4.7 Article

A carbon-rich g-C3N4 with promoted charge separation for highly efficient photocatalytic degradation of amoxicillin

期刊

CHINESE CHEMICAL LETTERS
卷 32, 期 9, 页码 2787-2791

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2021.01.012

关键词

Carbon-rich g-C3N4; Photocatalysis; Built-in electron field; Charge separation

资金

  1. National Natural Science Foundation of China [41807340]
  2. National Key R&D Program of China [2019YFC0408200, 2016YFC0402505]
  3. National Water Pollution Control and Treatment Science and Technology Major Project [2017ZX07207002]

向作者/读者索取更多资源

A novel carbon-rich g-C3N4 nanosheets with large surface area were prepared by thermal polymerization method, exhibiting superior photocatalytic activity for amoxicillin degradation. Radical quenching experiments, intermediates analysis, and DFT calculation were used to propose the contaminant degradation mechanism. Reusing experiments demonstrated the material's high stability and applicability for pollutants treatment under various water matrix parameters.
A novel carbon-rich g-C3N4 nanosheets with large surface area was prepared by facile thermal polymerization method using urea and 1,3,5-cyclohexanetriol. Plenty of carbon-rich functional groups were introduced into the surface layers of g-C3N4, which constructed the built-in electric field (BIEF) and resulted in improved charge separation; therefore, the carbon-rich g-C3N4 displayed superior photocatalytic activity for amoxicillin degradation under solar light. The contaminant degradation mechanism was proposed based on radical quenching experiments, intermediates analysis and density functional theory (DFT) calculation. Moreover, the reusing experiments showed the high stability of the material, and the amoxicillin degradation under various water matrix parameters indicated its high applicability on pollutants treatment, all of which demonstrated its high engineering application potentials. (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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