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Time-resolved Auger–Meitner spectroscopy of the photodissociation dynamics of CS2
The photodissociation dynamics of UV excited CS2 are investigated using time-resolved Auger-Meitner (AM) spectroscopy. AM decay is initiated by inner-shell ionisation with a femtosecond duration x-ray (179.9 eV) probe generated by the FERMI free electron laser. The time-delayed x-ray probe removes a...
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Published in: | Journal of physics. B, Atomic, molecular, and optical physics Atomic, molecular, and optical physics, 2024-11, Vol.57 (21) |
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creator | Thompson, Henry J Plekan, Oksana Bonanomi, Matteo Pal, Nitish Allum, Felix Brynes, Alexander D Coreno, Marcello Coriani, Sonia Danailov, Miltcho B Decleva, Piero Demidovich, Alexander Devetta, Michele Faccialà, Davide Feifel, Raimund Forbes, Ruaridh Grazioli, Cesare Holland, David M P Piseri, Paolo Prince, Kevin C Rolles, Daniel Schuurman, Michael S Simoncig, Alberto Squibb, Richard J Tenorio, Bruno N C Vozzi, Caterina Zangrando, Marco Callegari, Carlo Minns, Russell S Di Fraia, Michele |
description | The photodissociation dynamics of UV excited CS2 are investigated using time-resolved Auger-Meitner (AM) spectroscopy. AM decay is initiated by inner-shell ionisation with a femtosecond duration x-ray (179.9 eV) probe generated by the FERMI free electron laser. The time-delayed x-ray probe removes an electron from the S(2p) orbital leading to secondary emission of a high energy electron through AM decay. We monitor the electron kinetic energy of the AM emission as a function of pump-probe delay and observe time-dependent changes in the spectrum that correlate with the formation of bound, excited-state CS2 molecules at early times, and CS + S fragments on the picosecond timescale. The results are analysed based on a simplified kinetic scheme that provides a time constant for dissociation of approximately 1.2 ps, in agreement with previous time-resolved x-ray photoelectron spectroscopy measurements. |
doi_str_mv | 10.1088/1361-6455/ad7e89 |
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AM decay is initiated by inner-shell ionisation with a femtosecond duration x-ray (179.9 eV) probe generated by the FERMI free electron laser. The time-delayed x-ray probe removes an electron from the S(2p) orbital leading to secondary emission of a high energy electron through AM decay. We monitor the electron kinetic energy of the AM emission as a function of pump-probe delay and observe time-dependent changes in the spectrum that correlate with the formation of bound, excited-state CS2 molecules at early times, and CS + S fragments on the picosecond timescale. The results are analysed based on a simplified kinetic scheme that provides a time constant for dissociation of approximately 1.2 ps, in agreement with previous time-resolved x-ray photoelectron spectroscopy measurements.</description><identifier>ISSN: 0953-4075</identifier><identifier>ISSN: 1361-6455</identifier><identifier>EISSN: 1361-6455</identifier><identifier>DOI: 10.1088/1361-6455/ad7e89</identifier><identifier>CODEN: JPAPEH</identifier><language>eng</language><publisher>IOP Publishing</publisher><subject>Atom and Molecular Physics and Optics ; Atom- och molekylfysik och optik ; Auger spectroscopy ; free electron lasers ; time-resolved x-ray spectroscopy</subject><ispartof>Journal of physics. B, Atomic, molecular, and optical physics, 2024-11, Vol.57 (21)</ispartof><rights>2024 The Author(s). 