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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

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

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

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