2023
DOI: 10.1007/s12274-022-5131-7
|View full text |Cite
|
Sign up to set email alerts
|

New insight into pyrrolic-N site effect towards the first NIR window absorption of pyrrolic-N-rich carbon dots

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

0
14
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 14 publications
(14 citation statements)
references
References 56 publications
0
14
0
Order By: Relevance
“…Correspondingly, the peaks of pyridine N, pyrrolic N, and graphite N are also obtained from their high-resolution N 1s XPS envelopes (third column in Figure ). A sequential decrease of pyridine N and increase of pyrrolic N in CQDs-3-1, CQDs-7-2, CQDs-9-1, and CQDs-7-1 (Table S2) can explain why CQDs-7-1 has a strongest absorption in the long wavelength. ,, At last, two peaks at 532 and 531 eV are discerned from the high-resolution O 1s XPS spectra (fourth column in Figure ), attributed to the C–O and CO bonds, respectively. The deconvoluted results (Table S3) indicate that the carbonyl bond increases in the order of CQDs-3-1, CQDs-7-2, CQDs-9-1, and CQDs-7-1.…”
Section: Resultsmentioning
confidence: 95%
See 2 more Smart Citations
“…Correspondingly, the peaks of pyridine N, pyrrolic N, and graphite N are also obtained from their high-resolution N 1s XPS envelopes (third column in Figure ). A sequential decrease of pyridine N and increase of pyrrolic N in CQDs-3-1, CQDs-7-2, CQDs-9-1, and CQDs-7-1 (Table S2) can explain why CQDs-7-1 has a strongest absorption in the long wavelength. ,, At last, two peaks at 532 and 531 eV are discerned from the high-resolution O 1s XPS spectra (fourth column in Figure ), attributed to the C–O and CO bonds, respectively. The deconvoluted results (Table S3) indicate that the carbonyl bond increases in the order of CQDs-3-1, CQDs-7-2, CQDs-9-1, and CQDs-7-1.…”
Section: Resultsmentioning
confidence: 95%
“…Differences in chemical states between various CQDs are also discussed. Considering that the addition of UR is relatively low when preparing CQDs-3-1, it is not surprising that these CQDs have lower N-doping and pyrrolic N. On the other hand, overcarbonization would occur for CQDs-7-2 due to the longer reaction time, which results in a high content of aryl C. Although both UV–vis absorption spectra (Figure a) and NMR spectra (Figure ) of CQDs-7-1 and CQDs-9-1 are very similar, the results of FTIR and XPS demonstrate that the former has more amide groups and pyrrolic N, which play a vital role in increasing the absorption of long wavelength. ,, This contributes to the formation of photothermal CQDs. Combining the FTIR, NMR, and XPS results, the CQDs prepared under the optimal parameters (CA/UR = 1/7, 150 °C, and 1 h) were schematically depicted (Figure S3) and applied in the following research works.…”
Section: Resultsmentioning
confidence: 95%
See 1 more Smart Citation
“…Carbon dot (CDs)-derived ligands in this investigation were screened for their inhibitory ability against ACE2, with the optimized structure shown in Figure . Pyridinic-N, Pyrrolic-N, and Graphitic-N CDs are a variation of N-doped CDs, which are attractive to be explored in previous studies and applications. ,, The results of docking using YASARA software on the four ligand compounds and ACE2 yielded data with binding energy values. The binding energy is calculated using an empirical equation as shown in eq …”
Section: Resultsmentioning
confidence: 99%
“…Pyridinic-N, Pyrrolic-N, and Graphitic-N CDs are a variation of N-doped CDs, which are attractive to be explored in previous studies and applications. 35 , 43 , 44 The results of docking using YASARA software on the four ligand compounds and ACE2 yielded data with binding energy values. The binding energy is calculated using an empirical equation as shown in eq 1 .…”
Section: Resultsmentioning
confidence: 99%