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Title: Pump-probe spectroscopy of molecules driven by infrared field in both ground and excited electronic states

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.2393234· OSTI ID:20864349
;  [1]
  1. Theoretical Chemistry, Roslagstullsbacken 15, Royal Institute of Technology, S-106 91 Stockholm (Sweden) and Departmento de Quimica, Universidade Federal de Minas Gerais, Av. Antonio Carlos 6627, CEP-31270-901, Belo Horizonte, MG (Brazil)

Pump-probe spectra of molecules driven by strong infrared (IR) field in both ground and excited states are studied theoretically. The role of the final state interaction becomes important when pump and probe pulses overlap, and the Rabi frequency is comparable with the lifetime broadening of the excited state and the duration of the pump pulse. Our theoretical approach is applied to x-ray absorption of nitrogen molecule and valence photoionization of carbon monoxide. It is shown that IR-x-ray pump-probe spectroscopy can directly evidence the delocalization of core hole.

OSTI ID:
20864349
Journal Information:
Journal of Chemical Physics, Vol. 125, Issue 20; Other Information: DOI: 10.1063/1.2393234; (c) 2006 American Institute of Physics; Country of input: International Atomic Energy Agency (IAEA); ISSN 0021-9606
Country of Publication:
United States
Language:
English