Abstract <p>Monitoring of heavy metal ions Pb<sup>2+</sup> is a meaningful topic due to their high toxicity and serious damage on human health and ecological environment. In this paper, iron doped polymeric dopamine micro/nanospheres modified glassy carbon electrodes (Fe@PDA/GCE) were prepared and for the first time applied in heavy metal Pb<sup>2+</sup> detection. Differential pulse voltammetry (DPV) method was used for the quantitative determination of lead. The results showed that Fe@PDA/GCE exhibited excellent detection performance for Pb<sup>2+</sup>, with a wide concentration response linear range of 0.05–110 μM (10.4–22 792 μg L<sup>–1</sup>) and a low detection limit of 2.9 nM (0.6 μg L<sup>–1</sup>) (S/N = 3). This performance is comparable to or even superior to the reported electrochemical platforms for Pb<sup>2+</sup> determination. We attributed the improvement to the enrichment effect and charge transfer ability of Fe@PDA toward Pb<sup>2+</sup>. Fe@PDA/GCE also shared many advantages such as good reproducibility, anti-interference capability and low cost, allowing actual samples detection with recovery 95.9–104.0% and RSD 1.8–2.2%. Therefore, the Fe@PDA/GCE electrochemical sensors have good application prospect in water environment monitoring.</p>

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Preparation of Iron Doped Polymeric Dopamine Micro/Nanosphere and Its Application in Lead Ion Electrochemical Sensing

  • Hong Sun,
  • Chuan Yao,
  • Shixing Zhang,
  • Haiyan Xiong,
  • Kaibo You,
  • Shicheng Wang,
  • Junyan Wang,
  • Kejun Guo,
  • Leipin Shi,
  • Junqi Zhou

摘要

Abstract

Monitoring of heavy metal ions Pb2+ is a meaningful topic due to their high toxicity and serious damage on human health and ecological environment. In this paper, iron doped polymeric dopamine micro/nanospheres modified glassy carbon electrodes (Fe@PDA/GCE) were prepared and for the first time applied in heavy metal Pb2+ detection. Differential pulse voltammetry (DPV) method was used for the quantitative determination of lead. The results showed that Fe@PDA/GCE exhibited excellent detection performance for Pb2+, with a wide concentration response linear range of 0.05–110 μM (10.4–22 792 μg L–1) and a low detection limit of 2.9 nM (0.6 μg L–1) (S/N = 3). This performance is comparable to or even superior to the reported electrochemical platforms for Pb2+ determination. We attributed the improvement to the enrichment effect and charge transfer ability of Fe@PDA toward Pb2+. Fe@PDA/GCE also shared many advantages such as good reproducibility, anti-interference capability and low cost, allowing actual samples detection with recovery 95.9–104.0% and RSD 1.8–2.2%. Therefore, the Fe@PDA/GCE electrochemical sensors have good application prospect in water environment monitoring.