2022
DOI: 10.1016/j.aca.2021.338685
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Facile synthesis of yellowish-green emitting carbon quantum dots and their applications for phoxim sensing and cellular imaging

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Cited by 27 publications
(7 citation statements)
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“…To further analyze the surface group and chemical structure of the N‐CQDs, fourier transform infrared (FTIR) and X‐ray photoelectron spectroscopy (XPS) were performed. FTIR spectrum of the N‐CQDs was shown in Figure 3b, showing characteristic bands of ‐OH/N−H, C=O/C=C, C−N, C−O−C, and C−O at 3420, 1580, 1393, 1273 and 1074 cm −1 , respectively [37,38] . The FTIR results validated the N‐CQDs embedding of the carboxyl, hydroxyl, and amino groups.…”
Section: Resultsmentioning
confidence: 58%
See 1 more Smart Citation
“…To further analyze the surface group and chemical structure of the N‐CQDs, fourier transform infrared (FTIR) and X‐ray photoelectron spectroscopy (XPS) were performed. FTIR spectrum of the N‐CQDs was shown in Figure 3b, showing characteristic bands of ‐OH/N−H, C=O/C=C, C−N, C−O−C, and C−O at 3420, 1580, 1393, 1273 and 1074 cm −1 , respectively [37,38] . The FTIR results validated the N‐CQDs embedding of the carboxyl, hydroxyl, and amino groups.…”
Section: Resultsmentioning
confidence: 58%
“…FTIR spectrum of the N-CQDs was shown in Figure 3b, showing characteristic bands of -OH/NÀ H, C=O/C=C, CÀ N, CÀ OÀ C, and CÀ O at 3420, 1580, 1393, 1273 and 1074 cm À 1 , respectively. [37,38] The FTIR results validated the N-CQDs embedding of the carboxyl, hydroxyl, and amino groups. The presence of hydrophilic groups on the N-CQDs, especially OÀ H and C=O, ensures their hydrophilicity and stability in aqueous systems.…”
Section: Chemistryselectmentioning
confidence: 59%
“…In particular, phenylenediamines and diaminonaphthalenes were exploited for achieving different emission colors (Table ). For example, several green fluorescent CDs have been prepared by hydrothermal treatment of citric acid with p -phenylenediamine. , Yuan et al obtained five different CDs, exhibiting fluorescence from blue to red, by ethanol solvothermal treatment of 1,5-diaminonaphthalene or 2,3-diaminonaphthalene and different reaction conditions (Figure ). …”
Section: Ca-cd Classesmentioning
confidence: 99%
“…The concentration of all species was maintained at 40 mmol L −1 . After optimization of the experimental conditions, the sensing was performed, following a well-established assay 41 Briefly, 500 μL of prepared B,N-Cdot (5.0 μg mL −1 ) were transferred to a quartz cuvette, and aliquots of NaNO 2 stock solution (concentrations of 0.1, 0.01, and 0.001 mol L −1 ) and PBS solution pH 7.4 were added, resulting in a final volume of 2 mL for all samples and obtaining a NO 2 − range varying from 0.00 to 50.00 (mmol L −1 ). The emission spectra were recorded after 2 min of incubation at 340 nm excitation, and the PL intensity at 435 nm was used for NO 2 − quantification.…”
Section: Sensing Experimentsmentioning
confidence: 99%