Conference paper
Time-resolved transition state spectroscopy
J.H. Glownia, J. Misewich, et al.
QELS 1989
Third-order, nonresonant, difference-frequency (2ω1 − ω2) mixing in Xe gas was used to generate femtosecond-time-scale UV pulses, tunable near 193 nm. Subsequent amplification of these pulses in an ArF excimer gain module led to the production of ≃300-fs, ≃300-µJ optical pulses at 193 nm. © 1992 Optical Society of America.
J.H. Glownia, J. Misewich, et al.
QELS 1989
Ph. Avouris, D.S. Bethune, et al.
Journal of Photochemistry
P.P. Sorokin, J.H. Glownia, et al.
Physical Review A - AMO
J. Misewich, J.H. Glownia, et al.
Chemical Physics Letters