Search Results (100)

CuO/TiO₂ is a highly active visible-light-driven photocatalyst. The precise structural regulation of TiO₂ and the quantum dot-scale loading strategy of CuO have long been researching hotspots and challenges. This work presents an ingenious synthetic strategy, leveraging the photoinduced superhydrophilicity and dark-induced reversible hydrophobicity of TiO₂, coupled with carbon quantum dots (CQDs) as “seeds” to induce the in situ synthesis of CuO quantum dots (CuO QDs). Specifically, CuO QDs with an average diameter of 5–10 nm were successfully anchored onto TiO₂ nanowire arrays (TNWAs) with a diameter of 10–15 nm. By adjusting the dosage of “seeds” (CQDs), the loading amount of CuO QDs can be effectively controlled. Corresponding characterizations were performed, including ultraviolet-visible-near-infrared (UV-Vis-NIR spectroscopy) for optical absorption properties, photoluminescence (PL) spectroscopy for photoluminescent behavior, electron paramagnetic resonance (EPR) spectroscopy for free radical generation capability, and bisphenol A (BPA) degradation assays for photocatalytic performance. Loading 4.78 wt% CuO QDs can effectively inhibit the recombination of electron–hole pairs in TNWAs. Simultaneously, it prolongs the lifetime of charge carriers (photoelectrons) and enhances the yields of hydroxyl radicals (•OH) and superoxide radicals (•O₂⁻). The BPA degradation efficiency of the CuO QDs/TNWA composite is 2.4 times higher than that of TNWAs. Furthermore, we found that the loading of CuO QDs significantly modulates the depletion layer width of the P–N heterojunction, and the underlying mechanism has been discussed in detail. Full article

Quantum dots (QDs) composed of the narrow-bandgap semiconductor PbTe were incorporated into the depletion region of p–n junctions based on wide-bandgap II–VI semiconductors (p-ZnTe/n-CdTe). The heterostructures were grown by molecular beam epitaxy (MBE) on semi-insulating GaAs (100) substrates. The depletion region was engineered by depositing 20 alternating thin layers of CdTe and PbTe, then thermal annealing under ultrahigh vacuum. As revealed by cross-sectional scanning electron microscopy (SEM), the initially continuous PbTe layers transformed into arrays of zero-dimensional nanostructures, namely PbTe QDs. The formation of PbTe QDs in a CdTe matrix arises from the structural mismatch between the zinc blende and rock-salt crystal structures of the two materials. Electron beam-induced current (EBIC) scans confirmed that the QDs are localized within the depleted charge region between the p-ZnTe and n-CdTe layers. The resulting wide-gap diodes containing narrow-band QDs show pronounced sensitivity to infrared radiation in the spectral range of 1–4.5 μm, with a peak responsivity of approximately 8 V/W at a wavelength of ~2.0 μm and a temperature of 200 K. A red-shift in the cutoff wavelength when temperature decreases indicates that the infrared (IR) response is governed by band-to-band optical transitions in the PbTe QDs. In addition, the devices show sensitivity to visible radiation, with a maximum responsivity of 20 V/W at 0.69 μm. These results demonstrate that wide-bandgap p–n junctions incorporating narrow-bandgap QDs can function as dual-wavelength (visible and infrared) photodetectors, with potential applications in two-color detection and infrared solar cells. Full article

The total antioxidant capacity (TAC) of food products is a key parameter for assessing food quality and safety. In this work, iron-doped carbon dots (Fe-CDs) were successfully prepared using waste coffee grounds as a precursor with a satisfactory fluorescence quantum yield of 9.6%. The Fe-CDs exhibited exceptional peroxidase-like activity, which can oxidize colorless 3,3′,5,5′-tetramethylbenzidine (TMB) to form blue oxTMB. Concurrently, oxTMB induced an inner filter effect, quenching the fluorescence of Fe-CDs. After being added to antioxidants such as glutathione, ascorbic acid, and L-cysteine, the generated reactive oxygen species (ROS) are consumed, thereby preventing the oxidation of TMB. The color of the mixed solution changed from dark to light blue, accompanied by the fluorescence recovery of Fe-CDs. Nevertheless, these three antioxidants possessed remarkable differences in ROS elimination capability, which resulted in different signal responses in absorption and fluorescence, and were successfully used for constructing the colorimetric/fluorescent dual-channel sensor array. Furthermore, the sensor array signals were processed using principal component analysis to achieve simultaneous detection of glutathione, ascorbic acid, and L-cysteine, and were able to effectively discriminate between mixtures and individual antioxidants. The constructed sensor array was successfully applied for the TAC detection in various foods (including vegetables, fruit, and beverages) and for the precise differentiation of antioxidants in milk samples. Overall, the prepared sensor array exhibited outstanding potential in detecting food quality. Full article

