Carbon Dot - An Updated Review

ZnCl2 Enabled Synthesis of Highly Crystalline and Emissive Carbon Dots with Exceptional Capability to Generate O2⋅–

Subject of study. The study focuses on luminescent carbon nanoparticles, specifically carbon dots, based on citric acid, formamide, and various chiral molecules. Aim of study. The aim is to assess the influence of chiral molecules used in the synthesis of carbon dots on optical transitions in the long-wavelength spectral region and to investigate the mechanism underlying the circular dichroism signal of these nanoparticles. Method. Carbon dot samples were synthesized using two methods: (i) a one-step solvothermal synthesis of carbon dots from citric acid, formamide, and various chiral molecules and (ii) a two-step method involving the solvothermal synthesis of achiral carbon dots from citric acid and formamide, followed by surface treatment with L-cysteine. Absorption and luminescence spectroscopy methods were employed to study the chemical structure and optical properties of the carbon dots. The chiroptical properties of the obtained samples were analyzed using circular dichroism spectroscopy. Main results. The addition of various chiral molecules to a mixture of precursors during one-step synthesis enabled the fabrication of carbon dots with different chemical compositions, including variations in surface groups and types of emission centers in the spectral region of 350–700 nm. The use of L-phenylglycine and L-tryptophan in the one-step synthesis was shown to lead to the formation of nanoparticles with optical transitions in both short- and long-wavelength regions of the spectrum. The addition of L-glutathione during the one-step synthesis resulted in the formation of carbon dots with short-wavelength emission, while the addition of L-cysteine did not alter the emission characteristics of achiral carbon dots based on citric acid and formamide. The optical properties of the chiral carbon dots obtained using the two-step synthesis method with L-cysteine remained unchanged compared with those of the achiral carbon dots synthesized from citric acid and formamide. The circular dichroism spectra of all the samples showed a signal at ∼250nm, which was attributed to the derivatives of the chiral precursors attached to the surface of the nanoparticles, irrespective of the preparation method. Practical significance. Chiral carbon dots hold promise in biomedicine as sensors, luminescent biomarkers, and other applications due to their biocompatibility and non-toxicity. The results obtained in this work will serve as a foundation for the further fabrication and investigation of chiral carbon nanoparticles with long-wavelength luminescence.

Carbon dots (CDs) have outstanding optical properties, biocompatibility, and photostability, making them attractive for imaging applications. A facile and green one-step hydrothermal synthesis method is proposed, which can be safely used in a wide range of applications such as chemical sensing, bioimaging, and optoelectronics. In this study, we report green synthesis of carbon dots from bitter orange juice (Citrus Aurantium) by hydrothermal treatment for the first time. We studied effects of time, temperature, and pH on fluorescence of CDs, characterized them using various spectroscopic and microscopic methods, and evaluated their toxicity to different cell lines. Identifying an optimum reaction condition of 180 ºC for 7 h heating gave CDs that showed pH-dependent fluorescence, with the largest fluorescence at a pH of 7.0. The CDs were 1-2 nm in size with a spherical morphology and negative surface charge. The CDs showed a high quantum yield of 19.9 %, reasonable photostability, excellent water solubility, and long fluorescence lifetime. A one step hydrothermal rout led to various hydrophilic functional groups on the surface of the CDs. Our results showed that the CDs were non-toxic over a large concentration range and effective for imaging of cells, indicating their potential as imaging probes in medical diagnostics and biosensor applications.

Boron doping can effectively induce solid-state fluorescence (SSF) in carbon dots (CDs); however, research on the intrinsic mechanism underlying this phenomenon is lacking. Herein, a design strategy for boron-doped furan-based CDs is proposed, CDs with aggregation-induced emission (AIE) properties are synthesized, and the mechanism by which boron atom dopants induces SSF and room-temperature phosphorescence (RTP) is elucidated. The morphology and structural characterization of the CDs indicate that boron doping leads to structural twisting of the CDs. The AIE phenomenon of CDs arises from the inhibition of the twisted structure motions and a reduction in the nonradiative relaxation rate during the aggregation process. In addition, CDs with twisted structures exhibit a smaller overlap between the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO), effectively reducing the singlet-triplet splitting energy (ΔEST). CDs embedded in microcrystalline cellulose (MCC) exhibit green RTP because the nonradiative transitions are suppressed, and the excited triplet species remain stable. For the first time, this study reveals the structure-activity relationship between the twisted structure and optical properties of CDs, providing a new approach for the preparation of solid-state light-emitting CDs.

