\Sigma_u^{+},\,v'=6)$ intermediate-state nuclear wavefunction into the final vibrational states of H$_2^{+}(X\,^{2}\Sigma_g^{+})$. The present work establishes the fundamental concepts required to access coupled electron--nuclear dynamics in molecules using $\omega$--$2\omega$ coherent control schemes currently available at free-electron laser facilities.

physics.chem-ph↗

arXiv2026

Breakdown of the isotropic asymptotic approximation in two-colour photoionisation

The Wigner delay is defined as the energy derivative of the scattering phase of a particle in a given potential, unveiling the time taken (or gained) due to the interaction. The characterisation of this delay plays a central role in attosecond science, where the time resolution allows to gain information on the time interval required for a photoelectron to be emitted into the continuum after the absorption of a single photon. Attosecond interferometric techniques, based on two-colour (extreme ultraviolet and near-infrared) photoionisation schemes, cannot provide a direct measurement of the Wigner delay, because the low-frequency photon contributes with an additional delay, which is imprinted on the outgoing photoelectron. The isolation of the Wigner delay is usually achieved by appealing to the asymptotic approximation, which assumes that the two-photon delay is separable into a Wigner and a near-infrared-induced phase and provides a universal analytical expression for the latter. In this study, we introduce a self-referencing approach based on the implementation of non-consecutive extreme ultraviolet harmonics, in order to test the validity of the asymptotic approximation. We demonstrate its breakdown by observing a deviation of a few tens of milliradians (corresponding to a few attoseconds) between its predictions and the experimentally measured phases of the sideband oscillations generated in our scheme, in agreement with full-dimensional simulations.

physics.atom-ph↗

arXiv2025

Dichroic Electron Emission Patterns from Oriented Helium Ions

We report a joint experimental and theoretical study using a combination of polarization-controlled free-electron-laser (FEL) and near-infra\-red (NIR) pulses in a synchronized two-color photo\-ionization scheme. Excited He$^+$ ions, created by extreme ultraviolet (XUV) circularly polarized radiation from the XUV-FEL FERMI in the oriented $3p\, (m\!=\!+1)$ state, are exposed to circularly polarized 784-nm NIR radiation with peak intensities from $10^{12}\,\rm W/cm^2$ to $\rm 10^{13}\,W/cm^2$. The angular distribution of the ejected electrons exhibit a strong dichroism depending on the NIR intensity. While the co-rotating case is defined by a single path, for the counter-rotating case, there are two dominant pathways whose relative strength and phase difference are determined.

physics.atom-ph↗

arXiv2025

Shake-down spectroscopy as state- and site-specific probe of ultrafast chemical dynamics

Tracking the multifarious ultrafast electronic and structural changes occurring in a molecule during a photochemical transformation is a challenging endeavor that benefits from recent experimental and computational progress in time-resolved techniques. Measurements of valence electronic states, which provide a global picture of the bonding structure of the molecule, and core electronic states, which provide insight into the local environment, traditionally require different approaches and are often studied separately. Here, we demonstrate that X-ray pulses from a seeded free-electron laser (FEL) enable the measurement of high-resolution, time-resolved X-ray photoelectron spectra (XPS) that capture weak satellite states resulting from shake-down processes in a valence-excited molecule. This approach effectively combines the advantages of both valence- and core-state investigations. We applied this method to investigate photoexcited CS$_2$ molecules, where the role of internal conversion (IC) and intersystem crossing (ISC) in determining the pre-dissociation dynamics is controversial. We present XPS spectra from photoexcited CS$_2$, obtained at the FERMI FEL. High-resolution measurements, compared to the corresponding spectra obtained from accurate multireference quantum chemical calculations, reveal that shake-down satellite channels are highly sensitive to both valence electronic and geometric changes. Previous studies of the pre-dissociation dynamics have led to uncertain assignments of the branching between singlet and triplet excited states. We derive a propensity rule that demonstrates the spin-selectivity of the shake-downs. This selectivity allows us to unequivocally assign contributions from the bright and dark singlet excited states, with populations tracked along the pre-dissociation dynamic pathway.

physics.chem-ph↗

arXiv2025

Plasmon-Induced Tuning of Cerium Oxidation States in Au@CeO$_x$ Core@Shell Nanoparticles

