Search Results (99)

In clinical applications of surface-enhanced Raman spectroscopy (SERS) immunosensors, accurately determining analyte biomarker concentrations is essential. This study presents a non-invasive approach for quantifying various breast cancer biomarkers—including human epidermal growth factor receptor II (HER-II) (2+, 3+ (I), 3+ (II), 3+ (III), and positive IV) and CA 15-3—using a directional, plasmonically active, label-free SERS sensor. Each stage of sensor functionalization, conjugation, and biomarker interaction was verified by UV–Vis spectroscopy. Atomic force microscopy (AFM) characterized the morphology of gold nanourchin (GNU)-immobilized printed circuit board (PCB) substrates. An enhancement factor of ≈ 0.5 × 10⁵ was achieved using Rhodamine 6G as the probe molecule. Calibration curves were initially established using standard HER-II solutions at concentrations ranging from 1 to 100 ng/mL and CA 15-3 at concentrations from 10 to 100 U/mL. The SERS signal intensities in the 620–720 nm region were plotted against concentration, yielding linear sensitivity with R² values of 0.942 and 0.800 for HER-II and CA15-3, respectively. The same procedure was applied to breast cancer serum (BCS) samples, allowing unknown biomarker concentrations to be determined based on the corresponding calibration curves. SERS data were processed using the filtfilt filter from scipy.signal for smoothing and then baseline-corrected with the Improved Asymmetric Least Squares (IASLS) algorithm from the pybaselines.Whittaker library. Principal Component Analysis (PCA) effectively distinguished the sample groups and revealed spectral differences before and after biomarker interactions. Key Raman peaks were attributed to functional groups including N–H (primary and secondary amines), C–H antisymmetric stretching, C–N (amines), C=O antisymmetric stretching, NH₃⁺ (amines), carbohydrates, glycine, alanine, amides III, C=N stretches, and NH₂ in primary amides. Full article

For their use as chemical sensors, the optimization of the performance of polymeric materials is a critical step in their development for the desired application. The main objective of this work was to identify the best-suited materials to develop a sensor for carbonyl monitoring based on fluorescence. Two categories of materials were compared: acrylate-based materials, obtained by radical polymerization, and silicate-based materials, obtained by sol-gel synthesis. The performances of these materials in terms of yield of polymerization, carbonyl adsorption capacity and fluorescence property were compared. More precisely, the influence of various synthesis parameters such as polymerization type, radical polymerization initiation method, the nature of the functional monomer and the molar ratio of the different reactants was assessed. On the first hand, among acrylate-based materials, the one based on 4-vinylaniline showed better adsorption capacity compared to those based on 3-vinylaniline and 2-vinylaniline. Moreover, materials obtained by UV-polymerization showed a better adsorption capacity compared to those obtained by thermally initiated polymerization. On the other hand, the silicate-based material provided a better synthesis reproducibility, a higher adsorption capacity and a higher fluorescence intensity compared to its acrylate-based counterparts. Finally, contrary to the acrylate-based materials tested, the adsorption capacity and fluorescence properties of silicate-based materials were stable over time. Full article

This study reports a gate-tunable three-terminal optoelectronic synaptic device based on an Al/ZnO nanoparticles (NPs)/SiO₂/Si structure for neuromorphic in-sensor memory applications. The ZnO NP film, fabricated via spin coating, exhibited strong UV-induced excitatory post-synaptic current (EPSC) responses that were modulated by gate voltage through charge injection across the SiO₂ dielectric rather than by conventional field effect. Optical stimulation enabled short-term synaptic plasticity, with paired-pulse facilitation (PPF) values reaching 185% at a gate voltage of −5.0 V and decreasing to 180% at +5.0 V, confirming gate-dependent modulation of synaptic weight. Repeated stimulation enhanced learning efficiency and memory retention, as demonstrated by reduced pulse numbers for relearning and slower EPSC decay. Wickelgren’s power law analysis further revealed a decrease in the forgetting rate under negative gate bias, indicating improved long-term memory characteristics. A 3 × 3 synaptic device array visualized visual memory formation through EPSC-based color mapping, with darker intensities and slower fading observed under −5.0 V bias. These results highlight the critical role of gate-voltage-induced charge injection through the SiO₂ dielectric in controlling optical potentiation and electrical depression, establishing ZnO NP-based optoelectronic synaptic devices as promising platforms for energy-efficient, light-driven neuromorphic computing. Full article

