Attosecond metrology of vacuum-ultraviolet high-order harmonics generated in semiconductors via laser-dressed photoionization of alkali metals

Abstract Semiconductor crystals driven by strong mid-infrared pulses offer advantages for studying many-body physics and ultrafast optoelectronics via high-harmonic generation. While the process has been used to study solids in the presence strong mid-infrared fields, its potential as an attosecond...

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Main Authors: Arjun Nayak, Debobrata Rajak, Balázs Farkas, Camilio Granados, Philipp Stammer, Javier Rivera-Dean, Theocharis Lamprou, Katalin Varju, Yann Mairesse, Marcelo F. Ciappina, Maciej Lewenstein, Paraskevas Tzallas
Format: Article
Language:English
Published: Nature Portfolio 2025-02-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-025-56759-0
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author Arjun Nayak
Debobrata Rajak
Balázs Farkas
Camilio Granados
Philipp Stammer
Javier Rivera-Dean
Theocharis Lamprou
Katalin Varju
Yann Mairesse
Marcelo F. Ciappina
Maciej Lewenstein
Paraskevas Tzallas
author_facet Arjun Nayak
Debobrata Rajak
Balázs Farkas
Camilio Granados
Philipp Stammer
Javier Rivera-Dean
Theocharis Lamprou
Katalin Varju
Yann Mairesse
Marcelo F. Ciappina
Maciej Lewenstein
Paraskevas Tzallas
author_sort Arjun Nayak
collection DOAJ
description Abstract Semiconductor crystals driven by strong mid-infrared pulses offer advantages for studying many-body physics and ultrafast optoelectronics via high-harmonic generation. While the process has been used to study solids in the presence strong mid-infrared fields, its potential as an attosecond light source is largely underexplored. We demonstrate that high-harmonics emitted from zinc-oxide crystals produce attosecond pulses, measured through spectroscopy of alkali metals. Using a cross-correlation approach, we photoionize Cesium atoms with vacuum-ultraviolet high-harmonics in the presence of a mid-infrared laser field. We observe oscillations in the photoelectron yield, originating from the instantaneous polarization of atoms by the laser field. The phase of these oscillations encodes the attosecond synchronization of the high-harmonics and is used for attosecond pulse metrology. This source opens new spectral windows for attosecond spectroscopy, enabling studies of bound-state dynamics in natural systems with low ionization energies, while facilitating the generation of non-classical entangled light states in the visible-VUV.
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issn 2041-1723
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spelling doaj-art-4736a74767924b9cba2933759729cfd72025-02-09T12:44:30ZengNature PortfolioNature Communications2041-17232025-02-011611810.1038/s41467-025-56759-0Attosecond metrology of vacuum-ultraviolet high-order harmonics generated in semiconductors via laser-dressed photoionization of alkali metalsArjun Nayak0Debobrata Rajak1Balázs Farkas2Camilio Granados3Philipp Stammer4Javier Rivera-Dean5Theocharis Lamprou6Katalin Varju7Yann Mairesse8Marcelo F. Ciappina9Maciej Lewenstein10Paraskevas Tzallas11ELI-ALPS, ELI-Hu Non-Profit Ltd.ELI-ALPS, ELI-Hu Non-Profit Ltd.ELI-ALPS, ELI-Hu Non-Profit Ltd.Department of Physics, Guangdong Technion - Israel Institute of TechnologyICFO - Institut de Ciencies Fotoniques, The Barcelona Institute of Science and TechnologyICFO - Institut de Ciencies Fotoniques, The Barcelona Institute of Science and TechnologyFoundation for Research and Technology-Hellas, Institute of Electronic Structure & LaserELI-ALPS, ELI-Hu Non-Profit Ltd.Université de Bordeaux–CNRS–CEA, CELIA, UMR5107Department of Physics, Guangdong Technion - Israel Institute of TechnologyICFO - Institut de Ciencies Fotoniques, The Barcelona Institute of Science and TechnologyELI-ALPS, ELI-Hu Non-Profit Ltd.Abstract Semiconductor crystals driven by strong mid-infrared pulses offer advantages for studying many-body physics and ultrafast optoelectronics via high-harmonic generation. While the process has been used to study solids in the presence strong mid-infrared fields, its potential as an attosecond light source is largely underexplored. We demonstrate that high-harmonics emitted from zinc-oxide crystals produce attosecond pulses, measured through spectroscopy of alkali metals. Using a cross-correlation approach, we photoionize Cesium atoms with vacuum-ultraviolet high-harmonics in the presence of a mid-infrared laser field. We observe oscillations in the photoelectron yield, originating from the instantaneous polarization of atoms by the laser field. The phase of these oscillations encodes the attosecond synchronization of the high-harmonics and is used for attosecond pulse metrology. This source opens new spectral windows for attosecond spectroscopy, enabling studies of bound-state dynamics in natural systems with low ionization energies, while facilitating the generation of non-classical entangled light states in the visible-VUV.https://doi.org/10.1038/s41467-025-56759-0
spellingShingle Arjun Nayak
Debobrata Rajak
Balázs Farkas
Camilio Granados
Philipp Stammer
Javier Rivera-Dean
Theocharis Lamprou
Katalin Varju
Yann Mairesse
Marcelo F. Ciappina
Maciej Lewenstein
Paraskevas Tzallas
Attosecond metrology of vacuum-ultraviolet high-order harmonics generated in semiconductors via laser-dressed photoionization of alkali metals
Nature Communications
title Attosecond metrology of vacuum-ultraviolet high-order harmonics generated in semiconductors via laser-dressed photoionization of alkali metals
title_full Attosecond metrology of vacuum-ultraviolet high-order harmonics generated in semiconductors via laser-dressed photoionization of alkali metals
title_fullStr Attosecond metrology of vacuum-ultraviolet high-order harmonics generated in semiconductors via laser-dressed photoionization of alkali metals
title_full_unstemmed Attosecond metrology of vacuum-ultraviolet high-order harmonics generated in semiconductors via laser-dressed photoionization of alkali metals
title_short Attosecond metrology of vacuum-ultraviolet high-order harmonics generated in semiconductors via laser-dressed photoionization of alkali metals
title_sort attosecond metrology of vacuum ultraviolet high order harmonics generated in semiconductors via laser dressed photoionization of alkali metals
url https://doi.org/10.1038/s41467-025-56759-0
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