Quenching of the Photoluminescence of Gold Nanoclusters Synthesized by Pulsed Laser Ablation in Water upon Interaction with Toxic Metal Species in Aqueous Solution

Autor: Tahir, Fernando Lazaro Freire Jr, Ricardo Q. Aucelio, Marco Cremona, Juliana da S. Padilha, Giancarlo Margheri, Quaid Zaman, Guilherme C. Concas, Mariana Gisbert, Sajjad Ali, Carlos A. T. Toloza, Yordy E. Licea, Tatiana D. Saint’Pierre, Rafael S. Carvalho, Rajwali Khan, Gino Mariotto, Nicola Daldosso, Geronimo Perez, Tommaso Del Rosso
Jazyk: angličtina
Rok vydání: 2023
Předmět:
Zdroj: Chemosensors, Vol 11, Iss 2, p 118 (2023)
Druh dokumentu: article
ISSN: 2227-9040
DOI: 10.3390/chemosensors11020118
Popis: Sensors for the detection of heavy metal ions in water are in high demand due to the danger they pose to both the environment and human health. Among their possible detection approaches, modulation of the photoluminescence of gold nanoclusters (AuNCs) is gaining wide interest as an alternative to classical analytical methods based on complex and high-cost instrumentation. In the present work, luminescent oxidized AuNCs emitting in both ultraviolet (UV) and visible (blue) regions were synthesized by pulsed laser ablation of a gold target in NaOH aqueous solution, followed by different bleaching processes. High-resolution electron microscopy and energy-dispersive X-ray scattering confirmed the presence of oxygen and gold in the transparent photoluminescent clusters, with an average diameter of about 3 nm. The potentialities of the bleached AuNCs colloidal dispersions for the detection of heavy metal ions were studied by evaluating the variation in photoluminescence in the presence of Cd2+, Pb2+, Hg2+ and CH3Hg+ ions. Different responses were observed in the UV and visible (blue) spectral regions. The intensity of blue emission decreased (no more than 10%) and saturated at concentrations higher than 20 ppb for all the heavy metal ions tested. In contrast, the UV band emission was remarkably affected in the presence of Hg2+ ions, thus leading to signal variations for concentrations well beyond 20 ppb (the concentration at which saturation occurs for other ions). The limit of detection for Hg2+ is about 3 ppb (15 nmol/L), and the photoluminescence intensity diminishes linearly by about 75% up to 600 ppb. The results are interpreted based on the ligand-free interaction, i.e., the metallophilic bonding formation of Hg2+ and Au+ oxide present on the surface of the UV-emitting nanoclusters.
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