Search Results (808)

Magneto-fluorescent carbon quantum dots (CQDs) promise compact, dual-readout nanomaterials; however, achieving pronounced photoluminescence alongside magnetic functionality in a simple, scalable formulation remains difficult, especially for emerging doped CQDs. Here, we report Fe-doped carbon quantum dots (Fe-CQDs) as an emerging quantum-dot platform that integrates fluorescence with magnetic-resonance (MR) relaxometry within a single ultrasmall, carbonaceous nanostructure. To enable this, Fe-CQDs are prepared through a straightforward two-step, low-temperature route that uses a magnetic deep eutectic solvent precursor followed by mild carbonization in air at atmospheric pressure. Under UV excitation, the Fe-CQDs display bright blue emission centered at 439 nm, and their optical behavior is characterized by UV-Vis absorption, photoluminescence spectroscopy, and fluorescence microscopy. Meanwhile, dynamic light scattering indicates a narrowly distributed nanoscale hydrodynamic diameter, and X-ray diffraction together with FT-IR supports a carbonaceous framework enriched with oxygenated surface functionalities, consistent with aqueous dispersibility and environmentally responsive photophysics in water, while XPS supports Fe incorporation in an Fe(III)-dominated chemical environment. Importantly, Fe incorporation enables intrinsic MR relaxometric readout, establishing an intrinsic fluorescence/MR dual modality. As a proof-of-concept, Fe-CQDs were tested with a representative per- and polyfluoroalkyl substance (PFAS), showing parallel fluorescence and MR response trends at ppm levels in natural water matrices from Millerton Lake with Stern–Volmer analysis and a NaCl-based ionic strength control. Overall, these results position Fe-CQDs as a versatile magneto-fluorescent nanomaterial for dual-readout screening workflows and motivate future surface engineering and dopant tuning to improve selectivity and expand toward multi-modal readouts. Full article

In order to achieve rapid and qualitative detection of soluble heavy metal ions, nitrogen-doped fluorescent carbon quantum dots (N-CQDs) were synthesized using chitin extracted from shrimp and crab shells as the carbon source. The structural, morphological, and optical properties of the synthesized N-CQDs were systematically characterized using transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FTIR), Raman, X-ray photoelectron spectroscopies (XPS), ultraviolet-visible (UV-Vis) absorption spectroscopy and fluorescence spectroscopy. The resulting N-CQDs exhibited a carbonization yield of 54.46% and a fluorescence quantum yield of 34.33%. Their morphology, structure and optical properties were thoroughly characterized using a range of analytical techniques. The synthesized N-CQDs exhibited excellent fluorescence properties, and remarkable stability. When applied for metal ion detection, the N-CQDs displayed a distinct and selective fluorescence quenching response exclusively toward Fe³⁺ ions. The detection limit for Fe³⁺ at room temperature was 4.04 μmol/L. Furthermore, due to the inherent nitrogen present in the acetyl amino groups of chitin, nitrogen doping was achieved without the need for external dopants during the hydrothermal synthesis process. Owing to their high stability, low cost and low toxicity, the N-CQDs synthesized in this study provide a promising fluorescence sensing platform with excellent selectivity for Fe³⁺ detection, achieved through precise control of surface functional groups. Full article

Microlasers are innovative photonics devices that have recently attracted attention for their unique characteristics, including compactness, broad spectral emission, and low lasing threshold. These properties are beneficial in biophotonics as these lasers can interact with biological materials without causing damage, especially for optical biosensing applications. Among the optical materials recently used as gain media in microlasers are organic dyes, rare-earth ions, fluorescent proteins, and semiconductors, including quantum dots and perovskites. Moreover, different optical cavities and current laser configurations have increased the versatility of microlasers. Recently, digital sensing methods based on novel algorithms, machine learning, and neural networks have been combined with microlaser systems to enhance their accuracy and expand their applications. This work provides a comprehensive review of recent progress in microlasers, covering gain media, microcavity types, and their applications in biophotonics, including conventional spectral-based sensing and new digital approaches for the biomedical field. Full article

