4.7 Article

Highly sensitive fluorescence sensor for mercury(II) based on boron- and nitrogen-co-doped graphene quantum dots

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 566, 期 -, 页码 357-368

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2020.01.092

关键词

Boron- and nitrogen-co-doped graphene quantum dots; Graphene oxide; Absolute photoluminescence quantum yield; Fluorescence sensor; Mercury ions

资金

  1. National Natural Science Foundation of China [51262027]
  2. State Key Laboratory of Solidification Processing in NWPU [SKLSP201754]
  3. Science and Technology Project Gansu Province [17JR5RA082]
  4. Research Project of Higher Education in Gansu Province [2017A-002]

向作者/读者索取更多资源

In this work, we invented a new method to synthesize boron- and nitrogen-co-doped graphene quantum dots (B, N-GQDs). This synthesis method was more reliable, simple, and environmentally friendly than the bottom-up methods reported in the current literature that use citric acid or other organic materials as the carbon source. Instead, B, N-GQDs were synthesized from graphene oxide (GO) by a top-down method. The obtained B, N-GQDs showed a bright blue luminescence under a UV lamp at 365 nm, and the absolute photoluminescence quantum yield (PLQY) was 5.13%. Because mercury(II) ions (Hg2+) are highly toxic and can seriously affect the ecological environment and human health, the detection of low-concentration Hg2+ and the establishment of rapid, accurate and sensitive methods for detecting Hg2+. are of great significance to the activities of life, including those of humans. Therefore, using the good luminescence properties of B, N-GQDs, we invented a new type of fluorescence sensor that can detect Hg2+. The sensor was very sensitive to Hg2+, had a good linear relationship in the concentration range of 0.2-1 mu M, and exhibited a minimum limit of detection of 6.4 nM. Furthermore, this approach was successfully applied to the detection of Hg2+ in real environmental water samples. (C) 2020 Elsevier Inc. All rights reserved.

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