Sensitive Surface-enhanced Raman Scattering Research Articles

A dual-mode strategy for diacetyl detection based on colorimetry and surface-enhanced Raman scattering

Diacetyl is an important food additive with rich creamy flavor whose excessive intake may cause various diseases. Herein, for the first time, we designed a dual-mode method for diacetyl detection based on colorimetry and surface-enhanced Raman scattering (SERS) technology. Diacetyl exhibited excellent oxidase-like catalytic activity under light-mediated condition, facilitating the oxidation of colorless 3,3′,5,5′-tetramethylbenzidine (TMB) to blue ox-TMB for colorimetric detection. Notably, diacetyl could control the oxidation process of TMB by simply adjusting light irradiation, unlike traditional enzymatic reactions that required terminators to stop the reaction. Interestingly, ox-TMB was an ideal Raman marker for SERS analysis. Then, a three-dimensional flower-like zinc oxide/silver (ZnO/Ag) for sensitive SERS detection was prepared, which exhibited outstanding SERS effect with a high enhancement factor of 1.89 × 108 due to effective charge transfer and synergistic effect between ZnO and Ag. Based on these, SERS method was constructed to indirectly detect diacetyl, which has not been reported due to low Raman activity of diacetyl. The linear ranges of colorimetry and SERS were 0.5–60 μM and 10−9-10−5 M respectively, with detection limits of 0.41 μM and 0.73 nM. Obviously, the dual-mode strategy combined the simplicity and practicality of colorimetry and the high sensitivity of SERS, offering great potential applications in practical samples.

Enhancing SERS Sensitivity in N‐Graphene Hydrangea by Synergistic Charge‐Transfer and Excitation Light Absorption

Surface‐enhanced Raman scattering (SERS) is a versatile spectroscopic technique, which plays a crucial role in enhancing analytical sensitivity, investigating interfacial reaction mechanisms, enabling biosensing, and fostering efficient catalysis. Currently, the common SERS substrates are primarily metal nanostructures, which entail high manufacturing costs, complex processes, and the metal surface undergo change over time and with environmental conditions. These issues limit the development of SERS technology. In this work, a nitrogen‐doped graphene (N‐graphene) hydrangea was synthesized on a silicon (Si) substrate using plasma‐assisted chemical vapor deposition (PACVD), forming an N‐graphene hydrangea/Si hybrid structure as a SERS substrate. This substrate offers the advantages of high stability, ultra‐sensitivity, and reusability. The three‐dimensional nano‐cavity structure of graphene can increase the interaction between light and graphene, resulting in an increased localized electric field. Combining theoretical simulation analysis, the introduction of nitrogen (N) elements adjusts the Fermi level of graphene, promoting efficient charge transfer. In practical scenarios, Di(2‐ethylhexyl) phthalate (DEHP), a commonly used plasticizer, has raised concerns due to its potential as an endocrine disruptor and carcinogen. The as‐prepared SERS substrate achieves a remarkable detection limit of as low as 10−8 m for DEHP, providing significant support for environmental conservation and human health.

Multifunctional engineering on the ultrasensitive driven-dual plasmonic heterogenous dimer system of 1D semiconductor for accurate SERS sensitivity and quantitation

Self-assembled functional nanomaterials with electromagnetic (EM) hot spots and chemical (CM) enhancement have been recognized as a key in surface-enhanced Raman scattering (SERS) analysis. Herein, a dual-hybrid plasmonic coupling SERS sensor composed of rutile TiO2 nanorod arrays (r-TNRs), Au nanospheres (AuNSs), and Ag nanocubes (AgNCs) has been designed to achieve ultrasensitive detection and obtain unique molecular fingerprints. The AgNCs/AuNSs/r-TNRs-based SERS chip shows an extremely promising SERS enhancement factor (EF) of 1.2 ×1011, detectability at sub-picomolar concentrations (down to the single-molecule level, 10-13 M), and excellent signal reproducibility with a relative standard deviation (RSD) of 3.4 %. Furthermore, this system has been applied for fingerprint detection in complex mixtures, demonstrating impressive specificity and accuracy. The photocatalytic decomposition efficiency of the AgNCs/AuNSs/r-TNRs platform reaches approximately ∼99 % within 20 min. Additionally, the Raman intensity of crystal violet only declined by 15 % after 21 days, illustrating the outstanding stability of the as-proposed ternary SERS sensor.

