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Photo catalytic degradation of imidachloprid under solar light using metal ion doped TiO2 nano particles: Influence of oxidation state and electronic configuration of dopants

机译:金属离子掺杂TiO2纳米粒子在太阳光下光催化降解吡虫啉:氧化态和掺杂剂电子构型的影响

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摘要

Anatase TiO2 was doped with metal ions like Th4+, V5+ and Mo6+ and tested for the degradation of imidachloprid under solar light. X-ray diffraction results inferred that all the dopants stabilized the anatase phase irrespective of their nature, oxidation state and ionic size. The undoped and transition metal ion doped TiO2 were completely transformed to rutile phase at 700 °C while rare earth Th4+ doped sample completely transformed to rutile phase at 1,000 °C. The rare earth dopant stabilized the anatase phase by hindering the growth of crystallite size. Among the photo catalysts used, Th4+ (0.06)-TiO2 showed highest activity and its efficiency was 2.8 times higher than that of Degussa P-25. The Th4+ ion lowered the band gap of TiO2 to 2.6 and 2.5 eV facilitating solar light absorption. Detrapping of the trapped charge carriers depends on electronic configuration and the oxidation state of the dopants.
机译:锐钛矿型TiO2掺杂有Th4 +,V5 +和Mo6 +等金属离子,并在太阳光下测试了吡虫啉的降解。 X射线衍射结果表明,所有掺杂剂均稳定了锐钛矿相,而与它们的性质,氧化态和离子尺寸无关。未掺杂和过渡金属离子掺杂的TiO2在700°C时完全转变成金红石相,而稀土Th4 +掺杂的样品在1,000°C时完全转变成金红石相。稀土掺杂剂通过阻碍晶粒尺寸的增长来稳定锐钛矿相。在所用的光催化剂中,Th4 +(0.06)-TiO2表现出最高的活性,其效率是Degussa P-25的2.8倍。 Th4 +离子将TiO2的带隙降低到2.6和2.5 eV,促进了太阳光的吸收。被俘获的载流子的去俘获取决于电子结构和掺杂剂的氧化态。

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