Green-emitting Carbon Dots Research Articles

Portable real-time determination of Escherichia coli O157:H7 and Staphylococcus aureus based on smartphones and hydrogels

The aptamers functionalized orange-emission carbon dots (OCDs) and green-emission carbon dots (GCDs) had dual-emission peaks with single excitation. Tungsten disulfide nanosheets (WS2 NSs)-triggered fluorescence quenching achieved the ratiometric fluorescence determination of Escherichia coli O157:H7 (E. coli O157:H7) and Staphylococcus aureus (S. aureus) with wide ranges of 18–1.8 × 106 and 37–3.7 × 107 CFU/mL and low detection limits of 8 and 20 CFU/mL, respectively. The results in real sample with recoveries of 90–101 % and RSD < 4.12 % were no significant difference from standard plate counting method. Meanwhile, the dual-color CDs were further adopted in the smartphone-assisted hydrogel platform and achieved speedy, sensitive, portable and real-time determination of E. coli O157:H7 and S. aureus in real samples. This work has not only developed ratiometric fluorescence detection and constructed a portable hydrogel platform, but also provided a unique strategy in developing a time-efficient and easy-to-use portable device in food safety monitoring.

Synthesis of green fluorescent carbon dots using cysteine and maltose as ecofriendly ligands for the detection of venlafaxine anti-depression drug in pharmaceutical and plasma samples

In this work, the green emissive carbon dots (CDs) were fabricated using cysteine and maltose as bio-precursors via refluxing process. The emission and excitation peaks of fabricated cysteine-maltose CDs (CM-CDs) are noticed at 511 and 420 nm, respectively. The as-fabricated CM-CDs displayed average mean size of 3.63 ± 1.12 nm with uniform spherical shape and good quantum yield of 32.81 %. Importantly, the as-fabricated CM-CDs act as a sensor for venlafaxine an anti-depression drug sensing via a fluorescence “turn-off” mechanism. The fluorescence lifetime of CM-CDs was 1.34 ns. The as-fabricated CM-CDs were highly sensitive towards venlafaxine, displaying good linear range from 0.1 to 180 µM with the limit of detection of 75.15 nM. The fluorescence of CM-CDs was reduced with the interaction of venlafaxine, thereby favoring to develop CM-CDs-based cellulose paper sensor for venlafaxine assay. The fabricated sensor was effectively utilized for the quantification of venlafaxine in pharmaceutical and biological samples with good recovery rates (96.01––99.65 %).

High-efficiency laminated luminescent solar concentrators based on carbon dots and nanorings

Creation of novel fluorescent nanomaterials with high photoluminescence quantum yield (PLQY) will lead to high-efficiency luminescent solar concentrators (LSCs). Herein, two kinds of carbon dots (CDs), e.g., blue and green emissive CDs and one novel carbon nanorings (NRs) with yellow emission are synthesized by the solvothermal method. Diaminobenzenesulfonic acid is used as one main precursor to create blue, green emission carbon dots (B/GCDs) and yellow emission carbon nanorings (YCNRs). Importantly, the PLQYs of B/GCDs and YCNRs are 59.8±3.2 %, 12.2±0.7 % and 63.2±1.5 %, respectively. Moreover, B/GCDs and YCNRs are used as fluorescent nanomaterials to construct laminated LSCs with single-layer and double-layer through one-step photopolymerization technique. For single-layer laminated LSCs, YCNRs-based LSCs have the maximum external optical efficiency (ηopt), up to 3.05 %. Furthermore, for double-layer laminated LSCs, the LSCs based on BCDs and YCNRs achieve the highest ηopt of 4.09 %. Compared to single-layer laminated LSCs, the double-layer laminated LSCs show an increase of 34 % in ηopt. Their internal quantum efficiency (ηint) of 29.88 % and external quantum efficiency (ηext) of 25.18 % are obtained, respectively. The presented values are just for single-wavelength excitation. Thus, the synthesis of novel YCNRs with high PLQYs contributes to the optical performances at a large level. Remarkably, the optimal double-layer laminated LSCs show good transparency.