Nitrogen and sulfur-co-doped carbon dots (N, S-CDs) were synthesized using a simple, eco-friendly hydrothermal technique with L-cysteine as the precursor. The synthesis approach produced highly water-dispersible, heteroatom-doped CDs with surface functional groups comprising amine, carboxyl, thiol, and sulfonic acid. Data analysis of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and transmission electron microscopy (TEM) confirmed their amorphous nature, nanoscale dimensions (1–8 nm, average particle size of 2.6 nm), and surface chemistry. Optical examination revealed intense and pure blue fluorescence emission under UV excitation, with excitation-dependent emission behavior attributed to surface defects and heteroatom doping. The N, S-CDs were applied as fluorescent probes for detecting perfluorooctanesulfonic acid (PFOS), a notable component of the perfluoroalkyl substances (PFAS) family, demonstrating pronounced and concentration-dependent fluorescence quenching. A linear detection range of 3.33–20 µM and a limit of detection (LOD) of 2 µM were reported using the N, S-CDs probe. UV-Vis spectral shifts and dye-interaction investigations indicated that the sensing mechanism is regulated by non-covalent interactions, primarily electrostatic and hydrophobic forces. These findings confirm the potential of N, S-CDs to be used as effective optical sensors for detecting PFOS in environmental monitoring applications. Full article

IR-780 is a heptamethine cyanine dye that exhibits strong absorbance in the near-infrared region. Herein, we report IR-780 dye as a dual sensor for chromogenic cyanide detection and azide’s fluorogenic sensing in acetonitrile. Cyanide and hydroxide cause instant, dramatic color changes in the dye solution from green to yellow and dramatic spectral changes in the UV-Vis spectrum. The interaction of cyanide and hydroxide with the dye caused a dramatic decrease in the intensity of the strong absorption band at 780 nm and a concomitant band appearance at 435 nm. Other monovalent ions, including fluoride, chloride, bromide, iodide, dihydrogen phosphate, thiocyanate, acetate, and dihydrogen arsenate, caused no significant color or spectral changes. UV-Vis studies showed that the IR-780 dye is sensitive and selective to both ions. The detection limits for cyanide and azide are 0.39 µM and 0.50 µM, respectively. Interestingly, the IR-780 dye exhibited strong fluorescence at 535nm upon interaction with azide, while its initial emission at 809 nm was quenched. Both UV-Vis and fluorescence spectroscopy accomplished the detection of cyanide and azide using IR-780. Furthermore, the sensor’s effectiveness in fluorescence imaging of intracellular CN⁻ ions is demonstrated in live HeLa cells. Full article

A set of three-dimensional metal-organic frameworks, named MOF-76, belonging to the tetragonal P4₃22 space group, based on [Y(BTC)(H₂O)](DMF)_1.1 (1,3,5-benzenetricarboxylate) doped with Eu³⁺, Tb³⁺, and Eu³⁺/Tb³⁺ were obtained under solvothermal conditions and fully characterized by powder X-ray diffraction, thermal, and vibrational analyses. In addition, upon UV light excitation (280 nm), all the powdered samples exhibited fine 4f-4f transitions, of which the ⁵D₀ → ⁷F₂ (Eu³⁺) and ⁵D₄ → ⁷F₅ (Tb³⁺) were the most intense ones. All samples were photophysically analyzed by determining the luminescence lifetimes, and their emission colors were quantified by calculating their chromaticities and color purities. Moreover, the intrinsic quantum yield, radiative, and non-radiative constants were calculated and compared to establish a structure–property relationship. Specifically, the Eu/Tb co-doped sample was employed to monitor its hypersensitive emissions in the presence of small volatile organic compounds (VOCs), showing quenching or enhancement of emission in protic and non-protic solvents. Furthermore, DFT calculations were carried out to understand the energy transfer processes between the sensor and the respective analytes. These results are promising for the development of solid-state lighting devices and colorimetric chemical sensors for specific compounds. Full article

