Search Results (878)

A thin-film surface plasmon resonance (SPR) sensor is presented using a prism-coupled Kretschmann configuration and an optimized multilayer architecture incorporating black phosphorus (BP) as an ultrathin overlayer. The response is modeled at 633 nm under TM polarization using the transfer-matrix method. Low-concentration sensing conditions in the 1–5 ng/mL range are represented through small effective-refractive-index perturbations of the aqueous sensing medium, providing a preliminary optical framework for evaluating refractive-index response in biosensing-related scenarios. The coupling prism, Au film thickness, and Si₃N₄ spacer thickness are optimized to control resonance depth, linewidth, and angular shift. The optimized CaF₂/Au/Si₃N₄/BP configuration exhibits systematic condition-dependent displacement of the SPR minimum and an evanescent-field distribution that remains strongly localized at the sensing interface while extending into the sensing medium, enabling refractive-index interrogation. High angular sensitivity is obtained at low levels, reaching 517.62°/RIU at 2 ng/mL and 482.82°/RIU at 1 ng/mL, with quality factors above 120 RIU⁻¹ in the same regime. Composite indicators (figure of merit and contrast signal factor) peak at intermediate levels, whereas resonance broadening at higher levels reduces the quality factor and increases the inferred limit of detection, evidencing a sensitivity–resolution trade-off. Benchmarking against reported SPR platforms indicates that BP-assisted interface engineering provides a competitive low-level operating window within a preliminary refractive-index-sensing framework that is relevant to future biosensor design. These results motivate further experimental validation, including BP stabilization, surface biofunctionalization, and practical implementation under liquid-phase sensing conditions. Full article

Two-dimensional materials have broad application prospects in the field of optoelectronic devices. As a next-generation power electronic device, AlN materials have obvious advantages in power processing, and their monolayer structure has excellent optoelectronic properties, which is of great significance for the study of 2D AlN monolayers. Properties such as electronic and optical properties of metal-adsorbed AlN (M-AlN) systems have been systematically investigated using density functional theory from first principles. The results of the energy bands of the M-AlN system indicate that the adsorption of Al, Li, Ag, Au, Bi, Cr, Mn, Na, Pb, Sn, Ti, and K metals makes the monolayer AlN magnetic, the incorporation of two metals, Al and Li, is the transition of the monolayer AlN from a semiconductor to a semi-metal, and the introduction of K metal makes the monolayer AlN transition from a semiconductor to a metal. The work function of the M-AlN system shows that the introduction of the metal reduces the work function of the monolayer AlN, especially for K-AlN, which is reduced by 56.12% compared to the monolayer AlN. In addition, the results of the optical absorption spectra of the M-AlN system revealed that the introduction of the metals made the monolayer AlN exhibit high absorption peaks in the visible and near-infrared regions; in particular, the intensity of the absorption peaks of the Ti-AlN system at 557.8 nm reached 7.4 × 10⁴ cm⁻¹ and the intensity of the absorption peaks of the K-AlN system at 1109.3 nm reached 1.01 × 10⁵ cm⁻¹. This indicates that the introduction of Ti and K metal atoms enhances the absorption properties of monolayer AlN in the visible and near-infrared regions. Finally, the time-domain finite difference using spherical metal nanoparticles is used to excite the localized surface plasmon resonance, and the results show a small area of strong electric field around the electric field hotspot of Cr and Li particles, and a good concentration of the electric field strength in the x and y directions. In summary, the system of metal atoms adsorbed on AlN will be favorable for the design of spintronics, field-emitting devices and solar photovoltaic devices. Full article

