SearcharxivSearch

arXiv · 2601.05561

Phase-Controlled Ramsey Interference of XUV Photoelectrons

Abstract

We investigate Ramsey-type quantum interference in photoelectron momentum distributions generated by two time-delayed, linearly polarized extreme-ultraviolet (XUV) laser pulses. The electron dynamics are studied by solving the full-dimensional time-dependent Schr\"odinger equation within the single-active-electron approximation for neon initially prepared in a current-carrying $2p_+$ state. The coherent superposition of electron wave packets released by the two pulses gives rise to pronounced interference fringes in both energy-resolved spectra and angle-resolved momentum distributions. We demonstrate that the fringe positions are governed by a Ramsey phase accumulated during the interpulse delay, resulting in a linear dependence on the relative carrier-envelope phase and an inverse scaling of the fringe spacing with the delay time. By systematically varying the laser intensity, we establish that the observed modulations originate from temporal quantum interference rather than Autler--Townes splitting. Analysis of the time-resolved bound-state population dynamics reveals that carrier-envelope-phase dependent bound--bound coupling dominated by transient population transfer to the $2s$ state, which controls the interference contrast. The accumulated phase is further interpreted in terms of a dynamic Stark shift of the dressed bound states, which is quantitatively reproduced using a reduced two-level model.

Explore related subjects

Keep this discovery

BibTeXRIS

Neha Kukreti, Amol R Holkundkar. 2026-01-09. Phase-Controlled Ramsey Interference of XUV Photoelectrons. https://arxiv.org/abs/2601.05561

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Delay-engineered dynamical phases in a programmable non-Markovian spin oscillator

Non-Markovian dynamics offer a new route towards engineering non-equilibrium matter, where memory and feedback act as programmable resources for controlling order in time. Here we report the realization of a non-Markovian spin oscillator in a hot vapour $^{129}$Xe-Cs co-magnetometer with programmable feedback delay and gain. By tuning these parameters, we observe a hierarchy of dynamical phases, including time-crystalline response, nonlinear bifurcations, and frequency-comb formation. The measured spectra and phase boundaries are captured by linear stability analysis of delayed Bloch equations, revealing these phenomena as different manifestations of the same memory-induced instability structure. These results establish time-delayed feedback as a powerful strategy for controlling non-equilibrium phases, enabling quantum sensing, frequency referencing, and synchronization within a single spin-based platform.

physics.atom-ph

Non-stick vacuum wall collisions with a laser-coolable molecule

Molecular species that are suitable for direct laser cooling are typically considered lost or destroyed if they collide with an ambient temperature vacuum wall. Here, we study surface collisions with aluminum monofluoride (AlF), a laser-coolable molecule that survives this process with unusually high probability. We detect the outgoing AlF molecules from a single wall collision via Doppler-sensitive laser-induced fluorescence spectroscopy, using incoming supersonic (pulsed) and thermochemical (continuous) molecular beams. The angular, velocity and rovibrational level distributions of the outgoing molecules show near-complete thermalisation to the wall in a single collision event. We determine an upper limit to the surface residence time of about 5$~\mu$s, and by monitoring the decay in density of pulses of molecules loaded into a small storage volume, we deduce the surface sticking probability for different materials. For a siloxane-coated metallic surface, the sticking probability of AlF is about 0.015, allowing us to accumulate molecules from the thermochemical source into an ambient temperature storage vessel at densities near $10^{8}~$cm$^{-3}$. This provides a route to compact, portable traps for neutral molecules.

physics.atom-ph

Kinetic modeling of molecular beam formation in a cryogenic buffer-gas cell

Cryogenic buffer-gas cells are widely used to produce cold molecular beams, but the microscopic dynamics governing beam formation remain challenging to model. Here we present fully kinetic simulations of a cryogenic buffer-gas cell using the Direct Simulation Monte Carlo method implemented in the PICLas framework, treating the buffer gas and ablated molecules within a single unified model. We capture characteristic features of cryogenic buffer-gas sources, including plume cooling, directed transport toward the aperture, and the formation of a slow molecular beam, while also resolving energy transfer from the hot ablation plume to the helium buffer gas that is inaccessible to existing approaches relying on the background-gas approximation. Our results demonstrate that fully kinetic simulations can provide detailed insights into buffer-gas cell dynamics and open a route toward a systematic optimization of such sources.

physics.atom-ph