Fluorescent carbon dots have the advantages of good chemical stability, low toxicity, and surface functionalization, which has caused concern. In recent years, polymer carbon dots synthesize by polymer polysaccharides have become a new research hotspot. In this paper, a chitosan-based fluorescent polymer carbon dot material is synthesized by hydrothermal method and used for drug-loading research. We choose chitosan-graft-polyethylene glycol monomethyl ether and citric acid derivatives as the carbon sources for the carbon dots, because chitosan and polyethylene glycol are both a carbon source for carbon dots and a passivation reagent for carbon dots. Then the quantum yield of the polymeric carbon dots is increased. Polymer carbon dots can also retain the molecular structure of polyethylene glycol and chitosan, providing favorable conditions for its application in drug loading. The structural characterization is performed on P(CS-g-mPEG-CA)CDs by IR, UV, X-ray diffraction, photoelectron spectroscopy, transmission electron microscopy and photoluminescence spectra and pH stability test is carried out. The results show that the synthesized P(CS-g-mPEG-CA)CDs has higher fluorescence quantum yield(66.81%), longer fluorescence lifetime(15.247 ns), and better pH stability. Using Doxorubicin as a model drug, a load study was conducted using this polymer carbon dot. The results show that if the degree of substitution of mPEG is 11.9%, the maximum loading rate of polymer carbon dots is 51.3% and the maximum drug release rate is 28.7%. In addition, we also found that drug loading and release could be controlled by the grafting rate of mPEG. In addition, the cytotoxicity of polymer carbon dots on nasopharyngeal carcinoma cells(CNE-2) is evaluated using an MTT assay. The study shows that there is no obvious cytotoxicity of blank P(CS-g-mPEG-CA)CDs, and that the survival rate of CNE-2 cells decreases with the increase of drug-loaded micelles. The results show that the P(CS-g-mPEG-CA)CDs have a certain application prospect in the aspects of fluorescence labeling, drug delivery, fluorescent tracer system and controlled release.

Carbon dots (CDs) are known as the rising star of carbon-based nanomaterials and, by virtue of their unique structure and fascinating properties, they have attracted considerable interest in different fields such as biological sensing, drug delivery, photodynamic therapy, photocatalysis, and solar cells in recent years. Particularly, the outstanding electronic and optical properties of the CDs have attracted increasing attention in biomedical and photocatalytic applications owing to their low toxicity, biocompatibility, excellent photostability, tunable fluorescence, outstanding efficient up-converted photoluminescence behavior, and photo-induced electron transfer ability. This article reviews recent progress on the synthesis routes and optical properties of CDs as well as biomedical and photocatalytic applications. Furthermore, we discuss an outlook on future and potential development of the CDs based biosensor, biological dye, biological vehicle, and photocatalysts in this booming research field.

Developing highly fluorescent biogenic carbon dots (CDs) as molecular probes and cellular imaging agents with excellent cellular biocompatibility and water dispersibility can advance the scope of CDs in various biomedical applications. The present work aims to produce CDs from biological precursors such as natural amino acids. Due to their molecular recognition properties, the resultant CDs exhibit biocompatibility, polar functional groups, and selective molecule sensing. Microwave (MW)-assisted carbonization of L-tryptophan, L-glutamic acid, and their mixture led to the formation of CDs. However, the CDs derived from the mix of amino acids exhibited strong emission at 450 nm, with a quantum yield of 31.3%, and showed excellent stability under wide pH conditions. These CDs have a crystalline graphitic core, predominantly derived from the carbonization of the aromatic moiety intrinsic to L-tryptophan amino acid, while the partial carbonization of L-glutamic acid led to anchor polar functional groups on the CDs surface. These CDs were established as molecular probes for sensing the biomolecule cysteamine with enhanced sensitivity and remarkable cross-selectivity among the interfering metal ions, anions, and other thiols. To demonstrate these materials' cellular biocompatibility, the cell viability of MCF-7 and fibroblast cells was studied following their exposure to CDs. The studies revealed that the fluorescent CDs did not elicit cytotoxic effects on the cells at elevated concentrations. The CDs from the mixture of amino acids were efficiently internalized by MCF-7 cells, enabling efficient imaging of live cells. Overall, this study developed biogenic and cellular biocompatible CDs with robust luminescent properties and demonstrated their applications in biomolecular sensing, cellular uptake, and imaging.

Orange-red, green, and blue fluorescence carbon dots for white light emitting diodes

Fluorescent nitrogen-doped carbon dots (CDs) were prepared by a facile hydrothermal treatment from the waste biomass jackfruit peel. Structural, optical and morphological characterisation revealed that the functional groups on the surface of the CDs provided them with good aqueous solubility and excellent stability against different experimental conditions. From zeta potential analysis, the surface of the CDs was found to be negatively charged (-23.7mV). The synthesized CDs could emit blue light under UV radiation and they act as efficient sensors for various analytes like metal ions, antibiotics, and dyes, etc. The CDs displayed outstanding sensing activity for the analytes with a low detection limit by a static quenching process. Fluorescence enhancement was obtained in the presence of levofloxacin also owing to the formation of hydrogen bonds between the surface functional groups on CDs and levofloxacin.