Green‐Emissive Carbon Dots with a High Quantum Yield Applied for Photoconversion Film to Prevent from Blue Light Damage

AbstractHigh‐energy blue light is highly detrimental to health as it can penetrate the lens into the retina, potentially causing atrophy or even death of retinal pigment epithelial cells. To prevent the harmful effects of high‐energy blue light on our health, here the preparation of a photoconversion film specifically designed to block high‐energy blue light is reported, which is composed of green‐emissive carbon dots (G‐CDs) with a high photoluminescence quantum yield (PLQY = 95%) dispersed in polyvinyl alcohol (PVA) matrix. Notably, such a film (named as G‐CDs@PVA) not only converts an incident laser light with a short wavelength into a fluorescence with a longer wavelength, but also exhibits concentration‐dependent (0, 10, 20, and 30 wt.%) blue light barrier rate and green‐emissive intensity. With the increase of the concentration of G‐CDs in the film, the blue light barrier rate of the film as well as the maximum intensity of the green emission are also increased. When the concentration of G‐CDs reaches 30 wt.%, the blue light barrier rate of G‐CDs@PVA achieves up to 97%. Furthermore, G‐CDs@PVA film is attached to a blue light‐emitting diode (LED) chip to explore its practical application in the field of blocking blue light damage.

Synthesis and chromatographic isolation of blue, green, and orange emissive carbon dots with high quantum yields from Taraxacum

Carbon dots (CDs) have emerged as a novel class of fluorescent nanomaterials with superior optical properties and biocompatibility compared to traditional quantum dots. This study demonstrates a facile approach for synthesizing high quantum yield tricolor CDs from the natural precursor dandelion via a one-step solvothermal treatment. Chromatographic separation successfully yielded blue, green, and orange emissive CDs with emission peaks at 481 nm, 530 nm, and 587 nm respectively. Structural and optical characterization revealed the CDs possess excellent photostability, salt resistance, and thermal stability, alongside high quantum yields, measured at 43.8 %, 32.9 %, and 48.1 % for B-CDs, G-CDs, and O-CDs, respectively. Taking advantage of the unique properties of the tricolor CDs, their application in analytical sensing was explored using metal ion detection. The CDs displayed selective quenching responses towards Fe3+, Pb2+, and Sn4+ respectively, with strong anti-interference capabilities. This work provides a sustainable and efficient strategy for producing high-performance multicolor CDs, holding significant implications for reducing the synthesis cost of carbon dots and expanding their application spectrum.

Dopamine inspired lignin-derived green emissive carbon dots for pH sensing and metal ions separation

Lignin is the most abundant, but underutilization polyphenolic material on the earth. In this paper, an integrated platform for pH sensing and ions separation was prepared from lignin to make use of this abundant bioresource. Demethylation of enzymatic hydrolysis lignin was first achieved to mimic the catechol structure of dopamine. The demethylated lignin was then converted into carbon dots by a facile hydrothermal treatment. The as-prepared carbon dots emit green fluorescence with enhanced quantum yield, and exhibited pH-responsive color changes from yellow-green to blue. When incorporated into a chitosan aerogel, the pH-responsive property of the carbon dots was intact, whereas the adsorption capacity of the aerogel for Cu2+ ions was noticeably improved, which was owed to the abundant oxygen containing functional groups and unique optical properties of the as-prepared carbon dots. This study provides a feasible approach to convert lignin into fluorescent nanomaterials for pH sensing and metal ions recovery from wastewater.

The investigation of the interaction between fluorescent carbon dots labeling silk fibroin using a fluorescence microscope–surface plasmon resonance system

