Search Results (308)

Structural colors, generated by the physical interaction of light with micro- and nanostructured architectures, have emerged as an important platform in nanophotonics owing to their high color saturation, exceptional photostability, and long-term color durability. This review provides a comprehensive overview of recent advances in structural colors and establishes a unified classification framework based on their macroscopic angular optical responses. The intrinsic angular characteristics of four fundamental color-generation mechanisms are first distinguished, providing the physical basis for classifying structural colors into iridescent and non-iridescent systems. Representative iridescent architectures, including thin films, one-dimensional (1D) to three-dimensional (3D) photonic crystals, and diffraction gratings, are systematically reviewed, together with non-iridescent strategies based on independent plasmonic and dielectric resonators, quasi-amorphous structures, and engineered metasurfaces. Strategies for enhancing structural color visibility and saturation through absorption management are further discussed, particularly for suppressing undesired broadband and multiple-scattering backgrounds. Additionally, this review systematically summarizes quantitative methodologies for evaluating structural colors, including spectral metrics, CIE 1931 and CIE1976 color spaces, CIEDE2000 color difference, quantitative angular-response metrics, spatial resolution and pixel limits, and structural-order characterization using orientation parameters and two-dimensional fast Fourier transform (2D FFT) analysis. Particular attention is given to the quantitative assessment of angular stability through wavelength shifts and perceptual color differences, while recognizing that a universally accepted numerical boundary between iridescent and non-iridescent coloration has not yet been established. Representative functional applications are also reviewed, including self-cleaning coatings, passive daytime radiative cooling, label-free chemical and gas sensing, reflectometric interference spectroscopy (RIfS), surface-enhanced Raman scattering (SERS), and anti-counterfeiting. By integrating color-generation mechanisms, angular optical responses, quantitative evaluation methods, and functional applications, this review provides a unified framework for objectively comparing structural color platforms and highlights key trade-offs among color quality, angular stability, structural precision, durability, scalability, and multifunctionality, thereby providing design guidance for next-generation optical materials and devices. Full article

Early cancer detection can expand treatment options and improve patient survival, but it requires tests that can be repeated with minimal patient burden. Urine and saliva can be collected non-invasively and may contain cancer-associated nucleic acids, proteins, and extracellular vesicles. Clinical analysis of these body fluids is complicated by low biomarker abundance, inter-individual variation, and matrix components that interfere with surface-based sensing. Plasmonic nanoarray biosensors address some of these analytical constraints by concentrating local electromagnetic fields, supporting multiplexed optical readout, and accommodating surface chemistry and microfluidic handling. This review examines nanoarray architectures, fabrication methods, surface functionalization, and signal generation for cancer-associated biomarkers in urine and saliva. Localized surface plasmon resonance, surface-enhanced Raman scattering, and metal-enhanced fluorescence are discussed together with applications to bladder, prostate, pancreatic, oral, and head-and-neck cancers. Remaining barriers include biofouling, pre-analytical variation, fabrication reproducibility, limited validation using authentic biofluids, and incomplete sample-to-answer integration. Addressing these challenges through standardized biofluid processing, scalable nanoarray fabrication, and integrated microfluidic platforms will be essential for translating plasmonic nanoarray biosensors into clinically applicable cancer screening tools. Full article

Alzheimer’s disease (AD) is the most common neurodegenerative disorder worldwide. Early diagnosis of AD is crucial for delaying disease progression and improving patients’ quality of life. Blood biomarkers, particularly amyloid-beta (Aβ) and Tau proteins along with their phosphorylated isoforms, show advantages such as convenient sampling, minimal invasiveness, and excellent repeatability. However, the extremely low concentrations of AD biomarkers in blood impose stringent requirements on the sensitivity, specificity, and anti-interference capability of detection methods. Optical methods provide promising analytical platforms to address these challenges in view of their intrinsic merits of high sensitivity and selectivity; rapid response; and potential for miniaturization. This review systematically summarizes the latest advances in optical methods for the detection of the two core AD blood biomarkers (Aβ and Tau), covering techniques such as colorimetry, fluorescence, chemiluminescence, surface plasmon resonance (SPR), and surface-enhanced Raman scattering (SERS). The sensing principles, design strategies, and analytical performances of these methods are discussed, with special emphasis on different signal amplification strategies. In addition, several challenges and future prospects are provided with a primary focus on single-molecule detection, insufficient sensitivity and stability, lack of validation with large clinical cohorts, and absence of standardization. This review aims to provide researchers with guidance for the rational development of high-performance optical methods to achieve early diagnosis of AD. Full article

