The green and orange-red photoluminescent (PL) emissions characteristic of a porous silicon (PS) surface are excited with a variety of UV light sources and observed during and directly following the in situ (in solution) etching of a PS surface in a 20% HF in MeOH or 20% HF in H 2 O solution. Experimental observations of the time dependent behavior of this in situ PL are combined with a quantum chemical modeling of the low-lying electronic states of the silanone-based silicon oxyhydrides to suggest that the initially observed and relatively long-lived green PL, its subsequent transformation to a final orange-red emission, and its stabilization in an ethylene glycol solution are to be associated with oxyhydride electronic transitions and the chemical transformation of surface-bound oxyhydrides.
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Gole et al. (1998) studied this question.
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