4.7 Article

Effect of reaction temperature on structure and fluorescence properties of nitrogen-doped carbon dots

Journal

APPLIED SURFACE SCIENCE
Volume 387, Issue -, Pages 1236-1246

Publisher

ELSEVIER
DOI: 10.1016/j.apsusc.2016.07.048

Keywords

Nitrogen-free carbon dots; Nitrogen-doped carbon dots; Formation mechanism; Citric acid; Ammonia solution; Reaction temperaturea

Funding

  1. National Natural Science Foundation of China [21176169]
  2. International Science AMP
  3. Technology Cooperation Program of China [2012DFR50460]
  4. Shanxi Provincial Key Innovative Research Team in Science and Technology [2015013002-10]
  5. Shanxi Scholarship Council of China [2012-038]

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To investigate the effect of reaction temperature and nitrogen doping on the structure and fluorescence properties of carbon dots (CDs), six kinds of nitrogen-doped CDs (NCDs) were synthesized at reaction temperatures of 120, 140, 160, 180, 200 and 220 degrees C, separately, by using citric acid as carbon source and ammonia solution as nitrogen source. Nitrogen-free CDs (N-free CDs-180) was also prepared at 180 degrees C by using citric acid as the only carbon source for comparison. Results show that reaction temperature has obvious effect on carbonization degree, quantum yield (QY), ultraviolet-visible (UVvis) absorption and photoluminescence (PL) spectra but less effect on functional groups, nitrogen doping degree and fluorescence lifetime of NCDs. Compared with N-free CDs-180, NCDs-180 possesses enchanced QY and longer fluorescence lifetime. Doping nitrogen has obvious effect on UVvis absorption and PL spectra but less effect on particles sizes and carbonization degree. The formation mechanism of NCDs is explored: QY of NCDs depends largely on the number of fluorescent polymer chains (FPC), the competition between FPC formation on the surface of NCDs and carbon core growth leads to the change in number of FPC, and consequently to the NCDs with highest QY at appropriate hydrothermal temperature. (C) 2016 Elsevier B.V. All rights reserved.

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