Ultrasensitive amplification-free detection of circulating miRNA via droplet-based processing of SERS tag-miRNA-magnetic nanoparticle sandwich nanocomplexes on a paper-based electrowetting-on-dielectric platform.

MicroRNAs (miRNAs) have emerged as a promising class of biomarkers for early detection of various cancers, including ovarian cancer. However, quantifying miRNAs in human blood samples is challenging owing to the issues of sensitivity and specificity. In this study, hsa-miR-200a-3p of the miR-200a sub-family, which is a biomarker of ovarian cancer, was used as the analyte to demonstrate the analytical capability of an integrated biosensing platform using an extremely sensitive surface-enhanced Raman scattering (SERS) nanotag-nanoaggregate-embedded beads (NAEBs), magnetic nanoparticles (MNPs), a pair of highly specific locked nucleic acid (LNA) probes, and a semi-automated paper-based electrowetting-on-dielectric (pEWOD) device to provide labor-less and thorough sample cleanup and recovery. A sandwich approach where NAEBs are modified by one LNA-1 probe and MNPs are modified by another LNA-2 probe was applied. Then, the target analyte miRNA-200a-3p was introduced to form a sandwich nanocomplex through hybridization with the pair of LNA probes. The pEWOD device was used to achieve short cleanup time and good recovery of the nanocomplex, bringing the total analysis time to less than 30 min. The detection limit of this approach can reach 0.26 fM through SERS detection. The versatility of this method without the need for RNA extraction from clinical samples is expected to have good potential in detecting other miRNAs.

Microplasma-printed Au-based SERS sensing platform for ultra-sensitive chemical analyte detection

Direct and efficient fabrication of highly sensitive Au-based surface-enhanced Raman scattering (SERS) platforms is realized by integrating plasma with 3D printing technique.

A simple low-cost flexible plasmonic patch based on spiky gold nanostars for ultra-sensitive SERS sensing.

Recently, transparent and flexible surface-enhanced Raman scattering (SERS) substrates have received great interest for direct point-of-care detection of analytes on irregular nonplanar surfaces. In this study, we proposed a simple cost-effective strategy to develop a flexible SERS patch utilizing multibranched sharp spiked gold nanostars (GNS) decorated on a commercially available adhesive Scotch Tape for achieving ultra-high SERS sensitivity. The experimental SERS measurements were correlated with theoretical finite element modeling (FEM), which indicates that the GNS having a 2.5 nm branch tip diameter (GNS-4) exhibits the strongest SERS enhancement. Using rhodamine 6G (R6G) as a model analyte, the SERS performance of the flexible SERS patch exhibited a minimum detection limit of R6G as low as 1 pM. The enhancement factor of the SERS patch with GNS-4 was calculated as 6.2 × 108, which indicates that our flexible SERS substrate has the potential to achieve ultra-high sensitivity. The reproducibility was tested with 30 different spots showing a relative standard deviation (RSD) of SERS intensity of about 5.4%, indicating good reproducibility of the SERS platform. To illustrate the usefulness of the flexible SERS sensor patch, we investigated the detection of a carcinogenic compound crystal violet (CV) on fish scales, which is often used as an effective antifungal agent in the aquaculture industry. The results realized the trace detection of CV with the minimum detection limit as low as 1 pM. We believe that our transparent, and flexible SERS patch based on GNS-4 has potential as a versatile, low-cost platform for real-world SERS sensing applications on nonplanar surfaces.

Evidence of oxygen vacancy-mediated ultrahigh SERS sensitivity of Niobium pentoxide nanoparticles through defect engineering: theoretical and experimental studies.

