Nanoporous gold (np-Au) represents a novel nanostructured bulk material with very interesting perspectives in heterogeneous catalysis. Its monolithic porous structure and the absence of a support or other stabilizing agents opens up unprecedented possibilities to tune structure and surface chemistry in order to adapt the material to specific catalytic applications. We investigated three of these tuning options in more detail: change of the porosity by annealing, increase of activity by the deposition of oxides and change of activity and selectivity by bimetallic effects. As an example for the latter case, the effect of Ag impurities will be discussed. The presence and concentration of Ag can be correlated to the availability of active oxygen. While for the oxidation of CO the activity of the catalyst can be significantly enhanced when increasing the content of Ag, we show for the oxidation of methanol that the selectivity is shifted from partial to total oxidation. In a second set of experiments, two different metal-oxides were deposited on np-Au, praseodymia and titania. In both cases, the surface chemistry changed significantly. The activity of the catalyst for oxidation of CO was increased by up to one order of magnitude after modification. Finally, we used adsorbate controlled coarsening to tune the structure of np-Au. In this way, even gradients in the pore- and ligament size could be induced, taking advantage of mass transport phenomena.

Dimension changes on the order of 0.1% or above in response to an applied voltage have been reported for many types of materials, including ceramics, polymers, and carbon nanostructures, but not, so far, for metals. We show that reversible strain amplitudes comparable to those of commercial piezoceramics can be induced in metals by introducing a continuous network of nanometer-sized pores with a high surface area and by controlling the surface electronic charge density through an applied potential relative to an electrolyte impregnating the pores.

Nanostructured materials are governed by their surface chemical properties. This is strikingly reflected by np-Au. This material can be generated by corrosion of bulk Ag-Au alloys. Based on a self-organisation process, a 3 dimensional sponge like gold structure evolves with ligaments in the range of only a few tens of nanometers. Due to its continuous porosity, the material can be penetrated by gases which then adsorb and interact with the surface. In this perspective we will review potential applications of np-Au resulting from this effect, namely heterogeneous gas phase catalysis, surface chemistry driven actuation, and adsorbate controlled stability of the nanostructure. We will summarize the current knowledge about the low temperature oxidation of CO as well as the highly selective oxidation of methanol. Furthermore, we will address the question how surface chemistry can influence the material properties itself. In particular, we will deal with (a) the actuation of np-Au by the reversible oxidation of its surface using ozone and (b) the adsorbate controlled coarsening of ligaments, using annealing experiments under ozone or inert gas atmosphere.

Nanoporous metals prepared by the corrosion of an alloy can take the form of monolithic, millimeter-sized bodies containing approximately 1015nanoscale ligaments per cubic millimeter. The ligament size can reach down to the very limits of stability of nanoscale objects. The processes by which nanoporous metals are formed have continued to be fascinating, even though their study in relation to surface treatment, metal refinement, and failure mechanisms can be traced back to ancient times. In fact, the prospect of using alloy corrosion as a means of making nanomaterials for fundamental studies and functional applications has led to a revived interest in the process. The quite distinct mechanical properties of nanoporous metals are one of the focus points of this interest, as relevant studies probe the deformation behavior of crystals at the lower end of the size scale. Furthermore, the coupling of bulk stress and strain to the forces acting along the surface of nanoporous metals provide unique opportunities for controlling the mechanical behavior through external variables such as the electrical or chemical potentials.

Rayleigh instability of copper nanowires has been experimentally demonstrated. After annealing 30–50-nm-diam wires at temperatures between 400 and 600°C, different stages of the fragmentation process are observed by scanning electron microscopy. At 400°C, the wires start to fragment, forming shorter sections at 500°C, and finally decaying into a chain of nanospheres at 600°C. Average diameter and spacing of the spheres are in agreement with theoretical predictions. The Rayleigh instability applied to nanowires provides a structuring technique producing long chains of nanospheres, which should find interesting applications, for instance, by guiding light below the diffraction limit via coherent coupling of surface-plasmon polaritons.

