Deposition Of Silver Nanoparticles Research Articles

Target-mediated silver deposition-based electrochemical biosensor for highly sensitive detection of human chorionic gonadotropin

As a glycoprotein hormone, human chorionic gonadotropin (hCG) is an established marker for pregnancy test. On the basis of the target-mediated silver deposition (TSD), in this work, we report the development of an amplification-free electrochemical biosensor for the highly sensitive detection of hCG. The detection of hCG involves the use of the affinity peptide-modified electrode for hCG capture (the CGGSSPPLRINRHILTR peptide containing the hCG-binding domain of the PPLRINRHILTR sequence is used as the affinity peptide), the oxidation of the diol sites of the glycan chains on hCG hormones into aldehyde groups by NaIO4, and the deposition of silver nanoparticles (AgNPs) for the solid-state voltammetric stripping analysis. Due to the deposition of multiple AgNPs while the solid-state Ag/AgCl voltammetric process has a high signal-to-noise ratio, the TSD-based electrochemical biosensor can be applied to the highly sensitive detection of hCG without the need for signal amplification. Under optimal conditions, the stripping current increased linearly with an increasing hCG concentration over the range from 1.0 to 25 mIU/mL, with a detection limit of 0.45 mIU/mL. Owing to the high specificity of the hCG-binding peptide PPLRINRHILTR, this electrochemical hCG biosensor exhibits high selectivity. The results of the quantitative assay of hCG in urine samples at the concentrations of 25, 10, and 1.0 mIU/mL are desirable, indicating the good anti-interference capability. As the TSD-based electrochemical biosensor allows the amplification-free detection of low-abundance hCG, it is easy to use and cost-effective, showing great promise in point-of-care assay of hCG for pregnancy test.

Silver nanoparticles bridging liquid metal for wearable electromagnetic interference fabric

Stretchable conductive fibers are essential for the advancement of wearable electronic textiles. However, a significant challenge arises as their conductivity sharply decreases when stretched due to disruptions in electronic transport. Coating fibers with soft liquid metal (LM) has emerged as a promising solution. Despite this, there remains an urgent need to develop methods that enhance LM adhesion to substrates while facilitating efficient electron transport pathways. This study demonstrates a novel Ag-LM conductive network strategy for fabricating a thermoplastic polyurethane/polydopamine/silver-LM (TPU/PDA/Ag-LM) fiber membrane. This membrane exhibits outstanding stretchable electromagnetic interference (EMI) shielding performance and is produced through straightforward electrospinning, electroless depositing, and LM coating and activation. The TPU/PDA/Ag fiber membrane is initially prepared via polydopamine-assisted deposition of silver nanoparticles (AgNPs) on electrospun TPU fibers. The presence of AgNPs on the surface of TPU/PDA fibers enhances LM adhesion to the substrate and bridges adjacent LM to establish efficient conductive paths. This interaction benefits from the reactive alloying between AgNPs and LM, where the LM infiltrates the gaps among AgNPs, forming a distinctive LM-Ag alloy layer that uniformly coats the surface of TPU fibers. As anticipated, the unique three-dimensional (3D) interconnected LM-Ag conductive network remains intact during stretching, ensuring strain-invariant conductivity. The fabricated TPU/PDA/Ag-LM fiber membrane demonstrates exceptional EMI shielding effectiveness (SE) of 77.4 dB within the frequency range of 8.2–12.8 GHz and maintains an excellent EMI SE of 37.2 dB under extensive tensile deformation of 300%. Furthermore, the TPU/PDA/Ag-LM fiber membrane shows remarkable mechanical properties and stable Joule heating performance even under significant stretching.

Zinc oxide (ZnO) Enhanced with Silver (Ag) is Used to Improve the Photocatalytic Degradation of Phenol in Aqueous Solutions

Silver-modified zinc oxide (Ag/ZnO) photocatalysts were synthesized and characterized to evaluate their efficiency in degrading phenol under UV irradiation. X-ray fluorescence, surface area analysis, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and UV-visible reflectance spectroscopy confirmed successful deposition of metallic silver (Ag0) nanoparticles on the ZnO surface. The abundance of silver particles correlated directly with Ag concentration. Surface plasmon resonance bands indicated silver nanoparticle formation. Photocatalytic testing showed increased phenol degradation with Ag/ZnO versus pure ZnO, with 0.88 wt% Ag being optimal. Further experiments found 50 mg/L initial phenol and 0.15 g/L photocatalyst dosage optimized performance. Finally, almost complete elimination of phenol from drinking wastewater occurred after 180 minutes with the enhanced Ag/ZnO photocatalyst under UV irradiation.