Oxygen vacancy engineering in metal oxide-based semiconductors has emerged as an important area of research for sensing applications, such as Surface-enhanced Raman scattering (SERS), gas sensing, etc. It has the potential to replace high-cost and unstable noble metal-based substrates in the near future. However, improving the SERS enhancement factor in semiconductor-based substrates remains a challenge. In the present study, we demonstrate that oxygen vacancy engineering in Niobium pentoxide (Nb2O5) enables ultrahigh SERS sensitivity. Oxygen vacancies were induced and manipulated in the Nb2O5 nanoparticles via a facile high-energy ball milling method and post-growth oxygen annealing. A high enhancement factor (EF) of 5.15 × 107 was obtained for the Methylene Blue (MeB) molecule on the oxygen-deficient substrate with the lowest detection limit of 10-8 M, which is 2 orders of magnitude lower than the pristine substrate. Through a careful analysis of the experimental data and theoretical calculations, we investigated the underlying mechanism behind the high EF in SERS and showed that the SERS performance is directly proportional to the oxygen vacancy concentration in the Nb2O5 nanoparticles. Density functional theory (DFT) calculation suggests a strong coupling of the vibronic states and an increased charge transfer (CT) efficiency in the Nb2O5-MeB complex mediated through the vacancy-induced trap states in the defective Nb2O5 structure. Finite element method (FEM)-based simulations revealed a field enhancement factor of ∼4.17 × 102 that contributed to the SERS EF, while the remaining is contributed to the oxygen vacancy-mediated charge transfer, i.e., a factor of ∼1.23 × 105 is due to the high CT efficiency, the highest among the reported values. We believe that these findings offer valuable insights into the fabrication of defect-tailored cost-effective semiconductor-based SERS substrates for ensuing applications, such as trace dye detection.

Synthesis of Au@Ag core-shell nanocubes with finely tuned shell thicknesses for surface-enhanced Raman spectroscopic detection.

In this work, we describe a facile method for generating monodisperse Au@Ag core-shell nanocubes with well-controlled size and fine-tuned Ag shell thicknesses. In this synthesis method, Au nanocubes were prepared via the seed-mediated growth method. Then, Au@Ag nanocubes with the core-shell structure were prepared separately by reducing AgNO3 with AA using as-prepared Au nanocubes as seeds. The thickness of Ag shells could be finely tuned from 3.6 nm to 10.0 nm by varying the concentration of the AgNO3 precursor. By investigating the localized surface plasmon resonance (LSPR) properties of Au@Ag nanocubes in relation to the thickness of the Ag shell, we found that the intensity of the characteristic peak of Ag gradually increases and that of Au gradually decreases as the thickness of the Ag shell increases. Additionally, surface-enhanced Raman scattering (SERS) properties of Au@Ag core-shell nanocubes were evaluated using rhodamine 6G (R6G) as the probe molecule. Interestingly, Au@Ag nanocubes exhibit efficient SERS intensities compared to the Au nanocubes, and Ag shell with a thickness of about 8.4 nm exhibits the optimal SERS activity. In addition, our results also demonstrated that Au@Ag nanocubes with an Ag shell thickness of 8.4 nm exhibited high SERS sensitivity and are capable of probing the analyte down to 10-12 M. The results obtained here suggest that Au@Ag core-shell nanocubes might serve as a nanoprobe for SERS-based analytical and biosensing applications.

Block copolymer-templated surface-enhanced Raman scattering-active nanofibers for hydrogen sulfide detection

Metabolic disorders involving endogenous H2S have been linked to a variety of serious human diseases, particularly cancer. In this study, we employed nanofibers with surface-enhanced Raman scattering (SERS) activity for the detection of H2S within live cells. These nanofibers were chosen for their minimal invasiveness, high spatial resolution, and enhanced SERS sensitivity. To improve the performance of SERS, highly sensitive core-shell multibranched-Au NPs (MBAuNP)@Ag NPs were decorated on the nanofibers as SERS tags for H2S detection. A SERS probe named MBN, embedded between the Au core and Ag shell, was utilized for quantitative detection. These nanofibers exhibited excellent reproducibility (relative standard deviation (RSD) within 5.7 %) and demonstrated a strong linear relationship with sulfide concentrations ranging from 50 nM to 1 μM, with an estimated detection limit of 0.12 nM. As a proof of concept, the aforementioned nanofibers were successfully applied to detect endogenous H2S in living cells, offering a potential analytical method in the related research of detection.

The Geometry of Nanoparticle-on-Mirror Plasmonic Nanocavities Impacts Surface-Enhanced Raman Scattering Backgrounds.

Surface-enhanced Raman scattering (SERS) has garnered substantial attention due to its ability to achieve single-molecule sensitivity by utilizing metallic nanostructures to amplify the exceedingly weak Raman scattering process. However, the introduction of metal nanostructures can induce a background continuum which can reduce the ultimate sensitivity of SERS in ways that are not yet well understood. Here, we investigate the impact of laser irradiation on both Raman scattering and backgrounds from self-assembled monolayers within nanoparticle-on-mirror plasmonic nanocavities with variable geometry. We find that laser irradiation can reduce the height of the monolayer by inducing an irreversible change in molecular conformation. The resulting increased plasmon confinement in the nanocavities not only enhances the SERS signal, but also provides momentum conservation in the inelastic light scattering of electrons, contributing to the enhancement of the background continuum. The plasmon confinement can be modified by changing the size and the geometry of nanoparticles, resulting in a nanoparticle geometry-dependent background continuum in SERS. Our work provides new routes for further modifying the geometry of plasmonic nanostructures to improve SERS sensitivity.

