Au Ag Alloy Nanoparticles Research Articles

Engineering the Hot-Spots in Au-Ag Alloy Nanoparticles through Meniscus-Confined 3D Printing for Microplastic Detection.

The escalating concern surrounding microplastic (MP) pollution necessitates urgent attention and the development of rapid techniques for quantifying extremely low concentrations. Surface-enhanced Raman spectroscopy (SERS) has emerged as a promising method due to its simplicity, high sensitivity, and rapid quantification capabilities. Herein, the efficacy of gold-silver alloy nanoparticles (3DPAu-Ag) substrates for detecting poly(methyl methacrylate) (PMMA) and polystyrene (PS) MPs is investigated. The 3DPAu-Ag SERS substrates are fabricated using the meniscus-confined electrochemical 3D printing (MC-E3DP) process, employing a nozzle of 0.8 mm size with 2.5 V potential at a printing speed of 0.4 mm s-1. The proposed SERS substrates exhibit exceptional sensitivity and are capable of detecting PMMA concentrations as low as 0.2 μg mL-1 and PS concentrations of 1.2 μg mL-1 within the ranges of 1-103 μg mL-1 and 10-104 μg mL-1, respectively. Remarkable enhancement factors (EFs) of up to 3.2 × 104 for PMMA and 9.3 × 103 for PS are achieved, underscoring the substrates' effectiveness. Furthermore, the investigation demonstrates outstanding uniformity and reproducibility of the 3DPAu-Ag substrates, with relative standard deviation (RSD) values of only 4.1 and 6.4%, respectively, across 31 and 5 measurements. Additionally, a minimal 17% decrease in the initial SERS signal value after 5 weeks highlights the substrates' high stability. This not only highlights the superior quality of the substrates but also positions them ahead of previously reported works in the literature. Moreover, this study also comes up with a plausible mechanism for MPs SERS detection facilitated by the 3DPAu-Ag substrates, offering insights into the underlying processes. Overall, 3DPAu-Ag substrates show promise for sensitive, stable MP detection, which is crucial for environmental monitoring.

Poly(N‐Heterocyclic Carbene)‐Capped Alloy and Core‐Shell AuAg Bimetallic Nanoparticles

AbstractN‐Heterocyclic carbene (NHC)‐stabilized metal nanoparticles (NPs) have recently attracted considerable attention. While most efforts in the field have been devoted to the development of NHC‐tethered monometallic NPs and enhancing their stabilities under various conditions, their bimetallic counterparts are rare in the literature. Herein, we demonstrate that the covalent immobilization of Au and Ag atoms on polymerized NHCs is a powerful method to access bimetallic AuAg NPs. In addition, we show that while AuAg alloy NPs are often obtained via this method, the use of bimetallic polymeric substrates with lower Ag content, relative to Au, results in the formation of core–shell NPs with Au core and Ag shell. Application of these nanomaterials for oxygen reduction reaction is demonstrated with all materials exhibiting electrocatalytic activity. This work demonstrates for the first time that while bimetallic poly(NHC‐metal)s are viable substrates to access NHC‐stabilized bimetallic NPs, careful adjustment of metal content in the polymeric substrates can finetune the microstructure of the resulting NPs, i.e. alloy vs. core–shell.

A Green Synthesis of Au-Ag Alloy Nanoparticles using Polydopamine Chemistry: Evaluation of their Anticancer Potency Towards Both MCF-7 Cells and their Cancer Stem Cells Subgroup.

