Nitrogen-doped Carbon Dots Research Articles

Semiartificial Photosynthetic Nanoreactors for H2 Generation.

A relatively unexplored energy source in synthetic cells is transmembrane electron transport, which like proton and ion transport can be light driven. Here, synthetic cells, called nanoreactors, are engineered for compartmentalized, semiartificial photosynthetic H2 production by a Clostridium beijerinckii [FeFe]-hydrogenase (H2ase). Transmembrane electron transfer into the nanoreactor was enabled by MtrCAB, a multiheme transmembrane protein from Shewanella oneidensis MR-1. On illumination, graphitic nitrogen-doped carbon dots (g-N-CDs) outside the nanoreactor generated and delivered photoenergized electrons to MtrCAB, which transferred these electrons to encapsulated H2ase without requiring redox mediators. Compartmentalized, light-driven H2 production was observed with a turnover frequency (TOFH2ase) of 467 ± 64 h-1 determined in the first 2 h. Addition of the redox mediator methyl viologen (MV) increased TOFH2ase to 880 ± 154 h-1. We hypothesize that the energetically "uphill" electron transfer step from MtrCAB to H2ase ultimately limits the catalytic rate. These nanoreactors provide a scaffold to compartmentalize redox half reactions in semiartificial photosynthesis and inform on the engineering of nanoparticle-microbe hybrid systems for solar-to-chemical conversion.

Multifunctional fluorescence sensor based on nitrogen-doped carbon dots and its application for toxoflavin detection

Multifunctional fluorescence sensor based on nitrogen-doped carbon dots and its application for toxoflavin detection

DES-driven sustainable dual valorization of lignocellulose into carbon dots and porous biochar for effective wastewater remediation

Deep eutectic solvents (DES) are renowned for their effectiveness in deconstructing lignocellulose and extracting lignin, yet the challenges lie in lignin condensation and the disposal of the DES remnants after pretreatment. To overcome these issues, this work proposed a holistic strategy utilizing deep eutectic solvent (DES)-driven lignocellulose deconstruction to upgrade lignocellulose into nitrogen-doped carbon dots (CDs) and iron-decorated porous carbons, serving as photocatalysts and adsorbents, respectively. These nitrogen-doped CDs via the choline chloride/FeCl3 DES pretreatment exhibited abundant nitrogen/oxygen functional groups, enhancing photocatalytic activities and facilitating effective charge separation and transfer. The photocatalytic efficiency of the CDs on dyes reached 97 % under acidic conditions primarily, and free radical quenching experiments indicated that singlet oxygen was the dominant oxidant species. Moreover, the adsorption capabilities of Fe-decorated porous carbons for Congo red reached 2432.3 mg·g−1, surpassing most existing carbon materials. The adsorption mechanism was due to a synergistic effect including physical adsorption, coordination, hydrogen bonding, electrostatic, and π-π interactions. This study proposed a synergetic conversion of DES and lignocellulose into functional carbon materials for wastewater remediation, which inspired the development of a green and cost-effective biorefinery.

Multifunctional Nitrogen-Doped Carbon Dots to Inhibit the Aggregation of Aβ Peptide and Depolymerize the Aβ Fibrils by Modulating Reactive Oxygen Species.

Multifunctional nitrogen-doped carbon dots (N-CDs) were synthesized, and the morphology, composition, and spectral properties of N-CDs were characterized by multiple characterization techniques. The inhibition of β-amyloid (Aβ) peptide aggregation and the destruction of the Aβ fibril structure by N-CDs were also studied. The conformational transition and morphology of Aβ42 in the presence of N-CDs were monitored by far-UV circular dichroism (CD) spectroscopy and transmission electron microscopy (TEM). The results demonstrated that the prepared N-CDs could effectively inhibit Aβ42 peptide aggregation and depolymerize Aβ fibrils. Furthermore, the inhibition and disaggregation mechanism of existing Aβ42 fibrils by N-CDs was studied by electron paramagnetic resonance spectroscopy (EPR). The results showed that the modulation of reactive oxygen species (ROS) by N-CDs and multiple interactions between N-CDs and Aβ42 fibrils played a crucial part in restraining and reducing the aggregation of Aβ42. Our work demonstrates the therapeutic potential of N-CDs in suppressing Aβ42 peptide aggregation and destroying existing Aβ42 fibrils, which provides a new perspective strategy in the treatment of Alzheimer's disease (AD).

