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An electrochemiluminescence (ECL) biosensor was fabricated for the evaluation of prostate specific antigen (PSA). The sensor was developed by successively modifying glassy carbon electrode (GCE) electrodes with CdS/Chito/g-C3N4 nanocomposites and DNA1 was labeled at the 5′ end with thiol. The aptamer DNA was labeled at the 3′ end with a quencher ferrocene (Fc) was ligated to DNA1 by the principle of complementary base pairing. In the absence of PSA, the ECL intensity signal is effectively quenches through the energy transfer and photoexcitation electron transfer between CdS/Chito/g-C3N4 emitter and quencher Fc. After incubation with target PSA, the aptamer DNA interacts with PSA and then moved away from the electrode surface together, which will recover the ECL intensity. Under the optimal conditions, the ECL intensity increases linearly with the logarithm of PSA concentration in the range of 1 pg·mL−1 to 100 ng·mL−1, and the detection limit is 0.14 pg·mL−1 (S/N = 3). The biosensor has been successfully applied to the determination of PSA in serum sample. [ABSTRACT FROM AUTHOR]

CuAgSe is a promising thermoelectric (TE) material for its superior carrier mobility and ultralow lattice thermal conductivity. Herein, we present a scalable colloidal method to prepare monodisperse CuAgSe nanocrystals with high yield. The collected powder sample was washed by a sulfur-free reagent of NaNH2 to remove the surface organic ligands (CuAgSe-W) and then annealed (CuAgSe-W-A). Both kinds of ligand-free samples were then hot pressed into dense pellets to measure the TE property. The results revealed that the crystal structure of both samples changed from low-temperature β-phase to high-temperature α-phase at around 465 K. Sample CuAgSe-W shows interesting temperature-dependent transition from N-type to P-type, which could be potentially used as thermal control transistor. Sample CuAgSe-W-A does not display this transition state but it exhibits potential for intermediate temperature TE applications with a figure-of-merit zT reaching 0.68 at 566 K. [ABSTRACT FROM AUTHOR]

Copper-based chalcogenides that contain abundant, low-cost and environmentally-friendly elements, are excellent materials for numerous energy conversion applications, such as photocatalysis, photovoltaics, photoelectricity and thermoelectrics (TE). Here, we present a high-yield and upscalable colloidal synthesis route for the production of monodisperse ternary I-III-VI2 chalcogenides nanocrystals (NCs), particularly stannite CuFeSe2, with uniform shape and narrow size distributions by using selenium powder as the anion precursor and CuCl2•2H2O and FeCl3 as the cationic precursors. The composition, the state of valence, size and morphology of the CuFeSe2 materials were examined by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), transmission electron microscope (TEM) and high resolution transmission electron microscope (HRTEM), respectively. Furthermore, the TE properties characterization of these dense nanomaterials compacted from monodisperse CuFeSe2 NCs by hot press at 623 K were preliminarily studied after ligand removal by means of hydrazine and hexane solution. The TE performances of the sintered CuFeSe2 pellets were characterized in the temperature range from room temperature to 653 K. Finally, the dimensionless TE figure of merit (ZT) of this Earth-abundant and intrinsic p-type CuFeSe2 NCs is significantly increased to 0.22 at 653 K in this work, which is demonstrated to show a promising TE materialand makes it a possible p-type candidate for medium-temperature TE applications. [ABSTRACT FROM AUTHOR]

CdSe:Eu nanocrystals were successfully synthesized and characterized by transmission electron microscopy, X-ray powder diffraction, and X-ray photoelectric spectroscopy. The CdSe:Eu nanocrystals showed enhanced green electrochemiluminescence (ECL) intensity when compared to pure CdSe nanocrystals. Further, the nanocrystals were used to design an ECL immunosensor for the detection of carcinoembryonic antigen (CEA) that has a linear response over the 1.0 fg·mL to 100 ng·mL CEA concentration range with a 0.4 fg·mL detection limit. The assay was applied to the determination of CEA in human serum samples. [ABSTRACT FROM AUTHOR]

Graphene-like cobalt-nickel double hydroxide nanocomposites have been successfully prepared by a mild hydrolysis process at the room temperature. The samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and thermal gravimetric analysis. The results reveal that the as-prepared samples are composed of α-Co(OH) and α-Ni(OH), and contain numerous thin flakes with wrinkle structure, and the thickness of the flakes is ca. 1 nm. Magnetic measurements indicate that the as-prepared nanocomposites have a weak ferromagnetic behavior at the room temperature, which is due to a small content of metallic Co. The as-synthesized products emerge large specific surface area (260.1 m g) from the measurement of Brunauer-Emmett-Teller. Interestingly, compared to single components, the obtained nanocomposites have exhibited superiorly and enhanced catalytic activity to the hydrogenation of p-nitrophenol in the presence of excess sodium borohydride at room temperature. In addition, the adsorption property of the nanocomposites for methyl blue has also been examined. [ABSTRACT FROM AUTHOR]

A simple solvothermal route was explored to prepare hierarchical, nanostructured flower-like bismuth oxychlorides (BiOCl) by employing pyridine as the solvent. The volume ratios of distilled water to pyridine play an important role in the assembly of the BiOCl nanostructure from nanoplates to nanoflowers. The as-prepared BiOCl nanoflowers were characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy, high-resolution transmission electron microscopy, and nitrogen sorption. The resulting BiOCl nanoflowers with high specific surface area were phase-pure and self-assembled from thin nanoplates during the reaction process. In addition, the photocatalytic properties of the as-prepared samples were further investigated by photocatalytic decomposition of methyl orange (MO) dye, and it was found that the BiOCl nanoflowers showed a higher photocatalytic activity than that of TiO2(Degussa, P25) under modeling sunlight. [ABSTRACT FROM AUTHOR]

A simple solvothermal route was explored to prepare hierarchical, nanostructured flower-like bismuth oxychlorides (BiOCl) by employing pyridine as the solvent. The volume ratios of distilled water to pyridine play an important role in the assembly of the BiOCl nanostructure from nanoplates to nanoflowers. The as-prepared BiOCl nanoflowers were characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy, high-resolution transmission electron microscopy, and nitrogen sorption. The resulting BiOCl nanoflowers with high specific surface area were phase-pure and self-assembled from thin nanoplates during the reaction process. In addition, the photocatalytic properties of the as-prepared samples were further investigated by photocatalytic decomposition of methyl orange (MO) dye, and it was found that the BiOCl nanoflowers showed a higher photocatalytic activity than that of TiO2(Degussa, P25) under modeling sunlight. [ABSTRACT FROM AUTHOR]