RESUMO
An investigation into the performance of luminescence-based hyperspectral imaging (LHSI) for denim fiber bundle discrimination has been conducted. We also explore the potential of nitromethane (CH3NO2) -based quenching to improve discrimination, and we determine the quenching mechanism. The luminescence spectra (450-850 nm) and images from the denim fiber bundles were obtained with excitation at 325 or 405 nm. LHSI data were recorded in less than 5 s and subsequently assessed by principal component analysis or rendered as red, green, blue (RGB) component histograms. The results show that LHSI data can be used to rapidly and uniquely discriminate between all the fiber bundle types studied in this research. These non-destructive techniques eliminate extensive sample preparation and allow for rapid hyperspectral image collection, analysis, and assessment. The quenching data also revealed that the dye molecules within the individual fiber bundles exhibit dramatically different accessibilities to CH3NO2.
RESUMO
We carefully evaluate how porous silicon (pSi) surface oxidation by ozone (O(3)) and the resulting changes in nanocrystallite surface chemistries (e.g., SiOSi, SiH(x) (x = 1-3), O(y)SiH (y = 1-2), and SiOH) influence the pSi photoluminescence (PL). We discover a relationship between the pSi PL and the O(2)SiH band amplitude.
RESUMO
A high-throughput screening system has been developed to rapidly produce, screen, and assess the usefulness of organically modified silane (ORMOSIL)-based xerogel films formed on the surface of porous silicon (pSi) surfaces. The ORMOSILs tested include methyltriethoxysilane, n-octyltriethoxysilane, n-hexyltriethoxysilane, n-propyltriethoxysilane, 2-cyanoethyltriethoxysilane, phenyltriethoxysilane, benzyltriethoxysilane, vinyltriethoxysilane, tetraethoxysilane, and hexafluoroethyltriethoxysilane. Xerogel microarrays were pin-printed on the surface of O(3) oxidized pSi using a computer-controlled robotic pin-printer. The fragile pSi required careful pin-printing parameter optimization to simultaneously ensure sufficient sol application and limit pin-induced damage. These multi-functional xerogel-pSi microarrays were exposed to harsh conditions (0.1 mM NaOH, 15 min) to determine the extent to which the xerogel protected the pSi. Microarray assessment included multispectral photoluminescence and infrared imaging. Results demonstrate that the more hydrophobic/nonpolar xerogel films (n-octyltriethoxysilane, n-hexyltriethoxysilane) protect the pSi surface the most and maintained the pSi photoluminescence. Also, unlike xerogel material doped with a reporter molecule, the uniformity of the printed feature plays a role in the protection of the pSi material underneath. Areas with thinner xerogel distributions allowed the permeation of NaOH whereas the thicker areas prohibit pSi exposure to NaOH.