Limited chemotherapy efficacy and cancer stem cells (CSCs)-induced therapeutic resistance are major difficulties for tumour treatment. Adopting more efficient therapies to eliminate bulk-sensitive cancer cells and resistant CSCs is urgently needed. Based on the potential and functional complementarity of gold and silver nanoparticles (AuNPs or AgNPs) on tumour treatment, bimetallic NPs (alloy) have been synthesized to obtain improved or even newly emerging bioactivity from a combination effect. This study reported a facile, green and economical preparation of Au-Ag alloy NPs using biocompatible polydopamine (PDA) as a reductant, capping, stabilizing and hydrophilic agent. These alloy NPs were quasi-spherical with rough surfaces and recorded in diameters of 80 nm. In addition, these alloy NPs showed good water dispersity, stability and photothermal effect. Compared with monometallic counterparts, these alloy NPs demonstrated a dramatically enhanced cytotoxic/pro-apoptotic/necrotic effect towards bulk-sensitive MCF-7 and MDA-MB-231 cells. The underlying mechanism regarding the apoptotic action was associated with a mitochondria-mediated pathway, as evidenced by Au3+/Ag+ mediated Mitochondria damage, ROS generation, DNA fragmentation and upregulation of certain apoptotic-related genes (Bax, P53 and Caspase 3). Attractively, these Au-Ag alloy NPs showed a remarkably improved inhibitory effect on the mammosphere formation capacity of MCF-7 CSCs. All the positive results were attributed to incorporated properties from Au, Ag and PDA, the combination effect of chemotherapy and photothermal therapy and the nano-scaled structure of Au-Ag alloy NPs. In addition, the high biocompatibility of Au-Ag alloy NPs supported them as a good candidate in cancer therapy.

One-step synthesized multisize AuAg alloy nanoparticles with high SERS sensitivity in directly detecting SARS-CoV-2 spike protein

The coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in widespread disease transmission, challenging the stability of global healthcare systems. Surface-enhanced Raman scattering (SERS) as an easy operation, fast, and low-cost technology illustrates a good potential in detecting SARS-CoV-2. In the study, one-step fabrication of gold-silver alloy nanoparticles (AuAgNPs) with adjustable metal proportions and diameters is employed as SERS substrates. The angiotensin-converting enzyme 2 (ACE2) functionalized AuAgNPs are applied as sensor surfaces to detect SARS-CoV-2 S protein. By optimizing the SERS substrates, ACE2/Au35Ag65NPs illustrate higher performance in detecting the SARS-CoV-2 S protein with a limit of detection (LOD) of 10 fg/mL in both phosphate-buffered saline (PBS) and pharyngeal swabs solution (PSS). It also provides excellent reproducibility with a relative standard deviation (RSD) of 7.7 % and 7.9 %, respectively. This easily preparable and highly reproducible SERS substrate has good potential in the practical application of detecting SARS-CoV-2.

Nanoengineering of mono (Au, Ag) and bimetallic (Ag-Au) alloy nanoparticles for dye degradation and toxicity assessment

This research entails the synthesis and catalytic exploration of bimetallic nanoparticles combining silver (Ag) and gold (Au). The Au concentration was systematically varied (20%, 40%, 60%, and 80%), alongside the utilization of CTAB surfactant for nanoparticle stabilization. UV visible spectroscopic analysis confirmed the formation and stability of synthesized Au, Ag and bimetallic (Ag-Au) nanoparticles. FESEM further confirmed the formation of uniform sized Au and Ag nanoparticles. Integration of Au into Ag resulted in bimetallic (Ag-Au) alloy nanoparticles with smaller dimensions as compared to individual Au and Ag nanoparticles. EDX spectra and mapping verified the composition of each synthesized bimetallic nanoparticle variant. The catalytic potential of the synthesized nanoparticles was methodically explored using UV–visible spectroscopy. All the synthesized nanoparticles showcased excellent catalytic efficacy. The synergistic effect of the alloyed bimetallic nanoparticles was found promising. Assessment of dye toxicity pre- and post-degradation was conducted using the ECOSAR program, indicating a reduction in dye toxicity following degradation.

Study on fabrication and optical properties of monodisperse Ag-Au alloy nanostructure

This study addresses challenges in various fields by creating a new method for uniform, size- and composition-controlled Ag-Au alloy nanoparticles in organic solvents. Building on prior research, we demonstrate control over nanoparticle properties by varying complexing agents, surfactants, and reducing agents. Optimal conditions using surfactant SOA and reducing agent TBAB yielded small, monodisperse Ag nanoparticles ideal for alloying with Au. The reaction time significantly impacts final morphology and surface plasmon resonance (SPR) properties of the resultant Ag-Au alloy nanoparticles. Interestingly, Au nanoparticles formed under identical conditions shared a similar size with 60-minute Ag-Au alloys, evidenced by a single SPR peak at 520 nm. This control over Ag-Au nanoalloy composition and size opens doors for promising applications.