In this study, silver nanoparticles (Ag NPs) were synthesized on the surface of rutile-phase titanium dioxide (R-TiO₂) using a plasma-assisted technique. Comprehensive analyses were conducted to investigate the structural, morphological, optical, and electrical properties of the synthesized nanocomposites. Transmission electron microscopy (TEM) images revealed the uniform decoration of Ag NPs (average size: 29.8 nm) on the R-TiO₂ surface. X-ray diffraction (XRD) confirmed the polycrystalline nature of the samples, with decreased diffraction peak intensity indicating reduced crystallinity due to Ag decoration. The Williamson–Hall analysis showed increased crystallite size and reduced tensile strain, suggesting grain growth and stress relief. Raman spectroscopy revealed quenching and broadening of R-TiO₂ vibrational modes, likely due to increased oxygen vacancies. X-ray photoelectron spectroscopy (XPS) confirmed successful plasma-assisted deposition and the coexistence of Ag⁰ and Ag⁺ states, enhancing surface reactivity. UV-Vis spectroscopy demonstrated enhanced light absorption across the spectral range, attributed to localized surface plasmon resonance (LSPR), and a reduced optical bandgap. Dielectric properties, including dielectric constants, loss factor, and AC conductivity, were evaluated across frequencies (4–8 MHz) and temperatures (20–240 °C). The AC conductivity results indicated correlated barrier hopping (CBH) and overlapping large polaron tunneling (OLPT) as the primary conduction mechanisms. Composition-dependent dielectric behavior was interpreted through the Coulomb blockade effect. These findings suggest the potential of plasma assisted Ag NP-decorated R-TiO₂ nanostructures for photocatalysis, sensor and specific electro electrochemical systems applications. Full article

With the introduction of advanced Fiber Bragg Grating (FBG) technology, Fabry–Pérot (FP) interferometers have become widely used in fiber-optic ultrasound detection. In these applications, the slope of the reflectance is a critical factor influencing detection results. Due to the intensity limitations of the laser source in fiber-optic ultrasound detection, the reflectance of the FBG is generally increased to enhance the signal-to-noise ratio (SNR). However, increasing reflectance can cause the reflectance curve to deviate from a sinusoidal shape, which in turn affects the slope of the reflectance and introduces greater errors. This paper first investigates the relationship between the transmission curve of the FP interferometer and reflectance, with a focus on the errors introduced by simplified assumptions. Further research shows that in sensors with asymmetric reflectance slopes, their transmittance curves deviate significantly from sinusoidal signals. This discrepancy highlights the importance of achieving symmetrical slopes to ensure consistent and accurate detection. To address this issue, this paper proposes an innovative method to adjust the rear-end reflectance of the FP interferometer by combining stress modulation, UV adhesive, and a high-reflectivity metal disk. Additionally, by adjusting the rear-end reflectance to ensure that the transmittance curve approximates a sinusoidal signal, the symmetry of the slope is maintained. Finally, through practical ultrasound testing, by adjusting the incident wavelength to the positions of slope extrema (or zero) at equal intervals, the expected ultrasound signals at extrema (or zero) can be detected. This method converts the problem of approximating a sinusoidal signal into a problem of the slope adjustment of the transmittance curve, making it easier and more direct to determine its impact on detection results. The proposed method not only improves the performance of fiber-optic ultrasound sensors but also reduces costs, paving the way for broader applications in medical diagnostics and structural health monitoring. Full article

This paper deals with the evaluation of the combustion intensity of coal particles on the basis of measurement data (UV radiation) from a scanning point photodiode. UV radiation is measured using a custom UV scanner at different distances from the burner in the vertical combustion chamber. The designed scanner uses a sensitive silicon carbide (SiC) photodiode, and its dynamical properties are investigated in the present work. Subsequently, experiments are performed for coal particles at different combustion temperatures and at different measuring locations of the scanner. The measurement data are processed in the frequency domain using the proposed algorithm, and two indicators for evaluating the combustion intensity are proposed. The obtained results show that the proposed indicators provide unequivocal information about the combustion intensity as a function of the combustion temperature. Full article

