Studies of ultrafast molecular dynamics by femtosecond extreme ultraviolet absorption spectroscopy

Transient absorption spectroscopy is one of the most widely used experimental techniques for time-resolved studies of ultrafast phenomena. Recent advances in the generation of short-wavelength pulses of ultrashort duration have made transient absorption probing of atomic core level transitions possi...

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Main Author: Loh, Zhi-Heng
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2022
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Online Access:https://hdl.handle.net/10356/155541
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1555412023-02-28T19:59:51Z Studies of ultrafast molecular dynamics by femtosecond extreme ultraviolet absorption spectroscopy Loh, Zhi-Heng School of Physical and Mathematical Sciences Science::Chemistry Strong-Field Laser-Molecule Interaction Photodissociation Transient absorption spectroscopy is one of the most widely used experimental techniques for time-resolved studies of ultrafast phenomena. Recent advances in the generation of short-wavelength pulses of ultrashort duration have made transient absorption probing of atomic core level transitions possible. In this Highlight Review, we introduce our recent work on using extreme ultraviolet (XUV) transient absorption spectroscopy to investigate the ultrafast molecular dynamics induced by intense laser fields. While investigations of intense laser-molecule interaction have primarily focused on elucidating electron dynamics, it is important to understand the vibrational dynamics that are triggered by intense laser fields because of their coupling to electron dynamics. Probing the iodine 4d core level, our XUV transient absorption studies of iodoalkanes irradiated by intense laser fields elucidate ultrafast dissociative ionization dynamics and vibrational wave packet dynamics. Time-dependent XUV spectral shifts and global analysis of time-resolved XUV transient absorption spectra can be used to reconstruct CI dissociation dynamics and identify multiple dissociation channels. In addition, XUV transient absorption spectroscopy also unravels both small- and large-amplitude coherent vibrational motion, whose origin can be identified by analyzing the phase of the oscillatory XUV transition energies. Our studies show that XUV transient absorption spectroscopy is a powerful technique for the study of ultrafast molecular dynamics. Ministry of Education (MOE) Nanyang Technological University Accepted version Funding support from an NTU start-up grant, the NTU Nanyang Assistant Professorship, and the Ministry of Education Academic Research Fund (RG105/17 and MOE2018-T2-1-081) is gratefully acknowledged. 2022-03-03T05:26:51Z 2022-03-03T05:26:51Z 2021 Journal Article Loh, Z. (2021). Studies of ultrafast molecular dynamics by femtosecond extreme ultraviolet absorption spectroscopy. Chemistry Letters, 50(5), 965-973. https://dx.doi.org/10.1246/cl.200940 0366-7022 https://hdl.handle.net/10356/155541 10.1246/cl.200940 2-s2.0-85105804720 5 50 965 973 en RG105/17 MOE2018-T2-1-081 Chemistry Letters © 2021 The Chemical Society of Japan. All rights reserved. This paper was published in Chemistry Letters and is made available with permission of The Chemical Society of Japan. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Chemistry
Strong-Field Laser-Molecule Interaction
Photodissociation
spellingShingle Science::Chemistry
Strong-Field Laser-Molecule Interaction
Photodissociation
Loh, Zhi-Heng
Studies of ultrafast molecular dynamics by femtosecond extreme ultraviolet absorption spectroscopy
description Transient absorption spectroscopy is one of the most widely used experimental techniques for time-resolved studies of ultrafast phenomena. Recent advances in the generation of short-wavelength pulses of ultrashort duration have made transient absorption probing of atomic core level transitions possible. In this Highlight Review, we introduce our recent work on using extreme ultraviolet (XUV) transient absorption spectroscopy to investigate the ultrafast molecular dynamics induced by intense laser fields. While investigations of intense laser-molecule interaction have primarily focused on elucidating electron dynamics, it is important to understand the vibrational dynamics that are triggered by intense laser fields because of their coupling to electron dynamics. Probing the iodine 4d core level, our XUV transient absorption studies of iodoalkanes irradiated by intense laser fields elucidate ultrafast dissociative ionization dynamics and vibrational wave packet dynamics. Time-dependent XUV spectral shifts and global analysis of time-resolved XUV transient absorption spectra can be used to reconstruct CI dissociation dynamics and identify multiple dissociation channels. In addition, XUV transient absorption spectroscopy also unravels both small- and large-amplitude coherent vibrational motion, whose origin can be identified by analyzing the phase of the oscillatory XUV transition energies. Our studies show that XUV transient absorption spectroscopy is a powerful technique for the study of ultrafast molecular dynamics.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Loh, Zhi-Heng
format Article
author Loh, Zhi-Heng
author_sort Loh, Zhi-Heng
title Studies of ultrafast molecular dynamics by femtosecond extreme ultraviolet absorption spectroscopy
title_short Studies of ultrafast molecular dynamics by femtosecond extreme ultraviolet absorption spectroscopy
title_full Studies of ultrafast molecular dynamics by femtosecond extreme ultraviolet absorption spectroscopy
title_fullStr Studies of ultrafast molecular dynamics by femtosecond extreme ultraviolet absorption spectroscopy
title_full_unstemmed Studies of ultrafast molecular dynamics by femtosecond extreme ultraviolet absorption spectroscopy
title_sort studies of ultrafast molecular dynamics by femtosecond extreme ultraviolet absorption spectroscopy
publishDate 2022
url https://hdl.handle.net/10356/155541
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