Synthesis of nitrogen-doped carbon dot/ tin disulfide nanosheet composite electro-catalysts for dye-sensitized solar cells.

Nitrogen-doped carbon dots (N-CDs) and vertically-grown tin disulfide (SnS2) nanosheets are synthesized via hydrothermal method and chemical vapor deposition (CVD) technique, respectively. The SnS2 nanosheets are directly fabricated on flexible carbon cloth (CC), and then their basal planes are decorated with N-CDs. The as-prepared composite electrodes are used as the counter electrode for the application in dye-sensitized solar cells (DSSCs). The characterizations of N-CDs and SnS2 nanosheets are studied by high resolution transmission electron microscopy (HR-TEM), scanning electron microscopic (SEM), energy dispersive X-ray spectrometer (EDS), Raman spectrometer and X-ray photoelectron spectroscopy (XPS) ect. Moreover, the cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and photocurrent-density voltage (J-V) are utilized to understand the electro-catalytic performance of N-CDs/SnS2/CC composite counter electrode. The N-CDs/SnS2/CC composite electrode shows higher cathodic reduction current density and lower charge transfer resistance in CV and EIS measurements, respectively, as compared to those of the electrodes with N-CDs or SnS2 alone. Meanwhile, the DSSC using N-CDs/SnS2/CC exhibits cell efficiency (η) of 7.68%, which is higher than those of cells having SnS2/CC (η=7.54%) and N-CDs/CC (η=5.66%) counter electrodes, repectively; it also reaches 94% cell efficiency of the cell using Pt/CC counter electrode (η=8.15%). The design concept of the modification of the basal planes by defect-rich carbon dots (i.e., N-CDs) and highly-exposed edge sites (i.e., vertically-grown SnS2 nanosheets) makes promising route to enhance the performance of two-dimensional electro-catalysts.

Smartphone-assisted sensing platform based on dual-responsive nitrogen-doped carbon dots for enzyme-free and visual quantitative detection of Cu2+ and glyphosate

Rapid and selective detection of copper ion (Cu2+) and glyphosate (GLY) is crucial to environmental pollution control, especially when using a simple and portable device. In this study, an enzyme-free and visual fluorescence sensor based on nitrogen-doped carbon dots (N-CDs) is successfully designed, featuring strong blue fluorescence and excellent stability. The sensor shows a linear response to Cu2+ over a wide detection range of 0.048 to 40 μM with a low limit of detection (LOD, 48 nM), resulting in fluorescence quenching at 435 nm. Meanwhile, the rapid enhancement in fluorescence intensity of the quenched N-CDs/Cu2+ system can be triggered by GLY owing to the strong complexation between Cu2+ and GLY, with a LOD of GLY as low as 0.24 μM. Furthermore, we develop a smartphone-assisted sensing platform using N-CDs/polyvinyl alcohol films, which captures and analyzes fluorescence images to detect Cu2+ and GLY with sensitive LODs of 73 nM and 0.32 μM, respectively. Satisfactory recoveries, ranging from 94.0 % to 104.6 %, are achieved in real sample detection, implying the potential application in the field of enzyme-free and on-site pesticides detection.

Green synthesis of N-doped-carbon dots/ZnO for enhanced photocatalytic degradation of methylene blue dye: optimization of reaction parameters.

In this research work, nitrogen-doped carbon dots (N-CDs) adorned zinc oxide nanoparticles (N-CDs/ZnO) were successfully synthesized by a simple and cost-effective solution dispersion method and later on used as photocatalyst for decontamination of aqueous methylene blue (MB) dye on irradiation of UV light (300 W, 320-400nm) at room temperature. Both the N-CDs and ZnO were prepared through green technique utilizing non-toxic, inexpensive and eco-friendly precursors, namely Foeniculum vulgare and Psidium guajava leaf extract, respectively. All the synthesized samples exhibited crystalline nature with average diameter of particle 4.42nm, 12.38nm and 14.11nm corresponding to N-CDs, ZnO and N-CDs/ZnO, respectively. Further, band gap energy value (Eg) of 3.43, 2.76 and 2.49eV for N-CDs, ZnO and N-CDs/ZnO, respectively, were obtained by using Tauc's plot. The photocatalytic capability of the sample N-CDs/ZnO was compared with bare ZnO nanoparticles, utilizing identical experimental conditions. The results demonstrated that the composite exhibited notably higher photocatalytic degradation efficiency than bare ZnO nanoparticles up to 15.54%. Lower band gap value of N-CDs/ZnO was the major factor for exhibiting this behaviour, decreasing the recombination rate and thus enhancing the efficiency. Furthermore, N-CDs/ZnO exhibited 98.17% MB degradation under optimized conditions (0.03g, 5ppm, pH 10). The resultant N-CDs/ZnO exhibited good stability and decontamination efficiency up to five cycles with efficiency loss of only 7.89%. Along with, trapping experiments was conducted to analyze the role of active species involved for deep understanding of mechanism. The order of efficiency of active constituents was observed to be: •O2- > h+ > •OH. The study analyzed the non-toxic nature of treated water, revealing normal plant growth, suggesting its potential use in irrigation of parks and roadside areas. Overall, present research work obeys the green chemistry principles with the fabrication of highly efficient, eco-friendly, cost-effective photocatalyst N-CDs/ZnO by utilizing the green precursors for the whole research work.

