Surface topography and light scattering were measured on 15 samples ranging from those having smooth surfaces to others with ground surfaces. The measurement techniques included an atomic force microscope, mechanical and optical profilers, confocal laser scanning microscope, angle-resolved scattering, and total scattering. The samples included polished and ground fused silica, silicon carbide, sapphire, electroplated gold, and diamond-turned brass. The measurement instruments and techniques had different surface spatial wavelength band limits, so the measured roughnesses were not directly comparable. Two-dimensional power spectral density ͑PSD͒ functions were calculated from the digitized measurement data, and we obtained rms roughnesses by integrating areas under the PSD curves between fixed upper and lower band limits. In this way, roughnesses measured with different instruments and techniques could be directly compared. Although smaller differences between measurement techniques remained in the calculated roughnesses, these could be explained mostly by surface topographical features such as isolated particles that affected the instruments in different ways.

Toward a smart optical biosensor based on nanoporous anodic alumina (NAA): by modifying the pore geometry in nanoporous anodic alumina we are able to change the effective medium at will and tune the photoluminescence of NAA. The oscillations in the PL spectrum are converted into exclusive barcodes, which are useful for developing optical biomedical sensors in the UV-Visible region.

In this study, we report about the structural engineering and optical optimization of nanoporous anodic alumina rugate filters (NAA-RFs) for real-time and label-free biosensing applications. Structurally engineered NAA-RFs are combined with reflection spectroscopy (RfS) in order to develop a biosensing system based on the position shift of the characteristic peak in the reflection spectrum of NAA-RFs (Δλpeak). This system is optimized and assessed by measuring shifts in the characteristic peak position produced by small changes in the effective medium (i.e., refractive index). To this end, NAA-RFs are filled with different solutions of d-glucose, and the Δλpeak is measured in real time by RfS. These results are validated by a theoretical model (i.e., the Looyenga-Landau-Lifshitz model), demonstrating that the control over the nanoporous structure makes it possible to optimize optical signals in RfS for sensing purposes. The linear range of these optical sensors ranges from 0.01 to 1.00 M, with a low detection limit of 0.01 M of d-glucose (i.e., 1.80 ppm), a sensitivity of 4.93 nm M(-1) (i.e., 164 nm per refractive index units), and a linearity of 0.998. This proof-of-concept study demonstrates that the proposed system combining NAA-RFs with RfS has outstanding capabilities to develop ultrasensitive, portable, and cost-competitive optical sensors.

Modern‐day wonders of the world: Nanostructured films of plasmonic pyramid arrays (see picture) were prepared by the simple stamping of preformed homogeneous nanocolloids. These materials show very high efficiency as optical enhancers and can be exploited for the design of quantitative, cheap, portable, and ultrasensitive optical sensors with excellent reversibility.

Herein, we present an ultrasensitive, cost-competitive, and portable optical sensing system for detecting ionic mercury in environmental water. This analytical system combines structurally engineered and chemically modified nanoporous anodic alumina rugate filters (NAA-RFs) with reflection spectroscopy (RfS). The sensing performance of the proposed system is assessed through several tests, establishing its sensing performance (i.e., linear working range from 1 to 100 μM of Hg(2+), low limit of detection 1 μM of Hg(2+) ions (i.e., 200 ppb), and sensitivity of 0.072 nm μM(-1)), chemical selectivity (i.e., exposure to different metal ions Co(2+), Mg(2+), Ni(2+), Cu(2+), Pb(2+), Fe(3+), Ca(2+), Cr(6+), and Ag(+)) and metal ions binding mechanism (i.e., fitting to Langmuir and Freundlich isotherm models). Furthermore, the detection of Hg(2+) ions in tap and environmental water (River Torrens) is successfully carried out, demonstrating the suitability of this system for developing environmental point-of-analysis systems.

A cost-effective label-free optical biosensor based on gold-coated self-ordered nanoporous anodic alumina bilayers is presented. The structure is formed by two uniform nanoporous layers of different porosity (i.e., a top layer with large pores and a bottom layer with smaller pores). Each layer presents uniform pore size, regular pore distribution, and regular diameter along its pore length. To increase and improve the output sensing signals, a thin gold layer on the top surface was deposited. The gold layer increases the refractive index contrast between the nanoporous alumina layer and the analytical aqueous solution, and it results in a greater contrast in the interferometric spectrum and a higher sensitivity of the structure. From this structurally engineered architecture, the resulting reflectivity spectrum shows a complex series of Fabry-Pérot interference fringes, which was analyzed by the reflective interferometric Fourier transform spectroscopy (RIFTS) method. To determine the performance of this structure for biosensing applications, we tested bovine serum albumin (BSA) as the target protein. The results show a significant enhancement of the RIFTS peak intensity and position when a gold layer is on the top surface.

In this study, we demonstrate that an optimal design of the pore geometry and shape of sensing platforms based on nanoporous anodic alumina (NAA) photonic structures is critical to develop optical sensors with improved capabilities. To this end, two types of NAA photonic structures featuring different pore geometries (i.e., pore lengths and diameters) and shapes (i.e., straight and modulated pores) were produced, and their optical characteristics were assessed systematically by reflectometric interference spectroscopy. The geometric features (i.e., pore lengths, diameters, and shapes) were systematically modified in order to establish the optimization paths for the sensitivity, low limit of detection, and linearity of these optical sensing platforms. The obtained results reveal that an optimal design of these nanoporous photonic structures can enhance their sensitivity, achieve a lower limit of detection, and improve their linearity for both nonspecific and specific detection of analytes. Therefore, as this study demonstrates, the rational design of optical nanoporous sensing platforms is critical in the development of reliable, sensitive, robust, inexpensive, and portable optical systems for a broad range of sensing applications.

Herein, we present a smart enzymatic sensor based on nanoporous anodic alumina (NAA) and its photoluminescence (PL) in the UV−visible range. The asproduced structure of NAA is functionalized and activated in order to perform the enzyme immobilization in a controlled manner. The whole process is monitored through the PL spectrum and each stage is characterized by an exclusive barcode, which is associated with the PL oscillations. This characteristic property allows us to calculate the change in the effective optical thickness that takes place after each stage. This makes it possible to accurately detect and quantify the immobilized enzyme within the NAA structure. Finally, the NAA geometry (i.e., the pore length and its diameter) is optimized to improve the enzyme immobilization and its detection inside the pores. This enzymatic sensor can give quick and accurate measurements of enzyme levels, what is crucial in clinical enzymology to prevent and detect diseases at their primary stage.