CeO$_x$-based nanoforms are widely used in catalysis, or biomedical applications due to their redox activity and oxygen storage capacity. The key parameters determining their surface chemistry are the Ce$^{3+}$/Ce$^{4+}$ ratio and the ability to transition between Ce$^{4+}$ and Ce$^{3+}$ states. We synthesized Au@CeO$_x$ core@shell nanoparticles with different thicknesses of CeO$_x$ shells and different Ce$^{3+}$/Ce$^{4+}$ ratios through a photothermal reaction driven by localized surface plasmon resonances (LSPRs) at the Au nanoparticle surface induced by visible light. We introduce a way to further enhance the Ce$^{3+}$/Ce$^{4+}$ ratio in the shell by exposing the Au@CeO$_x$ nanoparticles to visible light using a green laser (532 nm, 50 mW). Our findings based on photoelectron spectroscopy indicate that the Ce$^{4+}$-to-Ce$^{3+}$ transition results from LSPR-induced superheating of the Au@CeO$_x$ interface, leading to the formation of oxygen vacancies and reduction of Ce$^{4+}$ ions. This process is reversible upon air exposure suggesting that the ability to transition between the Ce$^{4+}$ and Ce$^{3+}$ states is retained in the Au@CeO$_x$ nanoparticles. Our study presents the CeO$_x$-based nanoforms with a tunable cerium valence state ratio, highlighting the potential of plasmonic control in optimizing their photocatalytic and enzyme-mimetic properties.

cond-mat.mtrl-sci↗

arXiv2025

Unraveling the relaxation dynamics of Uracil: insights from time-resolved X-ray photoelectron spectroscopy

We report a study of the electronic and nuclear relaxation dynamics of the photoexcited RNA base uracil in the gas phase, using time-resolved core level photoelectron spectroscopy together with high level calculations. The dynamics was investigated by trajectory surface-hopping calculations, and the core ionization energies were calculated for geometries sampled from these. The molecule was excited by a UV laser and dynamics was probed on the oxygen, nitrogen and carbon site by core electron spectroscopy. Assuming a particular model, we find that the initially excited $S_2(ππ^*)$ state of uracil decays with a time constant of 17 $\pm$ 4 fs to the ground state directly, or to the $S_1(nπ^*)$ state via internal conversion. We find no evidence that the $S_1(nπ^*)$ state decays to the ground state by internal conversion; instead it decays to triplet states with a time constant of 1.6 $\pm$ 0.4 ps. Oscillations of the $S_1(nπ^*)$ state O 1s intensity as a function of time correlate with those of calculated C4=O8 and C5=C6 bond lengths, which undergo a sudden expansion following the initial $π\to π^*$ excitation. We also observe oscillations in the mean energy of the main line (core ionized ionic state), which we tentatively assign to dynamics of the hot ground state. Our calculations support our interpretation of the data, and provide detailed insight into the relaxation processes of uracil.

physics.chem-ph↗

arXiv2024

Strong-field quantum control in the extreme ultraviolet using pulse shaping

Tailored light-matter interactions in the strong coupling regime enable the manipulation and control of quantum systems with up to unit efficiency, with applications ranging from quantum information to photochemistry. While strong light-matter interactions are readily induced at the valence electron level using long-wavelength radiation, comparable phenomena have been only recently observed with short wavelengths, accessing highly-excited multi-electron and inner-shell electron states. However, the quantum control of strong-field processes at short wavelengths has not been possible, so far, due to the lack of pulse shaping technologies in the extreme ultraviolet (XUV) and X-ray domain. Here, exploiting pulse shaping of the seeded free-electron laser (FEL) FERMI, we demonstrate the strong-field quantum control of ultrafast Rabi dynamics in helium atoms with high fidelity. Our approach unravels a strong dressing of the ionization continuum, otherwise elusive to experimental observables. The latter is exploited to achieve control of the total ionization rate, with prospective applications in many XUV and soft X-ray experiments. Leveraging recent advances in intense few-femtosecond to attosecond XUV to soft X-ray light sources, our results open an avenue to the efficient manipulation and selective control of core electron processes and electron correlation phenomena in real time.

physics.atom-ph↗

arXiv2024

Circular Dichroism in Multiphoton Ionization of Resonantly Excited Helium Ions near Channel Closing

The circular dichroism (CD) of photoelectrons generated by near-infrared (NIR) laser pulses using multiphoton ionization of excited He$^+$ ions in the 3p(m=+1) state. The ions were prepared by circularly polarized extreme ultraviolet (XUV) pulses. For circularly polarized NIR pulses co- and counter-rotating relative to the polarization of the XUV pulse, a complex variation of the CD is observed as a result of intensity- and polarization-dependent Freeman resonances, with and without additional dichroic AC-Stark shifts. The experimental results are compared with numerical solutions of the time-dependent Schrödinger equation to identify and interpret the pronounced variation of the experimentally observed CD.