Tulathromycin (TULA) is primarily used for treating respiratory diseases in livestock. However, its misuse may lead to bacterial resistance and poses potential health risks such as chronic toxicity and allergic reactions through the food chain. Therefore, it is essential to develop rapid and accurate detection methods. In this study, two quantum dot-based fluorescent immunosorbent assays—direct competitive FLISA (dc-FLISA) and indirect competitive FLISA (ic-FLISA)—were established for detecting TULA residues in milk. The dc-FLISA exhibited a half-maximal inhibitory concentration (IC₅₀) of 1.99 ng·mL⁻¹, a limit of detection (LOD) of 0.018 ng·mL⁻¹, and a detection range of 0.058–69.18 ng·mL⁻¹. The ic-FLISA showed an IC₅₀ of 0.89 ng·mL⁻¹, an LOD of 0.005 ng·mL⁻¹, and a detection range of 0.019–42.65 ng·mL⁻¹. Spiked recovery tests in milk demonstrated recovery rates ranging from 97.41% to 101.02% for dc-FLISA and from 97.48% to 100.65% for ic-FLISA, with coefficients of variation below 10%. In summary, two simple, effective, rapid, and sensitive methods were successfully developed for detecting TULA residues in milk. Full article

Dual-emission photoluminescence (PL) nanoprobes provide improved analytical performance to develop a reliable and sensitive sensing platform for quantifying chloramphenicol in pharmaceutical samples, thereby ensuring therapeutic efficacy and patient safety. In this work, a dual-emission PL sensing platform combining carbon dots (CDs) and AgInS₂ quantum dots (QDs) capped with mercaptopropionic acid (MPA) was developed for the quantitative determination of chloramphenicol, resorting to chemometric methods for data analysis. CDs, CdTe QDs, and AgInS₂ QDs were synthesized and individually evaluated considering their photostability, PL response and kinetics of their interaction with the antibiotic. After this, two dual-emission probes, CDs/MPA-CdTe and CDs/MPA-AgInS₂, were prepared and assessed based on the complementarity of their individual emission features. The obtained kinetic PL dataset was processed using unfolded partial least squares (U-PLS) in order to explore the multidimensional information of the dual-emission systems and to evaluate the performance of both sensing platforms. CDs/MPA-AgInS₂ probe was demonstrated to be the most efficient sensing platform due to its better compromise between sensitivity and photostability, as well as its cadmium-free composition, allowing the implementation of a more environmentally friendly analytical methodology. The optimization of the U-PLS models involved the assessment of the kinetic acquisition time and different spectral regions. The results showed that reliable, sensitive and efficient quantification could be achieved within the first 5 min of interaction and using the full emission spectrum of the sensing probe. Additionally, different interaction mechanisms were observed for each nanomaterial in the combined probe, being static for the CDs/chloramphenicol interaction and dynamic for MPA-AgInS₂/chloramphenicol interaction, which supports the synergetic behavior of the combined probe. The proposed methodology was effectively applied to commercial pharmaceutical formulations, yielding accurate results with good figures of merit. Therefore, this approach can be used as a relevant alternative to existing methodologies for a rapid, robust, and environmentally friendly method for chloramphenicol quantification. Full article

The manuscript describes an optical sensing microplate for the high-throughput screening of imidazolinone herbicides in soil extracts. As far as we know, imprinted proteins (IPs) specific to imidazolinone herbicides have not been synthesized and used as a recognition element for their solid-phase extraction before. Imprinted bovine serum albumin (BSA) and glucose oxidase (GOx) were synthesized in the presence of imazamox as a template and then these IPs were immobilized at the bottom of microplate wells. The sorption capacity (Q) of aminated silica nanoparticles modified by IPs (IP–BIS) was 6.38 mg g⁻¹ while the imprinting factor ($IF$) equaled 2.6. The concentration of imazamox was determined by a “turn-off” solid-phase assay using alloyed CdZnSeS/ZnS quantum dots (QDs) as a component of fluorescent substrate. Alloyed CdZnSeS/ZnS QDs were stabilized in an aqueous phase by positively charged cysteamine that, as far we know, had not been used as this type of ligand before. Our method allows for determining the concentration of imazamox in the range of 0.5–9.2 μg mL⁻¹, with a limit of quantification limit of quantitation (LOQ) equal to 0.45 μg mL⁻¹ The sensing microplate enables parallel detection of up to 96 samples containing herbicides using standard fluorescence microplate readers or smartphones. The paper describes how such sensing microplates can be used for the analysis of artificially contaminated soil samples. The proposed approach combines pre-concentration of analyte at the IPs with its subsequent determination on a single analytical platform, thus allowing for both highly sensitive determination in laboratory conditions and mass screening in the field. Full article

