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In Situ Synthesis of Gold Nanoparticles without Aggregation in the Interlayer Space of Layered Titanate Transparent Films
Published on: January 17, 2017
Ta3N5 nanoparticles with enhanced photocatalytic efficiency under visible light irradiation
1State Key Lab of High Performance Ceramics and Superfine Microstructures, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, People's Republic of China.
Abstract:
Nanocrystalline Ta(3)N(5) particles with a surface area of more than 33 m(2)/g were synthesized by nitridation of nanosized Ta(2)O(5) particles using NH(3) as the reactant gas. It was found that nanocrystalline Ta(2)O(5) was converted into Ta(3)N(5) completely (by X-ray diffraction, XRD) at 700 degrees C within 5.0 h, which was much lower than the temperature 900 degrees C for the complete nitridation of micrometer-sized Ta(2)O(5) powder. The oxide precursor and the resulting nitride were characterized by XRD analysis, transmission electron microscopy, UV-vis diffuse reflectance spectra, and BET surface area techniques. The nitrogen contents in the prepared Ta(3)N(5) powders were quantitatively determined with a CHN elemental analyzer. Nanocrystalline Ta(3)N(5) showed an absorption edge of around 600 nm, and Ta(3)N(5) in the size of about 26 nm exhibited a blue shift of 15 nm in the adsorption edge. The photocatalytic activity of the prepared Ta(3)N(5) under UV-vis and visible light irradiation was compared to that of nanocrystalline TiO(2-x)N(x) using the photocatalytic degradation of methylene blue (MB) as a model reaction. The Ta(3)N(5) nanoparticles showed the significantly enhanced photocatalytic activity for the degradation of MB in comparison with the larger-sized Ta(3)N(5). Moreover, the nanocrystalline Ta(3)N(5) showed much higher photocatalytic activity under visible light irradiation compared with TiO(2-x)N(x) in the same size.
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