The design and development of fluorescent materials for detecting cancer-related enzymes are crucial for cancer diagnosis and treatment. Herein, we present a substituted rhodamine derivative for the chromogenic and fluorogenic detection of the cancer-relevant enzyme γ-glutamyltranspeptidase (GGT). Initially, the probe is non-chromic and non-emissive due to its spirolactam form, which hinders extensive electronic delocalization over broader pathway. However, selective enzymatic cleavage of the side-coupled group triggers spirolactam ring opening, resulting in electronic flow across the rhodamine skeleton, and reduces the band gap for low-energy electronic transitions. This transformation turns the reaction mixture from colorless to intense pink, with prominent UV and fluorescence bands. The sensor’s selectivity was tested against various human enzymes, including urease, alkaline phosphatase, acetylcholinesterase, tyrosinase, and cyclooxygenase, and showed no response. Absorption and fluorescence titration analyses of the probe upon incremental addition of GGT into the probe solution revealed a consistent increase in both absorption and emission spectra, along with intensified pink coloration. The cellular toxicity of the receptor was evaluated using the MTT assay, and bioimaging analysis was performed on BHK-21 cells, which produced bright red fluorescence, demonstrating the probe’s excellent cell penetration and digestion capabilities for intracellular analytical detection. Molecular docking results supported the fact that probe-4 made stable interactions with the GGT active site residues. Full article

Temperature and pressure sensors currently encounter challenges such as slow response times, large sizes, and insufficient sensitivity. To address these issues, we developed tetraphenylethylene (TPE)-doped polyvinylidene fluoride (PVDF) nanofiber membranes using electrospinning, with process parameters optimized through a convolutional neural network (CNN). We systematically analyzed the effects of PVDF concentration, spinning voltage, tip–to–collector distance, and flow rate on fiber morphology and diameter. The CNN model achieved high predictive accuracy, resulting in uniform and smooth nanofibers under optimal conditions. Incorporating TPE enhanced the hydrophobicity and mechanical properties of the nanofibers. Additionally, the fluorescent properties of the TPE-doped nanofibers remained stable under UV exposure and exhibited significant linear responses to temperature and pressure variations. The nanofibers demonstrated a temperature sensitivity of −0.976 gray value/°C and pressure sensitivity with an increase in fluorescence intensity from 537 a.u. to 649 a.u. under 600 g pressure. These findings highlight the potential of TPE-doped PVDF nanofiber membranes for advanced temperature and pressure sensing applications. Full article

Surface-enhanced Raman spectroscopy (SERS) is a promising and highly sensitive molecular fingerprint detection technology. However, the development of SERS nanocomposites that are label-free, highly sensitive, selective, stable, and reusable for gaseous volatile organic compounds (VOCs) detection remains a challenge. Here, we report a novel TiO₂NTs/AuNPs@ZIF−8 nanocomposite for the ultrasensitive SERS detection of VOCs. The three-dimensional TiO₂ nanotube structure with a large specific surface area provides abundant sites for the loading of Au NPs, which possess excellent local surface plasmon resonance (LSPR) effects, further leading to the formation of a large number of SERS active hotspots. The externally wrapped porous MOF structure adsorbs more gaseous VOC molecules onto the noble metal surface. Under the synergistic mechanism of physical and chemical enhancement, a better SERS enhancement effect can be achieved. By optimizing experimental conditions, the SERS detection limit for acetophenone, a common exhaled VOC, is as low as 10⁻¹¹ M. And the relative standard deviation of SERS signal intensity from different points on the same nanocomposite surface is 4.7%. The acetophenone gas achieves a 1 min response and the signal reaches stability in 4 min. Under UV irradiation, the surface-adsorbed acetophenone can be completely degraded within 40 min. The experimental results demonstrate that this nanocomposite has good detection sensitivity, repeatability, selectivity, response speed, and reusability, making it a promising sensor for gaseous VOCs. Full article