Aimed at addressing the increasingly serious problem of adulteration in Xihu Longjing, a catechin-targeted nano-enhanced visual and fluorescent dual-mode sensor array was constructed by nano porphyrins and quantum dots (QDs) for the precise analysis of Xihu Longjing from adjacent origins. This sensor array realizes the quantitative analysis of catechin enantiomers in Xihu Longjing through the selective combination of sensing units. It can accurately identify adjacent Xihu Longjing teas with different grades and storage times and can precisely detect samples with a low proportion of adulteration. At the same time, the flavor quality and antioxidant performance of Xihu Longjing tea can also be quantitatively evaluated. The dual-mode sensor array design proposed in this study provides a new idea for detecting minor differences in food authenticity and has significant application value for quality control in the tea industry. Full article

Optimal sensing devices exhibit a combination of key performance attributes, including an extensive detection limit, exceptional selectivity, high sensitivity, consistent repeatability, precise measurement, and rapid response times with efficient analyte flow. In recent years, biosensing platforms incorporating nanoscale materials have garnered considerable attention due to their diverse applications across various scientific and technological domains. The integration of nanoparticles (NPs) in biosensor design primarily bridges the dimensional gap between the signal transduction element and the biological recognition component, both of which operate at nanometer scales. The synergistic combination of NPs with electrochemical techniques has facilitated the development of biosensors characterized by enhanced sensitivity and superior analyte discrimination capabilities. This comprehensive analysis examines the evolution and recent advancements in nanomaterial (NM)-based biosensors, encompassing an extensive array of nanostructures. These consists of one-dimensional nanostructures including carbon nanotubes (CNTs), nanowires (NWs), nanorods (NRs), and quantum dots (QDs), as well as noble metal and metal and metal oxide nanoparticles (NPs). The article examines how advancements in biosensing techniques across a range of applications have been fueled by the growth of nanotechnology. Researchers have significantly improved biosensor performance parameters by utilizing the distinct physiochemical properties of these NMs. The developments have increased the potential uses of nanobiosensors in a wide range of fields, from food safety and biodefense to medical diagnostics and environmental monitoring. The continuous developments in NM-based biosensors are the result of the integration of several scientific areas, such as analytical chemistry, materials science, and biotechnology. This interdisciplinary approach continues to drive innovations in sensor design, signal amplification strategies, and data analysis techniques, ultimately leading to more sophisticated and capable biosensing platforms. As the field progresses, challenges related to the scalability, reproducibility, and long-term stability of nanobiosensors are being addressed through innovative fabrication methods and surface modification techniques. These efforts aim to translate the promising results observed in laboratory settings into practical, commercially viable biosensing devices that can address real-world analytical challenges across various sectors. Full article

Optical biosensors have emerged as a transformative technology for food safety monitoring. These devices combine biorecognition molecules with advanced optical transducers, enabling the detection of a wide array of food contaminants, including pathogens, toxins, pesticides, and antibiotic residues. This review comprehensively explores the principles, advancements, applications, and future trends of optical biosensors in ensuring food safety. The key advantages of optical biosensors, such as high sensitivity to trace contaminants, fast response times, and portability, make them an attractive alternative to traditional analytical methods. Types of optical biosensors discussed include surface plasmon resonance (SPR), interferometric, fluorescence and chemiluminescence, and colorimetric biosensors. SPR biosensors stand out for their real-time, label-free analysis of foodborne pathogens and contaminants, while fluorescence and chemiluminescence biosensors offer exceptional sensitivity for detecting low levels of toxins. Interferometric and colorimetric biosensors, characterized by their portability and visual signal output, are well-suited for field-based applications. Biosensors have proven invaluable in monitoring heavy metals, pesticide residues, and antibiotic contaminants, ensuring compliance with stringent food safety standards. The integration of nanotechnology has further enhanced the performance of optical biosensors, with nanomaterials such as quantum dots and nanoparticles enabling ultra-sensitive detection and signal amplification. Optical biosensors represent a vital advancement in the field of food safety, addressing critical public health concerns through their rapid and reliable detection capabilities. Continued interdisciplinary efforts in nanotechnology, material science, and device engineering are poised to further expand their applications, making them indispensable tools for safeguarding global food supply chains. Full article

