Abstract
In solids and viscous liquids, irreversible ultrafast dynamics, such as high-intensity processes and photo-induced chemical reactions, have to date proven difficult to study spectroscopically. In low-viscosity liquids, such processes can be monitored with conventional ultrafast techniques, so long as the liquid is flowed fast enough that each set of laser pulses interrogates a new portion of the sample. Such an approach is not practical in solids or viscous liquids, however.
© 1994 Optical Society of America
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