Au Alloy Research Articles

Using polarization sensitive SMLM to infer the interaction strength of dye-plasmonic nanosphere systems

Single-molecule microscopy is an effective tool for the characterization of fluorophore–plasmonic structure interaction. However, sophisticated evaluation is required as specific information is hidden in the emission. Here, we theoretically and experimentally investigated the emission polarization of rotationally mobile fluorophores near plasmonic Au–Ag alloy nanospheres. We developed an elaborate calculation based on the Mie theory, which considers the rotational mobility of dyes near spherical plasmonic nanoparticles of any size. Furthermore, we have created a simplified model that describes the emission’s degree of polarization within 10% accuracy in the case of small nanoparticles, when dipole approximation is valid. Our results indicate the close relation of the polarization degree of the emission, which can reach up to be ∼0.8 in the resonant case, to fluorescence scattering. DNA-PAINT single-molecule localization microscopy experiments conducted using AF488 and Atto647N dyes revealed that the measured polarization degree distribution followed the tendency predicted by calculations.

Detection of Skin, Cervical, and Breast Cancer Using Au–Ag Alloy and WS2-Based Surface Plasmon Resonance Sensor

Detection of Skin, Cervical, and Breast Cancer Using Au–Ag Alloy and WS2-Based Surface Plasmon Resonance Sensor

Biosynthesis of bimetallic Au-Ag nanoparticles using Abrus precatorius seed Extract: Analysis of photocatalytic, cytotoxic, and antibacterial activities

The present investigation aims to examine the bio-route preparation of gold-silver bimetallic nanoparticles using an aqueous seed extract of the Abrus precatorius plant. The bio-synthesized gold-silver bimetallic nanoparticles (AP-Au-Ag NPs) were characterized by various spectroscopic techniques. The surface plasmon resonance (SPR) peak at 555 nm for Au, 433 nm for Ag, and 546 nm for the Au-Ag alloy indicates that bimetallic NPs have been formed. FTIR data provided evidence of functional groups such as OH, CO, and NH2 (proteins, flavonoids, and carbohydrates). When making a bimetallic Au-Ag alloy, carbohydrates are useful as a capping agent and proteins as a reducing agent. The AP-Au-Ag NPs’ stability was assessed by looking at their negative zeta potential value of −21.5 mV. The spherical-shaped crystalline alloy AP-Au-Ag NPs was produced with an average particle size of 10 nm. The TEM images verified the presence of polydispersity in the AP-Au-Ag NPs. The synthesized alloy nanoparticles have a potential cytotoxic effect against MCF-7 cancer cell lines with an IC50 value of 25 ± 1.5 μg/mL and the AP-Au-Ag NPs were found to be a good antibacterial agent against gram-positive and gram-negative bacteria. During visible light photocatalysis, ciprofloxacin was not removed after 60 min of exposure when employing materials made of a pure monometallic nanoparticle. However, the use of bi-metallic nanoparticles made of gold and silver resulted in the breakdown of over 90% of the ciprofloxacin into minerals. The produced bi-metallic nanoparticles, composed of Au-Ag showed exceptional catalytic efficiency. The gold-silver alloyed nanoparticles showed the most promise and efficiency when compared to others.

Electrocatalytic ammonia synthesis on bimetallic AuPd porous structures

In industry, production of ammonia mainly relies on the intensive Haber-Bosch process, but it consumes high energy with low efficiency and generates a large number of green-house gases. Electrocatalytic nitrogen reduction reaction (ENRR), as an alternative method for fixing N2 under ambient conditions, provides a feasible strategy for sustainable development of N2 cycle storage and utilization of renewable energy. However, traditional nanocatalysts exhibit extremely poor ENRR performance due to low activity of the solid structure and intense hydrogen evolution reactions of single component. Herein, we design and prepare porous gold–palladium nanoalloys (pAuPdNs), which effectively enhance ENRR by the excellent catalytic activity of Au and the significant N2 fixation ability of Pd, as well as the nanoporous structure and synergistic effect between alloy components. The electrochemical results show the NH3 yield of the catalyst is as high as 43.6 μg·h−1·cm−2, and Faradaic efficiency reaches 43.8%, which are superior to the performances of most reported water-based ENRR electrocatalysts. Besides, the selectivity of 95% and stability also exhibit enhancement than numerous reported researches. As compared with solid alloy and porous Au or Pd structures, the superiority of pAuPdNs states the influence of alloying and porous structure. Hence pAuPdNs are proved to be the efficient, stable, and promising electrocatalysts for N2 reduction reaction at ambient temperature and atmospheric pressure.

