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Springer eBooks

Single-Shot Absorption Spectroscopy with Chirped Femtosecond Laser Pulses

Harald Schulz, Ping Zhou, Peter Kohns

Published Jan 1, 1996• 0 citations
Publisher
DOI
10.1007/978-3-642-80263-8_11

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Single-shot photoelectron spectroscopy of nonresonant two-color two-photon ionization of He has been carried out using an intense free-electron laser (FEL) at 59.7 nm and a femtosecond UV laser at 268 nm. By shot-by-shot analysis of photoelectron spectra, the cross section for nonresonant two-color ionization of He is determined to be ${\ensuremath{\sigma}}^{(2)}=4.1(6)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}52}$ cm4{}^{4}4 s. The cross-correlation trace derived from the nonresonant signals shows that the temporal resolution of the system is 0.36(3) ps, which is mainly governed by the timing jitter between the FEL and UV laser pulses.
Summary form only given. Coherent optical transients such as photon echo are a versatile method far measurement of the homogeneous absorption spectrum of molecular systems in the presence of strong inhomogeneous broadening. Such experiments require measurement of the decay of the optical coherence, typically accomplished by gradually varying the time delay between the excitation pulses. Time-domain information is then Fourier transformed to frequency domain by a computer. In this paper we demonstrate a new method that yields the homogeneous spectrum in a single shot of femtosecond laser pulse illumination by performing Fourier transformation of coherent optical transient signal with a lens. We apply this method to measure the homogeneous spectrum of dye molecules in a polymer film in a broad range of temperatures.