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B, Atomic, molecular, and optical physics</title><addtitle>JPhysB</addtitle><addtitle>J. Phys. B: At. Mol. Opt. Phys</addtitle><description>The photodissociation dynamics of UV excited CS2 are investigated using time-resolved Auger-Meitner (AM) spectroscopy. AM decay is initiated by inner-shell ionisation with a femtosecond duration x-ray (179.9 eV) probe generated by the FERMI free electron laser. The time-delayed x-ray probe removes an electron from the S(2p) orbital leading to secondary emission of a high energy electron through AM decay. We monitor the electron kinetic energy of the AM emission as a function of pump-probe delay and observe time-dependent changes in the spectrum that correlate with the formation of bound, excited-state CS2 molecules at early times, and CS + S fragments on the picosecond timescale. The results are analysed based on a simplified kinetic scheme that provides a time constant for dissociation of approximately 1.2 ps, in agreement with previous time-resolved x-ray photoelectron spectroscopy measurements.</description><subject>Atom and Molecular Physics and Optics</subject><subject>Atom- och molekylfysik och optik</subject><subject>Auger spectroscopy</subject><subject>free electron lasers</subject><subject>time-resolved x-ray spectroscopy</subject><issn>0953-4075</issn><issn>1361-6455</issn><issn>1361-6455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kMtKAzEYhYMoWKt7l_MAxuY6M1mW4g0qLlrXITP506a0kzCZUbrzHXxDn8QOI64OHD4Ohw-hW0ruKSnLGeU5xbmQcmZsAaU6Q5P_6hxNiJIcC1LIS3SV0o4QSktGJmi19gfALaSw_wCbzfsNtD9f36_guwbaLEWouzakOsRjFlzWbSGL29AF61MKtTedD01mj405-DoNxGLFrtGFM_sEN385Re-PD-vFM16-Pb0s5kvsaU46bG3Nia3yQsrCmQqUqABU4UqA0kjDWJU7ampRKG6UUQSsKRkFS6xTTlHBpwiPu-kTYl_p2PqDaY86GK83fdSnatPrBJoLxgQ58Xcj70PUu9C3zemdpkQPAvVgSw-29CiQ_wIZ7Wel</recordid><startdate>20241114</startdate><enddate>20241114</enddate><creator>Thompson, Henry J</creator><creator>Plekan, Oksana</creator><creator>Bonanomi, Matteo</creator><creator>Pal, Nitish</creator><creator>Allum, Felix</creator><creator>Brynes, Alexander D</creator><creator>Coreno, Marcello</creator><creator>Coriani, Sonia</creator><creator>Danailov, Miltcho B</creator><creator>Decleva, Piero</creator><creator>Demidovich, Alexander</creator><creator>Devetta, Michele</creator><creator>Faccialà, Davide</creator><creator>Feifel, Raimund</creator><creator>Forbes, Ruaridh</creator><creator>Grazioli, Cesare</creator><creator>Holland, David M P</creator><creator>Piseri, Paolo</creator><creator>Prince, Kevin C</creator><creator>Rolles, Daniel</creator><creator>Schuurman, Michael S</creator><creator>Simoncig, Alberto</creator><creator>Squibb, Richard J</creator><creator>Tenorio, Bruno N C</creator><creator>Vozzi, Caterina</creator><creator>Zangrando, Marco</creator><creator>Callegari, Carlo</creator><creator>Minns, Russell S</creator><creator>Di Fraia, Michele</creator><general>IOP Publishing</general><scope>O3W</scope><scope>TSCCA</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>F1U</scope><orcidid>https://orcid.org/0000-0002-0068-679X</orcidid><orcidid>https://orcid.org/0000-0002-7322-887X</orcidid><orcidid>https://orcid.org/0000-0001-6775-2977</orcidid><orcidid>https://orcid.org/0000-0002-8044-8969</orcidid><orcidid>https://orcid.org/0000-0002-3965-3477</orcidid><orcidid>https://orcid.org/0009-0007-2718-2229</orcidid><orcidid>https://orcid.org/0000-0001-8102-0799</orcidid><orcidid>https://orcid.org/0000-0003-2343-7566</orcidid><orcidid>https://orcid.org/0000-0003-1351-605X</orcidid><orcidid>https://orcid.org/0000-0003-2097-5991</orcidid><orcidid>https://orcid.org/0000-0002-4692-7018</orcidid><orcidid>https://orcid.org/0000-0001-5491-7752</orcidid><orcidid>https://orcid.org/0000-0002-6255-2041</orcidid><orcidid>https://orcid.org/0000-0002-0212-0191</orcidid><orcidid>https://orcid.org/0000-0002-5072-0394</orcidid><orcidid>https://orcid.org/0000-0002-3806-3475</orcidid></search><sort><creationdate>20241114</creationdate><title>Time-resolved Auger–Meitner spectroscopy of the photodissociation dynamics of CS2</title><author>Thompson, Henry J ; 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subjects | Atom and Molecular Physics and Optics Atom- och molekylfysik och optik Auger spectroscopy free electron lasers time-resolved x-ray spectroscopy |
title | Time-resolved Auger–Meitner spectroscopy of the photodissociation dynamics of CS2 |
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