Over the past two decades, organic semiconductors have attracted significant research interest due to their advantageous features, including low-cost fabrication, lightweight properties, and portability, for photonic device applications. In this study, nickel sulfide doped with cobalt $(\mathrm{N}\mathrm{i}\mathrm{S}/\mathrm{C}\mathrm{o})$ nanocomposites were successfully synthesized via a wet-chemical processing technique and used as a dopant in the active layer of thin-film organic solar cells (TFOSCs). The poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) blend was used as the active layer in this investigation. The devices were fabricated with $\mathrm{N}\mathrm{i}\mathrm{S}/\mathrm{C}\mathrm{o}$ nanocomposites at 1 wt%, 2 wt%, and 3 wt% in the active layer to determine the optimal dopant concentration. However, the experimental evidence clearly showed that the solar cell’s performance depends on the concentration of the $\mathrm{N}\mathrm{i}\mathrm{S}/\mathrm{C}\mathrm{o}$ nanocomposites. As a result, the highest power conversion efficiency (PCE) recorded in this experimental work was 6.11% at a 1% doping concentration, compared with 2.48% for the pristine reference device under AM 1.5G illumination (100 mW/cm²) in ambient conditions. The optical and electrical properties of the active layers are found to be strongly influenced by the inclusion of $\mathrm{N}\mathrm{i}\mathrm{S}/\mathrm{C}\mathrm{o}$ nanocomposites in the medium. However, the device doped with 1 wt% $\mathrm{N}\mathrm{i}\mathrm{S}/\mathrm{C}\mathrm{o}$ nanocomposite exhibits the highest absorption intensity, consistent with the better performance observed in this study, which can be attributed to the localized surface plasmon resonance (LSPR) effect. The optical and morphological characteristics of the synthesized $\mathrm{N}\mathrm{i}\mathrm{S}/\mathrm{C}\mathrm{o}$ nanocomposites were comprehensively analyzed using high-resolution transmission electron microscopy (HRTEM), high-resolution scanning electron microscopy (HRSEM), and additional complementary techniques. Full article

Surface-enhanced Raman scattering (SERS) has become an effective and sensitive analysis tool for the detection of various molecules. Nevertheless, it is a challenge to fabricate reusable SERS substrates for detecting gaseous molecules. Here, a self-calibrated and reusable SERS substrate has been developed for the quantitative analysis of n-butylamine. The obtained substrate enhances gas enrichment capability through the coordination interaction of Fe₂O₃ with the porous structure of ZIF-8, and strengthens the Raman signal intensity by the localized surface plasmon resonance of Ag nanoparticles. Ethanethiol is employed as an internal standard to enhance analysis accuracy. The substrate exhibits excellent quantitative analysis (linear correlation coefficient, R² = 0.996), signal uniformity (RSD = 6.3%), and batch reproducibility (RSD = 4.8%). Moreover, the substrate achieves self-cleaning through photocatalysis. After five cycles, the substrate retains high SERS activity (RSD = 3.13%), exhibiting excellent reusability. Full article

Sensitive and on-site detection of pesticide residues remains a critical challenge for food safety, particularly in developing regions where rapid screening tools are urgently needed. Herein, we report a flexible surface-enhanced Raman scattering (SERS) platform based on triangular silver nanoplates (TSNPs) integrated onto a polydimethylsiloxane (PDMS) substrate, enabling sensitive and conformal detection of paraquat residues on agricultural surfaces. TSNPs were synthesized via a seed-mediated photochemical growth method and formulated into a TSNP ink, which was directly deposited onto oxygen-plasma-treated and thiol-functionalized PDMS substrates. Owing to the highly anisotropic geometry and sharp edges of TSNPs, the flexible SERS substrate exhibits strong localized surface plasmon resonance (LSPR) enhancement and mechanically stable electromagnetic hot spots. Systematic optimization of TSNP optical absorbance revealed that uniform nanoplate distribution and optimal hotspot density were achieved at an absorbance of 2.0. The SERS performance was evaluated using rhodamine 6G under front-side and back-side illumination configurations, demonstrating good signal reproducibility and a detection limit of approximately 10⁻⁵ M. Notably, back-side illumination through the PDMS layer provided superior SERS responses due to improved optical transmission and light–matter interaction. The practical applicability was further demonstrated through back-side SERS detection of paraquat on aluminum foil as a model surface, achieving a lowest detectable concentration of 5 × 10⁻⁶ M, followed by damage-free detection on Chinese pear peels. This work highlights a reliable and nondestructive flexible SERS platform for on-site pesticide residue monitoring. Full article

The residual malachite green (MG) in aquatic products poses a severe threat to human health, thus an urgent need exists for the establishment of a rapid and accurate analytical method. In this work, a high-performance film based on a nano-network structure was developed for the highly sensitive detection of MG. This film employed the nanonetwork structure as its sensing substrate, and the network structure with a high specific surface area enabled efficient enrichment of MG molecules. The silver nanoparticles uniformly modified on the surface could produce a remarkable localized surface plasmon resonance effect, thereby significantly enhancing the signals of MG molecules adsorbed on its surface. The results showed that the film exhibited a low limit of detection (LOD) of 8.8 pM for MG, with a linear range from 10 to 5000 pM. In the detection of aquatic products, this film successfully achieved the rapid and accurate determination of MG in aquatic products, showing an excellent potential for practical applications. The nanonetwork-structured film developed in this work provides a reliable and sensitive technical solution for the trace detection of MG in aquatic products. Full article