Poly(N-Heterocyclic Carbene)-Capped Alloy and Core-Shell AuAg Bimetallic Nanoparticles.

N-Heterocyclic carbene (NHC)-stabilized metal nanoparticles (NPs) have recently attracted considerable attention. While most efforts in the field have been devoted to the development of NHC-tethered monometallic NPs and enhancing their stabilities under various conditions, their bimetallic counterparts are rare in the literature. Herein, we demonstrate that the covalent immobilization of Au and Ag atoms on polymerized NHCs is a powerful method to access bimetallic AuAg NPs. In addition, we show that while AuAg alloy NPs are often obtained via this method, the use of bimetallic polymeric substrates with lower Ag content, relative to Au, results in the formation of core-shell NPs with Au core and Ag shell. Application of these nanomaterials for oxygen reduction reaction is demonstrated with all materials exhibiting electrocatalytic activity. This work demonstrates for the first time that while bimetallic poly(NHC-metal)s are viable substrates to access NHC-stabilized bimetallic NPs, careful adjustment of metal content in the polymeric substrates can finetune the microstructure of the resulting NPs, i.e. alloy vs. core-shell.

Enhanced dielectric properties and electromagnetic interference shielding effectiveness of 3D hierarchical nanohybrid of Au-Ag@MoS2-rGO

Addressing the growing need for electromagnetic interference (EMI) shielding in GHz devices, this study presents a novel bimetallic Au-Ag@MoS2-rGO nanohybrid developed via hydrothermal and chemical processes. This work marks the first exploration of their dielectric properties and EMI shielding effectiveness. The composite, featuring uniformly dispersed Au-Ag alloy nanoparticles on MoS2-rGO nanosheets, significantly outperforms MoS2 and MoS2-rGO in EMI shielding, achieving over 38.1 dB in the X-band frequency range and blocking nearly 99.99% of electromagnetic power. This improvement is credited to the enhanced interfacial interactions, increased microwave absorption sites, and the formation of three-dimensional conductive bridges, boosting electrical conductivity and charge mobility. This efficient electromagnetic energy dissipation through a synergistic blend of conduction loss, polarization, and internal reflections suggests the potential for these advanced conductive metal-based materials in microwave absorbers and shielding applications.

Abstract 5757: Graphene quantum dots-covered AuAg alloy nanoparticles as drug delivery platforms for anticancer applications

Abstract Cancer continues to be a global health challenge, with millions suffering from its various forms. Prostate cancer, in particular, emerges as a significant health risk for men. Originating in the prostate gland—a small organ nestled in the male pelvis—this type of cancer the second most common cause of cancer-related deaths among men in the U.S. Despite numerous medical breakthroughs over the years, finding an effective treatment for prostate cancer remains a challenge. Our research is venturing into a new frontier in the fight against prostate cancer, focusing on an innovative method, it explores the potential of nanoparticles for targeted drug delivery. This targeted approach promises to not only intensify the therapeutic effect, but also minimize adverse side effects on healthy cells, ensuring a more balanced and effective treatment regimen. A key in this study is the drug Andrographolide (ADG), which has been previously recognized for its robust anti-cancer properties. However, one of its limitations is its hydrophobicity, which makes it challenging to administer due to solubility concerns. To navigate this challenge, we are pioneering the synthesis of AuAg (gold and silver) graphene quantum dots (GQDs) alloy nanoparticles. AuAg particles, in have been the subject of numerous studies due to their profound impact on cellular processes. By integrating a protective layer of GQDs, we aim to boost the nanoparticles' stability, all while preventing any potential release of harmful metallic ions. The primary objective of this advanced approach is to augment the solubility of andrographolide, paving the way for its targeted and efficient delivery to PC-3 cells. An integral part of our research involves determining the IC50 value, which is pivotal in indicating the concentration at which the drug can inhibit the growth of 50% of prostate cancer cells. Once the IC50 value for the AuAgGQDs is firmly established, our focus will shift to evaluating its effects on the morphology of Red Blood Cells (RBCs). By encapsulating andrographolide within the designed nanoparticles, such as AuAgGQDs and their derivatives, we aim to observe changes in morphology. If there is a change in morphology, it indicates successful drug encapsulation. Through this research, we are not just seeking a viable treatment method, but also aiming to expand the horizons of drug delivery systems. The insights gained from this study could very well revolutionize our understanding of therapeutic potential and underscore the importance of nanoparticles in the realm of biomedical applications. Citation Format: Alondra Del Mar Veloz Bonilla, Brad Weiner, Gerardo Morell, Nataniel Medina-Berríos. Graphene quantum dots-covered AuAg alloy nanoparticles as drug delivery platforms for anticancer applications [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2024; Part 1 (Regular Abstracts); 2024 Apr 5-10; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2024;84(6_Suppl):Abstract nr 5757.

