Doping effect of Europium (Eu3+) on flower-like ZnO nanostructures: shape variations, optical properties and its applicability in electrochemical sensing of heavy metal (Lead) ion detection

Hydrothermal synthesis has been effectively used to create pure and Europium (Eu 3+ ) doped (1, 3 & 5%) ZnO nanostructures. The as-synthesized structures were analyzed using a range of spectroscopic and microscopic techniques such as X-ray, UV–Vis, FTIR, PL, and SEM analysis. It was discovered t...

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Veröffentlicht in:Applied physics. A, Materials science & processing Materials science & processing, 2024-04, Vol.130 (4), Article 217
Hauptverfasser: Tahir, Asma, Want, Basharat
Format: Artikel
Sprache:eng
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Zusammenfassung:Hydrothermal synthesis has been effectively used to create pure and Europium (Eu 3+ ) doped (1, 3 & 5%) ZnO nanostructures. The as-synthesized structures were analyzed using a range of spectroscopic and microscopic techniques such as X-ray, UV–Vis, FTIR, PL, and SEM analysis. It was discovered that the shape of the fabricated flower-like ZnO nanostructures made of mixed compact clustered nanorods could be meticulously governed by changing the Eu 3+ dopant amount within the desired threshold. The distinctive photoluminescence (PL) properties indicate that energy is transferred from excited ZnO material, precisely at its band-gap (3.17 eV), to the Eu 3+ states through the luminescent defects present in the nanoparticles. Considering, the increasing presence of heavy metal ions poses a continuous risk to both human health and ecosystems, we introduced for the first time, an electrochemical spectroscopy analysis of Europium-doped ZnO (Eu 3+ : ZnO) as modifications to the glassy carbon electrodes for lead (Pb 2+ ) heavy metal ion detection. Electrochemical impedance spectroscopy, cyclic voltammetry, and square wave voltammetry were used to test the sensor’s sensing ability. Differential pulse voltammetry reveals the remarkable sensitivity towards Pb 2+ ions with a 0.002 µM detection limit. Graphical Abstract
ISSN:0947-8396
1432-0630
DOI:10.1007/s00339-024-07358-1