Low Ag Content Research Articles

Impact of Silver Incorporation and Flash-Lamp-Annealing on the Photocatalytic Response of Sputtered ZnO Films.

Thin films of silver-doped zinc oxide (SZO) were deposited at room temperature using a DC reactive magnetron co-sputtering technique using two independent Zn and Ag targets. The crystallographic structure, chemical composition and surface morphology of SZO films with different silver concentrations were correlated with the photocatalytic (PC) properties. The crystallization of the SZO films was made using millisecond range flash-lamp-annealing (FLA) treatments. FLA induces significant structural ordering of the wurtzite structure and an in-depth redistribution of silver, resulting in the formation of silver agglomerates. The wurtzite ZnO structure is observed for silver contents below 10 at.% where Ag is partially incorporated into the oxide matrix, inducing a decrease in the optical band-gap. Regardless of the silver content, all the as-grown SZO films do not exhibit any significant PC activity. The best PC response is achieved for samples with a relatively low Ag content (2-5 at.%) after FLA treatment. The enhanced PC activity of SZO upon FLA can be attributed to structural ordering and the effective band-gap narrowing through the combination of silver doping and the plasmonic effect caused by the formation of Ag clusters.

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.

Novel Ag@NH2-UiO-66(Zr) photocatalyst with controllable charge transfer pathways for efficient Cr(VI) remediation

Rational fabrication of core-shell photocatalysts to hamper the charge recombination is extraordinarily essential to enhance photocatalytic activity. In this work, core-shell Ag@NH2-UiO-66 (Ag@NU) Schottky heterojunctions with low Ag content (1 wt%) were constructed by a two-step solvothermal method and adopted for Cr(VI) reduction under LED light. Typically, the one with the Ag: NH2-UiO-66 mass ratio (1 : 100) led to 100% Cr(VI) removal within 1 h, superior to bare NH2-UiO-66 and Ag/NH2-UiO-66 (Ag was directly decorated on NH2-UiO-66 surface). The enhanced photocatalytic activity was related to the migration of the electrons on the CB of NH2-UiO-66 to Ag NPs through a Schottky barrier, and thus the undesired charge carriers recombination was avoided. This result was also evidenced by Density functional theory (DFT) calculations. The computational simulations indicate that the introduction of Ag effectively narrowed the band gap of NH2-UiO-66, facilitating the transfer of photo-generated electrons, expanding the light absorption area, and significantly enhancing photocatalytic efficiency. Most importantly, such a core-shell structure can inhibit the formation of •O2−, letting the direct Cr(VI) reduction by photo-excited e−. In addition, this structure can also protect Ag from being oxidized by O2. Ten cyclic tests evidenced the Ag@NU had excellent chemical and structural stability. This research offers a novel strategy for regulating the Cr(VI) reduction by establishing core-shell photocatalytic materials.

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.

Cobalt-silver catalyst with low metal content for highly efficient synthesis of methyl glycolate through synergistic effect

The Co-Agx/TiO2 catalysts with low mass content of Co and Ag were synthesized through the impregnation method and investigated for dimethyl oxalate (DMO) hydrogenation to methyl glycolate (MG). Remarkably, the Co-Ag0.7/TiO2 catalyst with an Ag concentration of 0.7 wt%, exhibited an impressive yield of MG of ∼94.4 %, surpassing the yields of MG obtained with Co/TiO2 (∼54 %) and Ag0.7/TiO2 (∼69 %) catalysts. Various characterizations elucidated that the exceptional catalytic performance of Co-Ag0.7/TiO2 can be ascribed to the synergy between Co and Ag, resulting in the formation of AgCoO2 as high active site can improve the adsorption and activation of DMO and H2 on catalyst surface. Additionally, the doping of a small amount of Ag regulated the contents of Lewis acidic and Brønsted acidic sites, leading to a high conversion of DMO and selectivity of MG. Furthermore, the excellent MG yield and long-term stability (at least 200 h) facilely obtained over our catalyst under mild reaction conditions guarantee a feasible prospect in the industrial application. This study not only unraveled the superior performance of the Co-Ag synergistic catalyst, but also carried significant implications for developing catalysts with low-content in DMO hydrogenation to MG.

