4.7 Article

Two 2D uranyl coordination complexes showing effective photocatalytic degradation of Rhodamine B and mechanism study

期刊

CHINESE CHEMICAL LETTERS
卷 32, 期 2, 页码 604-608

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2020.11.044

关键词

Uranyl-organic frameworks; Photocatalytic degradation; Coordination complexes; Photocurrent; Mechanism

资金

  1. National Science Foundations of China [21461001]
  2. Project of Jiangxi Provincial Department of Education [GJJ170436, GJJ180367]
  3. Natural Science Foundation of the Jiangsu Higher Education Institutions of China [19JKB150007]
  4. Doctoral Scientific Research Foundation of East China University of Technology [DHBK2019143]

向作者/读者索取更多资源

Two new hydrostable two-dimensional uranyl coordination complexes were synthesized hydrothermally, with complex 2 showing better performance in photocatalytic degradation of RhB and more stable photocurrent density compared to complex 1, indicating stronger ability to separate photoexcited charge carriers.
Two new hydrostable two-dimensional (2D) uranyl coordination complexes [(UO2)(5)(mu(3)-O)(2)(nbca)(2)].7H(2)O (1) and [(UO2)(3)(nbca)(2)(H2O)(3)].2H(2)O (2) (H(3)nbca = 5-nitro-1,2,3-benzenetricarboxylic acid) were hydrothermal synthesized. Single-crystal structural refinements reveal that both of the two complexes were formed by the packing of 2D uranyl coordination sheets via the hydrogen bonds. The nbca ligand coordinating to the uranyl polyhedron centers constructed the 2D sheets. There are UO8 hexagonal bipyramids and UO7 pentagonal bipyramids in 1 while only UO7 pentagonal bipyramids in 2. Photocatalytic degradation of rhodamine B (RhB) in aqueous solution was studied. Complex 2 possesses better performance than 1 with 96.2 % of the RhB was degraded in only 60 min. Mechanism studies reveal that the dissolved oxygens are essential to the RhB degradation. The photocurrent density of 2 is more stable than that of 1, which indicating the stronger ability to separate photoexcited electrons and hole pairs of 2. (C) 2021 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.

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