Laser-driven shock waves (0-5 GPa) can be generated at high repetition
rates (100/s) using a moderate-energy tabletop picosecond laser syste
m and a multilayered microfabricated shock target array. High spatial
resolution is needed to obtain high temporal resolution of the effects
of a steeply rising shock front on molecular materials. The needed sp
atial resolution is obtained using a sandwich arrangement with a thin
layer of sample material termed an ''optical nanogauge''. Experiments
with an anthracene nanogauge show that ultrafast vibrational spectrosc
opy can be used to determine the shock temperature, pressure, velocity
, and shock front rise time. Shock pulses can be generated with rise t
imes <25 ps, which generate irreversible shock compression, and with r
ise times of a few hundred picoseconds, which generate reversible comp
ression. These pulses, which have a duration of a few nanoseconds, are
termed ''nanoshock'' pulses. Nanoshock pulses produce large-amplitude
mechanical perturbations and can initiate and turn off thermochemical
reactions, produce highly excited vibrational populations, and heat a
nd cool condensed matter systems at tremendous rates. These applicatio
ns are illustrated briefly in nanoshock experiments on an energetic ma
terial and a heme protein. Using high repetition rate nanoshocks to st
udy large-amplitude molecular dynamics in molecular materials importan
t in chemistry and biology is the new wave in shock waves.