Molecular beam techniques are used to create nanoscale thin films composed
of different isotopes of amorphous solid water (ASW). The metastable ASW co
mposites are then heated above the glass transition temperature, T-g, and t
he extent of isotopic intermixing is determined using temperature programme
d desorption. The observed self-diffusion in the 150-160 K range is roughly
a millionfold greater than that expected for crystalline ice. The magnitud
e and temperature dependence of the self-diffusivity are consistent with an
amorphous solid that melts into a deeply supercooled liquid prior to cryst
allization. The overall temperature dependence for the diffusivity of liqui
d water, supercooled liquid water (238-273 K), and of ASW (150-160 K) is we
ll described by the Vogel-Fulcher-Tamman equation. These results suggest th
at ASW above its T-g is a deeply supercooled metastable extension of normal
liquid water prior to crystallizing near 160 K. Additionally, rapid H/D is
otopic exchange occurs in concert with the translational diffusive motion.
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