کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1489284 992303 2013 4 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Magnetic field-assisted synthesis of wire-like Co3O4 nanostructures: Electrochemical and photocatalytic studies
موضوعات مرتبط
مهندسی و علوم پایه مهندسی مواد سرامیک و کامپوزیت
پیش نمایش صفحه اول مقاله
Magnetic field-assisted synthesis of wire-like Co3O4 nanostructures: Electrochemical and photocatalytic studies
چکیده انگلیسی

Wire-like Co3O4 nanostructures were prepared by the combination of magnetic field-assisted hydrothermal reduction of cobalt ions and the subsequent ambient annealing at 500 °C. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were used to characterize the structure and morphological evolution of the products. The results show that the wire-like nanostructures possess diameters about 250 nm and lengths over 10 μm. The possible formation mechanism of the wire-like Co3O4 nanostructures is also proposed based on the SEM results. Galvanostatic methods were used to characterize the electrochemical properties. The measurements indicate that the wire-like Co3O4 nanostructures show larger discharge and charge capacities than that of spherical Co3O4 nanoparticles prepared in the absence of magnetic field. In addition, the photocatalytic activity of the products was investigated by measuring the photodegradation of methyl orange solution under ultraviolet radiation, which shows that both the wire-like and spherical products have a good photocatalytic activity.

Schematic illustration for the magnetic field-assisted growth of wire-like Co3O4 nanostructure.Figure optionsDownload as PowerPoint slideHighlights
► Co3O4 nanowires are prepared by magnetic field hydrothermal reduction and annealing.
► These Co3O4 nanowires possess enhanced capacitance.
► The Co3O4 nanowires have a good photocatalytic activity for methyl orange.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Materials Research Bulletin - Volume 48, Issue 1, January 2013, Pages 92–95
نویسندگان
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