synthesis and characterization of mn–c–codoped nanoparticles and photocatalytic degradation of methyl orange dye under sunlight irradiationmn-c-codoped纳米粒子的合成与表征及光催化降解甲基橙染料在阳光照射.pdfVIP
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synthesis and characterization of mn–c–codoped nanoparticles and photocatalytic degradation of methyl orange dye under sunlight irradiationmn-c-codoped纳米粒子的合成与表征及光催化降解甲基橙染料在阳光照射
Hindawi Publishing Corporation
International Journal of Photoenergy
Volume 2012, Article ID 767905, 7 pages
doi:10.1155/2012/767905
Research Article
Synthesis and Characterization of Mn–C–Codoped TiO2
Nanoparticles and Photocatalytic Degradation of Methyl Orange
Dye under Sunlight Irradiation
Wei Xin, Duanwei Zhu, Guanglong Liu, Yumei Hua, and Wenbing Zhou
Laboratory of Plant Nutrition and Ecological Environment Research,
Centre for Microelement Research of Huazhong Agricultural University, Wuhan 430070, China
Correspondence should be addressed to Guanglong Liu, liugl0924@
Received 25 July 2012; Revised 5 September 2012; Accepted 5 September 2012
Academic Editor: Jiaguo Yu
Copyright © 2012 Wei Xin et al. This is an open access article distributed under the Creative Commons Attribution License, which
permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Novel visible-light-active Mn–C–TiO2 nanoparticles were synthesized by modified sol-gel method based on the self-assembly tech-
nique using polyoxyethylenes orbitan monooleate (Tween 80) as template and carbon precursor and manganese acetate as man-
ganese precursor. The samples were characterized by XRD, FTIR, UV-vis diffuse reflectance, XPS, and laser particle size analysis.
The XRD results showed that Mn–C–TiO2 sample exhibited anatase phase and no other crystal phase was identified. High specific
surface area, small crystallite size, and small particle size distribution could be obtained by manganese and carbon codoped and
Mn–C–TiO exhibited greater red shift in absorption edge of samples in visible region than that of C–TiO and pure TiO . The
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