Entanglement in photoionisation reveals the effect of ionic coupling in attosecond time delays

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F25%3A10506078" target="_blank" >RIV/00216208:11320/25:10506078 - isvavai.cz</a>

Výsledek na webu

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=ky4cjbjgQE" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=ky4cjbjgQE</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1038/s41467-025-64182-8" target="_blank" >10.1038/s41467-025-64182-8</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Entanglement in photoionisation reveals the effect of ionic coupling in attosecond time delays

Popis výsledku v původním jazyce

Attosecond photoelectron interferometry, based on the measurement of photoelectron spectra generated by a two-colour field, provides access to the photoionisation dynamics of quantum systems. In general, due to the entanglement between the wave function of the emitted photoelectron and that of the parent ion, the dynamics driven by the infra-red field in the photoion can affect the properties of the photoemitted electronic wave packet, when the measurement protocol corresponds to the projection of the total time-dependent wave function onto a specific final state of the bipartite system. This is particularly relevant for molecules, due to their rich internal electronic and vibrational energy structure. Here we show how the polarisation of the ion influences the photoionisation dynamics by introducing an additional time delay in the photoelectrons emitted from CO2 molecules. The delay stems from the entanglement between the photoion and the photoelectron created in the photoionisation process.

Název v anglickém jazyce

Entanglement in photoionisation reveals the effect of ionic coupling in attosecond time delays

Popis výsledku anglicky

Attosecond photoelectron interferometry, based on the measurement of photoelectron spectra generated by a two-colour field, provides access to the photoionisation dynamics of quantum systems. In general, due to the entanglement between the wave function of the emitted photoelectron and that of the parent ion, the dynamics driven by the infra-red field in the photoion can affect the properties of the photoemitted electronic wave packet, when the measurement protocol corresponds to the projection of the total time-dependent wave function onto a specific final state of the bipartite system. This is particularly relevant for molecules, due to their rich internal electronic and vibrational energy structure. Here we show how the polarisation of the ion influences the photoionisation dynamics by introducing an additional time delay in the photoelectrons emitted from CO2 molecules. The delay stems from the entanglement between the photoion and the photoelectron created in the photoionisation process.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10300 - Physical sciences

Projekt

<a href="/cs/project/GF25-24428L" target="_blank" >GF25-24428L: Ultrafast electronic and nuclear dynamics in molecular photoionization studied by RABBITT</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2025

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Nature Communications

ISSN

2041-1723

e-ISSN

2041-1723

Svazek periodika

16

Číslo periodika v rámci svazku

1

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

9

Strana od-do

8554

Kód UT WoS článku

001586153800037

EID výsledku v databázi Scopus

2-s2.0-105017519804