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101.
We report the OMVPE growth and characterization of InAsSb/InAs strain balanced multiple quantum wells lattice-matched to GaSb substrates for potential application as mid-infrared detectors for wavelengths beyond 4 μmμm. Detailed transmission electron microscopy measurements were performed to evaluate the degree of Ga and Sb intermixing at the GaSb/InAsSb and InAs/InAsSb interfaces. Photoluminescence emission up to 5 μmμm was observed for superlattice structures with only 15% antimony. The dependence of PL on wavelength is red shifted compared to expectations based on type I band alignment.  相似文献   
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Abstract

A gas chromatography method is used to investigate the purity of dialkyl-diphenyl-diacetylene liquid crystal components and at the same time identify the structure and concentration of the major impurities.  相似文献   
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We analyse different error propagation mechanisms for conservativeand nonconservative time-integrators of nonlinear Schrödingerequations. We use a geometric approach based on interpretingwaves as relative equilibria.  相似文献   
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We present data for a comparison of a liquid-chromatographic method coupled with tandem mass spectrometry (LC-MS/MS) and a high-performance liquid-chromatographic method with column switching and UV spectrophotometric detection. The two methods were developed for determination of naltrexone and 6β-naltrexol in blood serum or plasma aiming to be used for therapeutic drug monitoring to guide the treatment of patients with naltrexone. For the high-performance liquid chromatography (HPLC)/UV detection, online sample cleanup was conducted on Perfect Bond C18 material with 2% (vol/vol) acetonitrile in deionized water. Drugs were separated on a C18 column using 11.5% (vol/vol) acetonitrile and 0.4% (vol/vol) N,N,N,N-tetramethylethylenediamine within 20 min. LC-MS/MS used naltrexone-d 3 and 6β-naltrexol-d 4 as internal standards. After protein precipitation, the chromatographic separation was performed on a C18 column by applying a methanol gradient (5–100%, vol/vol) with 0.1% formic acid over 9.5 min. The HPLC/UV method was found to be linear for concentrations ranging from 2 to 100 ng/ml, with a regression correlation coefficient of r 2?>?0.998 for naltrexone and 6β-naltrexol. The limit of quantification was 2 ng/ml for naltrexone and 6β-naltrexol. For the LC-MS/MS method the calibration curves were linear (r²?>?0.999) from 0.5 to 200 ng/ml for both substances, and the limit of quantification was 0.5 ng/ml. The concentrations measured by the two methods correlated significantly for both substances (r²?>?0.967; p?<?0.001). Both methods could be used for therapeutic drug monitoring. The HPLC/UV method was advantageous regarding automatization and costs, whereas LC-MS/MS was superior with regard to sensitivity.  相似文献   
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The spectroscopic application of a new broadband microelectromechanical-system-tunable vertical cavity surface-emitting laser with single-mode coverage of 60 nm (245 cm(-1)) in a single, continuous sweep is described. The operation of the device is illustrated with high-resolution spectra of CO and CO2 over 110 cm(-1) (27 nm) and 67 cm(-1) (17 nm), respectively, with the CO band shown for high-pressure scans between 1 and 3 bars (0.1-0.3 MPa). The achieved tuning range opens up new opportunities for tunable diode laser absorption spectroscopy. The spectra were compared with HITRAN-derived model calculations. The benefits of a sensor based on this laser are greater speed, laser power, and tuning range.  相似文献   
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JM Cline 《Pramana》2000,55(1-2):33-42
I review recent progress on the electroweak phase transition and baryogenesis, focusing on the minimal supersymmetric Standard Model as the source of new physics.  相似文献   
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