Investigation of Physicochemical Parameters That Influence Photocatalytic Degradation of Methyl Orange over TiO₂ Nanotubes

The photocatalytic degradation of a model textile dye, methyl orange (MO), using anodized titanium dioxide (TiO2) nanotubes has been investigated. The effects of light intensity, dye concentration, external bias, pH, and nanotube dimensions (length, diameter, and wall thickness) on MO photodegradation have been examined. The application of a minimal bias of +0.0 versus saturated calomel electrode (SCE) can enhance the dye degradation at least 10 times compared to unbiased conditions for dye concentrations between 20 and 100 μM. The overall initial dye degradation rate demonstrates three types of dependence on dye concentration over a range from 2.5−100 μM. For lower dye concentrations (2.5−40 μM) and natural pH (∼6.0) conditions, Langmuir−Hinshelwood (LH) kinetics was observed. The nanotubes diameter, calcination condition, and the anatase-to-rutile ratio in the crystalline TiO2 nanotubes together influence the photocatalytic and photoelectrochemical properties of the TiO2 nanotubes

Improved Photocatalytic Degradation of Textile Dye Using Titanium Dioxide Nanotubes Formed Over Titanium Wires

Titanium dioxide (TiO2) nanotubes formed by anodization over titanium wires show a significant improvement in photocatalytic activity compared to the nanotubes formed over foils. This is evident when the fractional conversion of a textile dye, methyl orange, increased from 19% over a foil to 40% over wires in the presence of nanotubes of identical dimensions illuminated over the same geometrical area. Higher degradation rates with Pt−TiO2 nanotubes over foils are matched by the Pt-free TiO2 nanotubes over the wires. The higher photocatalytic activity over the anodized wires can be attributed to the efficient capture of reflected and refracted light by the radially outward oriented TiO2 nanotubes formed over the circumference of the titanium wire. The formation of TiO2 nanotubes over wires can be considered as an effective alternate to improve photodegradation rates by avoiding expensive additives

Transmissive Nanohole Arrays for Massively-Parallel Optical Biosensing

A high-throughput optical biosensing technique is proposed and demonstrated. This hybrid technique combines optical transmission of nanoholes with colorimetric silver staining. The size and spacing of the nanoholes are chosen so that individual nanoholes can be independently resolved in massive parallel using an ordinary transmission optical microscope, and, in place of determining a spectral shift, the brightness of each nanohole is recorded to greatly simplify the readout. Each nanohole then acts as an independent sensor, and the blocking of nanohole optical transmission by enzymatic silver staining defines the specific detection of a biological agent. Nearly 10000 nanoholes can be simultaneously monitored under the field of view of a typical microscope. As an initial proof of concept, biotinylated lysozyme (biotin-HEL) was used as a model analyte, giving a detection limit as low as 0.1 ng/mL

Microretroreflector-Sedimentation Immunoassays for Pathogen Detection

Point-of-care detection of pathogens is medically valuable but poses challenging trade-offs between instrument complexity and clinical and analytical sensitivity. Here we introduce a diagnostic platform utilizing lithographically fabricated micron-scale forms of cubic retroreflectors, arguably one of the most optically detectable human artifacts, as reporter labels for use in sensitive immunoassays. We demonstrate the applicability of this novel optical label in a simple assay format in which retroreflector cubes are first mixed with the sample. The cubes are then allowed to settle onto an immuno-capture surface, followed by inversion for gravity-driven removal of nonspecifically bound cubes. Cubes bridged to the capture surface by the analyte are detected using inexpensive, low-numerical aperture optics. For model bacterial and viral pathogens, sensitivity in 10% human serum was found to be 10⁴ bacterial cells/mL and 10⁴ virus particles/mL, consistent with clinical utility