Search Results (161)

The biological effects of nanoparticles are closely related to their intracellular content and location, both of which are influenced by various factors. This study investigates the effects of surface charge on the uptake, intracellular distribution, and exocytosis of CdSe/ZnS quantum dots (QDs) in Raw264.7 macrophages. Negatively charged 3-mercaptopropanoic acid functionalized QDs (QDs-MPA) show higher cellular uptake than positively charged 2-mercaptoethylamine functionalized QDs (QDs-MEA), and serum enhances the uptake of both types of QDs via protein corona-mediated receptor endocytosis. QDs-MEA primarily enter the cells through clathrin/caveolae-mediated pathways and predominantly accumulate in lysosomes, while QDs-MPA are mainly internalized through clathrin-mediated endocytosis and localize to both lysosomes and mitochondria. Exocytosis of QDs-MPA is faster and more efficient than that of QDs-MEA, though both exhibit limited excretion. In addition to endocytosis and exocytosis, cell division influences intracellular QD content over time. These results reveal the charge-dependent interactions between QDs and macrophages, providing a basis for designing biocompatible nanomaterials. Full article

This study explores the optical properties of a close-packed monolayer composed of core/shell-alloyed CdSeS/ZnS quantum dots (QDs) of two different sizes and compositions. The monolayers were self-assembled in a stacked configuration at the water/air interface using Langmuir–Blodgett (LB) techniques. Under continuous 532 nm laser illumination on the red absorption edge of the blue-emitting smaller QDs (QD450), the red-emitting larger QDs (QD645) exhibited oscillatory temporal dynamics in their photoluminescence (PL), characterized by a pronounced blueshift in the emission peak wavelength and an abrupt decrease in peak intensity. Conversely, excitation by a 405 nm laser on the blue absorption edge induced a drastic redshift in the emission wavelength over time. These significant shifts in emission spectra are attributed to photon- and anisotropic-strain-assisted interlayer atom transfer. The findings provide new insights into strain-driven atomic rearrangements and their impact on the photophysical behavior of QD systems. Full article

Real-time, high-resolution monitoring of chemically diverse water pollutants remains a critical challenge for smart water management. Here, we report a fully integrated, multi-modal nano-sensor array, combining graphene field-effect transistors, Ag/Au-nanostar surface-enhanced Raman spectroscopy substrates, and CdSe/ZnS quantum dot fluorescence, coupled to an edge-deployable CNN-LSTM architecture that fuses raw electrochemical, vibrational, and photoluminescent signals without manual feature engineering. The 45 mm × 20 mm microfluidic manifold enables continuous flow-through sampling, while 8-bit-quantised inference executes in 31 ms at <12 W. Laboratory calibration over 28,000 samples achieved limits of detection of 12 ppt (Pb²⁺), 17 pM (atrazine) and 87 ng L⁻¹ (nanoplastics), with R² ≥ 0.93 and a mean absolute percentage error <6%. A 24 h deployment in the Cherwell River reproduced natural concentration fluctuations with field R² ≥ 0.92. SHAP and Grad-CAM analyses reveal that the network bases its predictions on Dirac-point shifts, characteristic Raman bands, and early-time fluorescence-quenching kinetics, providing mechanistic interpretability. The platform therefore offers a scalable route to smart water grids, point-of-use drinking water sentinels, and rapid environmental incident response. Future work will address sensor drift through antifouling coatings, enhance cross-site generalisation via federated learning, and create physics-informed digital twins for self-calibrating global monitoring networks. Full article

The current research developed an optical carbon dioxide (CO₂) sensor using anodized aluminum oxide (AAO) as the substrate. We developed an optical carbon dioxide (CO₂) sensor utilizing CdSe/ZnS quantum dots (QDs) as the fluorescent dye and Phenol Red as the pH indicator. The QDs acted as the CO₂-responsive fluorophore and were embedded in a polyimide butyl methacrylate (polyIBM) matrix. This sensing solution was applied to an anodized aluminum oxide (AAO) substrate, which provided a porous and stable platform for sensor fabrication. Photoluminescence measurements were conducted using the coated AAO substrate, with excitation from a 405 nm LED light source. The sensor exhibited red fluorescence emission at 570 nm and could detect CO₂ concentrations in the linear range of 0–100%. Experimental results showed that fluorescence intensity increased with CO₂ concentration, achieving a sensitivity of 211. A wavelength shift of 0.1657 nm/% was observed, indicating strong interactions among CO₂ molecules, Phenol Red, and the QDs within the AAO matrix. The sensor demonstrated a response time of 55 s and a recovery time of 120 s. These results confirm the effectiveness of this optical sensing approach in minimizing fluctuations from the excitation light source and highlight the potential of the AAO-supported QDs and Phenol Red composite as a reliable CO₂ sensing material. This advancement holds promise for applications in both medical and industrial fields. Full article

