4.7 Article

Graphitic carbon nitride quantum dots in situ coupling to Bi2MoO6 nanohybrids with enhanced charge transfer performance and photoelectrochemical detection of copper ion

Journal

JOURNAL OF ELECTROANALYTICAL CHEMISTRY
Volume 787, Issue -, Pages 66-71

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jelechem.2017.01.042

Keywords

Carbon nitride; Quantum dots; Bi2MoO6; Photoelectrochemical performances

Funding

  1. National Natural Science Foundation of China [21175061, 21375050, 21505055]
  2. Science Foundation of Jiangsu Province [BK20150486]
  3. Foundation of Jiangsu University [15JDG145]
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions [PAPD-2014-37]
  5. Qing Lan Project
  6. State Key Laboratory of Analytical Chemistry for Life Science [SKLACLS1504]

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Graphitic carbon nitride (g-C3N4) based nanohybrids have drawn considerable attentions due to superior performances. However, the photoactivity of bulk g-C3N4 is limited due to the recombination of its photogenerated electron-hole pairs. Graphitic carbon nitride quantum dots (g-CNQDs), as a newly developed semiconductor, are easily prepared and possess good stability, water-solubility and electronic properties. In this work, we explored the fabrication of nanohybrids by in situ coupling of g-CNQDs and Bi2MoO6 nanoparticles (NPs). The as prepared nanohybrids displayed nearly 3-fold and 6-fold enhanced photocurrent intensity than pure g-CNQDs and Bi2MoO6 NPs. This improvement was attributed to the accelerated charge transfer from the conduction band of g-CNQDs to that of Bi2MoO6. Based on the excellent photoelectrochemical (PEC) performances, the nanohybrids were successfully applied in the construction of Cu2+ PEC sensor. Under optimal conditions, the resulting sensor showed good performances with a wide linear range from 3 nM to 40 mu M and a good selectivity, which indicated that g-CNQDs/Bi2MoO6 nanohybrids could serve as a promising photoactive material for PEC sensing. (C) 2017 Elsevier B.V. All rights reserved.

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