The use of fluorescent carbon dots (CDs) as highly precise biolabeling probes has been widespread in the fields of live cell imaging and protein labeling due to their small size and excellent photoluminescence ability to accurately target specific molecules with surface chemical properties. However, there was a lack of research on the interaction between CDs and labeled molecules. In this work, we presented a novel investigation strategy, the fluorescence microscopy-surface plasmon resonance (FM-SPR) system, which combined the use of fluorescence microscopy and wavelength modulation surface plasmon resonance to study the interaction between CDs and labeled molecules in real-time. Using this system, simultaneously recorded the SPR signals and the fluorescence images on the surface of the FM-SPR sensor chip. We observed the dynamic curve and fluorescence images of the interaction between green emissive nitrogen-doped carbon dots (N-CDs) and silk fibroin (SF) in real-time. The kinetic parameters, the quantitative analysis, and the investigation of the binding could be achieved. The results showed a strong linear relationship between the change in SPR signals and the concentration of N-CDs, with a linear coefficient of 0.99913. The linear detection range was 2.5 μg/mL–100 μg/mL, and the real lowest detection limit reached 0.5 μg/mL. Additionally, the green fluorescence points in the imaging region on the FM-SPR sensor chip increased with the concentration of N-CDs, which was consistent with the change in SPR signals. Using this system we also acquired the association rate and dissociation rate of N-CDs to SF which were 2.65 × 10−5/s and 1.52 × 10−5/s, respectively. This demonstrated the effectiveness of our method in quantitatively analyzing SF labeled with N-CDs.

Blinking Carbon Dots as a Super-resolution Imaging Probe.

Single-molecule localization microscopy (SMLM) emerges as a powerful approach for super-resolution imaging that provides unprecedented resolution at the nanometer length scale. However, the development of appropriate probes with specific photophysical traits and characteristics is crucial for this approach. This study demonstrates two different fluorescent carbon dots (CDs) derived from the same molecular precursor─one emitting in red and the other in green─as a SMLM-based super-resolution imaging probe for different applications with an average localization precision of 20 nm and a resolution of 60 nm. Both the CDs exhibit spontaneous blinking with high photon count and low duty cycle but with different blinking cycles. The red emissive CDs with a lower blinking cycle are ideal for quantitative analysis, whereas green emissive CDs with a higher blinking cycle are ideal for high-resolution imaging. We show that the difference in blinking features is linked to their chemical compositions, and the presence of much denser trap states in red emitting CDs is responsible for the reduction of its blinking cycle. This study shows that CDs can be designed as a potential probe for SMLM-based super-resolution imaging for diverse bioimaging applications.

One-pot Synthesis of High-performance Green-emitting Carbon Dots for Cd2+ Sensing and Anti-counterfeiting Applications.

This study presents a facile one-pot solvothermal synthesis of high-performance green fluorescent carbon dots (G-CDs) using o-phenylenediamine and ethylenediamine as precursors. The G-CDs show excellent optical, temporal, and chemical stability. Notably, they exhibit the highest quantum yield of 24.2% in ethanol and a strong green emission peaking at 546nm under 440-490nm excitation. In addition, G-CDs have outstanding salt resistance and multi-solvent compatibility. Due to its bright photoluminescence, G-CDs can be used as a secure ink for anti-counterfeiting. More remarkably, Cd2+ ions can efficiently quench the fluorescence of G-CDs with a detection limit of 0.152 µmol/L, enabling accurate quantification of Cd2+ in water systems. The simple synthesis of high-performance G-CDs expands their applicability in sensing and bioimaging.

Green-emitting carbon dots as a "turn on" fluorescence bio-probe for highly sensitive and selective detection of lipase in human serum.

Enzyme activity assays play a crucial role in numerous fields, including biotechnology, the food industry, and clinical diagnostics. Lipases are particularly important enzymes due to their widespread use in lipid metabolism and esterification reactions. Here, we present a pioneering method for the sensitive and selective determination of lipase activity using green carbon dots (G-CDs) for first time. G-CDs are a fascinating class of carbon nanomaterials with unique optical properties and biocompatibility, making them ideal candidates for enzyme activity assays. This approach eliminates the need for traditional fluorophores or chromogenic substrates, reducing costs, fast response time (1 min), and environmental impact with a quantum yield (QY) of 7.42%. As designed, the G-CDs fluorescent probe turn-on demonstrated a reliable linear detection range from 0 to 9 mg/mL under ideal conditions, with detection limit of 0.01 mg/mL and limit of quantification (LOQ) of 0.045 mg/mL, respectively. Furthermore, the G-CDs system was thoroughly evaluated in human serum samples, showing recoveries ranging from 100.0 to 105.0%. These findings highlight the promising applicability of the G-CDs probe for lipase detection, yielding highly favorable results.