Framework-Induced Electrochemiluminescence Enhancement of an AIEgen-Based MOF Coupled with Heterostructured TiO2@Ag NPs as an Efficient Coreaction Accelerator for Sensitive Biosensing.

In conventional metal-organic framework (MOF) luminophore-involved electrochemiluminescence (ECL) systems, the aggregation-caused quenching commonly exists for the organic luminescent ligands, limiting the ECL efficiency and detection sensitivity. Herein, by employing the aggregation-induced emission luminogen (AIEgen) 1,1,2,2-tetra(4-carboxylbiphenyl)ethylene (H4TCBPE) as a ligand, one high-efficiency ECL emitter (Zr-MOF) was synthesized through a simple hydrothermal reaction. Compared with H4TCBPE monomers and their aggregates, the resultant Zr-MOF possesses the strongest ECL emission, which is mainly attributed to the framework-induced ECL enhancement. Specifically, the heterostructure was prepared by the deposition of silver nanoparticles on TiO2 microflowers and utilized as an efficient coreaction accelerator. Remarkably, the formative heterojunction can increase the interfacial charge transfer efficiency and promote the carrier separation, facilitating the oxidation of coreactant tripropylamine. In this way, a novel aptamer-mediated ECL sensing platform is constructed, achieving the sensitive analysis of adenosine triphosphate with a low detection limit of 0.17 nM. As a proof-of-concept study, this work may enlighten the rational design of new-type MOF-based ECL materials and expand the application scope of the ECL technology.

Structural Characteristics and Dielectric Properties of Deposited Silver Nanoparticles with Polypyrrole on PET Films for Dielectric Devices

Herein, (PPy-Ag)/PET composites, consisting of silver nanoparticles (AgNPs) and polypyrrole (PPy) coated on PET, were fabricated by the polymerization process and then the films were characterized by SEM and XRD techniques. The addition of PPy-Ag on the dielectric properties of PET were determined. The XRD proved the successful synthesis of the (PPy-Ag)/PET samples. The SEM results demonstrate the effect of Ag modified the characteristics of the composite, which confirmed the interaction of (PPy-Ag)/PET. The dielectric properties of the films in frequency of 50 Hz to 5.6 MHz were measured. The density energy was enhanced from 9.1 × 10−5 for PET to 5480 × 10−5 J m−3 for (PPy-Ag)/PET. Moreover, the relaxation time τr decreased from 1.7 × 10−5 for PET to 2.8 × 109 sec for (PPy-Ag)/PET. The obtained data confirm the incorporation of PPy-Ag by PET. This research has led to the development of novel physico-chemical properties in flexible polymeric nanocomposite films, which could be used in high-performance energy storage devices.

Multifunctional ultraelastic helical conductive yarn for motion detection and human-machine interaction

Featured with intrinsic lightweight, great flexibility, and easy integration into functional textiles or devices, the stretchable conductive fiber has attracted much attention in the realm of wearable electronics. However, the conductive fibers encounter a troublesome “trade-off” between high conductivity and large elasticity under large deformation, which restricts their widespread applications. Herein, we designed a multifunctional highly elastic helical conductive yarn (HCY) by electrospinning polyurethane (PU) nanofibers, polydopamine (PDA)-assisted silver nanoparticles (AgNPs) deposition and over-twisting. The introduction of a PDA mediated layer fosters strong bond between the conductive AgNPs and the elastic PU nanofibers matrix, showcasing robust structural stability and electrical performance. The hierarchically interlocked conductive structure confers high electrical conductivity to the stretchable HCY, enabling it to withstand large mechanical deformation, which achieves good recoverability within a range of 700 %, great durability (40000 times at deformation of 200 %) and maximum conductive tensile elongation up to 1200 %. Furthermore, the HCY also features excellent Joule-heating ability, great antibacterial performance, and functions as a rapid-response strain sensor (GFmax = 9.82), which is ideal for detecting human motion and enhancing human–machine interactions. This work provides a new path for developing advanced stretchable conductive materials, which is of great significance for versatile ultraelastic wearable electronic devices.

