Visible-Light Photocatalytic Activity of Fe and/or Ni Doped Ilmenite Derived-Titanium Dioxide Nanoparticles

光催化 材料科学 X射线光电子能谱 锐钛矿 二氧化钛 兴奋剂 金红石 微晶 掺杂剂 可见光谱 纳米颗粒 核化学 无机化学 催化作用 化学工程 纳米技术 冶金 化学 工程类 生物化学 光电子学
作者
Ge Li,Baodong Wang,Qi Sun,Wayne-Qiang Xu,Yi‐Fan Han
出处
期刊:Journal of Nanoscience and Nanotechnology [American Scientific Publishers]
卷期号:19 (6): 3343-3355 被引量:7
标识
DOI:10.1166/jnn.2019.16123
摘要

Pure TiO 2 nanoparticles and ones doped with Fe and/or Ni were successfully prepared by a co-precipitation method from ilmenite. The samples were structurally characterized by XRD, XPS, FT-IR, UV-vis, SEM, EDX, AAS and BET measurement. The XRD results showed that all samples were anatase TiO 2 , and no characteristic peaks of dopants were observed. The crystallite sizes of all doped TiO 2 nanoparticles were less than 20 nm and doping TiO 2 with metal ions can suppress the crystal growth of the particles. The XRD and XPS results indicated that TiO 2 was uniformly doped and its crystalline phase was not changed by doping. The specific surface area of Fe–Ni/TiO 2 is bigger than that of the un-doped TiO 2 . The pore size and pore volume of Fe–Ni/TiO 2 is smaller than that of the un-doped. UV-vis spectra of the samples showed that the absorption edge red shifted with increasing doped metal content. The photocatalytic activity was evaluated in oxidative degradation of methylene blue (MB) with H 2 O 2 under visible light irradiation. When doped with a single type of transition metal, the photocatalytic performance of Ni-doped samples was lower than that of Fe-doped ones. For the co-doped catalysts, the catalytic efficiency of 0.5%Fe 4 %Ni/TiO 2 was the highest, reaching 93.34% after 250 min. Metal doping enhanced the photocatalytic decomposition of methylene blue compared with that of pure TiO 2 by up to 1.5 times. The synergistic effects of the two metal ions improved the photocatalytic performance. The particles exhibited pronounced activity in degradation of MB as well as efficient recyclability. The photocatalytic degradation mechanism of methylene blue was analyzed.

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