4.7 Article

Engineering the nanoarchitecture and texture of polymeric carbon nitride semiconductor for enhanced visible light photocatalytic activity

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 401, 期 -, 页码 70-79

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2013.03.034

关键词

Carbon nitride; Pyrolysis of urea; Nanoarchitecture engineering; Texture; Visible light photocatalysis; Nitric oxide and RhB

资金

  1. Natural Science Foundation Project of CQ CSTC [cstc2012jjA20014]
  2. National Natural Science Foundation of China [51108487]
  3. Program for Young Talented Teachers in Universities of Chongqing Education Commission [[2011]65]
  4. Science and Technology Project from Chongqing Education Commission [KJ120701, KJTD201020, KJZH11214]
  5. National High Technology Research, Development Program (863 Program) of China [2010AA064905]
  6. Opening Project of Key Laboratory of Green Catalysis of Sichuan Institutes of High Education [LZJ1204]
  7. project from innovation team of environmental pollution control of CTBU

向作者/读者索取更多资源

In order to develop g-C3N4 for better visible light photocatalysis, g-C3N4 nanoarchitectures was synthesized by direct pyrolysis of cheap urea at 550 degrees C and engineered through the variation of pyrolysis time. By prolonging the pyrolysis time, the crystallinity of the resulted sample was enhanced, the thickness and size of the layers were reduced, the surface area and pore volume were significantly enlarged, and the band structure was modified. Especially for urea treated for 4 h, the obtained g-C3N4 nanosheets possessed high surface area (288 m(2)/g) due to the reduced layer thickness and the improved porous structure. A layer exfoliation and splitting mechanism was proposed to explain the gradual reduction of layer thickness and size of g-C3N4 nanoarchitectures with increased pyrolysis time. The as-synthesized g-C3N4 samples were applied for photocatalytic removal of gaseous NO and aqueous RhB under visible light irradiation. It was found that the activity of g-C3N4 was gradually improved as the pyrolysis time was prolonged from 0 min to 240 min. The enhanced crystallinity, reduced layer thickness, high surface area, large pore volume, enlarged band gap, and reduced number of defects were responsible for the activity enhancement of g-C3N4 sample treated for a longer time. As the precursor urea is very cheap and the synthesis method is facile template-free, the as-synthesized g-C3N4 nanoscale sheets could provide an efficient visible light driven photocatalyst for large-scale applications. (c) 2013 Elsevier Inc. All rights reserved.

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