Fe. Livingston et al., SURFACE AND BULK DIFFUSION OF HDO ON ULTRATHIN SINGLE-CRYSTAL ICE MULTILAYERS ON RU(001), The Journal of chemical physics, 108(5), 1998, pp. 2197-2207
The kinetics of HDO Surface and bulk diffusion on ultrathin (25-192 BL
; 96-700 Angstrom) single-crystal (H2O)-O-16 ice multilayers were stud
ied using a combination of laser-induced thermal desorption (LITD) pro
bing and isothermal desorption depth-profiling. The single-crystal hex
agonal ice multilayers were grown epitaxially on a single-crystal Ru(0
01) metal substrate with the basal (001) facet of ice parallel to the
Ru(001) surface. HDO surface diffusion on the single-crystal ice multi
layer was not observed within the resolution of the LITD experiment at
T=140 K. These LITD surface diffusion experiments yielded an upper Li
mit to the HDO surface diffusion coefficient of D-s less than or equal
to 1x10(-9) cm(2)/s at T= 40 K. The bulk diffusion coefficients were
measured along the c axis of the hexagonal ice crystal which is perpen
dicular to the (001) plane. HDO was observed to diffuse readily into t
he underlying (H2O)-O-16 ice multilayer. The measured HDO bulk diffusi
on coefficients ranged from D = 2.2(+/-0.3)x10(-16) cm(2)/s to D=3.9(/-0.4)x10(-14) cm(2)/s over the temperature range from 153 to 170 K. T
he HDO bulk diffusion coefficients-were measured for (H2O)-O-16 thickn
esses of 25-192 BL (1 BL=1.06x10(15) molecules/cm(2)) and initial HDO
adlayer thicknesses of 2-9 BL. The KDO bulk diffusion was independent
of (H2O)-O-16 him thickness and initial HDO coverage. Arrhenius analys
is of the temperature-dependent bulk diffusion coefficients yielded a
diffusion activation energy of E-A =17.0+/-1.0 kcal/mol and a diffusio
n preexponential of D-0=4.2(+/-0.8)x10(8) cm(2)/s. Compared with extra
polations from macroscopic diffusion kinetics obtained earlier at temp
eratures close to the melting point, these bulk diffusion coefficients
are larger and may reflect the perturbation of the ultrathin ice film
s induced by the nearby interfaces. The differences between these HDO
diffusion kinetics and recently measured kinetics for (H2O)-O-16 indic
ate that H/D exchange and molecular transport make comparable contribu
tions to the HDO diffusion coefficient. (C) 1998 American Institute of
Physics.