4.7 Article

Band Engineering and Morphology Control of Oxygen-Incorporated Graphitic Carbon Nitride Porous Nanosheets for Highly Efficient Photocatalytic Hydrogen Evolution

期刊

NANO-MICRO LETTERS
卷 13, 期 1, 页码 -

出版社

SHANGHAI JIAO TONG UNIV PRESS
DOI: 10.1007/s40820-020-00571-6

关键词

Graphitic carbon nitride nanosheet; Hollow morphology; Oxygen incorporating; Multiple thermal treatment; Photocatalytic hydrogen evolution

资金

  1. National Science Foundation of China [51772152, 51702129, 51572114, 51972150, 21908110, 51902161]
  2. Fundamental Research Funds for the Central Universities [30919011269, 30919011110, 1191030558]
  3. Key University Science Research Project of Jiangsu province [16KJB430009]
  4. Postdoctoral Science Foundation [2018M630527]
  5. China Scholarship Council [201708320150]
  6. Natural Science Foundation of Jiangsu Province [BK20190479, 1192261031693]

向作者/读者索取更多资源

Hollow oxygen-incorporated g-C3N4 nanosheet (OCN) with improved surface area was successfully fabricated by multiple thermal treatments. The OCN exhibited excellent photocatalytic hydrogen evolution activity.
Graphitic carbon nitride (g-C3N4)-based photocatalysts have shown great potential in the splitting of water. However, the intrinsic drawbacks of g-C3N4, such as low surface area, poor diffusion, and charge separation efficiency, remain as the bottleneck to achieve highly efficient hydrogen evolution. Here, a hollow oxygen-incorporated g-C3N4 nanosheet (OCN) with an improved surface area of 148.5 m(2) g(-1) is fabricated by the multiple thermal treatments under the N-2/O-2 atmosphere, wherein the C-O bonds are formed through two ways of physical adsorption and doping. The physical characterization and theoretical calculation indicate that the O-adsorption can promote the generation of defects, leading to the formation of hollow morphology, while the O-doping results in reduced band gap of g-C3N4. The optimized OCN shows an excellent photocatalytic hydrogen evolution activity of 3519.6 mu mol g(-1) h(-1) for similar to 20 h, which is over four times higher than that of g-C3N4 (850.1 mu mol g(-1) h(-1)) and outperforms most of the reported g-C3N4 catalysts.

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