Influence of bismuth addition on the physical and mechanical properties of low silver/lead-free Sn-Ag-Cu solder

The Sn–Ag–Cu (SAC) solders with low Ag content have been identified as promising candidates to replace the traditional Sn–Pb solder for flip-chip interconnects. This study examines the impact of incorporating Bi element on the microstructure, thermal behavior, and mechanical performance of low-silver-content Sn-1.5Ag-0.7Cu (SAC157) solder alloy. Besides using the conventional cross-sectioned microstructure image, X-ray diffraction (XRD), differential scanning calorimetry (DSC) and tensile stress- strain techniques were used to investigate the microstructure, thermal and mechanical properties after the addition of Bi, respectively. The results demonstrate that adding of Bi could refine the microstructure, optimize the thermal properties, and improve the tensile strength. Meanwhile, the ductility of the solder alloys reduced evidently in comparison to the Sn-1.5Ag-0.7Cu solder. From the microstructural analysis, 0.5 wt % Bi addition to SAC157 significantly enhanced the solid solution effect of Bi and refined β-Sn dendrite, as well as extended the eutectic area. Moreover, as the Bi addition increases to 5 wt %, finely dispersed bismuth precipitates within the β-Sn matrix, along with an enlarged eutectic area, lead to a remarkable enhancement in both ultimate tensile strength and yield strength. The electrical resistivity was characterized by the four-point probe technique. The results show that the electrical resistivity of Bi-modified SAC157 solder alloy decrease from 13.9 to 9.8 μΩ cm with the addition of 5 wt % Bi. These improvements can be attributed to the solid-solution and precipitation strengthening effects induced by the presence of bismuth. The results confirmed that the developed material is applicable as a potential high strength solder material in the context of advanced interconnecting applications.

Suppression of Ag dewetting in submicron Cu@Ag particles in paste for improving sinter bondability through surface modification

Operating temperature of a wide-bandgap semiconductor-based power device can reach 300 °C, which requires a next-generation die-attach sinter material. Ag-coated Cu (Cu@Ag) particles have been considered as a low-cost filler material in pastes for sinter bonding, replacing pure Ag particles. However, there are two main problems: out-diffusion of core Cu and Ag dewetting. Although the Ag shell is sufficiently thick, Ag dewetting induces accelerated out-diffusion of the core Cu and the resultant Cu oxidation through the formation of thin Ag coating parts. Accordingly, a surface-modification method using stearic acid was developed to suppress Ag dewetting and improve the sinterability of Cu@Ag particles. Sinter-bonding characteristics were examined using pastes containing surface-modified submicron Cu@Ag particles. Sinter bonding was conducted at 250 °C under 10 MPa for 1–10 min with N2 blowing using eight types of initial and surface-modified submicron Cu@Ag particles with Ag contents of 10, 20, 30, and 40 wt% (A10, A20, A30, and A40). The shear strength of the bondline containing surface-modified A10 exhibited 17.56 MPa when bonded for 3 min, compared with 11.67 MPa of the initial A10. After a bonding time of 10 min, the shear strength increased to 20.41 MPa. Surface-modified A10 (low Ag content), with the highest efficiency in Ag dewetting suppression, exhibited sinter-bonding characteristics similar to those of Cu@Ag particles with higher Ag contents without surface treatment. Surface-modified A20 provided a sufficient strength of 20.83 MPa after 3 min of bonding.

High-precision measurement of Ag isotopes for silicate rocks by MC-ICP-MS

A new protocol for the high-precision measurement of Ag isotopes for samples with low Ag contents by MC-ICP-MS.

