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Nitrogen-Doped Carbon Dots: A Facile and General Preparation Method, Photoluminescence Investigation, and Imaging Applications
Ist Teil von
Chemistry : a European journal, 2013-02, Vol.19 (7), p.2276-2283
Ort / Verlag
Weinheim: WILEY-VCH Verlag
Erscheinungsjahr
2013
Quelle
Wiley Online Library Journals Frontfile Complete
Beschreibungen/Notizen
Carbon dots (Cdots) are an important probe for imaging and sensing applications because of their fluorescence property, good biocompatibility, and low toxicity. However, complex procedures and strong acid treatment are often required and Cdots suffer from low photoluminescence (PL) emission. Herein, a facile and general strategy using carbonization of precursors and then extraction with solvents is proposed for the preparation of nitrogen‐doped Cdots (N‐Cdots) with 3‐(3,4‐dihydroxyphenyl)‐L‐alanine (L‐DOPA), L‐histidine, and L‐arginine as precursor models. After they are heated, the precursors become carbonized. Nitrogen‐doped Cdots are subsequently extracted into N,N′‐dimethylformamide (DMF) from the carbogenic solid. A core–shell structure of Cdots with a carbon core and the oxygen‐containing shell was observed. Nitrogen has different forms in N‐Cdots and oxidized N‐Cdots. The doped nitrogen and low oxidation level in N‐Cdots improve their emission significantly. The N‐Cdots show an emission with a nitrogen‐content‐dependent intensity and Cdot‐size‐dependent emission‐peak wavelength. Imaging of HeLa cells, a human cervical cancer cell line, and HepG2 cells, a human hepatocellular liver carcinoma line, was observed with high resolution using N‐Cdots as a probe and validates their use in imaging applications and their multicolor property in the living cell system.
Going dotty: A facile and general strategy involving the carbonization of precursors and their subsequent extraction with solvents is proposed for the preparation of nitrogen‐doped carbon dots (N‐Cdots) with multicolor emission (see figure). The emission mechanism of the Cdots was studied. Multicolor photoluminescence was validated in living cell systems.