Enhanced photocatalytic activity of transition metal ions Mn2+, Ni2+ and Zn2+ doped polycrystalline titania for the degradation of Aniline Blue under UV/solar light

被引:194
作者
Devi, L. Gomathi [1 ]
Kottam, Nagaraju [1 ]
Murthy, B. Narasimha [1 ]
Kumar, S. Girish [1 ]
机构
[1] Bangalore Univ, Cent Coll City Campus, Dept Post Grad Studies Chem, Bangalore 560001, Karnataka, India
关键词
Transition metal ion doped TiO2; Synergistic effect in the bicrystalline framework; Electronic configuration of dopant; Photocatalysis under UV/solar light; Aniline Blue; PHASE-TRANSFORMATION; TIO2; NANOPARTICLES; MESOPOROUS TIO2; DINITROGEN PHOTOREDUCTION; BICRYSTALLINE FRAMEWORK; HYDROTHERMAL SYNTHESIS; HOLLOW MICROSPHERES; LOW-TEMPERATURE; SIZED TIO2; ANATASE;
D O I
10.1016/j.molcata.2010.05.021
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Anatase TiO2 was doped with divalent transition metal ions like Mn2+, Ni2+ and Zn2+ and characterized by various analytical techniques. Powder X-ray diffraction revealed stabilization of anatase phase for Ni2+ and Zn2+ doped samples, while phase transformation from anatase to rutile was promoted due to Mn2+ inclusion. The rutile fraction increased with Mn2+ concentration due to the creation of surface oxygen vacancies. All the doped catalysts showed red shift in the band gap absorption to the visible region. The photocatalytic activities of these catalysts were evaluated in the degradation of Aniline Blue (AB) under UV/solar light. Among the photocatalysts, Mn2+ (0.06 at.%)-TiO2 showed enhanced activity, which is attributed to the synergistic effect in the bicrystalline framework of anatase and ruble. Further the unique half filled electronic structure of Mn2+ serves as a shallow trap for the charge carriers to enhance the photocatalytic activity. An insight to the mechanism of interfacial charge transfer in the mixed phase of anatase and rutile is explored, taking into consideration the theories of previous models. (C) 2010 Published by Elsevier B.V.
引用
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页码:44 / 52
页数:9
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