Multiwavelength SERS of Magneto-Plasmonic Nanoparticles Obtained by Combined Laser Ablation and Solvothermal Methods.

The present study introduces a novel method for the synthesis of magneto-plasmonic nanoparticles (MPNPs) with enhanced functionality for surface-enhanced Raman scattering (SERS) applications. By employing pulsed laser ablation in liquid (PLAL) to synthesize plasmonic nanoparticles and wet chemistry to synthesize magnetic nanoparticles, we successfully fabricated chemically pure hybrid Fe3O4@Au and Fe3O4@Ag nanoparticles. We demonstrated a straightforward approach of an electrostatic attachment of the plasmonic and magnetic parts using positively charged polyethylenimine. The MPNPs displayed high SERS sensitivity and reproducibility, and the magnetic part allowed for the controlled separation of the nanoparticles from the reaction mixture, their subsequent concentration, and their precise deposition onto a specified surface area. Additionally, we fabricated alloy based MPNPs from AgxAu100-x (x = 50 and 80 wt %) targets with distinct localized surface plasmon resonance (LSPR) wavelengths. The compositions, morphologies, and optical properties of the nanoparticles were characterized by using transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), UV-vis spectroscopy, and multiwavelength Raman spectroscopy. A standard SERS marker, 4-mercaptobenzoic acid (4-MBA), validated the enhancement properties of the MPNPs and found an enhancement factor of 2 × 108 for the Fe3O4@Ag nanoparticles at 633 nm excitation. Lastly, we applied MPNP-enhanced Raman spectroscopy for the analysis of the biologically relevant molecule adenine and found a limit of detection of 10-7 M at 785 nm excitation. The integration of PLAL and wet chemical methods enabled the relatively fast and cost-effective production of MPNPs characterized by high SERS sensitivity and signal reproducibility that are required in various fields, including biomedicine, food safety, materials science, security, and defense.

Controlled shrinkage surface driven by solvent evaporation for highly sensitive residual fungicides detection

In this study, a suite of novel surface-enhanced Raman scattering (SERS) substrates were fabricated based on the synergistic shrinkage surface of gelatin gels and silver nanoparticles (AgNPs). Based on the controllable evaporation rate of solvent in the gelatin gel, the arrangement of surface-loaded AgNPs showed to form a series of more compact nanogaps and serve as SERS hotspots induced by a significant gelatin shrinkage. The constructed Gelatin@AgNPs substrates demonstrated excellent SERS sensitivity with an enhancement factor of 1.83 × 105 and could to detect 10-9 M R6G prove molecule. These experimental results were in good agreement with the Finite-Difference Time-Domain (FDTD) simulations calculations. More critically, the Gelatin@AgNPs substrates could be as superb SERS platform for detecting the malachite green (MG) fungicides as low as 10-9 M concentrations in actual lake water, and expected to serve as a fast and simple method for highly sensitive hazardous contaminants and fungicides detection in aquaculture fields.

Recyclable magnetic nanoparticles combined with TiO2 enrichment and “Off” to “On” SERS assay for sensitive detection of alkaline phosphatase

