Searcharxiv⌕ Search

arXiv · 2610.24891

Hidden Perturbative Structure in Attosecond Streaking

Abstract

Attosecond streaking is inherently multiphoton, yet we uncover a hidden perturbative structure revealing the underlying continuum--continuum angular-momentum propensity. By filtering the inversion-odd response in helium streaking data at the IR fundamental, we isolate an angular distribution dominated by the $P_1$ and $P_3$ Legendre components, whose complex coefficients yield an effective $s/d$ two-photon amplitude ratio. Multichannel, two-electron time-dependent Schrödinger equation calculations demonstrate that the characteristic Fano propensity survives electron correlation. Incorporating the experimental XUV attochirp reproduces the measured emission-edge trend, while near-threshold calculations predict resonant amplitude and phase signatures associated with the bound He $np$ Rydberg series. This symmetry- and frequency-filtering approach offers a general spectroscopic framework with potential applications to atomic, molecular, and solid-state systems where attosecond streaking is established.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Jingsong Gao, Mahmudul Hasan, Zach Eisenhutt, Vladislav Serov, Hao Liang, Meng Han, Anatoli Kheifets. 2026-10-17. Hidden Perturbative Structure in Attosecond Streaking. https://arxiv.org/abs/2610.24891

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

KEEP EXPLORING

Related papers

Near-deterministic loading of molecular arrays by microwave-assisted collisions

Molecular tweezer arrays offer great prospects for quantum simulation, sensing, and computing, and would benefit from methods that enhance loading efficiency. Whereas light-assisted collisions underpin enhanced loading methods for atomic tweezer arrays, this approach cannot be directly extended to molecular arrays due to collisional loss. We show how this collisional loss can be suppressed by shelving molecules in rotationally or vibrationally excited states, so that a shelved molecule interacts with a newly loaded molecule through a repulsive van der Waals interaction. By introducing microwave assisted collisions, we show how to control the final states and the energy released in a collision between a pair of molecules. Following this controlled collision, one of the two molecules can be ejected, and we explore several strategies for ensuring deterministic ejection. Our schemes rely on currently available techniques for laser-coolable molecules, and we predict achievable filling fractions up to 96%, paving the way for scalable molecular arrays.

physics.atom-ph↗

Surface charges in a Rydberg atom-nanowaveguide hybrid quantum system

Hybrid quantum platforms based on highly excited Rydberg atoms coupled to nanophotonics devices offer a promising route toward scalable quantum networks and integrated quantum technologies. However, the close proximity of Rydberg atoms to dielectric nanostructures makes these systems particularly susceptible to uncontrolled surface electric fields that can lead to a degradation of the excitation process. Here, we experimentally investigate Rydberg excitation of laser-cooled $^{87}$Rb atoms via the evanescent field of an optical nanofiber in the presence of fiber-guided red- and blue-detuned light fields as used to trap ground state atoms in fiber-based dipole traps. We observe a time evolution of the Rydberg excitation spectrum when both the dipole trapping fields are on and the additional spectral features that appear can be suppressed by applying an external oscillating electric field to the system, strongly indicating that surface charge accumulation is responsible for the observed spectral feature. The experimental results are reproduced qualitatively by a model that incorporates DC energy level shifts arising from electric fields generated by charges deposited on the nanofiber surface. We identify Rydberg-ground state collisional ionization, which is enhanced by the dipole trapping fields, as the dominant mechanism for charge generation. These results provide new insight into charge dynamics at dielectric nanophotonic interfaces and establish practical guidelines for mitigating surface charge-induced electric fields in fiber-integrated Rydberg quantum systems.

physics.atom-ph↗

Fourier imaging of collective spontaneous emission modes in superradiant cold atomic clouds

We measure the spatial pattern associated with the superradiant emission from a cloud of cold 87Rb atoms using Fourier imaging. We observe a highly directional, ring-shaped emission structure, which corresponds to a single collective jump operator associated to the most superradiant mode of the ensemble. Using spatial filtering, we isolate this channel and find the typical superradiant burst with superlinear scaling of the intensity with atom number. We compare our results to two models that describe the competition between the various decay channels, finding good agreement. Our work shows that the collective jump operators introduced by Carmichael et al. [Optics Communications 179, 417 (2000)] can be measured and manipulated.

physics.atom-ph↗