This work investigates the use of two photoactive polymers, functionalized with quantum dots (QDs) (ZnS and CdTe/ZnS), to develop optical sensing hydrogel films through their interactions. It examines their responses to light stimulation for potential biological applications. The optical and morphological properties of the films were studied, revealing photoactive surfaces. The photoactive copolymers were synthesized based on poly(maleic anhydride-alt-2-methyl-2-butene), P(MAn-alt-2MB), and poly(maleic anhydride-alt-1-octadecene), P(MAn-alt-OD), by attaching the photochromic agent, 1-(2-hydroxyethyl)-3,3-dimethylindoline-6-nitrobenzo pyran (SP). Subsequently, QD nanoparticles (ZnS or CdTe/ZnS NPs) were incorporated into the polymer solutions in the presence of a crosslinker agent, and were then spin-coated onto glass substrates under suitable conditions to produce porous-patterned films. These films were created using a one-step bio-inspired process called the breath figure (BF) method. SEM images of QD-containing samples show a photoactive porous surface resulting from a synergistic interaction between the components. The reversibility of these macroscopic properties results from photoinduced transformations at the molecular level. The light-emitting properties of the films were characterized by blue and violet fluorescence under UV light. Advances in film-forming techniques enable the creation of functional structures with important applications, such as microstructured hydrogel films for biological uses. Full article

In this work, we synthesized blue-fluorescent nitrogen-doped carbon quantum dots (N-CQDs) via a facile, economical, and environmentally friendly one-pot synthesis, using citric acid as the carbon source and polyethyleneimine (PEI) as the nitrogen dopant. The as-prepared N-CQDs exhibited uniform size distribution, with an average diameter of approximately 3 nm and a quantum yield of up to 23.6%. Based on the mechanism of HClO-triggered static fluorescence quenching and oxidation of surface amine groups on the N-CQDs, we established a quantitative detection platform for hypochlorous acid (HClO). The proposed method demonstrated a linear response over the concentration range of 0–40 μmol/L, with a detection limit as low as 0.17 μmol/L. It also featured a rapid response time (within 2 min), high selectivity, and strong anti-interference capability against various common species, including Cl⁻, H₂O₂, NO₂⁻, NO₃⁻, TBHP, TBO•, Br⁻, I⁻, S²⁻, F⁻, O²⁻ and HO•. Furthermore, the probe was successfully applied to detect HClO in real-world samples such as river water and beer. Owing to its outstanding photostability and low toxicity, it proved highly effective for monitoring intracellular HClO in living cells. Full article

The selective detection of microplastics (MPs) in aquatic environments is hindered by particle size diversity and matrix-induced interferences. This study reports an excitation–emission matrix (EEM) fluorescence sensing platform using polyamide-derived carbon quantum dots (PACQDs; 0.5–2.6 nm) for the size- and concentration-resolved detection of polyethylene terephthalate MPs (PETMPs). PACQDs exhibited a pronounced fluorescence “turn-off” response upon PETMP interaction, governed by particle size (10–149 μm) and loading (4–8 g L⁻¹). Small PETMPs (10 μm) followed linear Stern–Volmer behavior, achieving a detection limit of 1.67 mg L⁻¹ in deionized water. Conversely, larger particles induced non-linear optical effects, including scattering-driven enhancement and inner-filter effects. Multivariate analysis using PCA and PARAFAC resolved three distinct components associated with surface-state quenching, scattering-mediated redistribution, and surface area-driven binding. Component-specific scores confirmed that PACQDs are most sensitive to small PETMPs, while larger particles primarily introduce optical interference. Selectivity tests showed distinct discrimination of PETMPs over polyamide and polypropylene. In tap water, significant matrix effects were corrected via matrix-matched calibration, achieving recoveries within 80–120%. This study establishes EEM-based multivariate fluorescence as a mechanism-informed strategy for PETMP sensing, highlighting the robust applicability of PACQDs for monitoring small PETMPs in real-world water matrices. Full article