physics.atom-ph↗

arXiv2024

Generation of entanglement using a short-wavelength seeded free-electron laser

Quantum entanglement between the degrees of freedom encountered in the classical world is challenging to observe due to the surrounding environment. To elucidate this issue, we investigate the entanglement generated over ultrafast timescales in a bipartite quantum system comprising two massive particles: a free-moving photoelectron, which expands to a mesoscopic length-scale, and a light-dressed atomic ion, which represents a hybrid state of light and matter. Although the photoelectron spectra are measured classically, the entanglement allows us to reveal information about the dressed-state dynamics of the ion and the femtosecond extreme ultraviolet pulses delivered by a seeded free-electron laser. The observed generation of entanglement is interpreted using the time-dependent von Neumann entropy. Our results unveil the potential for using short-wavelength coherent light pulses from free-electron lasers to generate entangled photoelectron and ion systems for studying spooky action at a distance.

quant-ph↗

arXiv2023

Control of ion-photoelectron entanglement and coherence via Rabi oscillations

We report a theoretical investigation of photoionization by a pair of coherent, ultrashort fundamental and second-harmonic extreme-ultraviolet pulses, where the photon energies are selected to yield the same photoelectron energy for ionization of two different sub-shells. This choice implies that the fundamental energy is equal to the difference in energy of the ionic states, and they are therefore coupled by the fundamental photon. By deriving analytical expressions using the essential-states approach, we show that this Rabi coupling creates coherence between the two photoelectron wave packets, which would otherwise be incoherent. We analyze how the coupling is affected by the parameters such as relative phase, pulse width, delay between the two pulses, the Rabi coupling strength, and photoelectron energy. Our discussion mostly considers Ne 2p and 2s photoionization, but it is generally valid for many other quantum systems where photoionization from two different shells is observed.

physics.atom-ph↗

arXiv2023

FEL stochastic spectroscopy revealing silicon bond softening dynamics

Time-resolved X-ray Emission/Absorption Spectroscopy (Tr-XES/XAS) is an informative experimental tool sensitive to electronic dynamics in materials, widely exploited in diverse research fields. Typically, Tr-XES/XAS requires X-ray pulses with both a narrow bandwidth and sub-picosecond pulse duration, a combination that in principle finds its optimum with Fourier transform-limited pulses. In this work, we explore an alternative xperimental approach, capable of simultaneously retrieving information about unoccupied (XAS) and occupied (XES) states from the stochastic fluctuations of broadband extreme ultraviolet pulses of a free-electron laser. We used this method, in combination with singular value decomposition and Tikhonov regularization procedures, to determine the XAS/XES response from a crystalline silicon sample at the L2,3-edge, with an energy resolution of a few tens of meV. Finally, we combined this spectroscopic method with a pump-probe approach to measure structural and electronic dynamics of a silicon membrane. Tr-XAS/XES data obtained after photoexcitation with an optical laser pulse at 390 nm allowed us to observe perturbations of the band structure, which are compatible with the formation of the predicted precursor state of a non-thermal solid-liquid phase transition associated with a bond softening phenomenon.

cond-mat.mtrl-sci↗

arXiv2022

Diffraction imaging of light induced dynamics in xenon-doped helium nanodroplets

We have explored the light induced dynamics in superfluid helium nanodroplets with wide-angle scattering in a pump-probe measurement scheme. The droplets are doped with xenon atoms to facilitate the ignition of a nanoplasma through irradiation with near-infrared laser pulses. After a variable time delay of up to 800 ps, we image the subsequent dynamics using intense extreme ultraviolet pulses from the FERMI free-electron laser. The recorded scattering images exhibit complex intensity fluctuations that are categorized based on their characteristic features. Systematic simulations of wide-angle diffraction patterns are performed, which can qualitatively explain the observed features by employing model shapes with both randomly distributed as well as structured, symmetric distortions. This points to a connection between the dynamics and the positions of the dopants in the droplets. In particular, the structured fluctuations might be governed by an underlying array of quantized vortices in the superfluid droplet as has been observed in previous small-angle diffraction experiments. Our results provide a basis for further investigations of dopant-droplet interactions and associated heating mechanisms.

physics.atm-clus↗

arXiv2022

High energy-resolution transient ghost absorption spectroscopy

We demonstrate the measurement of ultrafast dynamics using ghost spectroscopy and a pump-probe approach with an optical pump and a short-wavelength radiation probe. The ghost spectroscopy approach is used to overcome the challenge of the strong intensity and spectrum fluctuations at free-electron lasers and to provide high -spectral resolution, which enables the measurement of small energy shifts in the absorption spectrum. We exploit the high resolution to explore the dynamics of the charge carrier excitations and relaxations and their impact on the photoinduced structural changes in silicon by measuring the variation of the absorption spectrum of a Si(100) membrane near the silicon L2,3 edge and the accompanying edge shifts in response to the optical illumination.

