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Femtosecond spectroscopy with high-power tunable optical pulses

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Abstract

Femtosecond techniques permitting the generation of intense optical pulses tunable from the near UV to the near IR are presented. Implications for chemistry, biology, and solid-state physics are discussed. Specific cases are developed for applications such as the comparison of time-resolved polarization and absorption studies in photoexcited GaAs or malachite green in water.

© 1985 Optical Society of America

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