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Multi-channel photodissociation and XUV-induced charge transfer dynamics in strong-field-ionized methyl iodide studied with time-resolved recoil-frame covariance imaging

Allum Felix; Anders Nils; Brouard Mark; Bucksbaum Phil H; Burt Michael; Downes-Ward Briony; Grundmann Sven; Harries James; Ishimura Yudai; Iwayama Hiroshi; Kaiser Leon; Kukk Edwin; Lee Jason WL; Liu Xiaojing; Minns Russell S; Nagaya Kiyonobu; Niozu Akinobu; Niskanen Johannes; O'Neal Jordan T; Owada Shigeki; Pickering James; Rolles Daniel; Rudenko Artem; Saito Shu; Ueda Kiyoshi; Vallance Claire; Werby Nicholas; Woodhouse Joanne; You Daehyun; Ziaee Farzaneh; Driver Taran; Forbes Ruaridh

Multi-channel photodissociation and XUV-induced charge transfer dynamics in strong-field-ionized methyl iodide studied with time-resolved recoil-frame covariance imaging

Allum Felix
Anders Nils
Brouard Mark
Bucksbaum Phil H
Burt Michael
Downes-Ward Briony
Grundmann Sven
Harries James
Ishimura Yudai
Iwayama Hiroshi
Kaiser Leon
Kukk Edwin
Lee Jason WL
Liu Xiaojing
Minns Russell S
Nagaya Kiyonobu
Niozu Akinobu
Niskanen Johannes
O'Neal Jordan T
Owada Shigeki
Pickering James
Rolles Daniel
Rudenko Artem
Saito Shu
Ueda Kiyoshi
Vallance Claire
Werby Nicholas
Woodhouse Joanne
You Daehyun
Ziaee Farzaneh
Driver Taran
Forbes Ruaridh
Katso/Avaa
Final draft (4.416Mb)
Lataukset: 

Royal Society of Chemistry
doi:10.1039/D0FD00115E
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021042826719
Tiivistelmä

The photodissociation dynamics of strong-field ionized methyl iodide (CH3I) were probed using intense extreme ultraviolet (XUV) radiation produced by the SPring-8 Angstrom Compact free electron LAser (SACLA). Strong-field ionization and subsequent fragmentation of CH3I was initiated by an intense femtosecond infrared (IR) pulse. The ensuing fragmentation and charge transfer processes following multiple ionization by the XUV pulse at a range of pump–probe delays were followed in a multi-mass ion velocity-map imaging (VMI) experiment. Simultaneous imaging of a wide range of resultant ions allowed for additional insight into the complex dynamics by elucidating correlations between the momenta of different fragment ions using time-resolved recoil-frame covariance imaging analysis. The comprehensive picture of the photodynamics that can be extracted provides promising evidence that the techniques described here could be applied to study ultrafast photochemistry in a range of molecular systems at high count rates using state-of-the-art advanced light sources.

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