As an important enzyme in human tissues, abnormally alkaline phosphatase (ALP) is strongly associated with many diseases, particularly breast and prostate cancer. In this study, we proposed a rapid and sensitive surface-enhanced Raman scattering (SERS)-based biosensor for ALP detection. The biosensor utilized Fe3O4@Au@TiO2 nanoparticles (FAT NPs) as magnetic separation and enrichment materials to enrich grafted mediator Ag-4-mercaptophenylboronic acid (4-MPBA)-ascorbic acid 2-phosphate (AAP) NPs to form FAT-(AAP-4-MPBA-Ag) NPs, and 5,5′-dithiobis-(2-nitrobenzoic acid) (DTNB) was used as the internal standard tag molecule to prepare Au@DTNB@Ag as the signal source. The phosphate group in AAP was cleaved by ALP to form ascorbic acid (AA), which acts as a receptor for the boric acid to adsorb the 4-MPBA-Au@DTNB@Ag NPs. When the switch was “Off” to “On”, the Au@DTNB@Ag NPs were used to significantly improve the sensitivity of the proposed SERS platform, enabling detection as low as 1.17U/L of target ALP with a good linear range (R 2 = 0.991) of 2–10 U/L. Furthermore, the platform successfully detected ALP from 2 % human serum. The recoveries were 99.5–106 %. In addition, FAT-(AAP-4-MPBA-Ag) NPs could be transformed into FAT NPs to achieve recyclability by ultrasonication in acidic environments. Overall, this sensitive and fast SERS platform has promising potential for accurate and efficient identification of ALP from human serum.

Silver nanosphere array substrates fabricated by glancing angle deposition: Morphology, hot spots and SERS properties

The generation and exploitation of hot spots play a crucial role in the fabrication of highly sensitive surface-enhanced Raman scattering (SERS) substrates. In this work, silver nanosphere (AgNS) array substrates with various morphologies of polystyrene (PS) core/Ag shell were fabricated by reactive ion etching and glancing angle deposition technique on PS sphere templates. The electromagnetic field distribution (hot spots) of AgNS array was calculated by the finite difference time domain method. R6G and MB were used as probe molecules to investigate the effect of structure spacing on electric field enhancement. Under 785 nm excitation, an AgNS substrate with a gap of approximately 20 nm exhibited the best SERS enhancement, and the limit of detection reached 5 × 10−8 M for both analytes. For R6G and MB, the relative standard deviations (RSDs) were 2.39 % and 7.22 %, and the enhancement factors (EFs) were 7.25 × 108 and 7.68 × 107, respectively. These results serve as a reference for the development of new highly sensitive SERS sensors.

Core-shell metallic nanotube arrays for highly sensitive surface-enhanced Raman scattering (SERS) detection

Here, we demonstrate the application of highly ordered, periodic Ag/Au core-shell triangle nanotube arrays as an ultrasensitive and low-cost surface-enhanced Raman scattering (SERS) substrate for the first time. The arrays of core-shell nanotube, with an outer diameter of 1.5 μm, were fabricated using top-down wafer-scale lithography followed by sequential sputter deposition of Ag and Au. The SERS activity of various combinations of core-shell structures was evaluated. It was found that Ag-core nanotubes overlaid with the Au-shell resulted in the highest Raman intensity, where the enhancement factor for R6G as a probe molecule is determined to be 1.38 × 107. Meanwhile, the limit of detections for R6G and ketoprofen analytes was evaluated to be 10−10 and 10−6 M, respectively. Linear correlations between the SERS signal intensities and logarithmical scale of both analytes in different concentrations were also established, ranging 10−4–10−10 and 10−2–10−6 M for R6G and ketoprofen, respectively. The Raman R6G peak intensity mapping suggests our metal nanotube arrays act as effective plasmonic hotspots and, thus, are useful for SERS sensing applications.

Three-Dimensional MXene-AgNP Hollow Spheres for In Situ Surface-Enhanced Raman Scattering Detection of Catalysis Reactions.

MXenes are attractive candidates in the fields of surface-enhanced Raman scattering (SERS) and catalysis. However, most of the current studies on MXenes are based on blocks and nanosheets, limiting their SERS and catalytic properties. Herein, we have prepared 3D MXene hollow spheres wrapped with silver nanoparticles (Ti3C2-AgNP HSs) using a sacrificial template method, which exhibits excellent sensitivity with a low detection limit due to good light-trapping capability of the hollow sphere and strong localized surface plasmon resonance (LSPR) effect of AgNPs. Furthermore, it shows outstanding photocatalytic performance and realizes in situ SERS monitoring of the 4-nitrobenzenethiol (4-NTP) to 4-aminothiophenol (4-ATP) catalysis reaction. The finite-difference time-domain (FDTD) simulations confirm that 3D Ti3C2-AgNP hollow structures have stronger hot spots than 3D solid structures and higher SERS sensitivity for molecule detection. Therefore, it promises to be an excellent bifunctional material for highly sensitive SERS detection and the in situ monitoring of catalytic reactions.