Synergistic role of oxygen vacancy defect and plasmonics on modulating the photocatalytic activity of Ag/CuOx nanocomposites synthesized via solution plasma

Herein, an environmentally friendly green approach for the single-step synthesis of Ag/CuOx nanocomposite by generating plasma between two copper electrodes in an AgNO3 solution is reported. Morphological tunability of the CuOx nanoparticles from spindle to flower-like and then to wire-like is achieved by varying the concentration of the AgNO3 solution, which regulates toxic dye adsorption. Compositional analysis reveals the formation of oxygen vacancies, indicating the presence of sub-stoichiometric CuO due to the bombardment of plasma-generated species on the as-formed nanoparticle. The percentage of oxygen vacancies decreases with increasing the concentration of AgNO3 to fabricate the nanocomposites. At low Ag content in the Ag/CuOx nanocomposites, higher photocatalytic efficiency is observed than the bare CuOx nanoparticles, whereas for high Ag content, photocatalytic efficiency quenches. Electrochemical spectroscopy reveals an increase in the charge-transfer resistance with Ag content. A possible photo-degradation mechanism based on the trapping and transfer of photo-generated charge carriers between the defect-enriched CuOx and plasmonic Ag nanoparticles is presented. Charge carrier lifetime is investigated to support the photo-degradation mechanism. The effect of H2O2 on the photo-degradation by considering the band edge potential of CuOx nanoparticles is also discussed.

Efficient self-cleaning and antibacterial ceramics with ultra-low doping and high exposure of silver

The secondary bacterial infection of COVID-19 is known to contribute significantly to mortality rates. Silver (Ag)-based antibacterial ceramics have emerged as a prominent solution for daily antibacterial applications, aiming to minimize the reliance on disinfectants while safeguarding human health. However, the fabrication of Ag-based antibacterial ceramics with low Ag content, high dispersion, and high exposure still faces challenges. In this work, an innovative method was proposed to doping Ag nanoparticles (Ag NPs) into glass ceramics (GC) via a "melt-freeze" method, then efficient and stable Ag-doped antibacterial ceramics (GC-xAg@BiOCl) were fabricated through facile in-situ HCl etching GC. Results indicate that the low Ag content (0.03 mol%) and high dispersion of Ag NPs are fully exposed and anchored on the surface, and constructed Schottky junction Ag/BiOCl contributed to antibacterial and photocatalytic activity. The degradation rates of norfloxacin and methylene blue by GC-0.25Ag@BiOCl can reach 71.0% and 55.3% under visible light irradiation, respectively. Moreover, The GC-0.25Ag@BiOCl exhibited significant antibacterial activity against Escherichia coli (E.coli) and Staphylococcus aureus (S. aureus), with E.coli at 7.3 log10 cfu/mL and S. aureus at 7.0 log10 cfu/mL completely inactivated under visible light irradiation. Additionally, the antibacterial mechanism and charge transfer mechanism were explored.

Numerical evaluation of the mechanical response of Sn-Ag-Cu lead-free solders of various silver contents

PurposeThere are several lead-free solder alloys available in the industry. Over the years, the most favorable solder composition of tin-silver-copper (Sn-Ag-Cu [SAC]) has been vastly used and accepted for joining the electronic components. It is strongly believed that the silver (Ag) content has a significant impact on the solder mechanical behavior and thus solder thermal reliability performance. This paper aims to assess the mechanical response, i.e. creep response, of the SAC solder alloys with various Ag contents.Design/methodology/approachA three-dimensional nonlinear finite element simulation is used to investigate the thermal cyclic behavior of several SAC solder alloys with various silver percentages, including 1%, 2%, 3% and 4%. The mechanical properties of the unleaded interconnects with various Ag amounts are collected from reliable literature resources and used in the analysis accordingly. Furthermore, the solder creep behavior is examined using the two famous creep laws, namely, Garofalo’s and Anand’s models.FindingsThe nonlinear computational analysis results showed that the silver content has a great influence on the solder behavior as well as on thermal fatigue life expectancy. Specifically, solders with relatively high Ag content are expected to have lower plastic deformations and strains and thus better fatigue performance due to their higher strengths and failure resistance characteristics. However, such solders would have contrary fatigue performance in drop and shock environments and the low-Ag content solders are presumed to perform significantly better because of their higher ductility.Originality/valueGenerally, this research recommends the use of SAC solder interconnects of high silver contents, e.g. 3% and 4%, for designing electronic assemblies continuously exposed to thermal loadings and solders with relatively low Ag-content, i.e. 1% and 2%, for electronic packages under impact and shock loadings.

