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Defect Formation in Surface Modified TiO_2 Nanostructures

机译:表面改性的TiO_2纳米结构中的缺陷形成

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The defect formation in surface modified TiO_2 has been studied. Anatase TiO_2 structures in the 3-20 nm range formed by a wet chemical technique were surface modified and nitridation of the highly reactive TiO_2 nanocolloid surface was achieved by a quick and simple treatment in alkyl ammonium compounds. The nitriding process was also accompanied by a metal surface coating process using electroless plating techniques, resulting in a thin metal surface layer on the modified TiO_2 nanostructures. The crystal structure of the resultant TiO_(2-x)N_x nano-colloids remained anatase and the freshly prepared samples exhibited a strong light emission near 560nm (2.21 eV), which red shifted to 660 nm (1.88 eV) and dropped in intensity with aging in the atmosphere. This behavior was also evident in some of the combined nitridized and metal coated TiO_2 nano-colloids. Electron Spin Resonance performed on these samples identified a resonance at g = 2.0035, which increased significantly with nitridation. This resonance is attributed to an oxygen hole center created near the surface of the nanocolloid, which correlates well with the observed optical activity.
机译:研究了表面改性TiO_2中缺陷的形成。对通过湿化学技术形成的3-20 nm范围内的锐钛矿型TiO_2结构进行了表面改性,并通过在烷基铵化合物中进行快速简单的处理实现了高反应性TiO_2纳米胶体表面的氮化。氮化过程还伴随着使用化学镀技术的金属表面涂覆过程,从而在改性的TiO_2纳米结构上产生了一层薄的金属表面层。所得TiO_(2-x)N_x纳米胶体的晶体结构保持为锐钛矿型,新鲜制备的样品在560nm(2.21 eV)附近显示出强光发射,红色移至660 nm(1.88 eV),强度随在大气中老化。这种行为在某些氮化和金属包覆的TiO_2纳米胶体中也很明显。在这些样品上进行的电子自旋共振确定了在g = 2.0035的共振,该共振随氮化而显着增加。该共振归因于在纳米胶体表面附近产生的氧孔中心,该氧孔中心与观察到的光学活性很好地相关。

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