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Photocatalytic activity of TiO_2 doped with Zn~(2+) and V~(5+) transition metal ions: Influence of crystallite size and dopant electronic configuration on photocatalytic activity

机译:Zn〜(2+)和V〜(5+)过渡金属离子掺杂的TiO_2的光催化活性:微晶尺寸和掺杂剂电子构型对光催化活性的影响

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Anatase TiO_2 was prepared by sol-gel method through the hydrolysis of titanium tetrachloride and doped with transition metal ions like V~(5+) and Zn~(2+). The photocatalysts were characterized by various analytical techniques. Powder X-ray diffraction studies revealed only anatase phase for the doped samples. The band gap absorption for the doped samples showed red shift to the visible region (~456nm) as confirmed by UV-vis absorption spectroscopy and diffuse reflectance spectral studies. The surface area of the Zn~(2+) doped samples were higher than the V~(5+) doped samples as observed by BET surface area measurements due to their smaller crystallite size. Scanning electron microscopy showed almost similar morphology, while energy dispersive X-ray analysis confirmed the presence of dopant in the TiO_2 matrix. The photocatalytic activities of these catalysts were tested for the degradation of Congo Red under solar light. Although both the doped samples showed similar red shift in the band gap, Zn~(2+) (0.06at.%) doped TiO_2 showed enhanced activity and its efficiency was five fold higher compared to Degussa P-25 TiO_2. This enhanced activity was attributed to smaller crystallite size and larger surface area. Further completely filled stable electronic configuration (d~(10)) of Zn~(2+) shallowly traps the charge carriers and detraps the same to the surface adsorbed species thereby accelerating the interfacial charge transfer process.
机译:通过四氯化钛的水解,溶胶-凝胶法制备了锐钛矿型TiO_2,并掺杂了过渡金属离子V〜(5+)和Zn〜(2+)。通过各种分析技术对光催化剂进行了表征。粉末X射线衍射研究表明,掺杂样品仅具有锐钛矿相。紫外可见吸收光谱和漫反射光谱研究证实,掺杂样品的带隙吸收显示红移至可见区(〜456nm)。通过BET表面积测量观察到,掺杂Zn〜(2+)的样品的表面积比掺杂V〜(5+)的样品的表面积高,因为它们的晶粒尺寸较小。扫描电子显微镜显示了几乎相似的形态,而能量色散X射线分析证实了TiO_2基质中存在掺杂剂。测试了这些催化剂的光催化活性对刚果红在太阳光下的降解。尽管两种掺杂样品在带隙中都显示出类似的红移,但是Zn〜(2+)(0.06at。%)掺杂的TiO_2显示出增强的活性,其效率是Degussa P-25 TiO_2的五倍。这种增强的活性归因于较小的微晶尺寸和较大的表面积。 Zn〜(2+)的进一步完全填充的稳定电子构型(d〜(10))浅地俘获了电荷载流子,并将其释放到表面吸附的物质上,从而加速了界面电荷转移过程。

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