Perspectives of magnetic nature carbon dots in analytical chemistry: From separation to detection and bioimaging

As a relatively new type of fluorescent carbon-based nanomaterials, multicolor carbon dots (MCDs) have attracted much attention because of their excellent biocompatibility, tunable photoluminescence (PL), high quantum yield, and unique electronic and physicochemical properties. The multicolor emission characteristics of carbon dots (CDs) obviously depend on the carbon source precursor, reaction conditions, and reaction environment, which directly or indirectly determines the multicolor emission characteristics of CDs. Therefore, this review is the first systematic classification and summary of multiple regulation methods of synthetic MCDs and reviews the recent research progress in the synthesis of MCDs from a variety of precursor materials such as aromatic molecules, small organic molecules, and natural biomass, focusing on how different regulation methods produce corresponding MCDs. This review also introduces the innovative applications of MCDs in the fields of biological imaging, light-emitting diodes (LEDs), sensing, and anti-counterfeiting due to their excellent PL properties. It is hoped that by selecting appropriate adjustment methods, this review can inspire and guide the future research on the design of tailored MCDs, and provide corresponding help for the development of multifunctional MCDs.

The Emerging Development of Multicolor Carbon Dots.

Photocatalytic reduction of CO2 and degradation of Bisphenol-S by g-C3N4/Cu2O@Cu S-scheme heterojunction: Study on the photocatalytic performance and mechanism insight

Carbon dots (CDs) as the advancing fluorescent carbon nanomaterial have superior potential and prospective. However, the ambiguous photoluminescence (PL) mechanism and intricate structure-function relationship become the greatest hindrances in the development and applications of CDs. Herein, red emissive CDs were synthesized in high yield from o-phenylenediamine (oPD) and catechol (CAT). The PL mechanism of the CDs is considered as the molecular state fluorophores because 5,14-dihydroquinoxalino[2,3-b] phenazine (DHQP) is separated and exhibits the same PL properties and behavior as the CDs. These include the peak position and shape of the PL emission and PL excitation and the emission dependence on pH and solvent polarity. Both of them display close PL lifetime decays. Based on these, we deduce that DHQP is the fluorophore of the red emissive CDs and the PL mechanism of CDs is similar to DHQP. During the PL emission of CDs, the electron of the molecule state can transfer to CDs. The formation process of DHQP is further confirmed by the reaction intermediates (phthalazine, dimers) and oPD. These findings provide insights into the PL mechanism of this type of CDs and may guide the further development of tunable CDs for tailored properties. 

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Chuang He

Papers

The synthetic strategies, photoluminescence mechanisms and promising applications of carbon dots: Current state and future perspective