首页> 外文期刊>Applied Surface Science >Ultra-trace (parts per million-ppm) W~(6+) dopant ions induced anatase to rutile transition (ART) of phase pure anatase TiO_2 nanoparticles for highly efficient visible light-active photocatalytic degradation of organic pollutants
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Ultra-trace (parts per million-ppm) W~(6+) dopant ions induced anatase to rutile transition (ART) of phase pure anatase TiO_2 nanoparticles for highly efficient visible light-active photocatalytic degradation of organic pollutants

机译:超痕量(百万分之几)的W〜(6+)掺杂离子可诱导相纯锐钛矿TiO_2纳米粒子从锐钛矿向金红石转变(ART),用于高效可见光活性光催化降解有机污染物

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A series of novel photocatalysts were synthesized by incorporating tungsten (W6(+)) ions in to the lattice of pure anatase TiO2 nanoparticles with ultra-trace concentrations (ppm) such as 10 ppm, 50 ppm, 90 ppm and 120 ppm using a simple one-step hydrothermal method under identical conditions. X-ray diffraction (XRD) studies, revealed a spectacular structural phase transformation from anatase to ruffle on doping and associated morphological changes are seen by scanning electron microscopy (SEM). The phase transformation is promoted with the increase of W concentration up to 50 ppm and inhibited thereafter. Microstructural lattice distortions due to the presence of W6(+) ions are monitored by high-resolution transmission electron microscopy (HR-TEM). The valence band X-ray photoelectron spectra (XPS), Ultraviolet photoelectron spectra (UPS) and UV-Vis absorption studies confirm the reduction of band gap for W doped TiO2 mixed phase nanoparticles. The doping causes an enhanced visible light absorption. Room temperature photoluminescence (PL) spectroscopy ensures an oxygen vacancy mediated phase transformation. The photocatalytic performances of the W doped TiO2 catalysts are evaluated for the degradation of Rhodamine B (RhB), Methylene blue (MB) and Methyl orange (MO) aqueous solutions under visible-light irradiation. The efficiency of photocatalytic degradation of the dyes gradually increased with the content of W6+ ions (fill 50 ppm) and then decreased which is consistent with the structural and optical studies. The control experiments, showed possible oxidative species, are hydroxyl (center dot OH-) and oxygen (center dot O-2(-)) radicals while the earlier plays a dominant role. The resuability tests performed for five cycles demonstrate high stability and reusability of the photocatalysts. A possible synergistic mechanism based on the impurity energy levels of W6(+) ions, oxygen vacancies and anatase-rutile heterojunction for the enhancement of the photocatalytic activity under visible-light irradiation is proposed.
机译:通过使用简单的方法将钨(W6(+))离子掺入具有超痕量浓度(ppm)(例如10 ppm,50 ppm,90 ppm和120 ppm)的纯锐钛矿型TiO2纳米颗粒的晶格中,合成了一系列新型光催化剂。相同条件下的一步水热法。 X射线衍射(XRD)研究表明,掺杂后从锐钛矿到皱纹具有惊人的结构相变,并且通过扫描电子显微镜(SEM)可以看到相关的形态变化。随着W浓度增加到50 ppm,相变得到促进,此后被抑制。通过高分辨率透射电子显微镜(HR-TEM)监测由于W6(+)离子的存在而引起的微晶格畸变。价带X射线光电子能谱(XPS),紫外光电子能谱(UPS)和UV-Vis吸收研究证实了W掺杂的TiO2混合相纳米粒子的带隙减小。掺杂导致增强的可见光吸收。室温光致发光(PL)光谱可确保氧空位介导的相变。评估了掺W的TiO2催化剂在可见光照射下若丹明B(RhB),亚甲基蓝(MB)和甲基橙(MO)水溶液的光催化性能。染料的光催化降解效率随着W6 +离子含量(填充50 ppm)而逐渐增加,然后降低,这与结构和光学研究一致。对照实验表明,可能的氧化物质为羟基(中心点OH-)和氧(中心点O-2(-))自由基,而更早的则起主导作用。进行了五个循环的可重用性测试证明了光催化剂的高稳定性和可重用性。提出了基于W6(+)离子的杂质能级,氧空位和锐钛矿-金红石型异质结的可能的协同机制,以提高可见光照射下的光催化活性。

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