کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1640957 1517207 2016 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Hydrothermal synthesis of novel CoFe2O4/BiVO4 nanocomposites with enhanced visible-light-driven photocatalytic activities
موضوعات مرتبط
مهندسی و علوم پایه مهندسی مواد فناوری نانو (نانو تکنولوژی)
پیش نمایش صفحه اول مقاله
Hydrothermal synthesis of novel CoFe2O4/BiVO4 nanocomposites with enhanced visible-light-driven photocatalytic activities
چکیده انگلیسی


• A novel CoFe2O4/BiVO4 nanocomposite was synthesized by a facile hydrothermal method.
• The composite exhibited a high activity for MB degradation under visible light.
• The improved photocatalytic activity can be attributed to effective separation of photo-generated electrons and holes.

The novel CoFe2O4/BiVO4 nanocomposites were firstly synthesized by a facile hydrothermal method. The photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET)-specific surface area, UV–vis diffuse reflectance spectrophotometer (UV–vis DRS), and X-ray photoelectron spectroscopy (XPS). The photocatalytic activities of all samples were evaluated based on the photocatalytic degradation of methylene blue (MB) under visible light irradiation. The results indicated that the photocatalytic activity of the CoFe2O4:BiVO4 nanocomposite with the mole ratio of 0.2:0.8 was higher than that of pure CoFe2O4 and pure BiVO4. The enhanced photocatalytic activity could be attributed to the formation of a composite, which suppressed the recombination of photogenerated electron-hole pairs. The formation of hydroxyl radicals (OH
• ) was found as the oxidizing reactive species to cause the degradation of the MB. Based on the results, a reasonable mechanism of photocatalysis on CoFe2O4/BiVO4 nanocomposite under visible light was proposed.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Materials Letters - Volume 181, 15 October 2016, Pages 86–91
نویسندگان
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