Supported nanoparticles containing more than one metal have a variety of applications in sensing, catalysis, and biomedicine. Common synthesis techniques for this type of material often result in large, unalloyed nanoparticles that lack the interactions between the two metals that give the particles their desired characteristics. We demonstrate a relatively simple, effective, generalizable method to produce highly dispersed, well-alloyed bimetallic nanoparticles. Ten permutations of noble and base metals (platinum, palladium, copper, nickel, and cobalt) were synthesized with average particle sizes from 0.9 to 1.4 nanometers, with tight size distributions. High-resolution imaging and x-ray analysis confirmed the homogeneity of alloying in these ultrasmall nanoparticles.
To determine whether the method of "strong electrostatic adsorption" (SEA) can be extended to the preparation of uniform and highly dispersed supported Ag catalysts, the adsorption of silver diammine, Ag(NH 3) 2 + , also known as Tollen's reagent, has been examined over five supports (i.e., SiO 2 , γ-Al 2 O 3 , ZrO 2 , Nb 2 O 5 , and carbon) with different surface areas and PZCs. The speciation of Ag in solution was followed by UV-vis spectroscopy, Ag uptake as a function of the solution pH was determined by atomic absorption, and Ag particle size was determined by powder XRD and STEM. At the Ag concentrations, pH, and surface loadings employed, silver diammine complexes convert into soluble Ag(H 2 O) 2 + aquo complexes below pH 11 and hydrolyze to insoluble Ag 2 O above pH 11. The deposition of either Ag species over carbon at any pH appears to be reactive and results in large particles. The silver aquo complexes appear to adsorb via ion exchangenear the PZC of alumina, zirconia, and niobia but not silica, while the silver diammine complexes appear to adsorb electrostatically at high pH over all the oxides tested-niobia, silica, zirconia, and alumina in the order of ascending PZC. Niobia, which has the lowest PZC, adsorbs the highest surface density of Ag via both mechanisms. The particles obtained via electrostatic adsorption of Ag(NH 3) 2 + at high pH are somewhat smaller than those formed from Ag(H 2 O) 2 + ions at the lower pH values. In the absence of ammonia in solution at high pH, deposition of Ag aquo complexes occurs viasurface precipitation and gives large particles. In sum, SEA of silver ammine is demonstrated to be a simple, reproducible way to synthesize small particles on all supports but carbon.
Introduction: Poor or inconsistent adherence to daily oral pre-exposure prophylaxis (PrEP) has emerged as a key barrier to effective HIV prevention. The advent of potent long-acting (LA) antiretrovirals (ARVs) in conjunction with advances in controlled release technologies has enabled LA ARV drug delivery systems (DDS) capable of providing extended dosing intervals and overcome the challenge of suboptimal drug adherence with daily oral dosing. Areas covered: This review discusses the current state of the LA PrEP field, recent advances, and emerging technologies, including ARV prodrug modifications and new DDS. Technological challenges, knowledge gaps, preclinical testing considerations, and future directions important in the context of clinical translation and implementation of LA HIV PrEP are discussed. Expert opinion: The HIV prevention field is evolving faster than ever and the bar for developing next-generation LA HIV prevention options continues to rise. The requirements for viable LA PrEP products to be implemented in resource-limited settings are challenging, necessitating proactive consideration and product modifications during the design and testing of promising new candidates. If successfully translated, next-generation LA PrEP that are safe, affordable, highly effective, and accepted by both end-users and key stakeholders will offer significant potential to curb the HIV pandemic.
The demands of stricter diesel engine emission regulations have created challenges for current exhaust systems. With advances in low-temperature internal combustion engines and their operations, advances must also be made in vehicle exhaust catalysts. Most current diesel oxidation catalysts use heavy amounts of precious group metals (PGMs) for hydrocarbon (HC), CO, and NO oxidation. These catalysts are expensive and are most often synthesized with poor bimetallic interaction and dispersion. The goal of this work was to study the effect of aging on diesel emission abatement of Pt-Pd bimetallic nanoparticles precisely prepared with different morphologies: well dispersed core-shell versus well dispersed homogeneously alloyed versus poorly dispersed, poorly alloyed particles. Alumina and silica supports were studied. Particle morphology and dispersion were analyzed before and after hydrothermal treatments by XRD, EDX, and STEM. Reactivity as a function of aging was measured in simulated diesel engine exhaust. While carefully controlled bimetallic catalyst nanoparticle structure has a profound influence on initial or low temperature catalytic activity, the differences in behavior disappear with higher temperature aging as thermodynamic equilibrium is achieved. The metallic character of Pt-rich alumina-supported catalysts is such that behavior rather closely follows the Pt-Pd metal phase diagram. Nanoparticles disparately composed as well-dispersed core-shell (via seq-SEA), well-dispersed homogeneously alloyed (via co-SEA), and poorly dispersed, poorly alloyed (via co-DI) end up as well alloyed, large particles of almost the same size and activity. With Pd-rich systems, the oxidation of Pd also figures into the equilibrium, such that Pd-rich oxide phases appear in the high temperature forms along with alloyed metal cores. The small differences in activity after high temperature aging can be attributed to the synthesis methods, sequential SEA and co-DI which give rise, after aging, to a bimetallic surface enriched in Pd.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.