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.

Facile fabrication of Au-Ag alloy nanoparticles/Ag nanowires SERS substrates with bimetallic synergistic effect for ultra-sensitive detection of crystal violet and alkali blue 6B

The bimetallic nanostructure of Au and Ag can integrate two distinct properties into a novel substrate compared to single metal nanostructures. This work presents a rapid and sensitive surface-enhanced Raman scattering (SERS) substrate for detecting illegal food additives and dyes of crystal violet (CV) and alkali blue 6B (AB 6B). Au-Ag alloy nanoparticles/Ag nanowires (Au-Ag ANPs/Ag NWs) were prepared by solid-state ionics method and vacuum thermal evaporation method at 5μA direct current electric field (DCEF), the molar ratio of Au to Ag was 1:18.34. Many 40 nm-140 nm nanoparticles regularly existed on the surface of Ag NWs with the diameters from 80 nm to 150 nm. The fractal dimension of Au-Ag ANPs/Ag NWs is 1.69 due to macroscopic dendritic structures. Compared with single Ag NWs, the prepared Au-Ag ANPs/Ag NWs substrates show superior SERS performance because of higher surface roughness, the SERS active of Ag NWs and bimetallic synergistic effect caused by Au-Ag ANPs, so the limit of detections (LOD) of Au-Ag ANPs/Ag NWs SERS substrates toward detection of CV and AB 6B were as low as 10-16mol/L and 10-9mol/L, respectively. These results indicate that Au-Ag ANPs/Ag NWs substrates can be used for rapid and sensitive detection of CV and AB 6B and have great development potential for detection of illegal food additives and hazardous substances in the fields of environmental monitoring and food safety.

A Direct Dry Synthesis Route for High Purity Catalytic Nanoporous Metallic Films

Control of catalyst morphology is important because it affects many catalytic related properties such as, active sites, surface energy, and surface area, which can lead to tunable catalytic activity. Nanoporous metallic networks (NPMs), a morphology of interest for catalysis, contain many uncoordinated atoms at the surface and highly curved ligaments that can have a large effect on catalytic performance. Nanoporous self-supported metal structures have been synthesized in the past by dealloying of a master alloy,[1] which is a wet chemical method. This technique uses an Au-Ag alloy, from which Ag is etched away and which always results in NPMs containing residual amounts of the sacrificial metal (Ag) preventing the formation of high-purity structures. It follows that the catalytic properties of pure NPMs formed by dealloying can not be studied due to metal 'impurities' remaining in the structure. Although these 'impurities' contribute to catalytic activity and stability, it is difficult to control their amount and the systematic investigation of the 'impurity' effect is almost impossible for these NPMs.Here, we present results obtained by using physical vapor deposition, in the form of glancing angle deposition (GLAD), together with plasma etching to form nanoporous ultra-thin metal mesh structures, in a unique and facile dry synthesis method,[2] unlike most wet chemical synthesis methods used to prepare catalysts, which result chemical waste. The nanostructured metal mesh films are suitable for catalysis as they are extremely pure and highly porous, and contain high curvature ligaments, different crystal motifs, and many grain boundaries. We present nanoporous gold films (NPGF) prepared by our method as an example material. We show that the electrochemical structural stability of the NPGF is remarkably higher than that of dealloyed nanoporous gold, which is a result of the high amount of grain boundaries. Furthermore, the electrocatalytic performance of CH3OH oxidation is measured and the results show high catalytic activity for pure NPGF.[3] Our GLAD method can be applied to various metals and enables precise mixing or doping of different materials composing the NPMs. The high porosity, active sites, and potential elemental mixing will lead to new catalysts, especially suitable for CO2 reduction to fuels and value-added chemicals.[1] G. Wittstock, M. Bäumer, W. Dononelli, T. Klüner, L. Lührs, C. Mahr, L. V. Moskaleva, M. Oezaslan, T. Risse, A. Rosenauer, A. Staubitz, J. Weissmüller, A. Wittstock, Chem. Rev. 2023, 123, 6716.[2] H. Kwon, H.-N. Barad, A. R. Silva Olaya, M. Alarcón-Correa, K. Hahn, G. Richter, G. Wittstock, P. Fischer, ACS Appl. Mater. Interfaces 2023, 15, 5620.[3] H. Kwon, H.-N. Barad, A. R. Silva Olaya, M. Alarcón-Correa, K. Hahn, G. Richter, G. Wittstock, P. Fischer, ACS Catal. 2023, 11656.