Eco-friendly plant extract-assisted fabrication of CeO2@CH@Ag nanocomposite: A heterogeneous catalyst for organic pollutant remediation

This study explores the synthesis and application of a novel cerium oxide-chitosan-silver (CeO2@CH@Ag) nanocomposite as an efficient catalyst for the reduction of organic pollutants, including methyl orange (MO), congo red (CR), and 4-nitroaniline (4-NA). The nanocomposite was synthesized via a co-precipitation method, followed by in-situ deposition of silver nanoparticles on its surface. Comprehensive characterization techniques, including FTIR, XRD, FESEM, EDX, XPS and nitrogen sorption measurements, confirmed the successful incorporation of CeO₂ and silver within the chitosan matrix. The CeO2@CH@Ag nanocatalyst exhibited a high surface area of 58.081 m2/g, exhibiting remarkable catalytic activity, facilitating rapid reduction of the organic pollutants within 6 min using sodium borohydride as a reducing agent. Kinetic studies revealed pseudo-first-order reaction kinetics, with rate constants of 1.09, 0.38, and 0.58 min⁻1 for MO, CR, and 4-NA, respectively. The proposed mechanism involves the adsorption of dye molecules onto the catalyst's porous surface, followed by electron transfer from the reducing agent to the dye, facilitated by the redox properties of CeO2 and silver. The CeO2@CH@Ag nanocatalyst demonstrates the promising potential for efficient wastewater treatment and remediation of organic pollutants.

Ag nanoparticle-embedded fish scales as SERS substrates for sensitive detection of forever chemical in real samples

Biological materials with unique surface properties provide a new avenue for fabricating green and sensitive SERS-active substrates. Herein, we present a simple but efficient method to prepare surface-enhanced Raman scattering (SERS) substrates by depositing silver nanoparticles (AgNPs) on fish scale substrates using an evaporation-induced self-assembly method (EISA). Characterization of the formed flexible Ag-impregnated substrate proved outstanding SERS sensitivity, uniformity, and reproducibility properties, with a Raman enhancement factor of 1.3 × 106 and a relative standard deviation of 6.4 %. Using this powerful fish scale substrate, a toxic environmental pollutant perfluorooctane sulfonamide (PFOSA) was indirectly detected in lake water, soil, and human urine samples. Due to its chemical structure, it is difficult to detect low concentrations of PFOSA in real samples. Interestingly, malachite green (MG) was smartly used as the Raman label for PFOSA detection in real samples. One of the main appeals is that the concentration of PFOSA can be correlated with a decrease in the SERS signal of MG in real samples. In conclusion, the strategy employed and reproducible SERS substrates may have diverse applications in clinical and environmental analyses.

Enhanced Catalytic, Antioxidant, and Electrochemical Properties of Green‐Synthesized Graphene‐Silver Nanocomposite Utilizing Moringa Oleifera Leaf Extract

AbstractGraphene, a remarkable material known for its exceptional properties, can be efficiently produced through environmentally friendly methods using renewable resources and eco‐friendly solvents. Recent studies have highlighted the potential of leaf extracts as effective reducing and stabilizing agents in converting graphene oxide (GO) to graphene. This paper presents a green and cost‐effective approach for the effective deposition of silver nanoparticles (Ag NPs) onto the reduced graphene oxide (RGO) nanosheets. The process involves the co‐reduction of GO and AgNO3 in water using Moringa olifera leaf extract, resulting in the formation of a nanocomposite termed reduced graphene oxide‐silver (Ag‐RGO). The formation of RGO and Ag NP is confirmed through UV‐visible spectroscopy, XRD, and Raman spectroscopy techniques. TEM images revealed the morphology of the nanocomposite, depicting 2‐dimensional graphene sheets adorned with Ag NPs. FT‐IR analysis confirmed the removal of oxygenated functional groups from GO, indicating graphene formation. The synthesized Ag‐RGO nanocomposite exhibited significant catalytic, antioxidant, and electrochemical properties. This study underscores the utilization of natural ingredients as sustainable alternatives for producing multifunctional graphene‐silver nanocomposites.

