期刊
OPTICS LETTERS
卷 47, 期 10, 页码 2410-2413出版社
Optica Publishing Group
DOI: 10.1364/OL.457070
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Recent advances in femtosecond vacuum ultraviolet (VUV) pulse generation have allowed for new possibilities in ultrafast time-resolved spectroscopy. In this study, 60 fs VUV pulses were generated at the 7th harmonic of Ti:sapphire with a pulse energy of over 50 al and a repetition rate of 1 kHz. The pulses, produced using noncollinear four-wave difference-frequency mixing in argon, were pre-chirp compensated for material dispersion with xenon, resulting in almost transform-limited pulses delivered to the experimental chamber.
The recent advances in femtosecond vacuum UV (VUV) pulse generation, pioneered by the work of Noack et al., has enabled new experiments in ultrafast time-resolved spectroscopy. Expanding on this work, we report the generation of 60 fs VUV pulses at the 7th harmonic of Ti:sapphire with more than 50 al of pulse energy at a repetition rate of 1 kHz. The 114.6 nm pulses are produced using noncollinear four-wave difference-frequency mixing in argon. The non-collinear geometry increases the phase-matching pressure, and results in a conversion efficiency of similar to 10(-3) from the 200 nm pump beam. The VUV pulses are pre-chirpcompensated for material dispersion with xenon, which has negative dispersion in this wavelength range, thus allowing almost transform-limited pulses to he delivered to the experimental chamber.
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