NH2-MIL-101(Fe)/N-CNDs as a visible light photocatalyst for degradation of fluoroquinolone antibiotics in water

A microwave-assisted-hydrothermal approach has been employed to synthesize NH2-MIL-101(Fe) – (Fe-MOF) in composition with the Nitrogen-doped Carbon Nanodots - (N-CNDs) as a visible light photocatalyst. The octahedral structure of Fe-MOF was confirmed via microscopic and X-ray powder diffraction analysis. The composite with 30% N-CNDs exhibited the highest degradation efficiency of 97.9% for Ciprofloxacin (CIP) under visible light irradiation. Also, it shows a higher photocurrent response than bare Fe-MOF material. Also, EIS analysis reveals a smaller arc for the composite material, which suggests higher charge transfer properties. Based on the transient photocurrent measurements and EIS analysis, it could be stated that the improved photocatalytic activity of Fe-MOF@30%N-CNDs composite is due to the enhanced charge transfer properties caused by the introduction of N-CNDs. The photoactivity studies were tested using the LC-MS technique.

A cotton swab platform for fluorescent detection of aluminum ion in food samples based on aggregation-induced emission of carbon dots.

A novel portable cotton swab based on nitrogen-doped carbon dots (NCDs) for Al3+ detection was constructed for the first time. NCDs with bright green fluorescence were prepared by hydrothermal method with phenylhydrazine hydrochloride and 3-hydroxy-2-naphthoic acid hydrazide as precursors. The surface of NCDs was exposed to abundant functional groups (such as amino, carboxyl, hydroxyl, etc.), which was helpful for the formation of complexes between NCDs and Al3+. In the presence of Al3+, the aggregation of NCDs obviously induced their fluorescence enhancement due to the aggregation-induced emission (AIE) of NCDs. Furthermore, the quantum yield (QY) of NCDs was enhanced by 12 times with Al3+, and the fluorescence lifetime was increased by 7.54ns. The fluorescence intensity was linearly correlated with the concentration of Al3+ (2.5-300μM), and the limit of detection was 0.76μM. Moreover, for the portable way, cotton swabs were successfully employed to construct the sensors for the detection of Al3+ in food samples. This proposal haspotential for the application in food analysis.

3D printing of aligned silk fibroin microfibers covered with nitrogen-doped carbon dots for anti-counterfeiting

Counterfeiting has serious economic and social consequences, prompting researchers worldwide to develop innovative and highly secure anti-counterfeiting methods, including the use of various polymer printing techniques and the integration of functional materials to create patterns with customized designs that are easy to detect and cannot be falsified. Composite inks made of silk fibroin microfibers and polyvinyl alcohol or polyethylene glycol were developed to produce patterns with the microstructures aligned in the direction of extrusion during the 3D printing process. Fibroin microfibers were obtained via high temperature treatment and used as a precursor for carbon dot synthesis. This approach allowed the microfiber structure to be maintained and be amenable to the synthesis of carbon dots doped with N-heteroatom on its surface, resulting in a material that fluoresces bright blue when irradiated at 365 nm but remains invisible in normal lighting conditions.

Novel, Speedy, and Eco-Friendly Carboxymethyl Cellulose-Nitrogen Doped Carbon Dots Biosensors with DFT Calculations, Molecular Docking, and Experimental Validation.

