Syntheses of Novel Lanthanide Metal-Organic Frameworks for Highly Efficient Visible-Light-Driven Dye Degradation

被引:90
|
作者
Xia, Qiansu [1 ]
Yu, Xiaodan [1 ]
Zhao, Hongmei [1 ]
Wang, Siping [1 ]
Wang, Hong [2 ]
Guo, Zhifen [1 ]
Xing, Hongzhu [1 ]
机构
[1] Northeast Normal Univ, Coll Chem, Prov Key Lab Adv Energy Mat, Changchun 130024, Jilin, Peoples R China
[2] Jilin Prov Lin Chang Environm Technol Serv Co Ltd, Changchun 130012, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
COORDINATION POLYMERS; PHOTOCATALYTIC ACTIVITY; RADICAL POLYMERIZATION; IRON TEREPHTHALATE; WATER OXIDATION; REDUCTION; COMPLEXES; CATALYSTS; FORMATE; MOF;
D O I
10.1021/acs.cgd.7b00504
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Series of lanthanide metal-organic frameworks (Ln-MOFs) have been solvothermally synthesized using an anthracene-derived dicarboxylate ligand. The synthesized Ln-MOFs (Ce, Tb, Dy) show characteristics of broad-band visible-light absorption and efficient photoinduced charge generation. For the first time, Ln-MOFs have been employed as visible-light photocatalysts for rhodamine B (RhB) degradation in the presence of oxidant of hydrogen peroxide (H2O2). Results show that these Ln-MOFs are highly efficient for visible-light-driven RhB degradation in aqueous solution. The degradation reactions show notable reaction rate constants. It is interesting to observe that the premixing between Ln-MOFs and H2O2 is vital to improve photocatalytic performance, indicating the advantage of porous MOF catalysts. This study not only presents rare examples of visible-light-driven MOF photocatalysts constructed from lanthanide ions, but also reveals that the H2O2-involved advanced oxidation process is feasible for enhancing photocatalytic performance of aqueous dye degradation.
引用
收藏
页码:4189 / 4195
页数:7
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