Quantum dots combine advantages such as strong processability via solution methods, wide color gamut coverage, and precise emission color coordinates, making them highly promising for applications in optoelectronic devices. However, they face limitations such as insufficient fluorescence intensity and low far-field extraction efficiency. Plasmonic nanocavities based on metallic nanostructures offer an efficient platform for regulating light–matter interactions. In this study, we constructed a tilted plasmonic nanocavity structure composed of a silver nanocube, CdSe/CdS nanorods, and a single-crystal silver microplate. An Al₂O₃ isolation layer prepared via atomic layer deposition was used to control the nanocavity gap, precisely matching the plasmonic resonance mode with the 620 nm fluorescence emission of the quantum dots. This coupling system significantly enhances the radiative rate in the emission band and the electric field strength in the excitation band, achieving a 187-fold luminescence enhancement of the quantum dot. Additionally, leveraging the nano-antenna effect, the fluorescence exhibits upward directional emission. Experimental and simulation results confirm the high-efficiency enhancement and directional control of quantum dot fluorescence by the tilted nanocavity, providing new insights for the integrated application of quantum dots in displays, quantum communication, and other fields. Full article

Lignin from Phaleria macrocarpa (Mahkota Dewa) fruit, a bioactive-rich cultivated medicinal biomass, was employed as a renewable precursor for lignin quantum dots (LQDs). A simple, aqueous, catalyst-free two-step route (lignin to lignin nanoparticles to LQDs) is demonstrated, enabling the valorization of non-food lignin into photoluminescent nanomaterials. The resulting LQDs were predominantly amorphous with short-range graphitic ordering and a narrow particle size distribution (3–5 nm). Structural and chemical analyses indicated a partially graphitized carbon framework enriched with oxygenated surface functionalities, which is consistent with their bright blue–green emission (λ_em of 490 nm; average fluorescence lifetime of 4.51 ns). Hydrothermal carbonization induced a blue shift in the UV–Vis absorption profile, resulting in a main band at 288 nm with a shoulder at 312 nm. The LQDs exhibited high cytocompatibility toward L929 mouse fibroblasts (93.1 ± 6.5% viability at 24 h) and were readily internalized by cells, facilitating green fluorescence live-cell imaging as a proof-of-concept. Antibacterial activity was observed against both Gram-positive and Gram-negative strains, supporting dual biofunctional performance. Overall, this study established a green and scalable route for converting P. macrocarpa fruit lignin into multifunctional LQDs, with potential applications in circular-bioeconomy such as antimicrobial/active coatings and optical sensing in agro-industrial contexts. Full article