Carboxymethyl cellulose (CMC) was prepared from sugarcane bagasse (SB) in minutes using a novel microwave method. Additionally, nitrogen-doped carbon dots (N-CDs) were synthesized from SB using the same microwave technique. These materials were crosslinked with CaCl2 to prepare antibacterial/antifungal hydrogel sensors. In this regard, both CMC@Ca and CMC@Ca-N-CDs exhibited antibacterial activity against Escherichia coli (Gram negative), while only CMC@Ca-N-CDs demonstrated antibacterial activity against Staphylococcus aureus (Gram positive). Moreover, both materials showed antifungal activity against Candida albicans. The molecular docking study demonstrated that CMC@Ca-N-CDs showed good binding with proteins with short bond length 2.59, 2.80, and 1.97 A° for Escherichia coli, Staphylococcus aureus, and Candida albicans, respectively. These binding affinities were corroborated by the observed inhibition zone diameters. Furthermore, fluorescence microscope revealed distinct imaging patterns between Gram-positive and Gram-negative bacteria, as well as pathogenic yeast (fungi). CMC@Ca-N-CDs emitted blue light when exposed to Escherichia coli and Candida albicans (i.e., CMC@Ca-N-CDs/Escherichia coli and Candida albicans), whereas it emitted bright-red light when exposed to Staphylococcus aureus (i.e., CMC@Ca-N-CDs/Staphylococcus aureus). This disparity in the fluorescence-emitted colors is due to the difference in the cell wall of these microorganisms. Additionally, DFT calculations were conducted to substantiate the robust chemical interactions between CMC, Ca2+, and N-CDs.

Tangerine peel-derived nitrogen-doped carbon dots incorporated chitosan/pullulan-based active packaging film for bread packaging

Citrus peel waste carbon dots based on nitrogen-doped (N-TanCD) were developed by a hydrothermal strategy to deliver active packaging fillers and characterized by transmission electron microscopy, photoluminescence, and Fourier transform infrared analyses. The addition of N-TanCD into chitosan-pululan (CS/Pul@N-TanCD) polymer blend amplified the tensile strength of the composite film by 22.8 %, whereas the antioxidant activities against DPPH and ABTS reached 62.7 % and 91.6 %, respectively. The proposed film showed blocked 98.8 % of UV-A and 100 % of UV-B without affecting the film’s transparency. The CS/Pul@N-TanCD film lowered the contamination of L. monocytogenes and E. coli by more than 4 and 5 log CFU/mL, respectively. Sliced bread was packaged using CS/Pul-based films and stored for 12 days at 50 % relative humidity and 25 °C to investigate changes in the quality of the bread. It was found that bread packaged with CS/Pul film integrated with N-TanCD maintained excellent bread quality relating to appearance, moisture content, hardness, weight loss, and total viable bacterial count.

Rapid microwave preparation of nitrogen doped carbon dots and their applications as highly sensitive nanoprobe for hematin

In this work, nitrogen-doped carbon dots (NCDs) were obtained by microwave rapid preparation method with lipase and guanidine hydrochloride as precursors in only 6 min. In order to achieve high sensitivity detection of hematin, based on obtained NCDs as a nanoprobe, a new detection method based on photoluminescence (PL) change was developed. Further studies have shown that the sensing strategy relied on the inner filter effect to selectively quench the PL emission of NCDs at 379 nm by hematin under 320 nm excitation. The nanoprobe had a wide linear range (0.2–13 μmol/L) and a detection limit of 0.07 μmol/L. The method was effectively applied to the identification of hematin in human blood samples. The proposed nanoprobe has the characteristics of simple and efficient design. It can achieve rapid and accurate detection, which is very suitable for real-time analysis of blood samples to facilitate diagnosis.

Electrochemiluminescence of Carbon Dots and Nitrogen-Doped Carbon Dots from a Microwave-Assisted Method

This research focuses on the use of carbon dots (CDs) and nitrogen-doped carbon dots (NCDs) synthesized using a microwave-assisted method as electrochemiluminescence (ECL) luminophores. CDs have been synthesized using citric acid, while various concentrations of nitrogen-doped CDs have been successfully obtained by varying the amount of urea from 1 to 3 g with citric acid to produce NCD1, NCD,2 and NCD3. The ECL mechanism of CDs and NCDs on screen-printed electrodes has been studied using cyclic voltammetry (CV). ECL emission from as-prepared CDs and NCDs was observed in PBS with potassium persulfate (K2S2O8) as a co-reactant. The addition of potassium chloride (KCl) as a supporting electrolyte displays fast electroreduction of CDs and K2S2O8 to expedite the generation of CDs and peroxydisulfate radicals that simultaneously increase ECL intensity. Furthermore, as the concentration of nitrogen-doped CDs increases, so does the intensity of the ECL. NCD3 shows the highest ECL intensity by an increment of 86.4% in comparison to CDs in PBS with the addition of K2S2O8 and KCl. Finally, optimization of ECL measurement was carried out in terms of CV potential range, concentration of luminophore, supporting electrolyte, and co-reactant using NCD3 luminophore. The CV potential range at 0 to -2 V shows 50 mV of early CV reverse onset potential that resulted in an increase of 52.9% ECL intensity. Meanwhile, 30x dilution of NCD3, 0.1 M of supporting electrolyte KCl, and 0.1 M of co-reactant K2S2O8 show the optimum value to obtain high ECL intensity.