physics.optics↗

arXiv2022

Extreme ultraviolet wave packet interferometry of the autoionizing HeNe dimer

Femtosecond extreme ultraviolet wave packet interferometry (XUV-WPI) was applied to study resonant inter-atomic Coulombic decay (ICD) in the HeNe dimer. The high demands on phase stability and sensitivity for vibronic XUV-WPI of molecular-beam targets are met using an XUV phase-cycling scheme. The detected quantum interferences exhibit vibronic dephasing and rephasing signatures along with an ultrafast decoherence assigned to the ICD process. A Fourier analysis reveals the molecular absorption spectrum with high resolution. The demonstrated experiment shows a promising route for the real-time analysis of ultrafast ICD processes with both high temporal and spectral resolution.

physics.atm-clus↗

arXiv2022

Time-resolved Ultrafast Interatomic Coulombic Decay in Superexcited Sodium-doped Helium Nanodroplets

The autoionization dynamics of superexcited superfluid He nanodroplets doped with Na atoms is studied by extreme-ultraviolet (XUV) time-resolved electron spectroscopy. Following excitation into the higher-lying droplet absorption band, the droplet relaxes into the lowest metastable atomic $1s2s$ $^{1,\,3}$S states from which Interatomic Coulombic Decay (ICD) takes places either between two excited He atoms or between an excited He atom and a Na atom attached to the droplet surface. Four main ICD channels are identified and their time constants are determined by varying the delay between the XUV pulse and a UV pulse that ionizes the initial excited state and thereby quenches ICD. The time constants for the different channels all fall in the range $\sim$1~ps indicating that the ICD dynamics are mainly determined by the droplet environment. A periodic modulation of the transient ICD signals is tentatively attributed to the oscillation of the bubble forming around the localized He excitation. The ICD efficiency depends on the total number of excited states in a droplet rather than the density of excited states pointing to a collective enhancement of ICD.

physics.atm-clus↗

arXiv2022

High-resolution absorption measurements with free-electron lasers using ghost spectroscopy

We demonstrate a simple and robust high-resolution ghost spectroscopy approach for x-ray and extreme ultraviolet absorption spectroscopy at free-electron laser sources. Our approach requires an on-line spectrometer before the sample and a downstream bucket detector. We use this method to measure the absorption spectrum of silicon, silicon carbide and silicon nitride membranes in the vicinity of the silicon L2,3-edge. We show that ghost spectroscopy allows the high-resolution reconstruction of the sample spectral response using a coarse energy scan with self-amplified spontaneous emission radiation. For the conditions of our experiment the energy resolution of the ghost-spectroscopy reconstruction is higher than the energy resolution reached by scanning the energy range by narrow spectral bandwidth radiation produced by the seeded free-electron laser. When we set the photon energy resolution of the ghost spectroscopy to be equal to the resolution of the measurement with the seeded radiation, the measurement time with the ghost spectroscopy method is shorter than scanning the photon energy with seeded radiation. The exact conditions for which ghost spectroscopy can provide higher resolution at shorter times than measurement with narrow band scans depend on the details of the measurements and on the properties of the samples and should be addressed in future studies.

physics.ins-det↗

arXiv2022

Studying ultrafast Rabi dynamics with a short-wavelength seeded free-electron laser

Rabi oscillations are periodic modulations of populations in two-level systems interacting with a time-varying field. They are ubiquitous in physics with applications in different areas such as photonics, nano-electronics, electron microscopy, and quantum information. While the theory developed by Rabi was intended for fermions in gyrating magnetic fields, Autler and Townes realized that it could also be used to describe coherent light-matter interaction within the rotating wave approximation\cite. Although intense nanometer-wavelength light-sources have been available for more than a decade, Rabi dynamics at such short wavelengths have not been observed directly. Here we show that femtosecond extreme-ultraviolet pulses from a seeded free-electron laser can drive Rabi oscillations between the ground state and an excited state in helium atoms. The measured photoemission signal revealed an Autler-Townes doublet as well as an avoided crossing, phenomena that are both trademarks of quantum optics. Using theoretical analyses that go beyond the strong-field approximation, we found that the ultrafast build-up of the doublet structure follows from a quantum interference effect between resonant and non-resonant photoionization pathways. Given the recent availability of intense attosecond and few-femtosecond extreme-ultraviolet pulses, our results offer opportunities to carry out ultrafast manipulation of coherent processes at short wavelengths using free-electron lasers.

quant-ph↗