79 research outputs found

    Optical Properties of ZnP2 Nanoparticles in Zeolite

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    We report that for the first time the nanoparticles of II-V semiconductor (ZnP2) were prepared and studied. ZnP2 nanoparticles were prepared by incorporation into zeolite Na-X matrix. Absorption, diffuse reflection (DR) and photoluminescence (PL) spectra of the ZnP2 nanoclusters incorporated into the supercages of zeolite Na-X were measured at the temperature 77 K. Five bands B1-B5 are observed in both the DR and PL spectra demonstrating the blue shift from the line of free exciton in bulk crystal. We attribute the B1-B5 bands to some stable nanoclusters with size less than the size of zeolite Na-X supercage. We observed Stokes shift of the PL bands from the respective absorption bands. The nonmonotonic character of its dependence on the cluster size can be explained as the result of competition of the Frank-Condon shift and the shift due to electronic relaxation.Comment: Submitted to Microporous and Mesoporous Material

    Effect of shell thickness on exciton and biexciton binding energy of a ZnSe/ZnS core/shell quantum dot

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    The exciton and biexciton binding energy have been studied for a ZnSe/ZnS core/shell quantum dot using WKB (Wentzel-Kramers-Brillouin) approximation. The exciton binding energy increases for small shell thickness and for large thickness, the binding energy again starts decreasing. A similar result is obtained for biexcitons where for thicker shells, the biexciton attains antibonding.Comment: 5 Figure

    Fabrication, Study of Optical Properties and Structure of Most Stable (CdP2)n Nanoclusters

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    CdP2 nanoclusters were fabricated by incorporation into pores of zeolite Na-X and by laser ablation. Absorption and photoluminescence (PL) spectra of CdP2 nanoclusters in zeolite were measured at the temperatures of 4.2, 77 and 293 K. Both absorption and PL spectra consist of two bands blue shifted with respect to bulk crystal. We performed the calculations aimed to find the most stable clusters in the size region up to size of the zeolite Na-X supercage. The most stable clusters are (CdP2)6 and (CdP2)8 with binding energies of 9.30 eV and 10.10 eV per (CdP2)1 formula unit respectively. Therefore, we attributed two bands observed in absorption and PL spectra to these stable clusters. The Raman spectrum of CdP2 clusters in zeolite was explained to be originated from (CdP2)6 and (CdP2)8 clusters as well. The PL spectrum of CdP2 clusters produced by laser ablation consists of the asymmetric band with low-energy tail that has been attributed to emission of both (CdP2)8 cluster and CdP2 microcrystals.Comment: Accepted for publication in Physica E: Low-dimensional Systems and Nanostructure

    Optical Properties and Structure of Most Stable Subnanometer (ZnAs2)n Clusters

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    ZnAs2 nanoclusters were fabricated by incorporation into pores of zeolite Na-X and by laser ablation. Absorption and photoluminescence spectra of ZnAs2 nanoclusters in zeolite were measured at the temperatures of 4.2, 77 and 293 K. Both absorption and PL spectra consist of two bands which demonstrate the blue shift from the line of free exciton in bulk crystal. We performed the calculations aimed to find the most stable clusters in the size region up to size of the zeolite Na-X supercage. The most stable clusters are (ZnAs2)6 and (ZnAs2)8 with binding energies of 7.181 eV and 8.012 eV per (ZnAs2)1 formula unit respectively. Therefore, we attributed two bands observed in absorption and PL spectra to these stable clusters. The measured Raman spectrum of ZnAs2 clusters in zeolite was explained to be originated from (ZnAs2)6 and (ZnAs2)8 clusters as well. The PL spectrum of ZnAs2 clusters produced by laser ablation consists of a single band which has been attributed to emission of (ZnAs2)8 cluster.Comment: Article accepted for publication in Physica B: Physics of Condensed Matte

    Cell therapies in the clinic

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    Cell therapies have emerged as a promising therapeutic modality with the potential to treat and even cure a diverse array of diseases. Cell therapies offer unique clinical and therapeutic advantages over conventional small molecules and the growing number of biologics. Particularly, living cells can simultaneously and dynamically perform complex biological functions in ways that conventional drugs cannot; cell therapies have expanded the spectrum of available therapeutic options to include key cellular functions and processes. As such, cell therapies are currently one of the most investigated therapeutic modalities in both preclinical and clinical settings, with many products having been approved and many more under active clinical investigation. Here, we highlight the diversity and key advantages of cell therapies and discuss their current clinical advances. In particular, we review 28 globally approved cell therapy products and their clinical use. We also analyze >1700 current active clinical trials of cell therapies, with an emphasis on discussing their therapeutic applications. Finally, we critically discuss the major biological, manufacturing, and regulatory challenges associated with the clinical translation of cell therapies

    Robust estimation of bacterial cell count from optical density

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    Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals <1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data
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