( General Student Poster Award Winner, 2nd Place) Template-Assisted Fabrication of Transparent SERS Sensor with Uniform Au-Ag Nanoparticle Electrodeposition

Surface-enhanced Raman spectroscopy (SERS) is a very powerful tool for analyzing molecular interactions and provides unique spectral fingerprint information about chemical bondings.[1] SERS enhances weak Raman scattering signals through surface-localized plasmon resonance (LSPR) of the plasmonic metal nanoparticles. Arbitrarily distribution of plasmonic metal nanoparticles can result in a non-uniform SERS enhancement effect (EF) and low reproducibility, which hinders the practical application of this ultra-sensitive analysis technology.[2] The development of a cost-effective, highly reliable, and highly reproducible SERS sensor with precisely controlled nanoparticle size and distribution is still a challenge.[3] Electron beam lithography (EBL) is commonly used to achieve well-controlled nanoscale patterns, which can be used as a top-down SERS sensor fabrication technique.[2] However, the time-consuming and extremely costly method makes the SERS sensor not easily accessible.In this research, we propose a template-assisted fabrication process by electrodepositing nanoparticles into nanoarrays on a transparent ITO surface. This method precisely controls the surface morphology and provides high reproducibility without relying on EBL techniques. For the fabrication process, first, a layer of sol-gel SiO2 solution was spin-coated onto the ITO surface, and an array of nano-pillars was used to imprint the nanopattern to the sol-gel solution layer, to realize the nano-ordered uniformly distributed nanoarrays. (Fig.1) For the plasmonic material, Au-Ag alloy was deposited into the nanoarray due to its high durability and high SERS EF.[4] The use of a pulse current deposition, additives, and self-assembled monolayer (SAM) was also discussed from the perspective of altering the surface property of the ITO surface, to achieve dense and smooth filling of deposits in the nanoarray. The SERS sensor fabricated was tested with Janus Green B (JGB) and demonstrated a good SERS EF and good signal uniformity. We believe this sensor is widely applicable for different systems, further optimization and application of this sensor can bring us one step closer to the quantitative analysis by SERS. The fabricated sensor should be especially useful in electrochemical reaction analysis and biomolecular sensing.[1] Fleishmann et al., Phys. Lett., 26, 163(1974)[2] Lee et al., Chemical Society reviews., 48, 731(2019)[3] Shi et al., 66, 6525(2018)[4] B. Liu et al., 55 , 117104(2016) Figure 1

Monitoring the Dynamics of the Galvanic Replacement Reaction to Develop Free-Standing Electrocatalysts

