Attosecond control of dissociative ionization of O(2) molecules
Siu, W. ; Kelkensberg, F. ; Gademann, G. ; Rouzee, A. ; Johnsson, Per LU
; Dowek, D.
; Lucchini, M.
; Calegari, F.
; De Giovannini, U.
and Rubio, A.
, et al.
(2011)
In Physical Review A (Atomic, Molecular and Optical Physics)
84(6).
- Abstract
- We demonstrate that dissociative ionization of O(2) can be controlled by the relative delay between an attosecond pulse train (APT) and a copropagating infrared (IR) field. Our experiments reveal a dependence of both the branching ratios between a range of electronic states and the fragment angular distributions on the extreme ultraviolet (XUV) to IR time delay. The observations go beyond adiabatic propagation of dissociative wave packets on IR-induced quasistatic potential energy curves and are understood in terms of an IR-induced coupling between electronic states in the molecular ion.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/2316294
- author
- Siu, W.
; Kelkensberg, F.
; Gademann, G.
; Rouzee, A.
; Johnsson, Per
LU
; Dowek, D.
; Lucchini, M.
; Calegari, F.
; De Giovannini, U.
and Rubio, A.
, et al. (More)
- Siu, W.
; Kelkensberg, F.
; Gademann, G.
; Rouzee, A.
; Johnsson, Per
LU
; Dowek, D.
; Lucchini, M.
; Calegari, F.
; De Giovannini, U.
; Rubio, A.
; Lucchese, R. R.
; Kono, H.
; Lepine, F.
and Vrakking, M. J. J.
(Less)
- organization
- publishing date
- 2011
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Physical Review A (Atomic, Molecular and Optical Physics)
- volume
- 84
- issue
- 6
- article number
- 063412
- publisher
- American Physical Society
- external identifiers
-
- wos:000298113300005
- scopus:83655191039
- ISSN
- 1050-2947
- DOI
- 10.1103/PhysRevA.84.063412
- language
- English
- LU publication?
- yes
- id
- a663a9b6-914e-4a42-a4f2-1a3b8038c9c0 (old id 2316294)
- date added to LUP
- 2016-04-01 09:47:31
- date last changed
- 2022-04-19 19:40:17
@article{a663a9b6-914e-4a42-a4f2-1a3b8038c9c0,
abstract = {{We demonstrate that dissociative ionization of O(2) can be controlled by the relative delay between an attosecond pulse train (APT) and a copropagating infrared (IR) field. Our experiments reveal a dependence of both the branching ratios between a range of electronic states and the fragment angular distributions on the extreme ultraviolet (XUV) to IR time delay. The observations go beyond adiabatic propagation of dissociative wave packets on IR-induced quasistatic potential energy curves and are understood in terms of an IR-induced coupling between electronic states in the molecular ion.}},
author = {{Siu, W. and Kelkensberg, F. and Gademann, G. and Rouzee, A. and Johnsson, Per and Dowek, D. and Lucchini, M. and Calegari, F. and De Giovannini, U. and Rubio, A. and Lucchese, R. R. and Kono, H. and Lepine, F. and Vrakking, M. J. J.}},
issn = {{1050-2947}},
language = {{eng}},
number = {{6}},
publisher = {{American Physical Society}},
series = {{Physical Review A (Atomic, Molecular and Optical Physics)}},
title = {{Attosecond control of dissociative ionization of O(2) molecules}},
url = {{https://lup.lub.lu.se/search/files/1245680/2371850.pdf}},
doi = {{10.1103/PhysRevA.84.063412}},
volume = {{84}},
year = {{2011}},
}