Deciphering H2-induced low-temperature NOx adsorption on Ag/Al2O3: Expanding the operating temperature range of ethanol-SCR system for effective NOx abatement

Despite the advantages of the catalytic reduction of NOx by hydrocarbons, typical Ag/Al2O3 suffers from limited low-temperature activity in response to cold-start periods. In this study, the promotional effect of H2 on NOx adsorption on Ag/Al2O3 was investigated to address the low-temperature NOx emissions. H2 significantly enhanced NOx accumulation on Ag/Al2O3 below 200 °C, with desorption occurring at high temperatures. The H2-temperature-programmed reduction (H2-TPR) results showed the formation of silver oxide on metallic Ag species by H2+O2, serving as the primary site for H2-induced NOx adsorption, while the single-atom Ag species (Ag+) remained nearly unchanged. Ag/Al2O3 with low Ag loading (1–2 wt%) exhibited lower NOx adsorption capacities compared to the case with high Ag loading (4 wt%) owing to the low metallic Ag content. Diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) studies identified diverse surface-adsorbed species related to H2-induced NOx adsorption. Nitrite, bridging nitrate, and bidentate nitrate contributed to low-temperature NOx desorption, whereas monodentate nitrate contributed to high-temperature desorption. Finally, we demonstrated exceptionally-high NOx reduction activity by synergistically combining the NOx trapping ability of Ag/Al2O3 with its deNOx capability through ethanol with H2, covering a wide temperature range of 100–350 °C under transient conditions at a high space velocity of 100,000 h−1.

How Can Biological and Chemical Silver Nanoparticles Positively Impact Physio-Chemical and Chloroplast Ultrastructural Characteristics of Vicia faba Seedlings?

Through interactions with plant cells, silver nanoparticles (AgNPs) with both biological and chemical origins can stimulate physiological and metabolic processes in plants. To ensure their safe application in the food chain, it is necessary to investigate their effects on plant systems. Therefore, the effects of chemical AgNPs (chem-AgNPs) and biologically synthesized AgNPs (bio-AgNPs) at different levels (i.e., 0, 10, and 50 ppm) on physiological and biochemical traits {i.e., root and shoot growth traits, photosynthetic pigments (Chl a, Chl b, carotenoids, and total pigments), soluble sugars, total carbohydrates, starch, H2O2, and antioxidant enzyme activities} of Vicia faba L. seedlings were investigated. AgNPs were biosynthesized from silver nitrate (AgNO3) by a green synthesis approach using Jatropha curcas seed extract. The synthesized AgNPs were characterized by UV-vis spectroscopy, transmission electron microscopy (TEM), zeta potential, Fourier-transform infrared spectra (FT-IR), and X-ray diffraction (XRD). The results showed that bio-AgNPs at 10 ppm resulted in the highest growth, physiological, and biological traits of faba bean seedlings in comparison with those obtained from both AgNO3 and chem-AgNPs treatments. On the other hand, all AgNPs treatments adversely affected the chloroplast ultrastructure, however, fewer negative effects were obtained with the application of 10 ppm bio-AgNPs. In addition, the roots and shoots of seedlings contained the lowest Ag content under different treatments at 10 ppm AgNPs in comparison to the highest level of AgNPs (50 ppm), which indicates that additional studies should be incorporated to ensure safe use of lower concentrations of bio-AgNPs in seed priming. In conclusion, the application of biogenic nanoparticles at 10 ppm can be recommended to enhance plant growth and the productivity of strategic crops.

