Li Ge, Wang Bao-Dong, Sun Qi, Xu Wayne-Qiang, Han Yi-Fan
National Institute of Clean-and-Low-Carbon Energy, Beijing 102211, China.
State Key Laboratory of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, China.
J Nanosci Nanotechnol. 2019 Jun 1;19(6):3343-3355. doi: 10.1166/jnn.2019.16123.
Pure TiO₂ 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 TiO₂, and no characteristic peaks of dopants were observed. The crystallite sizes of all doped TiO₂ nanoparticles were less than 20 nm and doping TiO₂ with metal ions can suppress the crystal growth of the particles. The XRD and XPS results indicated that TiO₂ was uniformly doped and its crystalline phase was not changed by doping. The specific surface area of Fe-Ni/TiO₂ is bigger than that of the un-doped TiO₂. The pore size and pore volume of Fe-Ni/TiO₂ 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 H₂O₂ 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%Fe₄%Ni/TiO₂ was the highest, reaching 93.34% after 250 min. Metal doping enhanced the photocatalytic decomposition of methylene blue compared with that of pure TiO₂ 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.
采用共沉淀法从钛铁矿中成功制备了纯TiO₂纳米颗粒以及掺杂了铁和/或镍的TiO₂纳米颗粒。通过XRD、XPS、FT-IR、UV-vis、SEM、EDX、AAS和BET测量对样品进行了结构表征。XRD结果表明,所有样品均为锐钛矿型TiO₂,未观察到掺杂剂的特征峰。所有掺杂TiO₂纳米颗粒的晶粒尺寸均小于20 nm,金属离子掺杂TiO₂可抑制颗粒的晶体生长。XRD和XPS结果表明,TiO₂被均匀掺杂,掺杂后其晶相未发生变化。Fe-Ni/TiO₂的比表面积大于未掺杂的TiO₂。Fe-Ni/TiO₂的孔径和孔体积小于未掺杂的TiO₂。样品的UV-vis光谱表明,随着掺杂金属含量的增加,吸收边发生红移。在可见光照射下,以H₂O₂氧化降解亚甲基蓝(MB)来评估光催化活性。当掺杂单一类型的过渡金属时,Ni掺杂样品的光催化性能低于Fe掺杂样品。对于共掺杂催化剂,0.5%Fe₄%Ni/TiO₂的催化效率最高,250分钟后达到93.34%。与纯TiO₂相比,金属掺杂使亚甲基蓝的光催化分解增强了1.5倍。两种金属离子的协同效应提高了光催化性能。这些颗粒在MB降解中表现出显著活性以及高效的可回收性。分析了亚甲基蓝的光催化降解机理。