This study aimed to evaluate the effects of fruit position, light exposure and fruit surface temperature (FST) on apple fruit colour development and fruit quality at harvest, including sunburn damage severity. This was achieved by undertaking two experiments in a high-density planting of the dark-red apple ANABP 01 in Tatura, Australia. In the 2020–2021 growing season an experiment was conducted to draw relationships between fruit position and fruit quality parameters. Here, sample fruit position and level of light exposure were respectively determined using a static LiDAR system and a portable quantum photosynthetically active radiation (PAR) sensor. At harvest the sample fruit were analysed for percentage red colour coverage, objective colour parameters (L*, a*, b*, hue angle and chroma), sunburn damage, fruit diameter (FD), soluble solids concentration (SSC), flesh firmness (FF) and starch pattern index (SPI). A second experiment was conducted in the 2021–2022 growing season and focused on how fruit shading, light exposure and the removal of ultraviolet (UV) radiation affected the FST, colour development and harvest fruit quality. Five treatments were distributed among sample fruit: fully shaded with aluminium umbrellas, shaded for one month and then exposed to sunlight until harvest, exposed for one month and then shaded until harvest, covered with a longpass UV filter and a control treatment. The development of colour in this dark-red apple cultivar was highly responsive to aspects of fruit position, and the intensity and quality of light exposure. The best-coloured fruit were exposed to higher quantities of PAR, exposed to both PAR and UV radiation simultaneously and located higher in the tree canopy. Fruit that were fully exposed to PAR and achieved better colour development also displayed higher FST and sunburn damage severity. Full article

Increasing concern over the safety of consumable products, particularly aquatic products, due to freshness issues, has become a pressing issue. Therefore, ensuring the quality and safety of aquatic products is paramount. To address this, a dual-mode colorimetric–fluorescence sensor utilizing Ce-MOF as a mimic peroxidase to detect H₂S was developed. Ce-MOF was prepared by a conventional solvothermal synthesis method. Ce-MOF catalyzed the oxidation of 3,3’,5,5’-tetramethylbenzidine (TMB) by hydrogen peroxide (H₂O₂) to produce blue oxidized TMB (oxTMB). When dissolved, hydrogen sulfide (H₂S) was present in the solution, and it inhibited the catalytic effect of Ce-MOF and caused the color of the solution to fade from blue to colorless. This change provided an intuitive indication for the detection of H₂S. Through steady-state dynamic analysis, the working mechanism of this sensor was elucidated. The sensor exhibited pronounced color changes from blue to colorless, accompanied by a shift in fluorescence from none to light blue. Additionally, UV–vis absorption demonstrated a linear correlation with the H₂S concentration, ranging from 200 to 2300 µM, with high sensitivity (limit of detection, LOD = 0.262 μM). Fluorescence intensity also showed a linear correlation, ranging from 16 to 320 µM, with high selectivity and sensitivity (LOD = 0.156 μM). These results underscore the sensor’s effectiveness in detecting H₂S. Furthermore, the sensor enhanced the accuracy of H₂S detection and fulfilled the requirements for assessing food freshness and safety. Full article

The surfactant cetyltrimethylammonium bromide (CTAB) induces the aggregation of gold nanoclusters (GNCs), leading to the development of a proposed fluorometric technique for detecting thiocyanate (SCN⁻) ions based on an anti-aggregation mechanism. This approach is straightforward to execute, highly sensitive, and selective. A significant quenching effect occurs in fluorescence upon using the aggregation agent CTAB in GNCs synthesis, resulting in a transition from intense red fluorescence to dim red. The decrease in fluorescence intensity of GNCs in the presence of CTAB is caused by the mechanism of fluorescence quenching mediated by aggregation. As the levels of SCN⁻ rise, the fluorescence of CTAB-GNCs increases; this may be detected using spectrofluorometry or by visually inspecting under UV irradiation. The recovery of red fluorescence of CTAB-GNCs in the presence of SCN⁻ enables the precise and discerning identification of SCN⁻ within the concentration range of 2.86–140 nM. The minimum detectable concentration of the SCN⁻ ions was 1 nM. The selectivity of CTAB-GNCs towards SCN⁻ ions was investigated compared to other ions, and it was demonstrated that CTAB-GNCs exhibit exceptional selectivity. Furthermore, we believe that CTAB-GNCs have novel possibilities as favorable sensor candidates for various industrial applications. Our detection technique was validated by analyzing SCN⁻ ions in milk samples, which yielded promising results. Full article