The
persistent photoconductivity (PPC) of high-quality SnO2(101) films grown by molecular beam epitaxy (MBE) was investigated
as a function of atmosphere, carrier concentration (n) and temperature (T = 300–10 K). The decay
of the persistent photocurrent induced by sub-band-gap (405 nm) illumination
was well described by the Kohlrausch stretched-exponential function,
with the largest characteristic recovery times (τ) achieved
in high-vacuum conditions, and a steady decrease in τ observed
at increasing pressures above 1 Torr. This is consistent with the
accepted PPC model involving the light-induced desorption and postillumination
readsorption of an acceptor-like surface adsorbate, and the associated
removal and reformation of a near-surface electron depletion layer.
However, no difference in τ was found in 100% N2 and
100% O2 atmospheres, which is surprising given the dominant
acceptor role usually assigned to adsorbed oxygen species, in particular
O2
– superoxide ions. In contrast, a significant
decrease in τ was observed in humid N2, with a smaller
decrease found in air, suggesting that water vapor plays a dominant
role in the PPC of high-quality MBE SnO2 films. An almost
100-fold increase in τ with increasing n from
∼1016 to ∼1019 cm–3 was observed, with the photocurrent consistent with a simple parallel
conduction model involving the decrease in the thickness of the electron
depletion layer from ∼80 to ∼1 nm with n. Temperature-dependent measurements from 300 to 10 K revealed a
significant decrease in τ with decreasing T that matched the temperature dependence of n, while
the presence of two different recovery mechanisms was observed at T below 100 K.