Dual-spot ratiometric microfluidic paper-based analytical device for accuracy and precision improvement

Instrumental and environmental fluctuations are common sources of error in smartphone-based optical detection, significantly affecting the accuracy of analytical measurements. In this regard, spotting the sample and reference simultaneously and in close proximity compensates for the fluctuations. This “dual-spot” design is similar to the double-beam technique used in spectrophotometry, which reduces fluctuations in the results. The underlying hypothesis is that any instrumental and/or environmental factors influencing the color intensity in the detection zones will similarly impact the color intensity in the control zone under the same conditions. To test our design, a ratiometric microfluidic paper-based analytical device (μPAD), functionalized with a mixture of green-emissive carbon dots (CDs) and red-emissive ethidium bromide, was developed for the selective detection of ascorbic acid (AA). The green emission of the CDs is quenched by both AA and Fe3+; NaF was thus loaded onto the 3D connector as a masking agent to remove the interference effect of the Fe3+ ions. The color variations were monitored under a UV lamp, using a smartphone to capture the images, and the RGB intensities were processed using the Color Grab application. The proposed double-spot method greatly enhanced the analytical precision and accuracy of the device. A linear working range from 0 to 125 μM was obtained, and the limit of detection was 2.71 μM. The μPAD was successfully used for the detection of AA in human serum, with recoveries from 87.27 to 98.52 %.

Continuous monitoring of temperature and freshness in cold chain transport based on the dual-responsive fluorescent hydrogel

Comprehensive attention should be paid to the potential food spoilage in food transport. However, there is a problem of freshness destruction by repeated freezing and thawing during the cold chain transport. Herein, a fluorescent hydrogel with N-doped green-emitting carbon dots (N-GCDs), bovine serum albumin-gold nanoclusters (BSA-AuNCs) as fluorescent probes and polyvinyl alcohol-sodium alginate hydrogel as carrier matrix was developed to continuously detect temperature and freshness. Due to the solvatochromic effect of N-GCDs, when the temperature surpassed the threshold, the mixture of water and dimethyl sulfoxide underwent a phase transition and melted into the gel, changing the fluorescence color to realize the temperature monitoring. Then, due to the pH effect of BSA-AuNCs, the gel could respond to pH changes in food deterioration to monitor the food freshness. Thus, the changes of both fluorescence color and intensity of the hydrogel provides a new method for visual and portable authenticity of food freshness.

Highly sensitive fluoroprobe for detecting Sudan dyes in paprika utilizing carbon dot-embedded zeolitic imidazolate framework-8

In this manuscript, we synthesized CDs@ZIF-8 through a one-step, in-situ method by integrating green-emitting carbon dots (CDs) with zeolitic imidazolate framework-8 (ZIF-8). The resulting CDs@ZIF-8 was utilized as an ultrasensitive probe for detection, leveraging the inner filter effect. The analysis demonstrated the capability to detect Sudan dyes. Sudan I, for example, could be detected within a concentration range spanning from 0.25 to 70 μM, achieving a remarkable detection limit of 76.56 nM. This established method was effectively employed for detecting Sudan I in paprika. Compared with CDs, CDs@ZIF-8 exhibited a 3.32-fold increase in sensitivity and a wider detection range. This enhanced performance was attributed to the porous ZIF-8, which allowed for the enrichment of targets around CDs and avoided the aggregation of CDs. Additionally, embedding the CDs in ZIF-8 improved their pH stability. Our study provides a new approach for using CDs under limited conditions by leveraging metal–organic frameworks.

Zero Thermal Quenching Phenomenon of Green Emitting Carbon Dots with High Biocompatibility and Stable Multicolor Biological Imaging in a Hot Environment.

Carbon dots are emerging fluorescent nanomaterials with unique physical and chemical properties and a wide range of applications. Herein, we have designed and successfully synthesized thermally stable green emissive nitrogen-doped carbon dots (NCDs) with a photoluminescent quantum yield of 11.32% through facile solvent-free carbonization. NCDs demonstrated zero thermal quenching upon various temperatures modulating from 20 to 80 °C. The green emissive NCDs perform very stably even after heating them at 80 °C for 1 h. The thermal stability mechanism demonstrates that C═O and C═N functional groups control the particle aggregation and protect the fluorescent hub from photo-oxidation and thermal oxidation. Highly biocompatible CDs exhibit bright, stable, and multicolor emissions in T-ca cells under hot circumstances (25-45 °C). Additionally, NCDs offer long-term stability in the biosystem, as evidenced by the fact that the cell retains its brightness about 70% after prolonging the incubation time to 8 days. Furthermore, the fluorescent NCDs are utilized as in vivo imaging agents in the hot environment as they display bright and thermally stable imaging (27-45 °C) under 488 nm excitation. The results confirmed that the produced thermally stable NCDs could be used in biology and related medical fields that require hot environment imaging.

