Aschalew Kassu

Photoinduced grating formation in azo-dye-labeled phospholipid thin films by 244-nm light

Holographic gratings are recorded in azo-dye nitrobenzoxazole-labeled phospholipid thin films by use of 244-nm UV light. The gratings continue to grow for more than 1 h, even after the recording light is removed. The diffraction efficiency of these gratings shows extreme sensitivity to humidity and can increase reversibly by 2 orders of magnitude in air that is saturated with water vapor. This effect is related to the unique characteristics of phospholipid molecules that undergo hydration-dependent structural reorganization and self-assembly.

Detection of residual traces of explosives by surface enhanced Raman scattering using gold coated substrates produced by nanospheres imprint technique

Explosives detection for national and aviation security has been an area of concern for many years. In order to improve the security in risk areas, much effort has been focused on direct detection of explosive materials in vapor and bulk form. New techniques and highly sensitive detectors have been extensively investigated and developed to detect and identify residual traces that may indicate an individuals recent contact with explosive materials. This paper reports on the use and results of Surface Enhanced Raman Scattering (SERS) technique, to analyze residual traces of explosives in highly diluted solutions by using low-resolution Raman spectroscopy (LRRS). An evaluation of the detection sensitivity of this technique has been accomplished using samples of explosives such as Trinitrotoluene(TNT), Cyclotrimethylenetrinitramine (RDX) and HMX evaluated at different concentrations. Additionally, different SERS substrates have been studied in order to achieve the best enhancement of the Raman spectrum for residual amounts of materials. New substrates produced by gold-coated polystyrene nanospheres have been investigated. Two different sizes of polystyrene nanospheres, 625nm and 992nm, have been used to produce nanopatterns and nanocavities on the surface of a glass slide which has been coated with sputtered gold. Results from homemade substrates have been compared to a commercial gold-coated substrate consisting of an array of resonant cavities that gives the SERS effect. Sample concentration, starting from 1000ppm was gradually diluted to the smallest detectable amount. Raman spectrum was obtained using a portable spectrometer operating at a wavelength of 780nm.

Carbon Coating and Defects in CdZnTe and CdMnTe Nuclear Detectors

CADMIUM zinc telluride (CdZnTe) and cadmium manganese telluride (CdMnTe) are prime materials for detecting X-rays and gamma-rays at room temperature due to their high average atomic numbers that are essential to having high stopping-power for incident high-energy electromagnetic radiations. A major obstacle in developing CdZnTe and CdMnTe detectors lies in growing crystals free from defects, such as Te inclusions, dislocations, sub-grain boundary networks, and precipitates. We present the results of our study of the relationship between carbon coating of the growth ampoule and dislocations in CdZnTe and sub-grain boundary networks in CdMnTe, grown by Bridgman method. For the CdZnTe crystals, a carbon-coating of 2 μm on the ampoule generated fewer dislocations than did a thinner 0.2 - μm carbon-coated one. Furthermore, the ampoules design (normal- or tapered-shape) did not affect the densities of etch pits as much as did the thickness of the carbon-coating. For a CdMnTe ingot with a carbon coating of about 2 μm, created by cracking spectroscopic-grade acetone at ~ 900° C, we observed very few grain boundaries and grain-boundary networks.

Effect of Pore Size and Film Thickness on Gold-Coated Nanoporous Anodic Aluminum Oxide Substrates for Surface-Enhanced Raman Scattering Sensor.

A sensitive surface enhanced Raman scattering chemical sensor is demonstrated by using inexpensive gold-coated nanoporous anodic aluminum oxide substrates. To optimize the performance of the substrates for sensing by the Surface-enhanced Raman scattering (SERS) technique, the size of the nanopores is varied from 18 nm to 150 nm and the gold film thickness is varied from 30 nm to 120 nm. The sensitivity of gold-coated nanoporous surface enhanced Raman scattering sensor is characterized by detecting low concentrations of Rhodamine 6G laser dye molecules. The morphology of the SERS substrates is characterized by atomic force microscopy. Optical properties of the nanoporous SERS substrates including transmittance, reflectance, and absorbance are also investigated. Relative signal enhancement is plotted for a range of substrate parameters and a detection limit of 10−6 M is established.