Plasmonic biosensing technologies have emerged as powerful analytical tools for sensitive and label-free characterisation of biomolecular interactions and complex samples. The increasing demand for comprehensive molecular profiling has accelerated the development of multiplexing strategies that enable simultaneous analysis of multiple analytes and molecular interactions. This Feature Paper examines multiplexing through the complementary spatial, spectral, and temporal dimensions of multiplexing, together with their hybrid combinations and associated analytical trade-offs. Compared with other optical biosensing approaches, including interferometric, photonic, and fluorescence-based sensing platforms, plasmonic biosensors remain attractive owing to their combination of label-free detection, real-time interaction monitoring, sensitive interfacial analysis, and compatibility with multiplexed assay formats. This Feature Paper critically discusses current multiplexing strategies, focusing primarily on surface plasmon resonance (SPR), imaging SPR (SPRi), localised SPR (LSPR), surface-enhanced Raman scattering (SERS), and related nanoplasmonic biosensing approaches, together with recent advances in surface biofunctionalisation, antifouling interfaces, and molecular recognition strategies. Representative applications in biomedical diagnostics and non-clinical settings are highlighted, with examples such as liquid biopsy, glycoprofiling, extracellular vesicle profiling, and food and environmental analysis, alongside key challenges in reproducibility, standardisation, data interpretation, and clinical translation. In addition, selected non-plasmonic optical biosensing technologies are briefly discussed to position plasmonic biosensing within the broader landscape of multiplexed optical biosensing. This Feature Paper argues that the future of multiplexed plasmonic biosensing will depend less on further improvements in sensor performance than on robust, standardised analytical systems. Full article

In our prior research (2022), a Fe₃O₄@PDA@Au@GO composite was reported as a surface-enhanced Raman scattering (SERS) substrate for phenanthrene detection, with a detection limit of 10⁻⁷ g/L. The current study is a mechanistic follow-up investigation, which aims to explore the enhancement and enrichment mechanisms of the same substrate. By integrating density functional theory (DFT) calculations, adsorption experiments, and spectroscopic analyses (Raman, FTIR, XPS) before and after adsorption, the surface enhancement mechanism of the Fe₃O₄-PDA-Au-GO composite substrate is investigated. Our findings suggest that Fe₃O₄ enables efficient magnetic separation. The polydopamine (PDA) modification layer appears to enhance the uniformity and stability of the substrate surface, which is beneficial for uniform loading of Au nanoparticles (Au NPs). Graphene oxide (GO) and PDA are found to contribute to the effective enrichment of phenanthrene. Au NPs (mostly in the metallic Au⁰ state) may provide electromagnetic enhancement through localized surface plasmon resonance, and may also contribute to chemical enhancement through possible interactions with phenanthrene. Overall, the stepwise comparison presented in this study is consistent with the proposed roles of Au and GO in enhancing the SERS performance, which collectively improve the detection sensitivity. Full article

