4.4 Article

Improving Photoelectrochemical Performance of PbX (X=S, Se, Te) thin Films by Electro-oxidation for Cu2+ Detection

Journal

INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE
Volume 15, Issue 12, Pages 11976-11985

Publisher

ESG
DOI: 10.20964/2020.12.38

Keywords

Photoelectrochemical performance; Electro-oxidation; PbSe; Se; Cu2+ Detection

Funding

  1. National Natural Science Foundation of China [22064008]
  2. State Key Program of National Natural Science Foundation of China [51638006]
  3. Guangxi Natural Science Foundation [2017GXNSFAA198340]
  4. project of the high-level innovation team and outstanding scholar in the Guangxi colleges and universities
  5. Guangxi Colleges and Universities Key Laboratory of Food Safety and Detection, Guangxi Key Laboratory of Electrochemical and Magnetochemical Functional Materials
  6. Guangxi Key Laboratory of Environmental Pollution Control Theory and Technology

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This paper proposes an electro-oxidation method to improve the photoelectrochemical performance of PbX (X=S, Se, Te) thin films electrodeposited onto indium tin oxide (ITO)-coated glass. The PbX/ITO electrode was electro-oxidized using cyclic voltammetry scanning in the potential range of 0-1 V in NaNO3 solution. The photocurrent enhancement was observed in the electro-oxidized PbS/ITO, Pb Se/ITO, PbTe/ITO electrodes. Among these three electrodes, the electro-oxidized Pb Se/ITO electrode exhibited the strongest, most stable and reproducible photocurrent. The morphology and composition of the electro-oxidized Pb Se/ITO electrode were investigated by scanning electron microscopy (SEM) and X-ray powder diffraction (XRD). These results indicate that Se was formed on the surface of the PbSe thin film after the electro-oxidation. The enhancement of photocurrent of the Pb Se/ITO electrode could be attributed to the formation of Se-PbSe interface. In a HAc-NaAc buffer solution (pH 5.0), the SePb Se/ITO electrode exhibited a good photocurrent response to Cu2+ ions, with a dynamic range from 10 nM to 100 mu M and the limit of detection of 1.2 nM. The common metal ions at 100 times excess to Cu2+ (10 nM) did not interfere with the detection of Cu2+ within an error of 10%. The proposed method was applied for the detection of Cu2+ in municipal tap, river, and pond water samples, and the results are consistent with those obtained by atomic absorption spectrometry (AAS).

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