Tuning the morphology and chemical distribution of Ag atoms in Au rich nanoparticles using electrochemical dealloying.

Dealloying of Ag-Au alloy nanoparticles (NPs) strongly differs from the corresponding bulk alloy materials. Here, we have investigated the effects of potentiodynamic and potentiostatic dealloying on structure and distribution of residual Ag atoms for Au rich NPs. Two different sizes of Ag rich alloy NPs, 77 ± 26 nm Ag77Au23 and 12 ± 5 nm Ag86Au14, were prepared. 77 nm Ag77Au23 NPs form a homogeneous alloy, while 12 nm Ag86Au14 NPs show an Ag rich shell-Au rich core arrangement. The two groups of as-prepared NPs were dealloyed either under potentiodynamic (0.2-1.3 VRHE) or potentiostatic (0.9, 1.2, and 1.6 VRHE) conditions in 0.1 M HClO4. For the initial 77 nm Ag77Au23 NPs, both dealloying protocols lead to pore evolution. Interestingly, instead of homogenous Ag distribution, numerous Ag rich regions form and locate near the pores and particle edges. The critical dealloying potential also differs by ∼500 mV depending on the dealloying method. The initial 12 nm Ag86Au14 NPs remain dense and solid, but Ag distribution and thickness of the Au passivation layer vary between both dealloying protocols. When the Au passivation layer is very thin, the residual Ag atoms tend to segregate to the particle surface after dealloying. Due to the size effect, small NPs are less electrochemically stable and show a lower critical dealloying potential. In this systematic study, we demonstrate that the mobility of Au surface atoms and dealloying conditions control the structure and residual Ag distribution within dealloyed NPs.

Direct formate anion exchange membrane fuel cells with a PdAu bimetallic nanoparticle anode electrocatalyst obtained by metal vapor synthesis

Renewable energy can be stored in liquid e-fuels such as formate. Here Pd–Au alloy nanoparticles prepared by metal vapor synthesis show enhanced activity and efficiency for the re-transformation to electrical energy in direct formate fuel cells.

Surface-Enhanced Raman Scattering Studies of Au-Ag Bimetallic Nanoparticles with a Tunable Surface Plasmon Resonance Wavelength Synthesized by Picosecond Laser Irradiation

Here, we present a simple and green method of preparing Au-Ag bimetallic nanoparticles (NPs) with a tunable surface plasmon resonance (SPR) wavelength by using picosecond laser irradiation. Au-Ag alloy NPs have been produced by irradiating the solutions containing respective metallic salts in a polyvinyl alcohol (PVA) matrix using a picosecond laser in a single-step process. The SPR wavelength of the Au-Ag bimetallic NPs is observed to be shifted/changed with the Au-Ag concentration and the laser irradiation parameters. The Au-Ag NPs embedded in the PVA matrix are advantageous for Surface-Enhanced Raman scattering (SERS) applications. The estimated enhancement factors (EFs) were observed to vary as a function of conditions of the Au-Ag bimetallic alloy NPs synthesis and also on the concentration of Au at a fixed input fluence of irradiation. The SERS active platforms of Au-Ag bimetallic NPs showed EFs as high as of the order of 108 for Crystal Violet (CV) dye samples at nano molar concentrations. The present study demonstrates a simple, single-step, and green method that fabricates Au-Ag alloy-based nanocomposites suitable for SERS investigations with significantly higher orders of EFs.

