2021
DOI: 10.1007/s10895-020-02678-w
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Spontaneous Formation of Fluorescent Carbon Nanoparticles in Glutaraldehyde Solution and Their Fluorescence Mechanism

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Cited by 3 publications
(4 citation statements)
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“…The origin of this light emission can be attributed to a combination of transition states between the Si 3 N 4 and oxide (produced during the hydroxylation process), nitride dangling bonds, and probably also surface defects induced by the OH groups [ 29 , 30 ]. A similar PL response is observed when the samples are functionalized, where only a slight rise in PL intensity is measured, as expected due to the presence of the APTES and GTA molecules [ 30 , 31 ]. The PL signal increases even further when biotin is deposited on the functionalized surface.…”
Section: Resultssupporting
confidence: 74%
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“…The origin of this light emission can be attributed to a combination of transition states between the Si 3 N 4 and oxide (produced during the hydroxylation process), nitride dangling bonds, and probably also surface defects induced by the OH groups [ 29 , 30 ]. A similar PL response is observed when the samples are functionalized, where only a slight rise in PL intensity is measured, as expected due to the presence of the APTES and GTA molecules [ 30 , 31 ]. The PL signal increases even further when biotin is deposited on the functionalized surface.…”
Section: Resultssupporting
confidence: 74%
“…This higher signal includes the contribution of luminescence by the biotin molecules themselves [ 32 ]. Here, as indicated in Figure 4 , the characteristic wavelength at which biotin photoemits is 520 nm [ 31 , 33 , 34 ], which is closely around the maximum intensity peak (482 nm) of the PL signal of the biotinylated samples. These results, in addition to the previous findings, demonstrate the successful biotinylation of the Si 3 N 4 surfaces.…”
Section: Resultsmentioning
confidence: 96%
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“…In this structure, there is no remaining aldehyde band from the glutaraldehyde at 1720 cm −1 for (CO), and 2725 and 2825 cm −1 for Fermi resonance of the aldehyde group. [ 26 ] Otherwise, the spectrum of Mn‐DTOGA shows an imine peak at 1639 cm −1 , a weak NCS band (2055 cm −1 ), and a strong CS at 803 cm −1 due to the coordination bond formation between S and Mn atoms. Additionally, we confirmed the presence of acetate groups by the observation of a new band formed at CC (1445 cm −1 ) and CH 3 (1378 cm −1 ), even though a COOH band (≈1760 cm −1 ) overlapped a broad imine band.…”
Section: Resultsmentioning
confidence: 99%