Abstract
Red fluorescence is of great significance in biomedicine because of its high tissue penetration and low photodamage to organisms. While the carbon dots (CDs) obtained from o-phenylenediamine (oPD) mainly emit yellow fluorescence in a single reaction system, which greatly limits its development in long-wavelength applications. Here, we design a strategy to control the color of oPD-based CDs by only adding catalyst without changing the materials and conditions. The addition of the catalyst made the mass proportion of the obtained red CDs from less than 1% to 95.6%, and the conversion rate was up to 61.7%. The red CDs with a photoluminescence quantum yield of 29.99% have been successfully applied to live cell imaging. It is well known that catalysts can selectively change the reaction pathway and improve the reaction activity. In the process of oPD-based CD formation, we propose that the catalyst can activate the amino functional group, further accelerate the dehydrogenation and polymerization process, thus effectively increasing the sp2-conjugated domain and graphitic N content, which finally realizes the conversion of mixed CDs to single red CDs. This work provides a new idea for how to regulate the fluorescence of CDs without changing the materials and conditions in the future.
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