The nitrogen-vacancy (NV) center magnetic sensor, leveraging nitrogen-vacancy quantum effects, enables high-sensitivity magnetic field detection via optically detected magnetic resonance (ODMR). However, conventional single-point integrated devices suffer from limitations such as inefficient regional magnetic field detection and challenges in discerning the directional variations of dynamic magnetic fields. To address these issues, this study proposes an array- based architecture that innovatively substitutes the conventional 532 nm laser with quantum-dot light-emitting diodes (QLEDs). Capitalizing on the advantages of QLEDs—including compatibility with micro/nano-fabrication processes, wavelength tunability, and high luminance—a 2 × 2 monolithically integrated magnetometer array was developed. Each sensor unit achieves a magnetic sensitivity of below 26 nT·Hz^−1/2 and a measurable range of ±120 μT within the 1–10 Hz effective bandwidth. Experimental validation confirms the array’s ability to simultaneously resolve multi-regional magnetic fields and track dynamic field orientations while maintaining exceptional device uniformity. This advancement establishes a scalable framework for the design of large-scale magnetic sensing arrays, demonstrating significant potential for applications requiring spatially resolved and directionally sensitive magnetometry. Full article

Aquatic biomass—ranging from fish scales and crustacean shells to various algae species—offers an abundant, renewable source for carbon dot (CD) synthesis, aligning with circular economy principles. This review highlights recent studies for valorizing aquatic biomass into high-performance carbon-based nanomaterials—specifically aquatic biomass-based carbon dots (AB-CDs)—briefly summarizing green synthesis approaches (e.g., hydrothermal carbonization, pyrolysis, and microwave-assisted treatments) that minimize environmental impact. Subsequent sections highlight the varied applications of AB-CDs, particularly in biosensing (including the detection of marine biotoxins), environmental monitoring of water pollutants, and drug delivery systems. Physically AB-CDs show unique optical and physicochemical properties—tunable fluorescence, high quantum yields, enhanced sensitivity, selectivity, and surface bio-functionalization—that make them ideal for a wide array of applications. Overall, the discussion underlines the significance of this approach; indeed, transforming aquatic biomass into carbon dots can contribute to sustainable nanotechnology, offering eco-friendly solutions in sensing, environmental monitoring, and therapeutics. Finally, current challenges and future research directions are discussed to give a perspective of the potential of AB-CDs; the final aim is their integration into multifunctional, real-time monitoring and therapeutic systems—for sustainable nanotechnology innovations. 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

In this study, β-cyclodextrin (β-CD) functionalized graphene quantum dots (GQDs) was employed to augment the array of chiral recognition sites, thereby enhancing the affinity of GQDs/β-CD composite for imprinting molecules and realizing heightened chiral selectivity. The incorporation of GQDs/β-CD into the synthesis of molecularly imprinted polymers (MIPs), synergizing with the host-guest inclusion properties of β-CD and the abundant carboxyl groups of GQDs, enhanced the chiral recognition capacity of MIPs materials. Consequently, a novel MIPs/(GQDs/β-CD) sensor with chiral recognition capabilities tailored for D-carnitine was successfully fabricated. The binding mechanism between GQDs/β-CD and D-carnitine was elucidated via Ultraviolet-visible spectroscopy and Fourier transform infrared spectroscopy. The variation in the response signal (ΔI) of the probe molecule exhibited a linear correlation with the logarithm of D-carnitine concentration (lgC) in the range of 1.0 × 10⁻¹² mol/L to 1.0 × 10⁻⁹ mol/L, and the detection limit (3δ/S) was calculated as 2.35 × 10⁻¹³ mol/L. These results underscore a 7.15-fold enhancement in the selectivity of MIPs/(GQDs/β-CD) sensor for D-carnitine recognition. Moreover, the sensor presented commendable efficacy in real-world scenarios, yielding recovery rates ranging from 98.5% to 103.0% during the determination of D-carnitine content in real samples. Full article

