2023
DOI: 10.1016/j.carbon.2023.118086
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Ligand engineering with heterocyclic aromatic thiol doped carbon quantum dots

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Cited by 6 publications
(2 citation statements)
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“…two major contributions can be identified, at 566 nm and 625 nm, which can be associated with the formerly mentioned species. They suffered bathochromic shifts of 82 and 62 nm, respectively, proving the tunable photoluminescence properties of N-CDs [45][46][47].…”
Section: Photostability Testsmentioning
confidence: 90%
See 1 more Smart Citation
“…two major contributions can be identified, at 566 nm and 625 nm, which can be associated with the formerly mentioned species. They suffered bathochromic shifts of 82 and 62 nm, respectively, proving the tunable photoluminescence properties of N-CDs [45][46][47].…”
Section: Photostability Testsmentioning
confidence: 90%
“…two major contributions can be identified, at 566 nm and 625 nm, which can be associated with the formerly mentioned species. They suffered bathochromic shifts of 82 and 62 nm, respectively, proving the tunable photoluminescence properties of N-CDs [45][46][47]. The QY and fluorescence lifetime were also measured for both N-CDs, resulting in QYs of 2.3% when the synthesis lasted 2 h and 6.2% when it was left for 4 h. Fluorescence lifetimes of 2.59 ns for N-CDs and 3.04 ns for N-CDs were also observed when the reaction time was set at 2 h and when the reaction was maintained for 4 h.…”
Section: Optical Properties Of the Cdsmentioning
confidence: 92%