Lignin-Based N-Carbon Dots Anchoring NiCo2S4/Graphene Hydrogel Exhibits Excellent Performance as Anodes for Hybrid Supercapacitor.

A NiCo2S4/N-CDs/RGO ternary composite hydrogel was prepared via a one-step hydrothermal method, utilizing lignin-based nitrogen-doped carbon dots as a bridge connecting NiCo2S4 and graphene. The specific capacitance of NiCo2S4/N-CDs/RGO significantly outperforms that of the GH and NiCo2S4/RGO electrodes, achieving 1050 F g-1. The 3D mesh porous hydrogel structure mitigates NiCo2S4 nanoparticle aggregation, providing a larger specific surface area for enhanced charge storage. The abundant functional groups of N-CDs interact with Ni (II) and Co (III) cations, favoring NiCo2S4 particle synthesis. Additionally, an assembled solid-state asymmetric supercapacitor employing NiCo2S4/N-CDs/RGO as the positive electrode exhibited excellent energy density (68.4 Wh kg-1) and cycle stability (82% capacitance retention after 10,000 constant current charge-discharge cycles).

Discrimination of tetracycline in water using a fluorescence probe based on UiO-67 Encapsulated with NCDs

The large-scale production and abuse of antibiotics cause environmental pollution, threaten human health, and destroy the ecological balance. Efficient detection of these pollutants has emerged as a prominent topic in current research. In this study, we developed a novel material called UiO-67-NCDs by combining UiO-67 with nitrogen-doped carbon dots (NCDs) for sensing trace amounts of tetracycline (TC) in water. The NCDs were successfully introduced onto UiO-67 by the post-synthesis modification, resulting in a strong blue fluorescence at 445 nm. Thanks to the hydrogen bonding, π-π interactions and the internal filter effect (IFE) between UiO-67 and NCDs, UiO-67-NCDs was capable for TC sensing, exhibiting fluorescence quenching in 10 s with a limit of detection (LOD) of 32.9 nM (0–38 μM). The visual detection capabilities, high sensitivity, rapid detection time, and simplicity of the fluorescent probe make it a promising candidate for antibiotic detection in aqueous environments. This will further stimulate the interest of researchers in the in-depth study of MOFs and quantum dots and their applications in sensing.

Effective Determination of Diosmin Using Nitrogen Doped Carbon Dots as Probe Based on Internal Filtering Effect.

The establishment of a convenient and efficient testing method is crucial and needed for the monitoring of diosmin. In this study, nitrogen doped carbon dots (N-CDs) with the particle size distribution of 2.5-5.7nm and the average diameter of 4.1nm were successfully synthesized using a simple strategy. N-CDs exhibited excellent and stable fluorescence performance with the quantum yield of 22.33%. Correspondingly, a fluorescence analytical method was developed for diosmin determination using N-CDs as probe. UV-vis absorbance spectroscopy and the evaluation of internal filtering parameters verified that the mechanism causing the quenching of N-CDs was an internal filtering effect (IFE). The concentration of diosmin can be directly evaluated based on the quenched fluorescence intensities. After optimizing experimental conditions, it was found that the fluorescence quenching efficiency ((F0-F)/F0) of N-CDs exhibited a good linear relationship with the concentration of diosmin (CDiosmin) in the range of 3.0-50µg/mL. The limit of detection (LOD) was 0.86µg/mL based on 3σ/slope (n = 13). This method was successfully applied to accurately determine the content of diosmin in diosmin tablets and human plasma samples with good reproducibility. It stands out for its simplicity, speed, and acceptable determination performance.