Green synthesis of magnetic silver nanocomposite: the photocatalytic performance of nanocomposite to decolorize organic dyes

ABSTRACT The magnetite-silver nanocomposites (Fe3O4-Ag NCs) were synthesized via a facile and green process by Citrus sinensis peel extract. The deposition of silver nanoparticles (NPs) was confirmed by observing an absorption peak at the maximum wavelength at 422 nm in the suspension solution of samples, which is related to silver surface plasmon resonance (SPR). The characteristic diffraction patterns of Fe3O4 and Ag phases were characterized utilizing the XRD patterns and the average size of the crystals was 21 nm. The photocatalytic behavior of Fe3O4-Ag NCs was studied for the destruction of three organic dyes methyl green (MG), methyl orange (MO), and methylene blue (MB) below UV radiation. The effect of the amount of photocatalyst and volume of hydrogen peroxide as an oxidant in the process of dye degradation was also investigated. The complete degradation time of dyes MB, MG, and MO under UV irradiation in the presence of 0.002 g Fe3O4-Ag NCs were 57, 33, and 49 min, respectively. The time of degradation reactions showed the high photocatalytic performance of Fe3O4-Ag NCs. These results proved that the synergistic effect of magnetite in the role of supporting the silver NPs was a significant contribution to the excellent decolorization behavior of Fe3O4-Ag NCs.

In-situ deposition of silver nanoparticles onto glass by non-thermal plasma jet

In-situ deposition of silver nanoparticles onto glass by non-thermal plasma jet

Curvature-Insensitive Transparent Surface-Enhanced Raman Scattering Substrate Based on Large-Area Ag Nanoparticle-Coated Wrinkled Polystyrene/Polydimethylsiloxane Film for Reliable In Situ Detection.

Flexible and transparent surface-enhanced Raman scattering (SERS) substrates have attracted considerable attention for their ability to enable the direct in situ detection of analytes on curved surfaces. However, the curvature of an object can impact the signal enhancement of SERS during the measurement process. Herein, we propose a simple approach for fabricating a curvature-insensitive transparent SERS substrate by depositing silver nanoparticles (Ag NPs) onto a large-area wrinkled polystyrene/polydimethylsiloxane (Ag NP@W-PS/PDMS) bilayer film. Using rhodamine 6G (R6G) as a probe molecule, the optimized Ag NP@W-PS/PDMS film demonstrates a high analytical enhancement factor (AEF) of 4.83 × 105, excellent uniformity (RSD = 7.85%) and reproducibility (RSD = 3.09%), as well as superior mechanical flexibility. Additionally, in situ measurements of malachite green (MG) on objects with diverse curvatures, including fish, apple, and blueberry, are conducted using a portable Raman system, revealing a consistent SERS enhancement. Furthermore, a robust linear relationship (R2 ≥ 0.990) between Raman intensity and the logarithmic concentration of MG detected from these objects is achieved. These results demonstrate the tremendous potential of the developed curvature-insensitive SERS substrate as a point-of-care testing (POCT) platform for identifying analytes on irregular objects.

Penetrative Ionic Organic Molecular Cage Nanozyme for the Targeted Treatment of Keratomycosis.

Keratomycosis, caused by pathogenic fungi, is an intractable blinding eye disease. Corneal penetration is an essential requirement for conventional antifungal medications to address keratomycosis. Due to the distinctive anatomical and physiological structure of the cornea, the therapeutic efficacy is hampered by the inadequate penetration capacity. Despite the emergence of diverse antifungal drug delivery systems and advanced antifungal nanomaterials, it has remained challenging to achieve corneal penetration over the past decade. This study fabricates a penetrative ionic organic molecular cage-based nanozyme (OMCzyme) for treating keratomycosis. The synthesis of OMCzyme involved two steps. Initially, the ionic OMC is synthesized by a [2+3] cycloimination reaction of triformylphloroglucinol and 2,3-diaminopropionic acid. Subsequently, OMCzyme is fabricated by coordination of Fe2⁺ with carboxyl anions and phenolic hydroxyls in the organic cage, and further deposition of silver nanoparticles on the surface of OMC-Fe complex. The as-prepared OMCzyme demonstrates excellent water dispersion, peroxidase-like activity, in vitro and in vivo biocompatibility, and corneal penetration. Notably, the nanozyme displays targeted antifungal activity, effectively combating Fusarium solani with negligible cytotoxicity toward human corneal epithelial cells. The hybrid mimic is further demonstrated to be effective in treating keratomycosis in mice, indicating the potential of OMCzyme for curing fungal infectious diseases.

