Novel lanthanide coordination polymers based on mixed N,O-donor ligands and their visible-light-driven photocatalytic performance

被引:10
|
作者
Chen, Jun [1 ]
Kou, Weizhi [1 ]
He, Shunsheng [1 ]
Lin, Chenlan [1 ]
Wang, Xin [1 ]
Fu, Lianshe [2 ]
Yang, Ting-Hai [1 ]
机构
[1] Jiangsu Univ Technol, Sch Chem & Environm Engn, Jiangsu Lab Precious Met Proc Technol & Applicat, Changzhou 213001, Peoples R China
[2] Univ Aveiro, CICECO Aveiro Inst Mat, Dept Phys, P-3810193 Aveiro, Portugal
基金
中国国家自然科学基金;
关键词
Lanthanides; Coordination polymers; Photocatalytic degradation; Pyrazole carboxylic acid; Rare earths; METAL-ORGANIC FRAMEWORKS; CRYSTAL-STRUCTURES; DEGRADATION; DYE;
D O I
10.1016/j.jre.2022.01.004
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In the present work, we prepared three isostructural lanthanide (Ln) coordination polymers (CPs), namely [Ln (Hhpc) (phen) (NO3)] (Ln = Gd (1), La (2), Y (3), H(3)hpc = 5-hydroxy-1H-pyrazole-3-carboxylic acid, phen = 1,10-phenanthroline) by hydrothermal method. Their structures were characterized by single crystal X-ray diffraction, Fourier transform infrared spectrum, elemental analysis, powder X-ray diffraction and thermal gravimetric analysis. CPs 1-3 are isostrutural and exhibit two-dimensional (2D) wavy layered structure constructed from inorganic chains, in which equivalent eight coordinated Ln(3+) ions are linked through carboxylate groups. The three dimensional supramolecular structure is further formed by hydrogen bonding. The photocatalytic experiments show that CPs 2 and 3 exhibit good photocatalytic performances under visible light in degradation of methylene blue organic dye. The photocatalytic degradation efficiencies in 90 min are about 86.19% and 93.60% for CPs 2 and 3, respectively. The photocatalytic degradation mechanisms have been proposed through photoelectrochemical and trapping radical experiments. (c) 2022 Chinese Society of Rare Earths. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:85 / 90
页数:6
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