Hybrid nanomaterials that integrate surface functionality, colloidal stability, and efficient electron-transfer pathways are highly attractive for improving electrochemical sensing performance. Herein, we report the fabrication and evaluation of polyethyleneimine-functionalized gallium nitride nanoparticles (GaN) decorated with gold nanoparticles (GaN-PEI-Au) as a tunable electrode modifier for enhanced differential pulse voltammetry (DPV) detection of erythromycin. Branched polyethyleneimine was employed as a multifunctional interfacial layer to stabilize GaN dispersions, introduce amine-rich surface chemistry, and enable in situ gold nanoparticle formation at the GaN-PEI. The optimized GaN-PEI-Au material exhibited high colloidal stability, a characteristic Au localized surface plasmon resonance in the ~520–525 nm range, and well-defined Au nanoparticles attached to the GaN surface. When applied as an electrode coating, GaN-PEI-Au significantly enhanced the erythromycin oxidation response compared to bare Au and GaN-PEI interfaces, consistent with synergistic increases in electroactive surface area and interfacial charge-transfer efficiency. Under optimized DPV conditions, GaN-PEI-Au-modified electrodes enabled quantitative erythromycin determination with a linear range of 5 nM–2 µM (R² = 0.990), sensitivity of 1.32 × 10⁻³ µA nM⁻¹, and a limit of detection of 52.5 nM, while maintaining stable baseline behavior during repeated scans. The reported GaN-PEI-Au nanocomposites represent a robust platform for sensitive electrochemical detection of pharmaceutical compounds. Full article

Gold nanoparticles (AuNPs) were synthesized via two complementary routes, an inorganic surfactant-mediated method and a plant-extract-assisted biosynthesis, to elucidate how synthesis pathways influence nanoparticle physicochemical properties. In the inorganic route, hexadecyltrimethylammonium bromide (CTAB)-stabilized AuNPs were prepared using CTAB dissolution temperatures of 70–90 °C. UV–Vis spectroscopy showed localized surface plasmon resonance (LSPR) bands at 554–556 nm, while dynamic light scattering (DLS) indicated a decrease in hydrodynamic diameter from 110 to 97 nm with increasing dissolution temperature. Zeta potentials above +40 mV indicated strong electrostatic stabilization, and transmission electron microscopy (TEM) revealed ultrasmall Au cores with a narrow size distribution (2.4–3.0 nm) and a face-centered cubic crystal structure. In the biosynthetic route, AuNPs were obtained using aqueous Erythroxylum coca leaf extracts (1–4% w/v). The extracts exhibited a concentration-dependent red shift (~380 to ~420 nm), and biosynthesized AuNPs displayed LSPR bands in the 550–580 nm range. DLS yielded hydrodynamic diameters of 270–390 nm, with pronounced aggregation (3341 nm) at the lowest extract concentration. Under optimized conditions (HC5, n = 5), reproducible plasmonic and colloidal properties were obtained (maximum absorbance, localized surface plasmon resonance wavelength (λ_max) = 569.6 ± 1.7 nm; hydrodynamic diameter (D_H) = 237.6 ± 24.3 nm; absolute zeta potential (|ζ|)= 32.2 ± 2.6 mV). TEM analysis indicated predominantly quasi-spherical particles with a broader, log-normal size distribution, consistent with extract-mediated growth under heterogeneous organic capping environments. Full article

The plant hormone abscisic acid (ABA) plays an important role in crop growth and development, so it is urgent to establish a simple and sensitive method for the detection of ABA. (1) As one of the most sensitive spectral detection methods, surface-enhanced Raman spectroscopy (SERS) has made some progress in the detection of ABA, but it involved a complicated modification process of noble metal nanoparticles and was time-consuming. (2) In this work, a SERS and (local surface plasmon resonance) LSPR dual-signal aptamer (Apt) sensor based on the aggregation of dispersed (gold nanoparticles) AuNPs and the improved plasmonic coupling with formed SERS was developed and applied to the detection of the plant hormone ABA. Through the specific recognition of Apt and ABA, the prepared crystal violet (CV) and Apt modified AuNPs tended to aggregate in a high concentration salt solution, resulting in changes in LSPR characteristics of the detection system and enhanced SERS intensity of CV signal molecules. Thus, the quantitative relationship between ABA concentration and SERS intensity of signal molecule CV and the degree of absorbance change of AuNPs were established. (3) The linear range detection of SERS was 0.04~40 µM, the detection limit lod (LOD) was 17.6 nM, the linear range detection of LSPR was 0.4~80 µM, and the LOD was 36 nM. (4) The sensor has a good ability to detect ABA in the samples of common plants such as cucumber and tomato and has the characteristics of no chemical bond modification, more reliable detection results, and a universal detection platform. Full article