Occurrence and precipitation mechanism of silver in pyrite from chimney fragments in the Edmond hydrothermal field, Central Indian Ridge

The enrichment of precious elements including Au and Ag in submarine hydrothermal sulfide deposits attracts more and more attention. Previous studies indicate that Au and Ag combine distinctly different ligands under the physico-chemical conditions of submarine hydrothermal systems, therefore, the factors controlling their precipitation may be different. In general, silver mineralization has been much less studied than gold mineralization in submarine hydrothermal sulfide deposits. The Ag mineralization process and precipitation mechanism of submarine hydrothermal sulfide deposits formed at Mid-ocean Ridges are still poorly constrained. In this study, we studied the occurrence and precipitation mechanism of Ag in sulfide deposits of Edmond hydrothermal field, located on the intermediate-spreading Central Indian Ridge (CIR).Three ore-forming stages were identified in chimney fragments collected in the Edmond hydrothermal field. The corresponding minerals are (stage I) anhydrite + barite + colloidal/porous pyrite (Py1) + fine-grained sphalerite; (stage II) marcasite; (stage III) euhedral pyrite (Py2) + coarse-grained sphalerite + chalcopyrite + isocubanite. Py1, characterized by colloidal, porous, and micro-sized anhedral morphology, was usually overgrown by marcasite, which is, in turn, surrounded by euhedral-subhedral Py2, usually coexisting with coarse-grained sphalerite, chalcopyrite, and isocubanite. Compared to marcasite and Py2, only Py1 contains abundant native silver nanoparticles. LA-ICP-MS analyses suggest that Py1 contains higher Pb, Cu, Ag, Mn, Tl, Mo, Au, and lower Co as compared to Py2. In-situ LA-ICP-MS and nanoSIMS analyses indicate that Py1 with higher Ag contents (101–586 ppm) has larger variation in sulfur isotopic compositions (0.8 to 6.6‰) than those of Py2 with lower Ag contents (0.22–15.5 ppm; δ34S values: 2.1 to 4.8‰ for Fe-rich samples and 0 to 2.8‰ for Zn-rich samples).Texture, mineral assemblage, pyrite trace element and sulfur isotopic compositions indicate a progressive decrease on the degree of fluid-seawater mixing as the temperature gradually increases during the growth of the chimneys in Edmond hydrothermal field. Phase diagram analysis indicates that the increase in pH and in particular cooling, due to the mixing of the hot hydrothermal fluid with cold seawater, can significantly decrease the solubility of Ag and be the effective mechanisms of silver precipitation. Our results suggest that mixing of hydrothermal fluid with seawater is the main Ag precipitation mechanism for submarine hydrothermal sulfide deposits formed at Mid-ocean Ridges.

Biotransformation and bioaccessibility of active ingredients from Radix Astragali by Poria cocos during solid-state fermentation and in vitro digestion and antioxidant activity evaluation

