arXiv subjects

Kevin Gulu Xiong

Publications and source records attributed to Kevin Gulu Xiong.

3 recordsLinked to original sources

arXiv2026

Probing of Core Excitons in Solid NaF with Polarization-Selective Attosecond Time-Resolved Four-Wave Mixing Spectroscopy

Nonlinear Four-wave mixing processes are a powerful technique to unravel ultrafast dynamics in solid-state systems. Here, we employ attosecond four-wave mixing spectroscopy with one extreme ultraviolet (XUV) pump and two independently delayed, noncollinear near-infrared (NIR) probes to resolve the ultrafast decoherence of both dipole-allowed and dipole-forbidden core excitons at the Na+ L2,3 edge in sodium fluoride (NaF). The decoherence times of the core excitons are observed to be much faster than the 8 fs limit of the instrument response time, which is attributed to strong exciton-phonon coupling. Furthermore, polarization control of the NIR probes (Perpendicular and parallel polarizations) reveals that the bright core excitons exhibit s-like orbital angular momentum, while dark core excitons, reached by two-photon excitation, exhibit p-like angular momentum.

physics.chem-ph↗

arXiv2026

Background-free Tracking of Ultrafast Hole and Electron Dynamics with XUV Transient Grating Spectroscopy

Extreme ultraviolet (XUV) transient absorption (TA) and transient reflectivity (TR) spectroscopies enable element-specific insights into attosecond-timescale processes in solids. XUV transient grating spectroscopy (TGS) is an emerging tool that combines the advantages of both absorption and reflectivity while offering intrinsically background-free detection. Here, we implement XUV-TGS by generating a transient grating in germanium solid using two few-cycle near-infrared pulses and probing it with an attosecond XUV pulse, produced via tabletop high-harmonic generation. The spectrally resolved, diffracted XUV pulses directly visualize the separate ultrashort decay times of both photoexcited electrons and holes, without the need for iterative deconvolution. By combining XUV-TA and -TG spectroscopy, we extract the evolution of the complex refractive index, ñ, without the need for Kramers-Kronig reconstruction, as required in XUV-TR, allowing us to extract the roots of the induced optical response. We find reflectivity changes of up to 34% via the real part of ñ, whereas changes in the imaginary part only result in a variation in reflectivity of around 0.5%.

physics.optics↗

arXiv2024

Attosecond transient grating spectroscopy with near-infrared grating pulses and an extreme ultraviolet diffracted probe

Transient grating spectroscopy has become a mainstay among metal and semiconductor characterization techniques. Here we extend the technique towards the shortest achievable timescales by using tabletop high-harmonic generation of attosecond extreme ultraviolet (XUV) pulses that diffract from transient gratings generated with 500-1000 nm sub-5 fs near-infrared (NIR) pulses. We demonstrate the power of attosecond transient grating spectroscopy (ATGS) by investigating the ultrafast photoexcited dynamics in an Sb semimetal thin film. ATGS provides an element-specific, background-free signal, unfettered by spectral congestion, in contrast to transient absorption spectroscopy. With the ATGS measurements in Sb polycrystalline thin films, we observe the generation of coherent phonons and investigate the lattice and carrier dynamics. Among the latter processes, we extract carrier thermalization, hot carrier cooling, and electron-hole recombination, which are on the order of 20 fs, 50 fs, and 2 ps, timescales, respectively. Furthermore, simultaneous collection of transient absorption and transient grating data allows us to extract the total complex dielectric constant in the sample dynamics, including the real-valued refractive index, from which we are also able to investigate carrier-phonon interactions and longer-lived phonon dynamics. The outlined experimental technique expands the capabilities of transient grating spectroscopy and attosecond spectroscopies by providing a wealth of information concerning carrier and lattice dynamics with an element-selective technique, at the shortest achievable timescales.

physics.optics↗