The interaction between plasmonic nanoparticles and organic dye molecules plays an important role in varied photonic and optoelectronic applications. In this work, we systematically investigate the optical properties of a water-soluble perylenediimide derivative, N,N′-di(2-(trimethylammonium iodide) ethylene) perylenediimide (TAIPDI), in the presence of different concentrations of silver nanoparticles (AgNPs) under femtosecond (fs) laser excitation. The AgNPs were synthesized via the laser ablation technique. The influence of AgNP concentration on the linear, fluorescence, and nonlinear optical properties of the TAIPDI dye was explored through UV–visible absorption spectroscopy, fluorescence emission measurements, and open- and closed-aperture Z-scan techniques. The Ag NP–TAIPDI dye hybrid systems (Ag@TAIPDI nanocomposites) exhibited pronounced reverse saturable absorption and self-defocusing behavior, indicating a negative nonlinear refractive index. Both the nonlinear absorption coefficient and refractive index increased markedly with rising AgNP concentration, leading to a significant enhancement in the third-order nonlinear susceptibility. Fluorescence studies further revealed a concentration-dependent emission enhancement due to metal-enhanced fluorescence arising from surface plasmon resonance-induced local field amplification. The Ag@TAIPDI nanocomposites also demonstrated strong optical limiting performance, with the limiting threshold decreasing as the AgNP concentration increased. These findings highlight the synergistic role of plasmon–exciton coupling and thermal lensing in enhancing the nonlinear response of such nanocomposites. The results establish AgNPs–TAIPDI dye hybrid systems as promising materials for all-optical switching, optical limiting, and photonic device applications. Full article

Plasmonic nanostructures have been widely employed to improve upconversion luminescence performance; however, their impact on excitation pathways under multi-wavelength excitation is not yet fully understood. In this work, we constructed hybrid systems composed of gold nanorod arrays and NaYF₄:Yb³⁺/Ln³⁺ (Ln = Er³⁺, Tm³⁺) upconversion nanoparticles to systematically investigate upconversion behavior under dual-wavelength excitation at 808 and 976 nm. Contrary to the expected synergistic enhancement, our experimental results demonstrate that dual-wavelength excitation in the plasmonic hybrid structures produces different responses of upconversion emission. Measurements dependent on excitation power, along with the analysis of emission intensity ratio, indicate that plasmonic coupling under dual-wavelength excitation significantly enhances dissipative pathways that compete with upconversion processes. Notably, these effects strongly depend on the intrinsic energy-level structure of the lanthanide ions. In the Er³⁺-doped system, excitation at 808 nm facilitates population of higher-lying excited states, but the overall upconversion gain remains limited. In contrast, in the Tm³⁺-doped system, plasmonic coupling markedly amplifies stimulated emission and cross-relaxation processes, causing rapid depletion of high-energy state populations and substantial suppression of luminescence. These findings elucidate the competition between upconversion and dissipation processes governing plasmon-assisted upconversion under dual-wavelength excitation and provide a physical foundation for manipulating upconversion luminescence using multiple wavelengths. Full article

The global expansion of genetically modified (GM) crop cultivation has increased the demand for analytical platforms that can provide rapid, reliable, and cost-effective detection of GM-derived ingredients to support traceability, regulatory compliance, and accurate labeling. Conventional molecular assays such as polymerase chain reaction (PCR) and isothermal amplification are highly sensitive and specific but depend on sophisticated instrumentation and trained personnel, limiting their applicability in field settings. Here, we present a label-free and amplification-free nanobiosensor based on citrate-capped gold nanoparticles (AuNPs) for the direct colorimetric detection of the Cry1Ac gene associated with the MON87701 soybean event, without the use of polymerase chain reaction (PCR) or any enzymatic nucleic acid amplification step. The assay relies on the localized surface plasmon resonance (LSPR) of AuNPs, which induces a red-to-purple color transition upon hybridization between complementary DNA strands. Critical reaction parameters, including NaCl concentration, AuNP size, and ionic strength, were optimized to enable selective and reproducible aggregation. Integration with a Support Vector Machine (SVM) algorithm enabled automated spectral classification and semi-quantitative discrimination of GM content levels. The optimized AuNP–SVM system achieved high sensitivity (limit of detection ≈ 2.5 ng μL⁻¹, depending on nanoparticle batch), strong specificity toward Cry1Ac-positive sequences, and reproducible classification accuracies exceeding 90%. By eliminating enzymatic amplification steps, the proposed platform significantly reduces assay time, operational complexity, and instrumentation requirements, making it suitable for rapid on-site GMO screening. Full article