Radix Astragali is one of the most famous and frequently used health food supplements and herbal medicines. Among more than 227 components of Radix Astragali, Astragaloside IV (AG IV) is famous functional compound and is commonly used as a quality marker for Radix Astragali. However, the relatively low content of AG IV in Radix Astragali (< 0.04%, w/w) severely limits its application. The purpose of this study is to improve the biotransformation of AG IV and its bioaccessibility during in vitro digestion by Poria cocos solid fermenting Radix Astragali. The optimum fermentation conditions were as follows: Inoculation amount 8 mL; fermentation time 10 d; fermentation humidity 90%. Through fermentation, the content of AG IV was increased from 384.73 to 1986.49 μg/g by 5.16-fold. After in vitro digestion, the contents of genistin, calycosin, formononetin, AG IV, Astragaloside II (AG II) and total flavonoids in fermented Radix Astragali (FRA) of enteric phase II (ENTII) were 34.52 μg/g, 207.32 μg/g, 56.76 μg/g, 2331.46 μg/g, 788.31 μg/g, 3.37 mg/g, which were 2.08-fold, 2.51-fold, 1.05-fold, 8.62-fold, 3.22-fold and 1.50-fold higher than those of control, respectively. The Scanning electron microscopy (SEM) of FRA showed rough surface and porous structure. The DPPH and ABTS radical scavenging rate of FRA were higher than those of control. These results showed that the Poria cocos solid fermentation could increase the content of the AG IV in Radix Astragali and improve the bioaccessibility and antioxidant activity of Radix Astragali, which is providing new ideas for future development and utilization of Radix Astragali.

Effect of Ag modification on TiO2 and melem/g-C3N4 composite on photocatalytic performances

Here, the comparison of two different semiconductor materials is demonstrated, TiO2 and melem/g-C3N4 composites—modified with balls of approximately 5 nm Ag nanoparticles (NPs) as photocatalysts for the degradation of the model dye acid orange 7 (AO7). The melem molecule synthesized here is one of a series of organic compounds consisting of triazine ring compounds with a structure similar to that of melam and melamine. The photodegradation process of AO7 was carried out to examine all powder materials as a potential photocatalyst. Additionally, two different lamps of wavelengths 368 nm (UV light) and 420 nm (VIS light) were applied to compare the photodegradation tests. A new synthesis route for the acquisition of Ag NPs (Ag content 0.5, 1.0 and 2.5 wt%), based on a wet and low temperature method without the use of reducing reagents was proposed. The best photocatalytic performances under UV and VIS light were obtained for both, TiO2 and melem/g-C3N4 materials (new synthesis route) modified with a very low Ag content—0.5 wt%. The photodegradation activities using UV lamp (3 h, 368 nm irradiation) for samples with 0.5 wt% of Ag: TiO2 and melem/g-C3N4, in excess of 95 and 94%, respectively, were achieved. The highest photoactive materials melem/g-C3N4 with 0.5 and 1 wt% Ag revealed 98% of activity under the VIS lamp after 3 h long irradiation. Our work demonstrates a novel, environmentally acceptable, and cost-effective chemical strategy for preparation of photocatalysts suitable for degradation of organic contaminants in wastewater treatment.

Microstructure and morphology of the soldering interface of Sn–2.0Ag–1.5Zn low Ag content lead-free solder ball and different substrates

Eutectic Sn–Ag–Cu lead-free solder has limited applications due to cost and reliability issues. Sn–Ag–Zn solder has the advantages of low melting point, good mechanical properties and reliable welding interface. However, the research system of low silver content Sn–Ag–Zn solder is incomplete. In this paper, Sn–2.0Ag–1.5Zn low silver content alloy solder is soldered to different substrates. The interfacial reaction after soldering and the microstructure and reliability under different aging treatment conditions are studied. Sn–2.0Ag–1.5Zn solder is made into solder balls by direct melting method. The solder balls are placed in a solder strength tester to be heated and welded to the substrate, and then the solder joints are placed in a heating furnace for aging treatment. The results show that the solder is soldered to the bare Cu substrate, and a dense double-layer Intermetallic Compound (IMC) structure of Cu5Zn8 and Ag3Sn is formed at the interface after aging treatment. The double-layer structure blocks each other, limiting the development of copper-tin IMCs. The solder is soldered with the Cu substrate electroplated with Ni barrier layer, and the soldering interface forms a thin layer of Ni3Sn4 metal compound. After aging for 1000 h, the thickness of Ni3Sn4 is about 1 μm, the thickness of Ni barrier layer is kept at 2–3 μm, and the barrier effect of Ni barrier layer is stable. Sn–2.0Ag–1.5Zn solder has excellent loss performance in long aging treatment. It has good heat-resistance aging treatment, good quality of solder connection, high interface reliability and less environmental pollution. The low silver content in Sn–2.0Ag–1.5Zn solder results in a significant cost reduction. Coarse IMC Ag3Sn is not easily formed. The optimized ratio of Ag and Zn in Sn–2.0Ag–1.5Zn solder improves the strength and toughness of the solder joint. The performance has been improved, and it is a very promising alloy solder.