Hot Zone Empowered Highly Sensitive Surface-Enhanced Raman Scattering Analysis Using Au@HOF Nanoparticles

Hot Zone Empowered Highly Sensitive Surface-Enhanced Raman Scattering Analysis Using Au@HOF Nanoparticles

A surface-enhanced Raman scattering sensor for the detection of benzo[a]pyrene in foods based on a gold nanostars@reduced graphene oxide substrate.

In this study, a simple and sensitive surface-enhanced Raman scattering (SERS) sensor based on gold nanostars@reduced graphene oxide (AuNS@rGO) was successfully developed for the detection of benzo[a]pyrene in foods. The detection strategy involved benzo[a]pyrene adsorption on reduced graphene oxide, followed SERS detection of adsorbed molecules. Owing to the large electric fields generated by the gold nanostars under laser irradiation, which greatly amplified the Raman signals of benzo[a]pyrene, very high sensitivity for the target analyte was achieved. Under optimized conditions, the SERS sensor exhibited a wide linear detection range for benzo[a]pyrene (from 0.1μgL-1 to 10000μgL-1), with a low limit of detection of 0.0028μgL-1. Chicken samples spiked with benzo[a]pyrene were assayed using the sensor, with recoveries ranging from 89.20% to 100.80%. The benzo[a]pyrene content in roasted mutton sample was quantified using the SERS sensor and a reversed-phase high-performance liquid chromatography method, with similar results being obtained.

Highly Uniform Self-Assembly of Gold Nanoparticles by Butanol-Induced Dehydration and Its SERS Applications in SARS-CoV-2 Detection.

We report the development of a reproducible and highly sensitive surface-enhanced Raman scattering (SERS) substrate using a butanol-induced self-assembly of gold nanoparticles (AuNPs) and its application as a rapid diagnostic platform for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The butanol-induced self-assembly process was used to generate a uniform assembly of AuNPs, with multiple hotspots, to achieve high reproducibility. When an aqueous droplet containing AuNPs and target DNAs was dropped onto a butanol droplet, butanol-induced dehydration occurred, enriching the target DNAs around the AuNPs and increasing the loading density of the DNAs on the AuNP surface. The SERS substrate was evaluated by using Raman spectroscopy, which showed strong electromagnetic enhancement of the Raman signals. The substrate was then tested for the detection of SARS-CoV-2 using SERS, and a very low limit of detection (LoD) of 3.1 × 10-15 M was obtained. This provides sufficient sensitivity for the SARS-CoV-2 screening assay, and the diagnostic time is significantly reduced as no thermocycling steps are required. This study demonstrates a method for the butanol-induced self-assembly of AuNPs and its application as a highly sensitive and reproducible SERS substrate for the rapid detection of SARS-CoV-2. The results suggest the potential of this approach for developing rapid diagnostic platforms for other biomolecules and infectious diseases.

Magnetic MOF Substrates for the Rapid and Sensitive Surface-Enhanced Raman Scattering Detection of Uranyl.

With the widespread use of uranium in the nuclear industry, achieving rapid and sensitive detection of uranium contaminants is critical for reducing environmental pollution. Surface-enhanced Raman scattering (SERS), with its high sensitivity and unique fingerprint properties, has been used for the analysis of uranyl. However, the weak affinity of Au for uranyl remains a challenge in the development of spherical Au-based SERS substrates. The metal-organic framework (MOF) material ZIF-8 exhibits excellent adsorption capacity for uranyl and could overcome this limitation. In this study, ZIF-8 porous structures were modified on a magnetic SERS substrate, Fe3O4@SiO2@Au (FA), for the rapid and sensitive detection and analysis of the uranyl species. Uranyl was adsorbed by ZIF-8, allowing ready access to the hot spots in the interstices of Au nanoparticles (AuNPs). Symmetrically stretched vibrating bonds of O═U═O were detected at 829 cm-1 as the characteristic peak of uranyl by surface plasmon resonance between the AuNPs. The ZIF-8 coating had minimal influence on target detection as the detection limit for 4-MPY was only half an order of magnitude lower than before modification. The enhancement factor for uranyl reached 106. The substrate showed excellent sensing performance in a neutral or alkaline environment. It was used to detect uranyl in tap water and river water; rapid separation of the species from the water samples was achieved using an external magnet to extract radioactive waste. The proposed substrate offers a route for monitoring and detecting uranyl contamination and an approach for achieving rapid on-site detection, providing a promising application for environmental contaminant detection.