Colloidal quantum dots (QDs) provide an ideal platform for the development of integrated optoelectronic devices due to their excellent solution processability and size-tunable optical properties. In this paper, we investigate the self-assembly process of QD micro-rings based on the solution patterning method and the lasing phenomenon in the micro-rings. The characterization of the QD micro-rings demonstrates that they possess a high-quality morphological structure and excellent optical properties. The photoluminescence spectra of the QD micro-rings with different pump fluences are studied, and photon lasing with a narrow linewidth (0.3 nm) is found to have been achieved in the micro-rings above the threshold ($23 \mathsf{\mu }\mathrm{J} \mathrm{c}{\mathrm{m}}^{-2}$). The high coherence of the lasing in the QD micro-rings is revealed by angle-resolved photoluminescence (ARPL) spectra at room temperature. Moreover, the interference pattern of the coherent lasing obtained with Young’s double-slit interference method based on the far-field Fourier optical system in the ARPL spectrum reflects the distribution of the optical field in the QD micro-rings. Our research on the self-assembly of colloidal QDs and the lasing of QD micro-rings is expected to further promote the development of on-chip integrated QD optoelectronic devices. Full article

Vomitoxin is a member of the monotrichous mycotoxin family with a complex chemical structure and significant biological activity. This toxin has strong immunosuppressive toxic effects and can cause serious damage to human and animal health. In this study, an on-site immune detection method based on an immune SiO₂@QD fluorescent probe was developed, which realized the rapid and quantitative detection of emetic toxins in grains. Polyethyleneimine (PEI) is a polymer containing a large number of amino groups, and the binding of PEI to the surface of quantum dots can serve to regulate growth and provide functionalized groups. A SiO₂@QD nanotag with good dispersibility and a high fluorescence intensity was synthesized by combining a PEI interlayer on the surface of SiO₂ nanospheres. Utilizing the electrostatic adsorption of the amino group in PEI, CdSe/ZnS QDs were self-assembled on the surface of SiO₂ nanospheres. In the stability test, the SiO₂@QDs could maintain basically the same fluorescence intensity for 90 consecutive days in the dark at 4 °C, showing a high fluorescence stability. The fluorescence-enhanced QD immune probe was formed by coupling with anti-DON monoclonal antibodies through carbodiimide chemical synthesis. For the detection of spiked wheat flour samples, the immuno-SiO₂@QD fluorescent probe showed excellent sensitivity and stability, the detection limit reached 0.25 ng/mL, and the average recovery rate was 92.2–101.6%. At the same time, the immuno-SiO₂@QD fluorescent probe is simple to operate, is capable of rapid responses, and has great potential in the rapid detection of vomitoxins in grains. Full article

Based on dual-template molecular imprinting polymerization technology, a fluorescent molecularly imprinted polymer doped with CdSe/ZnS quantum dots was developed to construct a “Turn-on” fluorescence sensor for the rapid, sensitive, and specific detection of two biogenic amines. The biogenic amines bind to the quantum dots, which eliminates surface defects and enhances the fluorescence emission intensity of the quantum dots. By optimizing both the polymerization and detection processes, the results demonstrate that the sensor can detect biogenic amines within the range of 0.01–10 mmol/L, with a low detection limit of 14.57 μmol/L and a detection time of only ten minutes. Moreover, the sensor is cost-effective and does not require specialized instrument operation, offering a practical approach for the rapid detection of biogenic amines in complex food matrices. This study advances the development of simultaneous recognition and rapid detection technologies for multiple target molecules. Full article

The introduction of side-emitting lenses into white light-emitting diodes (LEDs) has enabled thin panel lighting technology based on LED technology, but also presents the disadvantage of low color rendering due to insufficient red components in the spectra of typical white LEDs. Additional application of remote quantum dot (QD) components such as QD films or caps presents the issues of increased numbers of components and higher costs. In this study, we incorporated red QDs directly into a lens placed on white LEDs and analyzed the effects of QD lenses on the optical characteristics of a lighting device through experiments and simulations. By incorporating red CdSe/ZnS QDs into UV-curable resin to fabricate QD lenses and applying them to white LEDs, we significantly improved the color rendering index and were able to adjust the correlated color temperature over a wide range between 2700 and 9900 K. However, as the concentration of QDs in the lens increased, scattering by the QD particles was enhanced, strengthening the Lambertian distribution in the intensity plot. Following the development of optical models for QD lenses under experimental conditions, comprehensive optical simulations of white LED lighting systems revealed that increasing the device height proved more effective than modifying TiO₂ scattering particle concentration in the diffuser plate for mitigating QD-induced bright spots and enhancing illumination uniformity. Full article

