Time-resolved extreme ultraviolet (XUV) transient absorption spectroscopy of iodomethane and iodobenzene photodissociation at the iodine pre-N4,5 edge is presented, using femtosecond UV pump pulses and XUV probe pulses from high harmonic generation. For both molecules the molecular core-to-valence absorption lines fade immediately, within the pump-probe time-resolution. Absorption lines converging to the atomic iodine product emerge promptly in CH3I but are time-delayed in C6H5I. We attribute this delay to the initial π → σ(*) excitation in iodobenzene, which is distant from the iodine reporter atom. We measure a continuous shift in energy of the emerging atomic absorption lines in CH3I, attributed to relaxation of the excited valence shell. An independent particle model is used to rationalize the observed experimental findings.
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http://dx.doi.org/10.1063/1.4955212 | DOI Listing |
Mid-infrared dual-comb spectroscopy offers significant advantages by combining the high sensitivity of mid-infrared spectroscopy with the high spectral resolution and rapid acquisition of the dual-comb method. However, its effective resolution, constrained by the inherent comb line spacing, hinders its ability to resolve narrow absorption features, common in critical applications such as sub-Doppler spectroscopy, low-pressure gas analysis, and construction of the atmospheric profile. To address this challenge, we present a synchronous offset frequency tuning method for the mid-infrared dual-comb system to improve effective resolution far beyond comb line spacing.
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College of Life Sciences, Jiangsu Collaborative Innovation Center for Solid Organic Waste Resource, Nanjing Agricultural University, Nanjing, 210095, PR China. Electronic address:
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