Catalytic and anti-cancer properties of platinum, gold, silver, and bimetallic Au-Ag nanoparticles synthesized by Bacillus sp. bacteria

Metallic nanoparticles play a significant role in the catalysis of chemical processes, besides, bimetallic nanoparticles with abundant active sites can reduce metallic nanoparticles toxicity in addition to increasing their catalytic performances. In this work, the platinum, gold, and silver nanoparticles are bio-synthesized using a native bacterium (GFCr-4). Also, the Au-Ag and Au@Ag bimetallic nanoparticles with alloy and core-shell structures, respectively, are biologically synthesized. To improve the synthesis, the effects of various factors like pH, temperature, electron donor, and ionic liquids were investigated. The as-synthesized nanoparticles were characterized with different techniques. The microscope images and dynamic light scattering (DLS) analysis confirm the uniform distribution of as-synthesized nanoparticles with average sizes of 25, 30, 47, 77, and 86 nm obtained for Ag, Au, Pt, Au-Ag alloy, and Au@Ag core-shell, respectively. The catalytic performances of as-synthesized nanoparticles were investigated. The Au-Ag alloy nanoparticles exhibit better catalytic performance than the as-synthesized metallic Au nanoparticles, according to the Gewald reaction. According to the photocatalytic study, the yield can be increased by up to 92% by using PtNPs in the presence of a green LED. Additionally, for the first time, PtNPs were utilized as an effective catalyst in a peroxyoxalate chemiluminescence (POCL) system in the presence of nuclear fast red (NFR) as a novel fluorophore. In addition, the results of the MTT (3-[4,5-dimethylthiazol-2-yl]−2,5 diphenyl tetrazolium bromide) assay revealed that the synthesized eco-friendly nanoparticles have a low effect on the lethality of 3T3 normal cells whereas MCF-7 cancer cells were inhibited up to 77.3% after treatment by PtNPs nanoparticles.

Experimental and theoretical study on one-step synthesis of AuAg alloy nanoparticle catalytic layer as highly stable non-enzymatic glucose sensing interface

Au-based non-enzymatic glucose sensor has excellent catalytic performance, but it is difficult to be applied to practice due to high cost. A facile method was developed to load three AuAg alloy nanoparticle catalytic layer on the fluorine-doped tin oxide conductive glass by calcination as the working electrodes for non-enzymatic glucose sensors in a single process. Scanning electron microscopy, energy dispersive spectrometer, X-ray diffraction, and N2-adsorption–desorption were used to characterize the samples. The electrochemical properties of the electrodes were studied by cyclic voltammetry and electrochemical impedance spectroscopy methods. The Au1Ag1 catalytic layer electrode prepared achieved ultra-high detection sensitivity for glucose, and demonstrated excellent stability, maintaining ∼90 % sensitivity after 30 days of storage in room-temperature air. The adsorption properties of various AuAg substrates on glucose molecules under alkaline conditions were investigated using density functional theory. For the same AuAg substrates, the Ag sites adsorbed glucose more strongly than the Au sites. The adsorption capacity of Ag sites on the AuAg substrates is superior to that of Au sites on the Au substrates, which means that the doping of Ag improves the adsorption capacity for glucose, qualitatively supporting the experimental results. Under alkaline synthetic conditions, the AuAg alloying dramatically enhances the sensitivity and stability of the non-enzymatic glucose sensor. Meanwhile, the preparation method of the sensor is simple and the cost is low. This paper provides research ideas and theoretical support for the performance improvement and cost reduction of noble metal-based non-enzymatic glucose sensors.