Surface-enhanced Raman spectroscopy scattering from gold-coated ceramic nanopore substrates: effect of nanopore size

Abstract. The dependence of magnitude of the electric near-field on the separation between metal nanoparticles for surface-enhanced Raman spectroscopy (SERS) substrates was experimentally verified. Diameters of gold-coated nanopores in a ceramic alumina substrate were varied to study the charge buildup near interparticle junctions and its effect on the enhancement factor due to SERS. The substrates were characterized by sensing a Rhodamine dye and calculating the associated Raman enhancement factors. Decreasing Au interparticle distance increases the electric near-field and shifts the plasmon resonance peak accordingly.

Short Distance Standoff Raman Detection of Extra Virgin Olive Oil Adulterated with Canola and Grapeseed Oils

A short distance standoff Raman technique is demonstrated for detecting economically motivated adulteration (EMA) in extra virgin olive oil (EVOO). Using a portable Raman spectrometer operating with a 785 nm laser and a 2-in. refracting telescope, adulteration of olive oil with grapeseed oil and canola oil is detected between 1% and 100% at a minimum concentration of 2.5% from a distance of 15 cm and at a minimum concentration of 5% from a distance of 1 m. The technique involves correlating the intensity ratios of prominent Raman bands of edible oils at 1254, 1657, and 1441 cm–1 to the degree of adulteration. As a novel variation in the data analysis technique, integrated intensities over a spectral range of 100 cm–1 around the Raman line were used, making it possible to increase the sensitivity of the technique. The technique is demonstrated by detecting adulteration of EVOO with grapeseed and canola oils at 0–100%. Due to the potential of this technique for making measurements from a convenient distance, the short distance standoff Raman technique has the promise to be used for routine applications in food industry such as identifying food items and monitoring EMA at various checkpoints in the food supply chain and storage facilities.

Photopatterning of polybutadiene substrates by interferometric ultraviolet lithography: fabrication of phospholipid microarrays.

Gratings are written holographically with low power (10 mW/cm(2)) 244 nm UV light on thin films of polybutadiene rubber polymer. The increase of hydrophilicity-wettability of polybutadiene films is measured over UV-exposed regions. Sequential fabrication of two orthogonal gratings results in hydrophilic microarrays having applications as functionalized substrates for immobilizing biomolecules. This is demonstrated by immobilizing a phospholipid in a microarray pattern.

Fabrication and characterization of a diffraction-grating transducer in thin polybutadiene rubber film for sensing dynamical strain

Surface relief gratings are holographically fabricated in thin polybutadiene rubber films produced by both spin coating and dip coating on glass and metal substrates. These thin-film gratings are characterized for their application as efficient transducers for detecting dynamic strain in solids. The performance of these rubber-grating transducers is compared to surface-mounted fiber Bragg gratings for a range of frequencies between 50 Hz and 30 kHz. Dynamic-strain sensitivity around 1 nepsilon/radicalHz is recorded for thin rubber-film grating transducers.

Standoff Raman measurement of nitrates in water

The identification and real time detection of explosives and hazardous materials are of great interest to the Army and environmental monitoring/protection agencies. The application and efficiency of the remote Raman spectroscopy system for real time detection and identification of explosives and other hazardous chemicals of interest, air pollution monitoring, planetary and geological mineral analysis at various standoff distances have been demonstrated. In this paper, we report the adequacy of stand-off Raman system for remote detection and identification of chemicals in water using dissolved sodium nitrate and ammonium nitrate for concentrations between 200ppm and 5000ppm. Nitrates are used in explosives and are also necessary nutrients required for effective fertilizers. The nitrates in fertilizers are considered as potential sources of atmospheric and water pollution. The standoff Raman system used in this work consists of a 2-inch refracting telescope for collecting the scattered Raman light and a 785nm laser operating at 400mW coupled with a small portable spectrometer.

Recycling of surface-enhanced Raman substrates by ultraviolet cleaning

Commercial substrates used for surface-enhanced Raman spectroscopy (SERS) are investigated for their reusability following cleaning with 254-nm UV light from a mercury lamp. SERS of Rhodamine 6G (Rh6G, a dye) and RDX (an explosive) is investigated. It is found that without UV irradiation, the substrate is usable only once, since it is not possible to dislodge the analyte either by prolonged immersion in distilled water or by ultrasonic cleaning. However, prolonged exposure to 254-nm UV followed by immersion in distilled water removes most of the analyte, making the substrate reusable for new SERS measurements. The technique of UV cleaning is demonstrated by recycling the same substrate several times and comparing SERS spectra taken after each cleaning cycle.