Nanostructured
Porous Si Optical Biosensors: Effect of Thermal Oxidation on Their
Performance and Properties
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Abstract
The influence of thermal oxidation
conditions on the performance of porous Si optical biosensors used
for label-free and real-time monitoring of enzymatic activity is studied.
We compare three oxidation temperatures (400, 600, and 800 °C)
and their effect on the enzyme immobilization efficiency and the intrinsic
stability of the resulting oxidized porous Si (PSiO<sub>2</sub>),
Fabry–Pérot thin films. Importantly, we show that the
thermal oxidation profoundly affects the biosensing performance in
terms of greater optical sensitivity, by monitoring the catalytic
activity of horseradish peroxidase and trypsin-immobilized PSiO<sub>2</sub>. Despite the significant decrease in porous volume and specific
surface area (confirmed by nitrogen gas adsorption–desorption
studies) with elevating the oxidation temperature, higher content
and surface coverage of the immobilized enzymes is attained. This
in turn leads to greater optical stability and sensitivity of PSiO<sub>2</sub> nanostructures. Specifically, films produced at 800 °C
exhibit stable optical readout in aqueous buffers combined with superior
biosensing performance. Thus, by proper control of the oxide layer
formation, we can eliminate the aging effect, thus achieving efficient
immobilization of different biomolecules, optical signal stability,
and sensitivity