Facile synthesis of N-doped TiO2 nanoparticles caged in MIL-100(Fe) for photocatalytic degradation of organic dyes under visible light irradiation

被引:90
作者
Huang, Jie [1 ]
Song, Haiyan [1 ]
Chen, Chunxia [1 ]
Yang, Yi [1 ]
Xu, Ningdi [1 ]
Ji, Xinzhen [1 ]
Li, Chunyu [1 ]
You, Jiang-An [1 ]
机构
[1] Northeast Forestry Univ, Coll Sci, Dept Chem, 26 Hexing Rd, Harbin 150040, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
N-TiO2; MIL-100(Fe); Caging; Photocatalytic degradation; Dyes; AZO-DYE; ADSORPTION; WATER; OXIDATION; FRAMEWORK; REMOVAL; HYBRID; PHARMACEUTICALS; NANOCOMPOSITE; CONVERSION;
D O I
10.1016/j.jece.2017.05.012
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A metal-organic frameworks (MOFs) matrix of MIL-100(Fe) loading N-doped TiO2 (N-TiO2) nanoparticles as a novel photocatalyst was successfully synthesized by a facile two-step strategy including preparation of neutral NTiO2 sol and caging N-TiO2 nanoparticles. The as-synthesized samples were characterized by a series of techniques including XRD, ICP, BET, UV-vis, XPS and TEM. Photocatalytic activity of the samples was assessed based on degradation of methylene blue or rhodamine B dye in model wastewater under visible-light irradiation. The as-synthesized samples essentially maintain the typical MOFs structure and porous property of MIL-100(Fe), which exhibits well confinement effect on TiO2 nanoparticles. A significant finding is that the quantum dots-like N-TiO2 nanoparticles (< 2 nm) with an appropriate mass percentage of 32% highly disperse in cages of MIL100(Fe) with 1.9 nm of pore size and obtain narrowed band gap. But agglomeration of N-TiO2 nanoparticles occurs as TiO2 content increases to 50%. Meanwhile, nitrogen atoms are successfully incorporated into the TiO2 lattice. The optimal catalyst obtains 99.1% and 93.5% of final removal rate, respectively for methylene blue and rhodamine B, presenting the enhanced photocatalytic performance by comparison with the pure MIL-100(Fe). The composite exhibits more excellent sedimentation efficiency and reusability than pure N-TiO2. A possible mechanism of the photocatalysis process is presented in detail.
引用
收藏
页码:2579 / 2585
页数:7
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