The development of anisotropic gold nanostructures supporting localized surface plasmon (LSP) resonances in the near-infrared (NIR) biological window is of great interest for diagnostic and therapeutic nanotechnologies. Here, we report gold open-shell nanoparticles (AuOSNs), a symmetry-broken nanoshell architecture exhibiting strong NIR surface-enhanced Raman scattering (SERS) activity. AuOSNs were fabricated via a surfactant-free strategy combining bottom-up silica sphere assembly with a simple top-down gold deposition process, without using highly cytotoxic surfactants such as cetyltrimethylammonium bromide (CTAB). Boundary element method (BEM) simulations revealed that the asymmetric open-shell geometry induces NIR LSP resonances with pronounced electromagnetic field localization near the opening edges, depending on excitation configuration. Consistent with these predictions, extinction spectra of AuOSNs dispersed in water showed an LSP resonance peak at ~793 nm, close to the 785 nm excitation wavelength for SERS. In aqueous dispersion, AuOSNs modified with 4-mercaptobenzoic acid (4-MBA) exhibited strong SERS activity with enhancement factors of ~10⁶. Furthermore, polyethylene glycol (PEG)-modified MBA/AuOSNs showed negligible cytotoxicity in vitro. SERS imaging confirmed that PEG/MBA/AuOSNs enable visualization of HeLa cells via characteristic MBA SERS signals. These results demonstrate that surfactant-free AuOSNs provide a biocompatible platform for NIR-excited SERS sensing and cellular imaging, highlighting their potential in plasmonic bioimaging applications. Full article

Photothermal therapy (PTT) is an emerging minimally invasive approach for cancer treatment that relies on photothermal agents capable of efficiently converting near-infrared (NIR) light into localized heat. In this work, silica–gold nanostructures (SGNs) were synthesized and systematically evaluated to investigate how silica core size influences the photothermal response of the SGNs and optimize their performance as a photothermal agent. SGNs were synthesized with silica cores ranging from 54 to 244 nm in diameter and coated with gold nanoparticles of 4–10 nm in size, enabling controlled tuning of their localized surface plasmon resonance within the NIR region. The morphology and composition were characterized by SEM, TEM, and EDS; optical properties were analyzed by UV-Vis spectroscopy. The SGNs photothermal response low-power laser irradiation at 852 nm and 1310 nm and temperature changes were monitored using a thermographic camera. A maximum temperature increase of 7.1 °C was observed for SGNs with a silica core diameter of approximately 77 nm under the 852 nm laser irradiation. Numerical simulations of the absorption efficiency showed good agreement with experimental UV–Vis spectra and thermal measurements, revealing a size-dependent shift of the absorption toward longer wavelengths for larger nanostructures. These results demonstrate that the photothermal response of silica–gold nanostructures can be rationally tuned through the control of core size and gold growth parameters, providing a framework for the design of wavelength-matched photothermal agents for PTT applications. Full article

The accurate monitoring and dynamic analysis of metal ions are of considerable practical significance in environmental toxicology and life sciences. Colorimetric analysis and surface-enhanced Raman scattering (SERS) sensing technologies, utilizing the aggregation effect of gold and silver nanoparticles (Au/Ag NPs), have emerged as prominent methods for rapid metal ion detection. While sharing a common plasmonic basis, these two techniques serve distinct yet complementary analytical roles: colorimetric assays offer rapid, instrument-free visual screening ideal for point-of-care testing (POCT), whereas SERS provides superior sensitivity and structural fingerprinting for precise quantification in complex matrices. Furthermore, the synergistic integration of these modalities facilitates the development of dual-mode sensing platforms, enabling mutual signal verification for enhanced reliability. This article evaluates contemporary optical sensing methodologies utilizing aggregation effects and their advancements in the detection of diverse metal ions. It comprehensively outlines methodological advancements from nanomaterial fabrication to signal transduction, encompassing approaches such as biomass-mediated green synthesis and functionalization, targeted surface ligand engineering, digital readout systems utilizing intelligent algorithms, and multimodal synergistic sensing. Recent studies demonstrate that these techniques have attained trace-level identification of target ions regarding analytical efficacy, with detection limits generally conforming to or beyond applicable environmental and health safety regulations. Moreover, pertinent research has enhanced detection linear ranges, anti-interference properties, and adaptability for POCT, validating the usefulness and developmental prospects of this technology for analysis in complicated matrices. Full article