Journal
INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE
Volume 15, Issue 12, Pages 11976-11985Publisher
ESG
DOI: 10.20964/2020.12.38
Keywords
Photoelectrochemical performance; Electro-oxidation; PbSe; Se; Cu2+ Detection
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Funding
- National Natural Science Foundation of China [22064008]
- State Key Program of National Natural Science Foundation of China [51638006]
- Guangxi Natural Science Foundation [2017GXNSFAA198340]
- project of the high-level innovation team and outstanding scholar in the Guangxi colleges and universities
- Guangxi Colleges and Universities Key Laboratory of Food Safety and Detection, Guangxi Key Laboratory of Electrochemical and Magnetochemical Functional Materials
- 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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