期刊
CHEMICAL PHYSICS
卷 366, 期 1-3, 页码 139-147出版社
ELSEVIER
DOI: 10.1016/j.chemphys.2009.09.021
关键词
Attosecond control; Dissociative ionization; Electron localization; Electron dynamics; Carbon monoxide; D-2
Laser pulses with stable electric field waveforms establish the opportunity to achieve coherent control on attosecond timescales. A first successful example of electron localization and its control could be demonstrated for the molecules D-2(+) and HD+. These molecules constitute simple model systems with only one electron and left the question open, whether electron localization in multi-electron systems can be achieved and controlled. In this context, we recently reported results where a high degree of light-waveform control over the directional emission of C+ and O+ fragments from the dissociative ionization of CO was observed [1]. Here, we compare and analyze the mechanisms leading to electron localization in the two different molecular systems D-2(+) and CO+. We use our recently introduced method for multi-electron systems that allows us to describe the formation of an electronic wavepacket and to follow its evolution during the dissociation process. (C) 2009 Elsevier B.V. All rights reserved.
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