As
non-toxic, elementally abundant, and low-cost luminophores,
silicon quantum dots (Si QDs) suit a wide variety of applications,
from luminescent devices, such as solar concentrators and light-emitting
diodes, to bioimaging. Nonthermal plasma-assisted decomposition of
silane gas is an efficient, relatively sustainable, and controllable
method for synthesizing Si QDs. However, as-synthesized Si QDs have
a high defect density and require additional passivation for utilization
in these settings. Liquid-based passivation methods, such as thermal
hydrosilylation, organically cap Si QDs but cannot prevent oxidation
upon exposure to ambient air. Native oxidation effectively passivates
the Si QDs and ensures long-term stability in air but typically requires
long exposures to ambient conditions. Here, we report the use of high-pressure
water vapor annealing (HWA) to quickly obtain Si/SiO2 core/shell
quantum dots with tunable photoluminescence (PL). We first show that
the injection of additional hydrogen gas, commonly used in synthesizing
organically capped Si QDs, is detrimental to achieving stable silica
shells. Then, we demonstrate that varying the applied pressure tunes
the PL quantum yield. At higher pressures, the formed silica shells
are fully thermally relaxed. Lastly, we report the influence of silica
shell thickness, with thicker silica shells leading to environmentally
stable quantum yields of >40%. Compared to both thermal hydrosilylation
and native oxidation, HWA is a convenient and rapid technique for
surface passivation.