Nanosized fluorescent carbon particles, namely, carbon dots (CDs), are a kind of fluorescent material that has drawn increasing attention in recent years. CDs have size-, surface chemistry-, and wavelength-dependent luminescence emission, which is different from traditional semiconductor-based quantum dots. Moreover, with excellent chemical stability, good biocompatibility, low toxicity, up-conversion emission, resistance to photo bleaching, as well as easy chemical modifications, CDs are promising for substantial applications in numerous areas: bioimaging, sensors, and energy-related devices. Herein, three kinds of fluorescent dots are reviewed: graphene quantum dots (GQDs), carbon nanodots (CNDs) and polymer dots (PDs). After the first reported CDs prepared from electrophoretic analysis and purification of fluorescent carbon nanotube fragments, there were hundreds of publications focusing on fluorescent CDs. Bioimaging was one of the most common applications of the CDs; therefore, in this review, most of the chosen reference papers were related to bioimaging based on CDs.

Smartphone-based portable device for rapid and sensitive pH detection by fluorescent carbon dots

Carbon dots (CDs) are usually smaller than 10 nm in size, and are meticulously formulated and recently introduced nanomaterials, among the other types of carbon-based nanomaterials. They have gained significant attention and an incredible interest in the field of nanotechnology and biomedical science, which is merely due to their considerable and exclusive attributes; including their enhanced electron transferability, photobleaching and photo-blinking effects, high photoluminescent quantum yield, fluorescence property, resistance to photo-decomposition, increased electrocatalytic activity, good aqueous solubility, excellent biocompatibility, long-term chemical stability, cost-effectiveness, negligible toxicity, and acquaintance of large effective surface area-to-volume ratio. CDs can be readily functionalized owing to the abundant functional groups on their surfaces, and they also exhibit remarkable sensing features such as specific, selective, and multiplex detectability. In addition, the physico-chemical characteristics of CDs can be easily tunable based on their intended usage or application. In this comprehensive review article, we mainly discuss the classification of CDs, their ideal properties, their general synthesis approaches, and primary characterization techniques. More importantly, we update the readers about the recent trends of CDs in health care applications (viz., their substantial and prominent role in the area of electrochemical and optical biosensing, bioimaging, drug/gene delivery, as well as in photodynamic/photothermal therapy).

A multifunctional guanosine-based carbon dots for dead microbial imaging and synergistic broad-spectrum antimicrobial therapy

To prepare fluorescent carbon dots for loading cationic anticancer drug through donor-quenched nanosurface energy transfer in visible sensing of drug release. Highly fluorescent carbon dots (CDs) were prepared by a facile hydrothermal approach from citric acid and o-phenylenediamine. The obtained CDs showed a high quantum yield of 46 % and exhibited good cytocompatibility even at 1 mg/ml. The cationic anticancer drug doxorubicin (DOX) can be loaded onto the negatively charged CDs through electrostatic interactions. Additionally, the fluorescent CDs feature reversible donor-quenched mode nanosurface energy transfer. When loading the energy receptor DOX, the donor CDs' fluorescence was switched "off", while it turned "on" again after DOX release from the surface through endocytic uptake. Most DOX molecules were released from the CDs after 6 h incubation and entered cell nuclear region after 8 h, suggesting the drug delivery system may have potential for visible sensing in drug release.

In this study, newly synthesized crystalline carbon dots shows the concentration and solvent‐dependent multicolor emission. The carbon dots have been characterized by several techniques like Fourier transformed infrared spectroscopy (FT‐IR), X‐ray photoelectron spectroscopy (XPS), UV‐visible and fluorescence spectroscopy, and field emission gun transmission electron microscopy (FEG‐TEM). The high polarity of the solvents and the high concentration of the carbon dots help it to aggregate which opens up a new red‐shifted emission band. It has been revealed that the Förster resonance energy transfer (FRET) between the dispersed and aggregated state of the carbon dots becomes the actual cause behind this change. These carbon dots selectively shows the white light emission in the dioxane. The particular polarity of the dioxane selectively helps for the coexistence of the blue and greenish‐yellow emission bands with the same intensity which eventually turns the emission very much near to white light. It has been found that the very minute amount of water present in dioxane (0.1 % V/V) can change the emission nature of the carbon dots. This observation has finally helped these carbon dots for highly selective and perceptible water detection in dioxane.