Direct measurements of interadsorbate vibrational energy flow between
Si-H stretching modes on hydrogen-terminated, stepped vicinal H/Si(111
) surface have been made. A two-colour picosecond infrared method has
been used in which one vibrational mode is pumped by a resonant infrar
ed pulse and other vibrational modes are probed by vibrationally reson
ant sum frequency generation to observe energy transfer. The surfaces
are prepared by chemical etching in HF solutions and have monohydride-
terminated (111)-(1X1) terraces with average terrace widths of ca. 5 a
toms, and dihydride-terminated steps. The results confirm that interad
sorbate energy transfer competes efficiently with slow multiphonon ene
rgy relaxation to the substrate. The energy flow is analysed to give a
kinetic model of the energy equilibration pathways. The model confirm
s that the fast relaxing dihydride-terminated steps (60-120 ps lifetim
e) drain a large fraction (ca. 2/3) of the terrace Si-H mode energy (t
he terrace mode intrinsic lifetime is fit to be ca. 1.4 ns). The model
is consistent with terrace-step energy transfer by dipole-dipole coup
ling between Si-H oscillators. The dipole coupling also causes normal-
mode delocalization, and unusual spectroscopic changes in pump-probe e
xperiments.