Colloidal quantum dots (QDs) have emerged as promising materials for the development of infrared photodetectors owing to their tunable band gaps, cost-effective manufacturing, and ease of processing. This paper provides a comprehensive overview of the fundamental properties of quantum dots and the operating principles of various infrared detectors. We review the latest advancements in short-wave infrared (SWIR), mid-wave infrared (MWIR), and long-wave infrared (LWIR) detectors employing colloidal quantum dots. Despite their potential, these detectors face significant challenges compared to conventional infrared technologies. Current commercial applications are predominantly limited to the near-infrared and short-wave bands, with medium- and long-wave applications still under development. The focus has largely been on lead and mercury-based quantum dots, which pose environmental concerns, underscoring the need for high-performance, non-toxic materials. Looking forward, the development of large array and small pixel detectors and improving compatibility with readout circuits are critical for future progress. This paper discusses these hurdles and offers insight into potential strategies to overcome them, paving the way for next-generation infrared sensing technologies. 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

Outlined is a proposal designed to culminate in the foundry fabrication of arrays of singly addressable quantum dot sources deterministically emitting single pairs of energy-time entangled photons at C-band wavelengths, each pair having negligible spin-orbit fine structure splitting, each pair being channeled into single mode pig-tail optical fibers. Entangled photons carry quantum state information among distributed quantum servers via I/O ports having two functions: the unconditionally secure distribution of decryption keys to decrypt publicly distributed, encrypted classical bit streams as input to generate corresponding qubit excitations and to convert a stream of quantum nondemolition measurements of qubit states into a classical bit stream. Outlined are key steps necessary to fabricate arrays of on-demand quantum dot sources of entangled photon pairs; the principles are (1) foundry fabrication of arrays of isolated quantum dots, (2) generation of localized sub-surface shear strain in a semiconductor stack, (3) a cryogenic anvil cell, (4) channeling entangled photons into single-mode optical fibers, (5) unconditionally secure decryption key distribution over the fiber network, (6) resonant excitation of a Josephson tunnel junction qubits from classical bits, and (7) conversion of quantum nondemolition measurements of qubit states into a classical bit. Full article

Single nucleotide polymorphisms (SNPs) present significant challenges in microbial detection and treatment, further raising the demands on sequencing technologies. In response to these challenges, we have developed a novel barcode-based approach for highly sensitive single nucleotide recognition. This method leverages a dual-head folded complementary template probe in conjunction with DNA ligase to specifically identify the target base. Upon recognition, the system triggers rolling circle amplification (RCA) followed by the self-assembly of CdSe quantum dots onto polystyrene microspheres, enabling a single-particle fluorescence readout. This approach allows for precise base identification at individual loci, which are then analyzed using a bio-barcode array to screen for base changes across multiple sites. This method was applied to sequence a drug-resistant mutation site in Helicobacter pylori (H. pylori), demonstrating excellent accuracy and stability. Offering high precision, high sensitivity, and single nucleotide resolution, this approach shows great promise as a next-generation sequencing method. Full article

The design of chemical sensors and probes is usually based on selective receptors for individual analytes, however, many analytical tasks are dedicated to multi-analyte sensing or recognizing properties of the sample related to more than one analyte. While it is possible to simultaneously use multiple sensors/receptors in such cases, multi-responsive probes could be an attractive alternative. In this work, we use thiomalic acid-capped CdTe quantum dots as a multiple-response receptor for the detection and quantification of six heavy metal cations: Ag(I), Cd(II), Co(II), Cu(II), Ni(II), and Pb(II) at micromolar concentration levels. Multiplexing is realized via multispectral fluorescence (so-called virtual sensor array). For such a sensing strategy, the effective decoding of the excitation–emission spectrum is essential. Herein, we show how various parameters of chemometric analysis by the Partial Least Squares method, such as preprocessing type and data structure, influence the performance of discrimination and quantification of the heavy metals. The established models are characterized by respective performance metrics (accuracy, sensitivity, precision, specificity/RMSE, a, b, R²) determined for both train and test sets in replicates, to obtain reliable and repeatable results. Full article