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The synthesis of trimetallic nanoparticles represents an emerging strategy to maximize catalytic performances in noble metal-based catalysts. However, the controllable synthesis of trimetallic nanomaterials as well as the exact role played by the addition of a third metal in their composition over catalytic performances remains unclear. In this paper, we describe the synthesis of trimetallic nanoshells having AgAuPd, AgAuPt, and AgPdPt compositions by a sequential galvanic replacement reaction approach between Ag nanospheres as sacrificial templates and the corresponding metal precursors, i.e., AuCl4 − (aq), PdCl4 2− (aq), and/or PtCl6 2− (aq). In each of these systems, the composition could be systematically tuned by varying the molar ratios between Ag and each metal precursor. Nanoshells having Ag56Au28Pd16, Ag78Au9Pt13, and Ag71Pd16Pt13 compositions were employed as model systems to investigate the effect of the addition of the third metal in their composition over the catalytic activities toward the 4-nitrophenol reduction. Our data demonstrate a significant enhancement in conversion percentages and thus the catalytic activities relative to the sum of their bimetallic counterparts, and this increase was dependent on the nature of the metals, corresponding to 826, 135, and 56 % for Ag56Au28Pd16, Ag78Au9Pt13, and Ag71Pd16Pt13 nanoshells relative to their bimetallic analogs. The results presented herein demonstrate the strong correlation between catalytic activity and composition in multimetallic nanoshells, and that the incorporation of a third metal may represent a promising approach to boost catalytic activities for a variety of transformations.

This study demonstrates that the precursor reduction kinetics can be employed to control the morphology and composition of bimetallic metal/metal oxides systems obtained by galvanic replacement reaction using metal oxides as sacrificial templates. This work investigated Cu2O as a proof-of-concept example, in which the relative rates of Cu2O oxidation by O2 and by noble metal precursors determined the morphology and composition of the products. We focused on three metal precursors with fast, medium, and slow reduction kinetics in the presence of Cu2O under aerobic conditions: PdCl42–, AuCl4–, and Ru3+, respectively. It was found that metal-oxide-based bowls, rattles, or dendrites can be obtained by simply changing the precursor reduction kinetics. These results provide novel insights over the versatility and mechanistic understanding of galvanic replacement to the synthesis of metal/metal-oxide bimetallic nanoparticles.

Nanorattles, comprised of a nanosphere inside a nanoshell, were employed as the next generation of plasmonic catalysts for oxidations promoted by activated O2 . After investigating how the presence of a nanosphere inside a nanoshell affected the electric-field enhancements in the nanorattle relative to a nanoshell and a nanosphere, the SPR-mediated oxidation of p-aminothiophenol (PATP) functionalized at their surface was investigated to benchmark how these different electric-field intensities affected the performances of Au@AgAu nanorattles, AgAu nanoshells and Au nanoparticles having similar sizes. The high performance of the nanorattles enabled the visible-light driven synthesis of azobenzene from aniline under ambient conditions. As the nanorattles allow the formation of electromagnetic hot spots without relying on the uncontrolled aggregation of nanostructures, it enables their application as catalysts in liquid phase under mild conditions using visible light as the main energy input.

In this work, a simple but powerful method for controlling the size and surface morphology of AgAu nanodendrites is presented. Control of the number of Ag nanoparticle seeds is found to provide a fast and effective route by which to manipulate the size and morphology of nanoparticles produced via a combined galvanic replacement and reduction reaction. A lower number of Ag nanoparticle seeds leads to larger nanodendrites with the particles' outer diameter being tunable in the range of 45-148 nm. The size and surface morphology of the nanodendrites was found to directly affect their catalytic activity. Specifically, we report on the activity of these AgAu nanodendrites in catalyzing the gas-phase oxidation of benzene, toluene and o-xylene, which is an important reaction for the removal of these toxic compounds from fuels and for environmental remediation. All produced nanodendrite particles were found to be catalytically active, even at low temperatures and low metal loadings. Surprisingly, the largest nanodendrites provided the greatest percent conversion efficiencies.

Metallic nanomaterials displaying hollow interiors as well as sharp tips/branches at their surface (such as hollow nanodendrites) are attractive, because these features enable higher surface-to-volume ratios than their solid and/or rounded counterparts. This paper describes a simple strategy for the synthesis of Ag-Au nanodendrites in 15 s using Ag nanospheres prepared in a previous synthetic step as seeds. Our approach was based on the utilization of Ag nanospheres as seeds for Au deposition by a combination of galvanic replacement reaction between Ag and AuCl4(-)(aq) and AuCl4(-)(aq) reduction using hydroquinone in the presence of polyvinylpyrrolidone (PVP) as a stabilizer and water as the solvent. The produced Ag-Au nanodendrites presented monodisperse sizes, and their surface morphologies could be tuned as a function of growth time. Owing to their hollow interiors and sharp tips, the Ag-Au nanodendrites performed as effective substrates for surface-enhanced Raman scattering (SERS) detection of 4-MPy (4-mercaptopyridine) and R6G (rhodamine 6G) as probe molecules. We believe that the approach described herein can serve as a protocol for the fast and one-step synthesis of Ag-Au hollow nanondendrites with a wide range of sizes, compositions, and surface morphologies for applications in SERS and catalysis.