Development of turn-on fluorescent sensor based on green emissive carnosine-modified tannic acid carbon dots for the selective detection of ascorbic acid

Ascorbic acid (AA) is an indispensable biological antioxidant with anti-aging potential in neurological disorders such as Parkinson’s and Alzheimer’s. Its abnormal concentrations in physiological fluids like human serum can lead to neurological complications. In this study, a turn-on fluorescent sensor was developed using dipeptide (i.e., carnosine) modification of the polyphenolic tannic acid (TA) carbon dots (CDs) (TATA-CDs) for AA detection. Blue-fluorescent TATA-CDs were synthesized using the hydrothermal treatment of the TA and ethylene glycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid (EGTA) as a nitrogen (N) dopant. TATA-CDs were functionalized with carnosine (TATA-Car CDs) using a facile stirring reaction. Their morphological and optical properties were studied via TEM, XRD, UV–Vis, and fluorescence spectroscopy. TATA-Car CDs displayed green fluorescence with excitation and emission wavelength maxima of 400 and 509 nm, respectively. These novel CDs are responsible for the selective turn-on fluorescence sensing of AA (0 to 15 nM) when mixed with copper (Cu2+) ions and deliver a low detection limit of 1.34 nM. The practicality and feasibility of TATA-Car CDs were investigated in human serum samples. From this perspective, the proposed fluorescent sensor is more suitable for the real-time monitoring of AA in different neurological disorders.

Hinge-like paper-based dual-channel enzyme-free ratiometric fluorescent microfluidic platform for simultaneous visual detection of carbaryl and glyphosate

On-site multi-pesticide residues detection is particularly urgent and challenging. Here, we fabricated an enzyme-free ratiometric fluorescent detection system in combination with a hinge-like dual-channel 3D microfluidic paper analytical device (3D μPAD) for simultaneous visual detection of carbaryl and glyphosate. Blue-emission 1-naphthol (Em. 470 nm) was hydrolyzed from carbaryl, while yellow-emission 2,3-diaminophenazine (Em. 570 nm) was produced with the aid of Cu2+ for glyphosate sensing. Inner-filter effect between 1-naphthol or 2,3-diaminophenazine and green-emission carbon dots (Em. 510 nm) realized two ratiometric fluorescent detection systems. Remarkable color variation of green–blue for carbaryl (50.00–1100 μΜ) and yellow–green for glyphosate (5.00–600 μΜ) were observed on a dual-channel 3D μPAD without crosstalk. Their detection limits were 1.11 and 0.63 μΜ, respectively. The strategy realized simultaneous visual detection of carbaryl and glyphosate in food/herbal with excellent accuracy (spiked recoveries, 91.00–107.2%), high precision (RSD ≤ 8.43%), and superior selectivity.

Synthesis of high-performance carbon dots from laurel leaves and their application in anti-counterfeit ink

Green-emitting carbon dots (G-CDs) with high quantum yield were successfully synthesized through a one-step bottom-up approach, utilizing laurel leaves as the carbon precursor, o-phenylenediamine (OPD) as the nitrogen source, and N,N-dimethylacetamide (DMAC) as the solvent. Structural characterizations unveiled the presence of abundant nitrogen-containing functional groups on the surface of G-CDs, significantly influencing their luminescent properties. The excitation and emission wavelengths of G-CDs were determined to be 467 nm and 508 nm, respectively, with a quantum yield of up to 49.9 %. Moreover, the emissions of G-CDs were found to be dependent on the excitation wavelength, suggesting a potential correlation between luminescence and particle size. Notably, the stability assessment demonstrated excellent salt resistance and strong photostability of the G-CDs. A brief discussion on the practical application of G-CDs in anti-counterfeit fluorescent ink highlighted their potential in this filed. This study presents a green synthesis strategy for producing high-performance carbon dots, reducing reliance on chemical reagents, lowering synthesis costs, and mitigating environmental pollution.