Controlling Threshold and Resistive Switch Functionalities in Ag‐Incorporated Organometallic Halide Perovskites for Memristive Crossbar Array

AbstractHalide perovskites (HPs) can be the effective functional materials for the sneak‐path current issue in the memristive crossbar array. Herein, an efficient strategy is proposed to integrate the HPs‐based bidirectional threshold and bipolar resistive switches (TS and RS). The resistance change characteristics from volatile threshold to nonvolatile resistive switching are modulated by controlling Ag doping concentration in the MAPbI3. HPs provide the diffusive condition and the quantity of Ag regulates the radius of its network. A low amount of Ag contributes to weak network with a short lifetime. However, when the amount of Ag increases, the conductive filament becomes more robust, showing a long lifetime. A MAPbI3:Ag TS with a low Ag content is developed, showing a steep switching slope (1 mV per decade), fast switching speed (&lt; 80 ns), and low off‐current (10 nA). And, a MAPbI3:Ag RS with a high Ag content is developed, showing multilevel storage capability and long retention time (1400 s). Finally, these TS and RS coupled into the 1S‐1R integrated component, resulting the development of the maximum crossbar array size to 1.4 × 1012. This study offers an efficient methodology for tailoring the resistance change characteristics and a promising strategy for practical HPs‐based memristive crossbar application.

Coupled and uncoupled to δ34S behavior of gold and silver in pyrite and marcasite from the low-sulfidation Sarnak gold deposit, SE Bulgaria

In this study, the contents of Au and Ag in five pyrite±marcasite samples from the Sarnak gold deposit, the respective δ34S, and the sample distances to the contact between metamorphic basement and overlying sedimentary cover were considered. We found that two samples from lower horizons (levels of 69 and 30 m below the contact) display relatively low Au and Ag contents, negative values of δ34SV-CDT (–3.14 and –6.42‰) and pronounced oscillatory zoning, resulting from oscillating contents of As. Three samples from higher horizons (levels of 8, 7 and 0 m below the contact) have higher Au and Ag contents, positive or slightly negative values of δ34SV-CDT (+0.5, +1.73 and –1.85‰) and poorly expressed or absent arsenian zoning. Two of them contain microscopic electrum and adularia. Based on these contrasting features we assume different mechanisms of precipitation: intense fluid-rock interaction for samples from lower horizons under steady conditions and boiling of fluid for samples from higher horizons under fluctuating conditions.

High strength CuAg foil with a nano-lamellar structure prepared via pulse electrodeposition in an environmental-friendly methanesulfonic acid-based bath

In this study, high strength CuAg foils with nano-lamellar structures were prepared using a pulse electrodeposition method in an environmental-friendly methanesulfonic acid (MSA)-based solution. In an MSA-based bath, the Ag+ ion acted as the source for solute atoms and as a brightening agent, which allowed the formation of compact and bright CuAg structures in an additive-free bath. The application of pulse plating led to the formation of a nano-lammellar structure, in which Cu-rich and Ag layers were repeatedly stacked. Because of the contribution of the Ag layer, the as-deposited CuAg foil exhibited a high ultimate tensile strength (927 MPa) even at a low Ag content (2.37 wt%). The strength of the CuAg foil was further improved with annealing at 100–250 °C owing to the stabilization of the phase boundary. Despite a high fraction of the phase boundary, the nanostructure was stably maintained even after annealing at 250 °C for 1 h.