2015
DOI: 10.1080/1536383x.2015.1018413
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Carbon Dots: From Intense Absorption in Visible Range to Excitation-Independent and Excitation-Dependent Photoluminescence

Abstract: Carbon dots (CDs) were hydrothermally synthesized using citric acid as carbon source and ethylenediamine as additive. The as-obtained CDs were then subjected to ultraviolet (UV) irradiation, resulting in ultraviolet-irradiated CDs (UVCDs). The morphology and size of CDs were characterized by transmission electron microscopy. Elemental analysis (EA) was employed to explore the composition of CDs. The surface functional groups of CDs were investigated with the help of Fourier transformation infrared spectroscopy… Show more

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Cited by 52 publications
(25 citation statements)
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References 47 publications
(90 reference statements)
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“…The weak peak in the silica‐CDs spectrum at 240 nm is attributed to the π‐π* transition within the aromatic sp 2 domains of the CDs’ core [5a,28a, 33] . The other weak peak at 325 nm might be ascribed to the n‐π* transition in the surface groups, i. e. the C=O or C−O bonds of the carboxyl (‐COOH) surface groups [28b,34] . The corresponding transitions for CDs are at 235 and 335 nm, consistent with the report of Li et al [5a] .…”
Section: Resultssupporting
confidence: 86%
“…The weak peak in the silica‐CDs spectrum at 240 nm is attributed to the π‐π* transition within the aromatic sp 2 domains of the CDs’ core [5a,28a, 33] . The other weak peak at 325 nm might be ascribed to the n‐π* transition in the surface groups, i. e. the C=O or C−O bonds of the carboxyl (‐COOH) surface groups [28b,34] . The corresponding transitions for CDs are at 235 and 335 nm, consistent with the report of Li et al [5a] .…”
Section: Resultssupporting
confidence: 86%
“…3a ). The prominent band is found in nearly all CDs and is generally assigned to the π-π ∗ transition of the aromatic hydrocarbon domains 27 , 54 56 . The peak position shifts slightly from 344 to 357 nm with increasing BPEI content.…”
Section: Resultsmentioning
confidence: 99%
“…Generally, the optical absorption peaks of CQDs in the UV-visible region is usually estimated as π-π * transition of sp 2 conjugated carbon and n-π * transition of hybridization with heteroatom such as N, S, P, etc. The absorption property can be manipulated through surface passivation or modification process (Zhao et al, 2015; Jiang et al, 2016; Li et al, 2018b; Anwar et al, 2019). Jiang et al developed a facile hydrothermal method to synthesize red, green and blue luminescent CQDs by using three isomers of phenylenediamines (Jiang et al, 2015).…”
Section: Physical and Chemical Propertiesmentioning
confidence: 99%