2017
DOI: 10.1016/j.carbon.2017.01.035
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Hydrothermal synthesis of fluorescent carbon dots from sodium citrate and polyacrylamide and their highly selective detection of lead and pyrophosphate

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Cited by 202 publications
(94 citation statements)
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“…These results are in fair agreement with the one obtained by Lu et al who prepared N-doped carbon dots from hydrothermal treatment of citric acid in the presence of poly ethylenimine and reported a 2θ value of 20° for CDs [33]. In an almost similar report, [34], XRD analysis of CDs obtained from hydrothermal treatment of sodium citrate and poly(acrylamide) exhibited a broad low intensity diffraction peak at 20.66°, indicating existence of amorphous carbon. Similarly, He et al prepared carbon dots from sodium salt of EDTA and reported a broad peak around 24.4°, corresponding to 0.363 nm interlayer spacing of CDs.…”
Section: Characterization Of N-cdssupporting
confidence: 91%
“…These results are in fair agreement with the one obtained by Lu et al who prepared N-doped carbon dots from hydrothermal treatment of citric acid in the presence of poly ethylenimine and reported a 2θ value of 20° for CDs [33]. In an almost similar report, [34], XRD analysis of CDs obtained from hydrothermal treatment of sodium citrate and poly(acrylamide) exhibited a broad low intensity diffraction peak at 20.66°, indicating existence of amorphous carbon. Similarly, He et al prepared carbon dots from sodium salt of EDTA and reported a broad peak around 24.4°, corresponding to 0.363 nm interlayer spacing of CDs.…”
Section: Characterization Of N-cdssupporting
confidence: 91%
“…The strong absorption peak at 1580 cm À1 is attributed to the C=Os tretching vibration and that of 1400 cm À1 is from COO-group. [22][23][24][25] The full survey XPS spectrum manifests that carbon,o xygen and sodium are presented at the surface of the obtained solid CDs (Figure 2b). The presence of the Na KLL peak suggests that Na is still bound to oxygen, which further confirms the existence of the carboxylate groups in the obtained solid CDs.…”
Section: Resultsmentioning
confidence: 96%
“…FT‐IR (Figure a) and XPS (Figure b–f) spectra are used to identify the chemical structure and elemental composition of the solid CDs. The broad absorption band between 3200 and 3700 cm −1 in the FT‐IR spectrum of the solid CDs is assigned to the stretching vibrations of O‐H, which is responsible for the hydrophilicity of CDs. The strong absorption peak at 1580 cm −1 is attributed to the C=O stretching vibration and that of 1400 cm −1 is from COO‐group .…”
Section: Resultsmentioning
confidence: 99%
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