Photoluminescence and cathodoluminescence ͑CL͒ spectra of stoichiometric and oxygen-deficient ZnO films grown on sapphire were examined. It was found that the intensities of the green and yellow emissions depend on the width of the free-carrier depletion region at the particle surface; the thinner the width, the larger the intensity. Experimental results and spectral analyses suggest that the mechanism responsible for the green ͑yellow͒ emission is the recombination of a delocalized electron close to the conduction band with a deeply trapped hole in the single ionized oxygen vacancy V o ϩ ͑the single negatively charged interstitial oxygen ion O i Ϫ) center in the particle.

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Using electrochemical etching of a polycrystalline 3C-SiC target and subsequent ultrasonic treatment in water solution, we have fabricated suspensions of 3C-SiC nanocrystallites that luminesce. Transmission electron microscope observations show that the 3C-SiC nanocrystallites, which uniformly disperse in water, have sizes in the range of 1-6 nm. Photoluminescence and photoluminescence excitation spectral examinations show clear evidence for the quantum confinement of 3C-SiC nanocrystallites with the emission band maximum ranging from 440 to 560 nm. Tunable, composite polystyrene/SiC film can be made by adding polystyrene to a toluene suspension of the 3C-SiC nanocrystallites and then coating the resulting solution onto a Si wafer.

. Overall, the Biotyper system generated significantly more accurate identifications than the Vitek MS IVD system (P ‫؍‬ 0.016; 177 versus 167 out of 181 specimens). The Biotyper system identified the minority species among polymicrobial blood cultures. We also compared the performance of an in-house extraction method with that of the Sepsityper on both MALDI-TOF MS systems. The in-house method generated more correct identifications at the genus level than the Sepsityper (96.7% versus 93.5%) on the Biotyper system, whereas the two methods exhibited the same performance level (88.0% versus 88.0%) on the Vitek MS IVD system. Our study confirmed the practical advantages of MALDI-TOF MS, and our in-house extraction method reduced the reagent cost to $1 per specimen, with a shorter turnaround time of 3 h, which is highly cost-effective for a diagnostic microbiology service. Bloodstream infection is a condition associated with high morbidity and mortality (1, 2). The rapid identification of bloodstream pathogens is critical to clinical management and the choice of appropriate antibiotic treatments (3, 4). Currently, microbiologic diagnosis of bacteremia relies on subculture of positive blood culture broths on solid medium for an 18-to 24-h incubation period followed by biochemical tests or an automated preformed enzyme assay for identification of the bacteria (5). In general, laboratory diagnosis of common pathogens requires 18 to 48 h, while diagnosis of fastidious organisms requires longer incubation and identification procedures. Although the use of modern techniques such as fluorescence in situ hybridization and PCR can shorten the identification time (6), these operations require specialized equipment and technical expertise and the targeted pathogens are limited in a single run (7). Therefore, the introduction of a simple, rapid, broad-spectrum, and cost-effective system for the identification of blood culture pathogens is imperative.Matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) was developed in the 1980s, and this technique had been widely used for biomolecule analysis in the chemical industry for over 10 years. In recent years, MALDI-TOF MS was introduced for bacterial identification, which revolutionized the diagnostic microbiology service (8). Two manufacturers, bioMérieux (Marcy l'Etoile, France) and Bruker Daltonics (Bremen, Germany), are marketing efficient MALDI-TOF systems, the Vitek-MS and the Microflex LT, respectively, that allow the identification of bacteria and yeasts in a few minutes instead of the hours required by traditional methods. The practical use of MALDI-TOF MS for microorganism identification directly from positive blood culture specimens has been substantiated by a number of studies (9-13). Generally, studies have shown high identification rates for various types of organisms with the use of MALDI-TOF MS . However, various organism isolation methods from blood were used in those studies and therefore method standardization is necessary. The...