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

机译:过渡金属离子mn2 +,Ni2 +和Zn2 +掺杂多晶二氧化钛在紫外/太阳光下降解苯胺蓝的光催化活性增强

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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 rutile. 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. © 2010 Elsevier B.V.
机译:锐钛矿型TiO2掺杂了二价过渡金属离子,如Mn2 +,Ni2 +和Zn2 +,并通过各种分析技术进行了表征。粉末X射线衍射揭示了掺杂Ni2 +和Zn2 +的样品的锐钛矿相稳定,而由于包含Mn2 +,促进了从锐钛矿到金红石的相变。金红石分数随Mn2 +浓度的增加而增加,这是由于表面氧空位的产生所致。所有掺杂的催化剂在带隙吸收中显示出红移到可见光区域。在紫外线/太阳光下苯胺蓝(AB)的降解中评估了这些催化剂的光催化活性。在光催化剂中,Mn2 +(0.06 at。)-TiO2显示出增强的活性,这归因于锐钛矿和金红石双晶构架中的协同作用。此外,Mn2 +的独特的半填充电子结构充当电荷载流子的浅陷阱,以增强光催化活性。考虑到先前模型的理论,探索了锐钛矿和金红石混合相中界面电荷转移的机理。 ©2010 Elsevier B.V.

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