Journal
ADVANCED OPTICAL MATERIALS
Volume -, Issue -, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adom.202300750
Keywords
carbon dots; colloidal nanomaterials; mercury sensing; time-resolved photoluminescence
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One of the UN Sustainable Development Goals is to ensure universal access to clean drinking water. Mercury (Hg) is considered to be one of the most dangerous water contaminants due to its immense toxicity and vast environmental impact. A nanosensor based on carbon dots (CDs) functionalized with carboxylic groups has been developed to monitor water quality, showing an ultrahigh sensitivity and selectivity in detecting Hg2+ concentration-dependent photoluminescence (PL) lifetimes. The selectivity is explained by significant perturbation of the CD photoexcited state upon Hg2+ binding, supported by light-induced electron paramagnetic resonance (LEPR) spectroscopy and time-dependent density functional theory (TD-DFT) calculations.
One of the UN Sustainable Development Goals is to ensure universal access to clean drinking water. Among the various types of water contaminants, mercury (Hg) is considered to be one of the most dangerous ones. It is mostly its immense toxicity and vast environmental impact that stand out. To tackle the issue of monitoring water quality, a nanosensor based on carbon dots (CDs) is developed, whose surface is functionalized with carboxylic groups. CDs show Hg2+ concentration-dependent photoluminescence (PL) lifetimes along with an ultrahigh sensitivity and selectivity. The selectivity of PL quenching by Hg2+ is rationalized by performing light-induced electron paramagnetic resonance (LEPR) spectroscopy showing significant perturbation of the CD photoexcited state upon Hg2+ binding. The experimental findings are supported by time-dependent density functional theory (TD-DFT) calculations. These unveiled the emergence of a low-lying charge transfer state involving a vacant 6s orbital of Hg2+ stabilized by relativistic effects.
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