The persistent accumulation of tetracycline (TC) antibiotics in aquatic environments poses severe ecological and public health risks, necessitating the development of multifunctional platforms capable of simultaneous detection and degradation. Herein, we report magnetically recoverable plasmonic Fe₃O₄/Cu₂O-Ag nanocomposites (NCs) that integrate visible-light-driven photocatalysis with ultrasensitive surface-enhanced Raman scattering (SERS) detection. Hierarchical flower-like Fe₃O₄ nanocrystals were employed as magnetic supports, followed by in situ growth of Cu₂O nanocrystals and controlled deposition of Ag nanocrystals. The optimized composite (FCA-2) exhibited enhanced visible-light absorption (E_g = 1.86 eV), suppressed electron–hole recombination, and improved photocurrent response, which were attributed to Schottky barrier formation at the Cu₂O-Ag interface and localized surface plasmon resonance (LSPR) effects. Under simulated solar irradiation, FCA-2 NCs achieved 91.79% degradation of TC within 60 min, following pseudo-first-order kinetics (k = 20.37 × 10⁻³ min⁻¹). Finite-difference time-domain (FDTD) simulations revealed that optimal Ag loading maximized plasmonic “hot spot” density, thereby enhancing electromagnetic field intensity and SERS performance. The FCA-2 substrate enabled ultrasensitive TC detection with a limit of detection of as low as 10⁻¹⁰ M. Moreover, the superparamagnetic Fe₃O₄ core allowed for rapid magnetic separation and sustained performance over multiple SERS–photocatalysis cycles, with negligible signal attenuation after 30 days. This work presents a rational strategy for constructing plasmonic magnetic NCs that synergistically couple photocatalytic remediation, ultrasensitive sensing, and magnetic recyclability, offering significant potential for integrated environmental monitoring and sustainable water treatment applications. Full article

Surface-enhanced Raman spectroscopy (SERS) has emerged as a transformative tool in biomedical diagnostics, offering a highly sensitive and non-invasive method for detecting molecular biomarkers at exceptionally low concentrations. This approach takes advantage of the plasmonic characteristics of customized metallic nanostructures that produce intense localized electromagnetic fields via localized surface plasmon resonance and facilitate electron transfer reactions that notoriously enhance the intrinsically weak Raman scattering signals of molecular entities which reside on or next to their surfaces. SERS-based assays have shown remarkable potential in detecting cancer biomarkers, circulating tumor DNA (ctDNA), and proteins at early stages, enabling timely and targeted intervention. Additionally, the combination of SERS with AI-driven data analysis has facilitated real-time diagnostics, enhancing the precision and efficiency of point-of-care testing. Despite its promising capabilities, challenges such as substrate fouling, signal degradation, and the need for better biocompatibility remain. Nevertheless, ongoing research in substrate development, coupled with advances in AI, positions SERS as a leading technology for future diagnostic tools. This paper explores the current state of SERS in biomedical applications, highlighting its potential to revolutionize diagnostics and personalized medicine while addressing the existing limitations and future research directions. Full article

We demonstrate a mechanism-oriented Surface-Enhanced Raman Scattering (SERS) platform based on a hybrid structure integrating monolayer molybdenum disulfide (MoS₂) and gold nanospheres (AuNSs) on an optical microfiber (MF). The microfiber serves as a whispering-gallery-mode (WGM) microcavity. Monolayer MoS₂, grown directly on the microfiber surface via chemical vapor deposition (CVD), provides a chemically active interface for molecular adsorption and charge-transfer-related chemical enhancement. Subsequently deposited AuNSs couple with the microfiber-supported WGM, leading to the formation of hybrid photonic–plasmonic modes. This coupling results in a narrowed scattering resonance and a localized electromagnetic hotspot near the AuNS–microfiber interface. The combined contribution of electromagnetic enhancement from the microfiber–AuNS hybrid cavity and chemical enhancement from the MoS₂ layer produces discernible Raman enhancement for Rhodamine 6G (R6G) molecules under proof-of-concept measurement conditions. This work provides a useful platform for studying SERS enhancement mediated by hybrid photonic–plasmonic modes and offers guidance for the future development of optimized fiber-based SERS sensors. Full article