Solution plasma synthesis of nitrogen-doped carbon dots from glucosamines: Comparative fluorescence modulation for dopamine detection

The intriguing fluorescence characteristics of carbon dots (CDs) have led to many sensor applications, particularly for dopamine (DA), a molecule linked to various diseases. This study prepares CDs from glucose and glucosamine (nitrogen-free and nitrogen-containing precursors) using a simple solution plasma process (SPP). We explore how nitrogen elements and counterions in glucosamine (hydrochloride and sulfate) affect CD properties and their ability to modulate fluorescence for DA detection. Glucosamine offers three advantages over glucose: (i) single-step CD synthesis via SPP, (ii) enhanced fluorescence of CDs, and (iii) improved fluorescence response to DA. We investigate the DA detection capabilities of N,S-CDs (from glucosamine sulfate) and N,Cl-CDs (from glucosamine hydrochloride). Both can sense DA with distinct photoluminescence responses. N,S-CDs show selectivity and fluorescence brightening upon DA interaction, with a detection limit of 33.05 μM. N,Cl-CDs demonstrate higher sensitivity with a lower detection limit of 0.1212 μM through fluorescence quenching. Silver ions (Ag+) may also contribute to N,Cl-CDs quenching; however, the observed color change to gray due to silver nanoparticle (AgNP) formation helps pinpoint the quenching substance. The varied photoluminescence responses arise from different surface functional groups: N,S-CDs have amino-rich surfaces, while N,Cl-CDs have conjugated carbonyl-rich surfaces. This study illustrates the mechanisms of DA detection and AgNP formation, suggesting the potential of CDs in medical diagnostics as selective tools for disease diagnosis. Additionally, we compare the DA sensing methodology of our CDs with existing literature, highlighting the advantages of our sensor.

Rational design of carbon dot nanozymes for ratiometric dual-signal and smartphone-assisted visual detection of nitrite in food matrices

Developing reliable nitrite (NO2−) sensors is essential for food safety and reducing health risks from NO2− exposure. In this study, we strategically designed nitrogen-doped carbon dot (N-CD) nanozymes to establish an accessible dual-signal ratiometric sensing system for detecting NO2− in food matrices. This system utilizes the photoluminescence and enzyme-like properties of N-CD nanozymes combined with NO2−-triggered diazotization reactions of substrates such as o-phenylenediamine (OPD) or 3,3′,5,5′-tetramethylbenzidine (TMB). The resulting N-CD/OPD and N-CD/TMB composites provide dual-mode detection—fluorescence and colorimetric—with high selectivity for NO2− and excellent resistance to interference. These sensors exhibit clear color changes under both ultraviolet and visible light, and can be combined with smartphones for visual, on-site detection of NO2−. By incorporating a ratiometric strategy, dual-signal output, and smartphone compatibility, our system achieved a low detection limit (≤ 1.92 μM) and satisfactory recovery rates (85.6–115 %) in environmental water and food samples. This highlights the potential of smartphone-assisted sensors for environmental monitoring and food safety applications. Our carbon dot-based platform offers a practical and effective solution for on-site NO2− detection, contributing valuable insights to the field.

Highly fluorescent nitrogen doped carbon dots as analytical probe for sensitive detection of curcumin through smartphone integrated 3D-printed platform: A new horizon in food safety

COVID-19 pandemic has significantly influenced the dietary habits of humans, emphasizing the incorporation of natural ingredients to enhance immunity towards viral and bacterial infections. Curcumin (Cur), a widely used traditional medicine in various Asian countries and a natural coloring agent, has gained popularity, leading to surge in its usage specially in post COVID-19 era. This surge has led to increased scrutiny of the potential side effects of excessive Cur use, with recent reports suggesting it may result in inactivation of DNA and reduce adenosine triphosphate levels, leading to health risks. In this work, we synthesized highly fluorescent nitrogen-doped carbon dots with a photoluminescence quantum yield of 72.9 % for the sensitive and selective detection of Cur. The developed fluorescent probe exhibits excellent sensory response towards Cur within a concentration range of 0.081–51.45 µM, achieving an ultra-low detection limit of 15.91 nM. The sensor was successfully tested on real food samples like ginger powder, turmeric powder, and curry powder, demonstrating good recovery rates. To assess the practicality of the sensor system, we developed a 3D-printed smartphone-integrated device platform for curcumin detection through fluorescence image analysis. This developed platform exhibited promising results, achieving a limit of detection (LoD) of 132.28 nM across a curcumin concentration range of 0.13–54.00 µM. This device platform holds significant potential for the development of efficient sensors for real-time detection of Cur in food samples.