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Crafting carbon quantum dots from acetone: dual purpose Fe sup(3+) ion and pH sensing platform

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dc.contributor.author D'Souza, L.F.B.
dc.contributor.author Jadhav, R.W.
dc.contributor.author Bhosale, S.V.
dc.contributor.author Bugde, S.T.
dc.date.accessioned 2024-09-24T07:10:35Z
dc.date.available 2024-09-24T07:10:35Z
dc.date.issued 2024
dc.identifier.citation Emergent Materials. NYP; 2024; NYP. en_US
dc.identifier.uri https://doi.org/10.1007/s42247-024-00792-0
dc.identifier.uri http://irgu.unigoa.ac.in/drs/handle/unigoa/7380
dc.description.abstract We developed a low-cost single-step reflux method to synthesize acetone-based sulfonated carbon dots (acetone-CQDs) using acetone as a sole precursor. The acetone-CQDs were purified via column chromatography and characterised by IR, XRD, NMR, TEM, and XPS techniques. We hypothesized that acetone-CQDs would exhibit strong fluorescence and be effective in sensing applications. The purified acetone-CQDs displayed strong green fluorescence, a size distribution of 2 to 9 nm, and a fluorescence quantum yield of 35 percent. They were successfully applied as fluorescent sensors for selective and sensitive detection of Fe sup(3+) ions in water. In addition, it was also demonstrated that the acetone-CQD could act as a sensitive pH sensor. The Stern-Volmer plot was drawn, from which the quenching constant was determined to be 1.02x10 sup(5) M sup(-1) and the quenching efficiency was 92 percent. The acetone-CQD was able to detect low concentrations of Fe sup(3+) ions, as the LOD obtained was 4.76 mu M. The fluorescence emission quenching was due to Photoinduced Electron Transfer (PET) from acetone-CQDs to the half-filled 3d orbital of Fe sup(3+) ions. These findings demonstrate the potential of acetone-CQDs as effective fluorescent sensors for the sensitive and selective detection of Fe sup(3+) ions in water as well as pH sensing. en_US
dc.publisher Springer en_US
dc.subject Chemistry en_US
dc.title Crafting carbon quantum dots from acetone: dual purpose Fe sup(3+) ion and pH sensing platform en_US
dc.type Journal article en_US
dc.identifier.impf cs


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