Femtosecond pulse induced predissociation dynamics in static electric fields

Literature Information

Publication Date 2005-01-11
DOI 10.1039/B415885G
Impact Factor 3.676
Authors

P. Marquetand, V. Engel


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Abstract

The quantum dynamics of NaI molecules in static electric fields is investigated. Upon femtosecond excitation, a wave packet is prepared which performs a quasi-bound motion in a coupled system of two electronic states. A detailed study of the influence of the external field on the molecular orientation on one hand, and the interplay between the rotational, vibrational and predissociation dynamics on the other, is presented. It is documented that polarization dependent pump–probe experiments are a powerful tool to follow the orientational dynamics in real time.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
Articles per Year: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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