Porous
silicon (PSi) thin films have been widely studied for biosensing
applications, enabling label-free optical detection of numerous targets.
The large surface area of these biosensors has been commonly recognized
as one of the main advantages of the PSi nanostructure. However, in
practice, without application of signal amplification strategies,
PSi-based biosensors suffer from limited sensitivity, compared to
planar counterparts. Using a theoretical model, which describes the
complex mass transport phenomena and reaction kinetics in these porous
nanomaterials, we reveal that the interrelated effect of bulk and
hindered diffusion is the main limiting factor of PSi-based biosensors.
Thus, without significantly accelerating the mass transport to and
within the nanostructure, the target capture performance of these
biosensors would be comparable, regardless of the nature of the capture
probe–target pair. We use our model to investigate the effect
of various structural and biosensor characteristics on the capture
performance of such biosensors and suggest rules of thumb for their
optimization.