Templated silver nanoparticle deposition on laser-induced periodic surface structures for SERS sensing

Organized assemblies of metal nanoparticles exhibit unique optical properties and can be used as platforms for surface-enhanced Raman scattering (SERS) to detect small amounts of analyte molecules. In this work, we demonstrate that using Yb:KGW femtosecond laser structuring of silicon wafer we can modify surface properties by creating laser-induced quasi periodic surface structures (LIPSS) of 850 ± 43 nm periodicity. We show that silicon with LIPSS is a suitable surface for direct nanoparticle deposition because of its superhydrophilic properties and the nanoparticle density affects the density of the hot spots contributing in the Raman enhancement. We have analyzed the influence of the silver nanoparticle deposition on the structured silicon surface conditions on their density and coverage. 101±8 nm size silver nanoparticles were deposited by two methods, namely drop casting colloidal solution at three different temperatures (4 °C, 21 °C, 35 °C) and their SERS enhancements were compared with the monolayers deposited by liquid-liquid interface. It was found that monolayer deposition on a structured surface was the best approach in the sense of even silver nanoparticles coverage which exhibited best SERS performance reaching a limit of detection of 10−7 M for 2-naphthalenethiol. The obtained LoD is comparable with that of commercial substrates available in the market.

Fabrication of PTFE + TiO2/Ag coatings on 316L/polydopamine with advanced mechanical, bio-corrosion, and antibacterial properties for stainless steel Catheters

This study explores the corrosion resistance and antibacterial properties of a PTFE + TiO2/Ag coating applied to 316 L stainless steel. To enhance adhesion, a polydopamine interlayer was chemically deposited onto the steel surface. The PTFE + TiO2 coating was subsequently applied through immersion, followed by the deposition of silver nanoparticles using a chemical method. Optimization of the polydopamine interlayer involved varying temperature, time, stirring speed, and drying parameters. The optimal conditions for the polydopamine interlayer were determined to be 60 °C for 1 h, 300 rpm stirring, and 24-h drying in a freeze dryer. Analytical results demonstrated that both the PTFE + TiO2 and PTFE/PTFE + TiO2/Ag coatings exhibited exceptional corrosion resistance, with corrosion currents of 3.3 × 10−5 and 3.2 × 10−4 μA/cm2, respectively. Antibacterial assessments showcased the remarkable ability of the PTFE/PTFE + TiO2/Ag coating, containing 5% silver content, to effectively inhibit bacterial penetration within a 6.5 mm radius. Furthermore, this coating displayed a water contact angle of 143°, classifying it as a hydrophobic coating. The photocatalytic efficiency (Rs) was determined to be 3.18 × 10−3 A/W, a performance level comparable to that of a standard UV sensor. These findings underscore the substantial enhancements in corrosion resistance, antibacterial performance, and hydrophobic characteristics achieved with the PTFE + TiO2/Ag coating, particularly through the novel optimization of the polydopamine interlayer. This coating exhibits great promise for multifunctional protective applications in diverse fields, particularly demonstrating its suitability for implants and bio-coatings.

Detection of water pollutants using super-hydrophobic porous silicon-based SERS substrates.

Super hydrophobic porous silicon surface is prepared using a wet chemical synthesis route. Scanning electron microscopic investigation confirms a correlation between pore size and reaction time. SERS substrates are prepared by silver nanoparticle deposition on porous silicon surface. They exhibit excellent characteristics in terms of sensitivity, reproducibility, stability, and uniformity. They could detect rhodamine 6G in femtomolar range with SERS enhancement factor of ~ 6.1 × 1012, which is best ever reported for these substrates. Molecule-specific sensing of water pollutants such as methylene blue, glyphosate, andchlorpyrifos, is demonstrated for concentrations well below their permissible limits along with excellent enhancement factors. Porous silicon substrate functionalized with Ag nanoparticles demonstrates to be a promising candidate for low-cost, long-life, reliable sensors for environmental conservation applications.

Colloidal carbon soot templated TiO2/Ag surface functionalized 3D printed metal brushes as new generation surface enhanced Raman scattering substrates

This present work demonstrated the functional transformation of 3D printed metal substrates into a new family of Surface-enhanced Raman Scattering substrates, a promising approach in developing SERS-based Point-of-care (PoC) analytical platforms. l-Powder Bed Fusion (l-PBF, Additive manufacturing or 3D printing technique) printed metal substrates have rough surfaces, and exhibit high thermal stability and intrinsic chemical inertness, necessitating a suitable surface functionalization approach. This present work demonstrated a unique multi-stage approach to transform l-PBF printed metal structures as recyclable SERS substrates by colloidal carbon templating, chemical vapor deposition, and electroless plating methods sequentially. The surface of the printed metal structures was functionalized using the colloidal carbon soot particles, that were formed by the eucalyptus oil flame deposition method. These carbon particles were shown to interact with the metals present in the printed structures by forming metal carbides and function as an adlayer on the surface. Subsequent deposition of TiO2 onto these templates led to strong grafting of TiO2 and retaining the fractal structure of the soot template onto the metal surface. Electroless deposition of silver nanoparticles resulted in the formation of fractally structured TiO2/Ag nanostructures and these functionalized printed metal structures were shown as excellent SERS substrates in enhancing the vibrational spectral features of Rhodamine B (RhB). The presence of TiO2 photocatalyst on the surface was shown to remove the RhB analyte from the surface under photochemical conditions, which enables the regeneration of SERS activity, and the substrate can be recycled. The migration of metals from the printed metal structures into the fractally ordered TiO2/Ag nanostructures was found to enhance the photocatalytic activity and increase the recyclability of these substrates. This study demonstrates the potential of 3D-printed Inconel metal substrates as next-generation recyclable SERS platforms, offering a substantial advancement over traditional colloidal, thin-film, flexible, and hard SERS substrates.

