RESUMO
In this work rod-like YMnO3 were successfully prepared by hydrothermal method. The crystal structure and morphology of prepared samples were characterized by X-ray diffraction, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The structural information was confirmed from Raman spectrum and the functional group of the sample was studied from FTIR spectrum. X-ray photoelectron spectroscopy studies confirm the formation and oxidation states of YMnO3. The optical properties of the prepared samples were investigated using UV-vis spectroscopy. The photocatalytic activity of YMnO3 nanorods was evaluated by degradation of methyl orange (MO) under both ultraviolet and visible-light irradiation. The result shows that the YMnO3 nanorods exhibit maximum photocatalytic activity in the degradation of MO.
RESUMO
The two-dimensional (2D) transition metal dichalcogenide nanosheet-carbon composite is an attractive material for energy storage because of its high Faradaic activity, unique nanoconstruction and electronic properties. In this work, a facile one step preparation of a molybdenum disulfide (MoS2) nanosheet-graphene (MoS2/G) composite with the in situ reduction of graphene oxide is reported. The structure, morphology and composition of the pure MoS2 and composites were comparatively analyzed by various characterization techniques. The electrochemical performance of the pure MoS2, graphene oxide and the MoS2/G composite electrode materials was evaluated by cyclic voltammogram, galvanostatic charge-discharge and electrochemical impedance spectroscopy. The MoS2/G composite showed a higher specific capacitance (270 F g(-1) at a current density of 0.1 A g(-1)) compared to the pure MoS2 (162 F g(-1)) in a neutral aqueous electrolyte. Moreover, the energy density of the composite electrode is also higher (12.5 Wh kg(-1)) with a high power density (2500 W kg(-1)) compared to the pure MoS2. In addition, the MoS2/G composite electrode showed excellent cyclic stability even after 1000 cycles. The enhancement in specific capacitance, excellent cyclic stability and high energy density of the composite electrode are mainly due to the interconnected conductive network of the composite as well as the synergetic effect of the pure MoS2 and graphene. The experimental results demonstrated that the MoS2/G composite is a promising electrode material for high-performance supercapacitors.
RESUMO
OBJECTIVES: Similar to other epithelia, urothelium in vivo has a hierarchal organization of cells each with specific gradients of differentiation. While distinct cell types have been described as important in bladder cancer in vitro, clonal and proliferative capacities of normal urothelial cells have not been characterized. MATERIALS AND METHODS: Three cell types and colony types were identified from primary porcine urothelial culture. Proliferative activity, patterns of apoptosis and differentiation, colony forming efficiency and ability to change phenotype with passage were determined and compared. RESULTS: Small, T-I colonies with large flattened (type-1) cells had low levels of proliferation and high levels of apoptosis. Large T-III colonies had a central area of small (type-3) cells surrounded by type-1 and type-2 cells. Proliferation and apoptosis were asymmetrically distributed in the periphery of T-II and T-III colonies. T-III colonies proved to be significantly more clonogenic and proliferative. With appropriate induction, type-1 cells were able to proliferate upon passage and form type-3 cells, yet long-term culture demonstrated that progeny of type-1 cells appeared to have inherited a clonogenic handicap. CONCLUSIONS: Type-3 cells in the centre of T-III colonies appear to harbour stem-like qualities with a relatively low proliferative and apoptotic index at homeostasis and the ability to become highly proliferative upon passage. This study demonstrates that distinct urothelial cell types with differing clonal capacities can be isolated from the bladder and these cells may have implications for tissue engineering and carcinogenesis.