Facile Microwave Synthesis of Efficient Green Emissive Carbon Dots Powder and Their Application in Visible Light Communication and White Light Emitting Devices

AbstractHighly green emissive solid‐state carbon dots (CDs) with photoluminescence quantum efficiency of 58% are prepared through a rapid microwave assisted heating method. Due to the spatial confinement from the biuret crystal matrix, aggregation among CDs is effectively suppressed, thus allowing the CDs to give efficient emission in the solid‐state. The CDs show excitation independent emission and mono‐exponential decay characteristics with a nearly constant lifetime of ≈13 ns upon varying the detected emissions, indicating the presence of a single type of emissive state in the CDs. Due to their high quantum efficiency and short lifetime, the obtained CDs are applied as the color conversion layer of a near‐ultraviolet micro light‐emitting diode (µLED) chip (405 nm) for visible light communication, achieving a modulation bandwidth of 165 MHz, which is much higher than the bandwidth of the conventional combination of Ce3+‐doped yttrium aluminum garnet phosphor with GaN LED. Moreover, the green emitting solid‐state CDs are applied to fabricate a prototype white LED device, which exhibits good lighting suitability with a color rendering index of 90.6 and a Commission Internationale de L'Eclairage chromaticity coordinates of (0.327, 0.332).

Facile synthesis of high-brightness green-emitting carbon dots with narrow bandwidth towards backlight display

High-performance carbon dots (CDs) allowing the application in high-end display devices are highly desirable and usually limited by the absence of simple and easy synthesis methods. In this work, we exploited an easy-to-implement strategy for the one-step synthesis of green-emitting CDs (G-CDs) with superb optical properties. The G-CDs were synthesized using m-phenylenediamine (m-PD) as a single precursor, and the reaction reacted at 180 °C for 12 h The resultant G-CDs exhibit high-purity and excitation-independent green fluorescence with the photoluminescence (PL) peak located at 516 nm, full width at half maximum (FWHM) of 46 nm, and PL quantum yield (QY) of ∼80% under the 470 nm excitation light. The G-CDs and corresponding composite film prepared with polyvinyl butyral (G-CDs@PVB) exhibit good PL stability after undergoing long-time storage for one year and 360 h exposure under 460 nm blue light. The G-CDs@PVB film was used as color-conversion materials in green-emitting light-emitting diode (LED) application, exhibiting a Commission internationale de l'Eclairage (CIE) chromaticity coordinate of (0.21, 0.44). The film was also used in CD-based liquid crystal display (CD-LCD) application, achieving a color gamut value of 85%. This work will offer a working basis for the synthesis of high-performance CDs as well as their application in displays.

Electrochemically synthesized green fluorescent carbon dots for quantitation of hypochlorite and carbendazim.

Green emission carbon dots (CDs) electrochemically prepared from 2,6-pyridinedicarboxylic acid and o-phenyl-enediamine were applied separately for the quantitation of hypochlorite and carbendazim. The characteristic and optical properties of the CDs were studied through fluorescence, UV-vis absorption, X-ray photoelectron spectroscopy, and transmission electron microscopy. The synthesized CDs were mainly 0.8-2.2 nm in size, with an average size of 1.5 nm. The CDs exhibited green luminescence centered at 520 nm when excited by 420 nm light. The green emission of the CDs is quenched after the addition of hypochlorite, mainly through the redox reaction between hypochlorite and hydroxyl groups on the CDs surface. Furthermore, the hypochlorite-induced fluorescence quenched can be prevented in the presence of carbendazim. The sensing approaches exhibit good linear ranges of 1-50 μM and 0.05-5 μM for hypochlorite and carbendazim, respectively, with low detection limits of 0.096 and 0.005 μM, respectively. Practicalities of the luminescent probes were separately validated by the quantitation of the two analytes in real sample matrix with recoveries ranging from 96.3 to 108.9% and the relative standard deviation values below 5.51%. Our results show the potential of the sensitive, selective, and simple CD probe for water and food quality control.