Green synthesis of fluorescent nitrogen/sulfur-doped carbon dots and investigation of their properties by HPLC coupled with mass spectrometry
A fast and green approach to synthesise ultrasmall nitrogen ( N ) and sulfur ( S )-doped carbon dots ( N , S -C-dots) by microwave-assisted pyrolysis of the precursors rice as carbon source and N -acetyl- l -cysteine (NAC) as N and S dopant has been developed. The obtained N , S -C-dots were fully c...
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Veröffentlicht in: | RSC advances 2014, Vol.4 (35), p.18065-18073 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A fast and green approach to synthesise ultrasmall nitrogen (
N
) and sulfur (
S
)-doped carbon dots (
N
,
S
-C-dots) by microwave-assisted pyrolysis of the precursors rice as carbon source and
N
-acetyl-
l
-cysteine (NAC) as
N
and
S
dopant has been developed. The obtained
N
,
S
-C-dots were fully characterised by elemental analysis, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, UV-vis absorption and photoluminescence (PL) spectroscopy. The undoped C-dots (derived from rice only) and
N
,
S
-C-dots possess different chemical compositions, sizes and spectral properties. With the assistance of high-performance liquid chromatography coupled with fluorescence detection (HPLC-FD), the effect of different mass ratios of NAC to rice (NAC/rice) on
N
,
S
-C-dots was investigated. Higher NAC/rice ratio benefits the generation of
N
,
S
-C-dots with stronger fluorescence emission. In addition, the HPLC separated
N
,
S
-C-dots fractions were collected and further characterised by mass spectrometry, UV-vis absorption and PL spectroscopy, showing that the structural changes induced by doping with heteroatoms
N
and
S
plays a key role in regulating the PL properties of the
N
,
S
-C-dots. This work highlights the merits of synthesising
N
,
S
-C-dots from readily available natural bioresources and applying modern HPLC-FD technology to study the effect of doped heteroatoms on
N
,
S
-C-dots properties. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/C4RA02170C |