Functionalization of silver nanoparticles coating cotton fabrics through hydrothermal synthesis for improved antimicrobial properties

Deposition of silver nanoparticles (AgNPs) on the surfaces of cotton fabric (CF) is an approach for producing antimicrobial textile products. CF-AgNPs composites were fabricated ex situ using a simple hydrothermal synthesis of AgNPs, while the fabric was surface modified using a plasma to improve adhesion prior to coating. The morphology and chemical composition of CF-AgNPs nanocomposites were examined using UV–vis spectrophotometry (UV–vis), x-ray diffraction (XRD), transmission electron microscopy (TEM) and field emission scanning electron microscopy (FESEM). Study results show uniform deposition of AgNPs on cotton fabrics. The CF-AgNPs composite material exhibits excellent laundering durability and antimicrobial performance against Gram-positive, Staphylococcus aureus and Gram-negative, Escherichia coli pathogens. These findings indicate that the developed fabric can be used in a wide range of biomedical applications, health care and various packaging systems.

Optimization of cotton SERS substrates based on different weave structures for surface trace detection

Cotton fabrics have been used to fabricate Surface-enhanced Raman spectroscopy (SERS) substrates due to their excellent properties such as flexibility, hygroscopicity, and large-scale production. The morphology of the SERS substrate has a great influence on the deposition of noble metal nanoparticles and affects the Raman-enhanced signal. Although numerous research reports have been conducted on SERS substrates made from cotton, there has been limited exploration on the impact of the weave structure of cotton fabric on SERS performance. Herein, the cotton SERS substrates were prepared by depositing silver nanoparticles (Ag NPs) on cotton fabrics with different weave structures by a simple vacuum-thermal evaporation method. The influence of substrate morphology on the deposition arrangement of Ag NPs and the enhancement of SERS performance was explored. The analysis findings demonstrate that the cotton SERS substrate displays exceptional Raman signal enhancement performance. Thereinto, the satin SERS substrate exhibited a stronger Raman signal due to its smoother surface favoring the deposition of Ag NPs. The limit of detection for p-aminothiophenol (PATP) was established at a low of 10−8 M, with an RSD value of 9.96%. Moreover, the satin SERS substrate demonstrated an enhancement factor of 5.18 × 105. In addition, it has excellent mechanical flexibility and good hygroscopicity, and thiram on the apple surface can be detected by simple wiping. Cotton SERS substrates show great potential in food safety analysis and monitoring. More importantly, this study provides assistance for the selection of SERS substrates for traditional cotton fabrics, and further promotes the broadening of the application fields of smart cotton fabrics.

Fabrication of Surface Enhanced Raman Spectroscopy based sensor using Ag NPs on copper tape flexible substrate

In this work, the authors have investigated the properties of thermally evaporated silver nanoarrays on copper tape (Ag/Cu) as flexible and reusable sensors for organic contaminants. Uniformly deposited silver nanoparticles (Ag NPs) with well-controlled sizes have formed by thermal evaporation. The deposition time is varied to obtain different morphology of the Ag nanoparticles. The Surface-enhanced Raman spectroscopy (SERS) efficiency has been optimized using Rhodamine 6G (R6G) as a test molecule. Morphological studies have also been carried out using scanning electron and atomic force microscopes. The Ag NPs on the copper tape-based sensor show a substantial enhancement in the order of 8.3x107 in the SERS signal for a deposition time of 10 s. Furthermore, we observe that as-prepared Ag/Cu tape can detect micro-molar alizarine red S (ARS), which exhibited excellent reproducibility as well. Hence, the flexible copper substrate proves to be a promising material for detecting environmental hazards at a meager cost.