The development of cost-effective and resource-rich materials is crucial for the practical application of microwave absorbers. This study demonstrates the successful fabrication of core-shell Fe and TiC nanoparticles encapsulated within carbon shells using the arc discharge method. The samples are designated as Fe3Ti1 and Fe1Ti3, where the numbers indicate the Fe-to-Ti mass ratio in the precursor (e.g., Fe1Ti3 = 1:3 by mass). In the arc discharge synthesis mechanism, the mass ratio of Fe to Ti in the raw material was adjusted from 3:1 to 1:3 to optimize the Fe/TiC/C interfaces under a CH₄ forming gas atmosphere. TEM analysis reveals spherical and polyhedral nanoparticles with diameters of 30–50 nm and a uniform carbon shell thickness of 3–4 nm. Raman spectroscopy shows that the Fe1Ti3 sample has a higher defect density (I_D/I_G = 1.13) compared to Fe3Ti1 (0.87), indicating a more disordered carbon structure. Magnetic measurements yield saturation magnetization values of 87 emu/g for Fe3Ti1 and 50 emu/g for Fe1Ti3, with coercivities of 190.72 Oe and 203.65 Oe, respectively. When composited with paraffin at 50 wt% loading, the Fe1Ti3 sample exhibits superior microwave absorption performance, achieving a minimum reflection loss (RL) of −25.22 dB at 8.23 GHz and an effective absorption bandwidth (RL ≤ −10 dB) of 4 GHz (6.5–10.5 GHz) at a thickness of 2.5 mm. This enhanced performance is attributed to the synergistic effect of multiple loss mechanisms, including conduction loss within the three-dimensional core-shell architecture, interfacial polarization at the heterojunctions between the core and the carbon shell, and magnetic loss induced by ferromagnetic behavior associated with defects in both the shell and carbon atomic layers. The magnetic loss in the (Fe/TiC)@C nanocomposites primarily arises from the natural resonance (at ~6.5 GHz) and exchange resonance (at ~12 GHz) of the Fe cores. The dielectric loss is primarily attributed to dipole, interfacial, and space charge polarization from TiC and the carbon shell, as well as multiple scattering effects between nanoparticles. Furthermore, far-field radar cross-section simulations substantiate that the Fe/TiC@C nanocomposite demonstrates excellent radar wave attenuation capability. Further, first principles simulations reveal that introducing Fe at the C/TiC interface induces strong charge redistribution and orbital hybridization, transforming a localized dielectric interface into a highly conductive and electronically coupled C/Fe/TiC system. This interfacial modulation enhances both dielectric loss (via charge transport and polarization) and magnetic loss (via Fe-induced magnetic interactions), thereby enabling optimized dielectric-magnetic synergy for broadband microwave absorption in (Fe/TiC)@C nanocomposites. Full article

Noble metal nanostructures based on localized surface plasmon resonance (LSPR) can induce metal-enhanced fluorescence (MEF) and surface-enhanced Raman scattering (SERS), significantly improving trace detection sensitivity for biomedical and chemical analysis. While self-assembly of noble metal nanoparticles offers simplicity and low equipment dependence, achieving large-area, uniform, and controllable nanostructures remains challenging. In this study, angle-dependent dip coating (ADDC) technology was employed to achieve efficient, controllable self-assembly of silver nanoparticles (AgNPs) on glass slides, establishing a fabrication process for MEF/SERS dual-functional substrates. A stable AgNPs-anhydrous ethanol suspension was prepared and extracted from an inclined substrate reservoir using a microfluidic syringe pump, enabling large-area uniform nanostructure assembly. Systematic investigation revealed that substrate inclination angle provides better morphology and fluorescence enhancement control than withdrawal flow rate. The silver nanostructured surface fabricated under a withdrawal flow rate of 16 mL/h and a substrate inclination angle of 30° exhibited a Cy3 detection limit as low as ${10}^{-1}$ nM, with an enhancement factor ranging from 19.14 to 28.66, as well as an R6G SERS detection limit of ${10}^{-10}$ M with an enhancement factor of 4.07 × ${10}^8$. This study confirms that ADDC technology enables simple, efficient, large-area uniform AgNPs self-assembly for superior dual-function enhancement substrates, offering a cost-effective and efficient strategy for highly sensitive trace detection. Full article