In this paper, we demonstrate a broadband and simultaneous waveguide array light source based on water-soluble CdSe/ZnS quantum dots (QDs). We initially measure the fluorescence intensity for various cladding solution concentrations along the fiber axis to assess their impact on the propagation loss; the experimental results show that the fluorescent intensity decreases with fiber length, with higher concentrations showing a more pronounced decrease. Then, we showcase a synchronous QD light source in an optofluidic chip that fluoresces in red, green, and blue (RGB) within a microfluidic channel. Finally, a 3 × 3 QD array of a fluorescent display on a single PDMS chip is demonstrated. The QD waveguide represents a compact and stable structure that is readily manufacturable, making it an ideal light source for advancing high-throughput biochemical sensing and on-chip spectroscopic analysis. Full article

Quantum dot light-emitting diodes (QLEDs) based on high-color-purity blue quantum dots (QDs) are crucial for the development of next-generation displays. I-III-VI type QDs have been recognized as eco-friendly luminescent materials for QLED applications due to their tunable band gap and high-stable properties. However, efficient blue-emitting I-III-VI QDs remain rare owing to the high densities of the intrinsic defects and the surface defects. Herein, narrow-band blue-emissive CuAlSe₂/Ga₂S₃/ZnS QDs is synthesized via a facile strategy. The resulting QDs exhibit a sharp blue emission peak at 450 nm with a full width at half maximum (FWHM) of 35 nm, achieved by coating a double-shell structure of Ga₂S₃ and ZnS, which is associated with the near-complete passivation of Cu-related defects (e.g., Cu vacancies) that enhances the band-edge emission, accompanied by an improvment in photoluminescence quantum yield up to 69%. QLEDs based on CuAlSe₂/Ga₂S₃/ZnS QDs are fabricated, exhibiting an electroluminescence peak at 453 nm with a FWHM of 39 nm, a current efficiency of 3.16 cd A⁻¹, and an external quantum efficiency of 0.35%. This research paves the way for the development of high-efficiency eco-friendly blue QLEDs. Full article

We propose a temperature-dependent optimization procedure for the second-nearest neighbor (2NN) sp³s* tight-binding (TB) theory parameters to calculate the effects of strain, structure dimensions, and alloy composition on the band structure of heterostructure spherical core/shell quantum dots (QDs). We integrate the thermoelastic theory of solids with the 2NN sp³s* TB theory to calculate the strain, core and shell dimensions, and composition effects on the band structure of binary/ternary CdSe/Cd(Zn)S and ZnSe/Zn(Cd)S QDs at any temperature. We show that the 2NN sp³s* TB theory with optimized parameters greatly improves the prediction of the energy dispersion curve at and in the vicinity of L and X symmetry points. We further used the optimized 2NN sp³s* TB parameters to calculate the strain, core and shell dimensions, and composition effects on the nanocrystal bandgaps of binary/ternary CdSe/Cd(Zn)S and ZnSe/Zn(Cd)S core/shell QDs. We conclude that the 2NN sp³s* TB theory provides remarkable agreement with the measured nanocrystal bandgaps of CdSe/Cd(Zn)S and ZnSe/Zn(Cd)S QDs and accurately reproduces the energy dispersion curves of the electronic band structure at any temperature. We believe that the proposed optimization procedure makes the 2NN sp³s* TB theory reliable and accurate in the modeling of core/shell QDs for nanoscale devices. Full article

Escherichia coli (E. coli) detection suffers from slow analysis time and high costs, along with the need for specificity. While state-of-the-art electrochemical biosensors are cost-efficient and easy to implement, their sensitivity and analysis time still require improvement. In this work, we present a paper-based electrochemical biosensor utilizing magnetic core-shell Fe₂O₃@CdSe/ZnS quantum dots (MQDs) to achieve fast detection, low cost, and high sensitivity. Using electrochemical impedance spectroscopy (EIS) as the detection technique, the biosensor achieved a limit of detection of 2.7 × 10² CFU/mL for E. coli bacteria across a concentration range of 10²–10⁸ CFU/mL, with a relative standard deviation (RSD) of 3.5781%. From an optical perspective, as E. coli concentration increased steadily from 10⁴ to 10⁷ CFU/mL, quantum dot fluorescence showed over 60% lifetime quenching. This hybrid biosensor thus provides rapid, highly sensitive E. coli detection with a fast analysis time of 30 min. This study, which combines the detection advantages of electrochemical and optical biosensor systems in a graphite-based paper sensor for the first time, has the potential to meet the needs of point-of-care applications. It is thought that future studies that will aim to examine the performance of the production-optimized, portable, graphite-based sensor system on real food samples, environmental samples, and especially medical clinical samples will be promising. Full article