Facile green synthesis of highly stable, water dispersible carbohydrate conjugated Ag, Au and Ag-Au biocompatible nanoparticles: Catalytic and antimicrobial activity

Highly stable carbohydrate conjugated silver, gold and bimetallic silver-gold alloy biocompatible and nearly monodisperse nanoparticles (NPs) have been synthesized through bio-reduction of aqueous solution of corresponding metal salt precursors mediated by aqueous extracts of a high altitude lichen, Lobaria retigera. The biomolecule accountable for the reduction, stabilization and capping of the metal nanoparticles is identified to be carbohydrates. The as-synthesized carbohydrate conjugated nanoparticles have excellent dispersibilty in water, phosphate, phosphate-buffered saline, and serum media. The resulting nanoparticles were completely stable for several months in water. The nanoparticles were characterized using UV–visible spectroscopy, TEM, EDX, FT-IR, powder XRD, DLS and CV study. Though mostly spherical in shapes, occasionally truncated triangular and rod shapes were also noted. The average particle sizes of Ag, Au and Ag-Au alloy nanoparticles as determined from TEM analysis are 14.5 nm, 11.7 nm and 16.3 nm, respectively. Cyclic voltammetry pointed to a relatively high electrode potential barrier for the synthesized nanomaterials. The prepared Ag, Au and Ag-Au alloy nanoparticles served as efficient catalysts for the degradation of hazardous pollutant dye, methyl orange (MO) with rate constat of 0.1496 min−1, 0.1049 min−1, and 0.1882 min−1. The bimetallic Ag-Au nanoparticles exhibited the most accelerated reduction with 90.6% degradation efficiency. The reduction kinetics for the reactions followed a pseudo-first order, kAu < kAg< kAu-Ag. The Ag and Ag-Au alloy NPs showed pronounced antimicrobial activity towards selected bacterial strains while AuNPs lacked any such activity.

Silver-Gold Alloy Nanoparticles (AgAu NPs): Photochemical Synthesis of Novel Biocompatible, Bimetallic Alloy Nanoparticles and Study of Their In Vitro Peroxidase Nanozyme Activity.

Facile synthesis of metal nanoparticles with controlled physicochemical properties using environment-friendly reagents can open new avenues in biomedical applications. Nanomaterials with controlled physicochemical properties have opened new prospects for a variety of applications. In the present study, we report a single-step photochemical synthesis of ~5 nm-sized silver (Ag) and gold (Au) nanoparticles (NPs), and Ag-Au alloy nanoparticles using L-tyrosine. The physicochemical and surface properties of both monometallic and bimetallic NPs were investigated by analytical, spectroscopic, and microscopic techniques. Our results also displayed an interaction between L-tyrosine and surface atoms that leads to the formation of AgAu NPs by preventing the growth and aggregation of the NPs. This method efficiently produced monodispersed NPs, with a narrow-sized distribution and good stability in an aqueous solution. The cytotoxicity assessment performed on breast cancer cell lines (MCF-7) revealed that the biofriendly L-tyrosine-capped AgNPs, AuNPs, and bimetallic AgAu NPs were biocompatible. Interestingly, AgAu NPs have also unveiled controlled cytotoxicity, cell viability, and in vitro peroxidase nanozyme activity reliant on metal composition and surface coating.

A Microshutter for the Nanofabrication of Plasmonic Metal Alloys with Single Nanoparticle Composition Control.

Alloying offers an increasingly important handle in nanomaterials design in addition to the already widely explored size and geometry of nanostructures of interest. As the key trait, the mixing of elements at the atomic level enables nanomaterials with physical or chemical properties that cannot be obtained by a single element alone, and subtle compositional variations can significantly impact these properties. Alongside the great potential of alloying, the experimental scrutiny of its impact on nanomaterial function is a challenge because the parameter space that encompasses nanostructure size, geometry, chemical composition, and structural atomic-level differences among individuals is vast and requires unrealistically large sample sets if statistically relevant and systematic data are to be obtained. To address this challenge, we have developed a microshutter device for spatially highly resolved physical vapor deposition in the lithography-based fabrication of nanostructured surfaces. As we demonstrate, it enables establishing compositional gradients across a surface with single nanostructure resolution in terms of alloy composition, which subsequently can be probed in a single experiment. As a showcase, we have nanofabricated arrays of AuAg, AuPd, and AgPd alloy nanoparticles with compositions systematically controlled at the level of single particle rows, as verified by energy dispersive X-ray and single particle plasmonic nanospectroscopy measurements, which we also compared to finite-difference time-domain simulations. Finally, motivated by their application in state-of-the-art plasmonic hydrogen sensors, we investigated PdAu alloy gradient arrays for their hydrogen sorption properties. We found distinctly composition-dependent kinetics and hysteresis and revealed a composition-dependent contribution of a single nanoparticle response to the ensemble average, which highlights the importance of alloy composition screening in single experiments with single nanoparticle resolution, as offered by the microshutter nanofabrication approach.