Hydrogen (H2) is well-known for its potential to become the future fuel and bring a more sustainable energy system [1]. The selective electrooxidation of organic compounds from biomass appears to be a possible substitute for the kinetically slow oxygen evolution reaction (OER) at the anode, which increases the electrical energy input for a conventional water electrolysis in alkaline media [2]. However, this approach is currently impeded by limited fundamental knowledge of the different active sites of electrocatalysts. The latter can be used to control selectivity at low potential and high current density to co-generate value-added products at the anode instead of CO2 by complete oxidation. Nanostructured gold-based multi-metal electrocatalysts can meet such objectives. Particularly in the electro-valorization of cellulosic biomass at electrode potentials unfavorable to C-C bond breaking and high overall cell voltage.To develop such electrocatalysts, we have initiated a multivariate methodology to study the dynamics of galvanic replacement between silver and gold. This procedure allows us to control nanoporosity and nanoalloying in the resulting gas diffusion electrode (GDE): GDE-Ag1-xAux. GDE-Ag represents the electrode upon which Ag particles were electrochemically grown prior to reaction with Au(III). Thermodynamically, silver with E°(Ag+/Ag) = 0.8 V vs SHE (standard hydrogen electrode) can be replaced by gold with E°(AuCl4 –/Au) = 1.0 V vs SHE according to: 3Ag + xKAuCl4(aq) → 3xAgCl + xKCl + Ag3-3xAux.[2,3] From a kinetic point of view, the challenge is to capture in real time the formation of metal cages of Ag-Au alloys after a '3by1' atomic exchange that introduces nanoporosity and electronic strain as silver and gold have a similar atomic radius. To interrogate the driving force behind this redox process, we have also established an electrochemical methodology to extract quantitative data, allowing detailed capture of the mixed electrochemical and mass transport (diffusion) kinetics. As the precipitation product AgCl leads to pore fouling, we have developed an efficient methodology to trigger its instant dissolution as soon as it is formed, thus promoting the production of a high-quality alloy. As shown in Figure 1, upon injection of a KAuCl4 solution into a degassed solution in contact with the GDE-Ag electrode, the open circuit potential (OCP) begins to change. This evolution is due to the modification of the electrochemical interface as silver atoms are progressively replaced by gold atoms. Thereby, leading to a regulated potential defined either by the Ag(I)/Ag redox couple, or by the Au(III)/Au pair. Interestingly, we found that the OCP variation logically depends on initial conditions such as Ag loading on the GDE, KAuCl4 concentration, Ag particle size, etc. This fundamental knowledge has led to the synthesis of efficient electrocatalysts for the oxidation of cellulose subunits in alkaline media with an onset electrode potential much lower than OER (E < 1 V vs RHE (reversible hydrogen electrode)). Indeed, the formation of an alloy phase, the creation of nanoporosity within it and the free-standing nature amplify, through synergistic and electronic effects, the electrocatalytic efficiency. Acknowledgments This work was funded by French National Research Agency (ANR-22-CE43-0004).

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.

Molecule Doping of Atomically Dispersed Cu–Au Alloy for Enhancing Electroreduction of CO to C2+ Products

Molecule Doping of Atomically Dispersed Cu–Au Alloy for Enhancing Electroreduction of CO to C₂₊ Products

State of the art on plasma-liquid route synthesis monometallic Au, bimetallic Au/Ag core–shell and alloy nanoparticles: Toxicological, сanalytical, antimicrobial activity for environmental control

Nanoparticles (Au monometallic, bimetallic structures Au-Ag alloy and Aucore – Agshell) were synthesized in aqueous solutions with traditional capping agent - sodium citrate, using a one-step (for monometalic and alloy structure) and two–step (for Aucore – Agshell NPs) liquid-phase anode type plasma process. The effects of parameters of synthesis: precursors concentration, the solution plasma process discharge time, molar contents Ag+/Au3+ for alloy NPs, and molar content of Ag+ for Au core NP to the characteristics of the synthesized NPs, including average size (the size distribution, polydispersity index), optical absorption properties ect.) were investigated. The synthesized nanoparticles have the following characteristics: Au NPs with λ=530–540 nm and d = 5–60 nm, the monometalic structure; Ag/Au with the λ=410–530 nm and d = 28–80 nm, bimatalic strucrure of alloy; NPs with significant blue-shift the λ=530→410 nm, depending the shell thickness (the thickness of the deposited Ag shells varied from ∼1–15 nm) and d = 21–35 nm for NPs core(Au)–shell(Ag). TEM images clearly confirm the effectiveness of a one- and two-step plasma-liquid treatment for the synthesis of monometallic Au NPs and the two different structures of the NPs (bimetallic structures Au-Ag alloy and Aucore@– Agshell). The effect of nanoparticle structure on antimicrobial and catalytic properties relative to their respective monometallic counterparts was demonstrated. Among the different investigated structure NPs only for bimetallic core−shell structured AucoreAgshell NPs was found strong synergistic effect for antimicrobial and catalytical activity.