CdSe/ZnS quantum dots (QDs) that were highly dispersed in porous glass showed a rapid decrease in the intensity of their photoluminescence (PL) in response to ozone at concentrations of 0–200 ppm in air (at room temperature and atmospheric pressure), followed by a similarly rapid recovery to full PL in air with no ozone. The response time of the PL quenching in the presence of ozone, and the recovery time to full PL in air after the ozone was removed, showed little dependence on the ozone concentration. Compared to conventional CdSe/ZnS QD films on planar glass substrates, the speed of ozone-induced decrease in the PL intensity of QDs increased, and the recovery speed of the PL intensity, once the ozone was removed from the air, was even more rapid compared to the recovery on planar glass. The 100% PL intensity recovery time in air was reduced to about 10% for CdSe/ZnS QDs that were dispersed in porous glass compared to CdSe/ZnS QD films on planar glass substrates. We hypothesize that this reflects the fact that ozone molecules that are adsorbed on the QD-layer-lined pore surfaces are quickly desorbed in ozone-free air, because the layer of CdSe/ZnS QDs is much thinner in the pores of porous glass than on a planar glass substrate. Thus, CdSe/ZnS QDs that were dispersed in porous glass showed a rapid response to ozone and a similarly rapid recovery in ozone-free air, which has not been seen in previous QD ozone gas sensors, indicating that they are promising as high-performance optical ozone sensor materials. Full article

The use of nanostructures to enhance the emission of single-photon sources has attracted some attention in the last decade due to the development of quantum technologies. In particular, the use of metallic and high-refractive-index dielectric materials has been proposed. However, the utility of moderate-refractive-index dielectric nanostructures to achieve more efficient single-photon sources remains unexplored. Here, a systematic comparison of various metallic, high-refractive-index and moderate-refractive-index dielectric nanostructures was performed to optimize the excitation and emission of a CdSe/ZnS single quantum dot in the visible spectral region. Several geometries were evaluated in terms of electric field enhancement and Purcell factor, considering the combination of metallic, high-refractive-index and moderate-refractive-index dielectric materials conforming to homogeneous and hybrid nanoparticle dimers. Our results demonstrate that moderate-refractive-index dielectric nanoparticles can enhance the photoluminescence signal of quantum emitters due to their broader electric and magnetic dipolar resonances compared to high-refractive-index dielectric nanoparticles. However, hybrid combinations of metallic and high-refractive-index dielectric nanostructures offer the largest intensity enhancement and Purcell factors at the excitation and emission wavelengths of the quantum emitter, respectively. The results of this work may find applications in the development of single-photon sources. Full article

Dopamine (DA) is a widely present, calcium cholinergic neurotransmitter in the body, playing important roles in the central nervous system and cardiovascular system. Developing fast and sensitive DA detection methods is of great significance. Fluorescence-based methods have attracted much attention due to their advantages of easy operation, a fast response speed, and high sensitivity. This study prepared hydrophilic and high-performance CdS/ZnS quantum dots (QDs) for DA detection. The waterborne CdS/ZnS QDs were synthesized in one step using the amphiphilic polymer PEI-g-C14, obtained by grafting tetradecane (C14) to polyethyleneimine (PEI), as a template. The polyacrylonitrile nanofiber membrane (PAN-NFM) was prepared by electrospinning (e-spinning), and a metal organic frame (ZIF-8) was deposited in situ on the surface of the PAN-NFM. The CdS/ZnS QDs were loaded onto this substrate (ZIF-8@PAN-NFM). The results showed that after the deposition of ZIF-8, the water contact angle of the hydrophobic PAN-NFM decreased to within 40°. The nanofiber membrane loaded with QDs also exhibited significant changes in fluorescence in the presence of DA at different concentrations, which could be applied as a fast detection method of DA with high sensitivity. Meanwhile, the fluorescence on this PAN-NFM could be visually observed as it transitioned from a blue-green color to colorless, making it suitable for the real-time detection of DA. Full article