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Nanoarchitectonics of neomycin-derived fluorescent carbon dots for selective detection of Fe sup(3+) ions

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dc.contributor.author Jadhav, R.W.
dc.contributor.author Khobrekar, P.P.
dc.contributor.author Bugde, S.T
dc.contributor.author Bhosale, S.V.
dc.date.accessioned 2022-10-21T06:37:08Z
dc.date.available 2022-10-21T06:37:08Z
dc.date.issued 2022
dc.identifier.citation Analytical Methods. 14(34); 2022; 3289-3298. en_US
dc.identifier.uri https://doi.org/10.1039/D2AY01040B
dc.identifier.uri http://irgu.unigoa.ac.in/drs/handle/unigoa/6897
dc.description.abstract The first-ever neomycin antibiotic-based carbon dots (Neo-CDs) were synthesized via a low-cost, eco-friendly, and single-step hydrothermal method using neomycin as a single precursor. The as-prepared Neo-CDs exhibited strong and stable blue fluorescence and were well characterized by TEM, UV-vis absorption, fluorescence emission, IR, XRD, Raman and XPS spectroscopy methods. The Neo-CDs showed a well-distributed size within the range of 4.5 to 7.8 nm, comprising various functional groups on the surface of the carbon core. The Neo-CDs exhibited exceptional emission behaviour, and fluorescence quantum yield was calculated to be 55 percent in double distilled water. Neo-CDs have been used as a fluorescent sensor for selective and sensitive detection of Fe sup(3+) ions in aqueous solution in the fluorescence turn-off mode. From the set of metal ions, only the Fe sup(3+) ion showed quenching of fluorescence due to photoinduced (PET) electron transfer from Neo-CDs to the half-filled 3d orbital of Fe sup(3+) ions. The limit of detection for Fe sup(3+) ions was calculated to be 0.854 mu M. Further, the quenching efficiency and Stern-Volmer quenching constant have been calculated which are about 94 percent and 5.6 x 10 sup(6) M sup(-1), respectively. en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Chemistry en_US
dc.title Nanoarchitectonics of neomycin-derived fluorescent carbon dots for selective detection of Fe sup(3+) ions en_US
dc.type Journal article en_US
dc.identifier.impf y


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