Electric field-induced assembly of Au-Ag alloy nanoparticles into nano-reticulation for ultrasensitive SERS.

This paper discusses a method for assembling Au-Ag alloy nanoparticles (NPs) using direct current (DC) electric field to fabricate highly active SERS substrates. Different nanostructures could be obtained by regulating the intensity and action time of DC electric field. Under the condition of 5mA*10 min, we obtained Au-Ag alloy nano-reticulation (ANR) substrate with excellent SERS activity (Enhancement factor on order of magnitude of 106). ANR substrate has excellent SERS performance due to the resonance matching between its LSPR mode and excitation wavelength. The uniformity of the Raman signal on ANR is greatly improved than bare ITO glass. ANR substrate also has the ability to detect multiple molecules: ANR substrate can respectively detect Rh6G and CV molecules with a concentration as low as 10-10 M and 10-9 M and the Raman spectral intensity of the probe molecules on the surface of the ANR substrate has good linear correlation with the molecular concentration (R2 > 0.95). In addition, ANR substrate can detect both thiram and aspartame (APM) molecules far below (thiram for 0.0024 ppm and APM for 0.0625 g/L) the safety standard, which demonstrate its practical application potential.

Two-Step Synthesis of Large Gold–Silver Alloy Nanoparticles via the Combination of Seeded Growth and Citrate Co-reduction

We report a novel two-step method for the synthesis of uniform quasi-spherical and monodisperse gold–silver alloy nanoparticles with diameters of approximately 80 nm. In step one, gold–silver alloy seeds (G0) with diameters of approximately 30 nm are synthesized by citrate co-reduction of gold acetate and silver nitrate. In step two, the seeds grow into large alloy nanoparticles with diameters of approximately 80 nm by the combination of seeded growth and citrate co-reduction of gold and silver precursors. Our method makes use of gold acetate (rather than chloroauric acid) as a gold precursor to avoid the formation of silver chloride precipitates during synthesis. To our knowledge, we are the first to prepare gold–silver alloy nanoparticles with diameters of above 70 nm using gold acetate as a gold precursor. The alloy seeds and seed-grown nanoparticles show good control of size and composition, which enables tuning of the plasmonic band of these gold–silver alloy nanoparticles. Gold and silver are distributed uniformly within the cores of all Au-Ag alloy nanoparticles, while the surface is enriched in silver. This silver-enriched surface layer is thicker and more prominent for 25% Au alloy nanoparticles than for 50% and 75% Au alloy nanoparticles.

Flexible Surface-enhanced Raman Scattering Strips Using Colloidal Ink of Gold-silver Alloyed Nanoparticles

Surface-enhanced Raman scattering (SERS) has been used for trace detection at the single-molecule level. The low-cost preparation of high-performance test strips has enabled the development of SERS techniques. In this study, oil-dispersible metal or alloy nanoparticles prepared by the Brust-Schiffrin method were used as "inks" in a ballpoint pen to handwrite SERS test strips on polytetrafluoroethylene (PTFE) membranes. Because of the good PTFE lipophilicity, the flexible substrates had good uniformity. The large laser damage threshold of the PTFE membrane also enabled increased laser powers for SERS testing. The Au and Ag alloy nanoparticle inks exhibited increased performance with larger proportions of Ag. The Au1Ag8 nanoparticles had the best properties, and those strips could detect 10-11-M Rhodamine 6G dyes in a 10-µL volume with an enhancement factor of 5.4×108. The SERS strips were used to demonstrate detection of malachite green, the use of which is prohibited in aquaculture and fish tanks.