Bilirubin is an important biomarker, where a small unbound fraction dissociated from albumin can cross the blood–brain barrier and induce neurotoxicity, such as kernicterus, at low nanomolar levels. Accurate detection of this low-level fraction remains challenging. Surface-enhanced Raman spectroscopy (SERS) enables label-free molecular detection; however, variations in the local refractive index (RI) at plasmonic hotspots can detune the resonance from the excitation wavelength, leading to signal fluctuations and limited quantitative reliability. Here, we present a multi-resonant nanolaminate SERS substrate designed to achieve RI-insensitive and robust signal enhancement. The vertically stacked metal–insulator–metal architecture provides broadband spectral overlap with both excitation and Raman scattering under dielectric loading, maintaining consistent enhancement across varying RI conditions. We demonstrate label-free bilirubin detection with a highly linear response over 10⁻⁹ to 10⁻⁴ M, achieving an R² value of 0.99. Compared with previously reported bilirubin SERS substrates relying mainly on single-resonant plasmonic enhancement, this RI-insensitive design offers improved quantitative reliability under dielectric environmental changes. These results highlight the importance of RI-insensitive SERS design for reliable quantification and provide a general strategy for robust SERS-based biosensing. Full article

Noble metal nanostructures provide versatile platforms for light manipulation through localized surface plasmon resonances (LSPRs). Among them, triangular silver nanoplates (AgNPTs) exhibit strong field-enhancement and spectral tunability, yet assembling them reproducibly on solids is challenging. We report a two-step functionalization strategy for constructing ordered AgNPT dimers on silica substrates, combining 3-aminopropyltriethoxysilane (APTES) anchoring with 1,4-butanedithiol bridging. AFM reveals face-to-face dimers with well-defined sub-nanometer gaps. Large-area AFM statistics collected over multiple regions (N = 80 nanoplates per condition) confirm reproducible and selective vertical dimerization. Extinction spectroscopy reveals sequential dielectric and coupling effects: thiol adsorption red-shifts the main resonance from 700 to 780 nm because of increased local refractive index and near-field damping, whereas dimerization partially restores it to ≈750 nm, consistent with plasmon hybridization within rigid ∼0.7 nm molecular gaps, where nonclassical moderation may occur but classical hybridization fully explains the observed shifts. Concomitantly, the extinction intensity doubles, following an exponential growth toward saturation during assembly. Surface-enhanced Raman scattering (SERS) measurements using 4-mercaptobenzoic acid (4-MBA) confirm a fourfold increase in the SERS enhancement factor from monolayer to bilayer, consistent with near-field coupling and hotspot formation at interplate junctions. Quantitative plasmon sensitivity analysis yields comparable results between experiments and finite-difference-time-domain simulations, confirming that the observed spectral shifts arise from near-field coupling and dielectric modulation rather than ensemble effects. This reproducible methodology enables precise tuning of NPT orientation, spacing, and optical response, providing a robust platform for enhanced sensing, SERS, and nanophotonic device engineering. 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

Time-resolved (TR) resonance Raman (RR) spectroscopy with continuous-wave excitation is a fundamental technique that has contributed substantially to the understanding of the structure and dynamics of retinal proteins. However, the underlying principles were developed about fifty years ago for instrumentation that is hardly in use anymore. Thus, the adaptation of the technique to the current state-of-the-art equipment is needed to satisfy the increasing demand for the spectroscopic characterization of novel retinal proteins. In this work, we focus on pump–probe TR RR experiments with a confocal spectrometer using a rotating cell. We define the parameters ensuring fresh-sample condition and the photochemical innocence of the probe beam as a prerequisite for studying retinal proteins that undergo a cyclic photoinduced reaction sequence. For the measurements of intermediate states and reaction kinetics, pump–probe experiments are required in which the two laser beams hit the flowing sample with a defined but variable delay time. An appropriate set-up for such two-beam experiments with a confocal spectrometer is proposed and tested in TR experiments of bacteriorhodopsin. The comparison with the results obtained with classical slit spectrometers using a 90-degree scattering illustrates the advantages and disadvantages of the confocal arrangement. It is shown that modern confocal spectrometers substantially decrease the spectra acquisition time but require a more demanding optical set-up. Furthermore, the extent of photoconversion by the pump beam is lower than for the 90-degree-scattering arrangement, which reduces the accuracy of kinetic measurements. Full article