The rapid and selective discrimination of microplastics (MPs) is a critical analytical challenge, particularly as current carbon quantum dot (CQD)-based sensors often rely on single-wavelength “turn-on/off” or staining mechanisms that lack polymer-specific resolution. This work addresses these limitations by presenting a mechanism-driven fluorescence sensing platform using ultra-fine polyamide-derived carbon quantum dots (PACQDs; ~1.4 nm) to identify three prevalent MPs: polyamide (PA), polypropylene (PP), and polyethylene terephthalate (PET). Excitation–emission matrix (EEM) spectroscopy reveals polymer-specific photophysical responses: PAMPs and PPMPs induce fluorescence enhancement of 11.66% and 11.43%, respectively, whereas PETMPs cause net quenching (−4.61%) alongside a distinct, red-shifted emission band. Despite a common scatter-dominated peak at 290/308 nm, quantitative discrimination is achieved via integrated intensity and red/blue emission ratios (0.0137 for PAMPs, 0.0098 for PPMPs, and 0.0072 for PETMPs). Multivariate analysis reinforces this discrimination. Parallel factor analysis (PARAFAC) resolves the EEM data into three fluorescent components representing the intrinsic CQDs core and two interaction-induced surface states with a rank 3 model reducing the relative reconstruction error from 0.1625 to 0.1285. Principal component analysis (PCA) yields clear separation of the polymer classes, with the first two principal components capturing ~88% of the total spectral variance. ATR–FTIR spectroscopy provides direct molecular evidence for the underlying mechanisms: amide–amide coupling and interfacial rigidification for PAMPs; hydrophobic interaction without spectral shifts for PPMPs; and a synergistic interaction involving hydrogen bonding and π–π stacking for PETMPs. In particular, these polymer-specific fluorescence fingerprints are largely preserved in tap water, despite elevated background intensity and partial contrast attenuation, demonstrating the resilience of the EEM–chemometric approach under realistic matrix conditions. Collectively, the strong agreement between fluorescence metrics, multivariate signatures, and interfacial chemistry establishes a robust structure–property framework and positions PACQDs as a rapid, label-free, and matrix-tolerant platform for reliable microplastic discrimination in environmental analysis. Full article

We present an optical deformation sensor additively manufactured via an embedded printing process that enables the direct integration of colloidal quantum dots into multimode silicone (PDMS) waveguides. The sensor consists of two parallel waveguide strands, one of which is locally functionalized with CdSe/CdS quantum dots serving as fluorescent emitters. When narrow-band UV light at 405 nm is coupled into the non-functionalized strand, structural deformation alters the conditions of total internal reflection, thereby changing the optical interaction between both strands. This leads to a deformation-dependent variation in the fluorescence shift-affected intensity ratio, which serves as a self-referenced signal for angle determination. Using ratiometric evaluation, angular deflections of up to 9.5° are detected with a resolution below 1° ($2\sigma$ confidence), representing the performance of an initial functional prototype. The embedded printing process allows the voxel-wise adjustment of the material composition within a viscoplastic support medium and thus the spatially resolved integration of quantum dot-functionalized silicone. Attenuation losses of $0.81\pm 0.02\mathrm{dB}/\mathrm{cm}$ at 625 nm confirm the optical suitability of the printed waveguides. This approach combines optical sensing and structural flexibility within a single manufacturing step and establishes a pathway toward fully integratable deformation-sensing elements for soft robotic and wearable systems. Full article

Paper-based analytical devices have emerged as a versatile and cost-effective platform for on-site chemical and biological analysis. The integration of fluorescence detection with smartphone imaging has significantly enhanced the analytical performance and portability of these systems, enabling sensitive, rapid, and user-friendly detection of diverse analytes. This review highlights recent advancements in paper-based fluorescence sensing technologies, focusing on their design principles, materials, and detection strategies. Emphasis is placed on the use of nanomaterials, quantum dots, and carbon-based fluorophores that improve sensitivity and selectivity in food, bioanalytical, and environmental applications. The role of smartphones as optical detectors and data processing tools is explored, underscoring innovations in image analysis, calibration algorithms, and app-based quantification methods. Full article

A new fluorescence detection method for PO₄³⁻ was developed through the in situ synthesis of cadmium sulfide quantum dots (CdS QDs). Without PO₄³⁻, the CdS QDs could not be effectively formed by only the S²⁻ and Cd²⁺ in the solution. As a stabilizer, PO₄³⁻ is an essential component to regulate the in situ synthesis of CdS QDs. The fluorescence intensity following the addition of different concentrations of PO₄³⁻ was monitored for quantification. Under optimum conditions, the fluorescence intensity shows a linear relationship with concentrations ranging from 3.0 to 300 µM, and a detection limit of 2.9 µM. This assay was successfully employed to assess PO₄³⁻ in tap water and wastewater. Compared with traditional methods, which require pre-synthesizing QDs and tethering them with recognition elements to achieve sample detection, the proposed method is simpler and quicker. It takes less than 5 min to complete PO₄³⁻ detection. Full article