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.

Widening the Gamut of Structural Colors of Gold via Insulator–Metal Bilayer Coatings

Tuning the color of Au has been a longstanding problem in the luxury industry. Conventional approaches, involving Au alloying, compromise purity and demand distinct alloy compositions for each hue. This study demonstrates a lithography‐free method for generating structural colors on a gold surface by adjusting the thickness of titanium dioxide, a high‐index dielectric. While color tuneability is limited if TiO2 is coated directly on the Au surface, a range of vivid colors can be generated if a 50−100 nm thick AuAl2 underlayer is used. AuAl2, an accepted alloy for purple gold, broadens the color gamut, providing a protective coating without diminishing gold purity. The reflectance dip of the bilayer structure exhibits a significant red shift with increasing thickness of the TiO2 layer, allowing diverse colors by TiO2 insulator tuning. Simulation studies corroborate experimental results, affirming that coating a TiO2 layer on the AuAl2 underlayer yields a wide range of colors. This method, based on thin‐film interference, shows promise for widespread use, offering a broad spectrum of structural colors in an industry striving for diverse Au color representation.

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.

Achieving high fatigue endurance of nanocrystalline Ni/Ni-W layered composites through thermally and mechanically-induced relaxations

Stabilizing non-equilibrium nanograin boundaries has been shown to enhance the strength of nanocrystalline metals. Nevertheless, a thorough comprehension of how these stable grain boundaries impact the fatigue behavior in nanocrystalline metallic layered composites with heterogeneous interfaces is currently lacking. Here, aiming to develop high-performance small components in microelectromechanical systems, we prepared nanocrystalline Ni/Ni-W layered composites that underwent various degrees of annealing treatment. Our results reveal that the Ni/Ni-W layered composites annealed at 200 °C exhibit significantly higher fatigue strength, surpassing that of the as-prepared composites by 40 % and the Pt-10 at.% Au alloy by 17 % which is one of the best candidates for the microelectromechanical systems switches at present. The enhanced fatigue strength is primarily attributed to the annealing-induced grain boundary relaxation and mechanically-induced structural relaxation. Grain boundary relaxation enhances the strength by improving GB stability, while the mechanically-induced structural relaxation results in the coarsening and expansion of triangular columnar grains towards the Ni-W layer during fatigue loading. As a result, the dispersive strain localized regions triggered by the triangular columnar grains undertook cyclic strain accumulation and weakened localized damage accumulation in Ni layers, and thus further improved the fatigue resistance. The finding of the underlying mechanisms may offer a promising approach for designing high-performance materials for microelectromechanical systems switches operating at elevated temperatures.

Influence of the barrier layer on the electrical properties of the V/Al-based Ohmic contact on n-type high-Al-fraction AlGaN

Influence of the barrier layer on the electrical properties of V/Al-based Ohmic contact is investigated by comparing the surface morphology and alloying results of V/Al/Ni/Au (with barrier Ni) and V/Al/Cr/Au (with barrier Cr) contacts on n-AlGaN (Al molar fraction&amp;gt;60%) after 850 °C annealing. Due to the clustering of Ni during annealing, a thin Al layer (AlOx) and a number of Al-Au alloy clusters are formed at the contact interface of n-AlGaN, which increases the contact resistance of the V/Al/Ni/Au Ohmic contacts. In contrast, the annealed V/Al/Cr/Au electrodes cover the surface uniformly, which not only contributes to the increased contact area, but also suppresses the formation of high resistance products. Thanks to the Cr barrier layer, the specific contact resistivity of V/Al-based Ohmic contact is reduced by 26%.