Nanoporous gold (NPG) is usually made by electrochemical dealloying of Ag from binary AgAu alloys. The resulting nanoscale ligaments are not very stable, and tend to coarsen with time by surface self-diffusion, especially in electrolyte, which may lead to inferior electrocatalytic properties. Addition of a small amount of Pt to the precursor alloy is known to refine and stabilize the nanoporous product (NPG-Pt). However, the mechanisms by which Pt serves to refine the microstructure remain poorly understood. The present study aims to expand our knowledge of the role of Pt by examining NPG-Pt at atomic resolution with Atom Probe Tomography (APT), as well as by aberration-corrected Transmission Electron Microscopy. Atomic level observation of Pt enrichment on ligament surfaces sheds light on the underlying mechanisms that give rise to Pt's refining effect. Owing to improved Ag retention with higher Pt content, NPG-Pt (made by dealloying AgAuPt) was shown to have the highest surface area-to-volume ratio, compared to NPG-Pt (made by dealloying AgAuPt). Quantitative estimates reveal up to 5-fold enrichment of Pt at nanoligament surfaces, compared to the precursor content, in NPG-Pt. The interface between the dealloyed layer and the substrate was captured by APT, for the first time. The findings of this investigation add insight into the functionality of NPG-Pt and its prospective catalytic performance.

Low-coordination sites, including edges, kinks, and defects, play an important role in oxygen-reduction electrocatalysis. Their role was studied experimentally and theoretically for various Pt surfaces. However, the roughness effect on similar-sized nanoparticles that could elucidate the role of low-coordination sites has attracted much less attention, with no studies on Pd nanoparticles. Here, using Br- adsorption/desorption, we introduce an effective approach to reduce surface roughness, yielding Pd nanoparticles with smoother surfaces and an increased number of (111)-oriented facets. The resulting nanoparticles have a slightly contracted structure and narrow size distribution. Pt monolayer catalysts that contain such nanoparticles as the cores showed a 1.5-fold enhancement in specific and Pt mass activities for the oxygen reduction reaction compared with untreated ones. Furthermore, a dramatic increase in durability was observed with bromide-treated Pd(3)Co cores. These results demonstrate a simple approach to preparing nanoparticles with smooth surfaces and confirm the adverse effect of low-coordination sites on the kinetics of the oxygen-reduction reaction.© 2011 American Chemical Society

Over the past decade, on-surface fabrication of organic nanostructures has been widely investigated for the development of molecular electronic components, catalysts, and new materials. Here, we introduce a new strategy to obtain alkyl oligomers in a controlled manner using on-surface radical oligomerisations that are triggered by electrons between the tip of a scanning tunnelling microscope and the Si(111)√3 ×√3 R30°-B surface. This electron transfer event only occurs when the bias voltage is below -4.5 V and allows access to reactive radical species under exceptionally mild conditions. This transfer can effectively 'switch on' a sequence leading to the formation of oligomers of defined size distribution thanks to the on-surface confinement of the reactive species. Our approach enables new ways to initiate and control radical oligomerisations with tunnelling electrons, leading to molecularly precise nanofabrication.

The microstructure of boron (B) and phosphorus (P) codoped silicon (Si) nanocrystals (NCs), cubic boron phosphide (BP) NCs and their mixed NCs (BxSiyPz NCs) has been studied using atom probe tomography (APT), transmission electron microscopy (TEM), and Raman scattering spectroscopy. The BxSiyPz NCs inherit superior properties of B and P codoped Si NCs such as high dispersibility in aqueous media and near infrared (NIR) luminescence and those of cubic BP NCs such as high chemical stability. The microanalyses revealed that BxSiyPz NCs are composed of a crystalline core and an amorphous shell. The core possesses a lattice constant between that of Si (diamond-cubic) and BP (cubic). The amorphous shell is comprised of B, Si and P, though the composition is not uniform and there are local B-rich, Si-rich and P-rich domains connected contiguously. The amorphous shell is proposed to be responsible for their superior chemical properties such as high dispersibility in polar solvents and high resistance to acids, and the crystalline core is responsible for the stable NIR luminescence.

Lu, N.; Du, K.; Lu, L.; Ye, H. Q. Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China.

Monolayer metal membranes have attracted research attention owing to their fascinating physical properties. Unlike layered materials with weak interlayer van der Waals bonding, metallic monolayer membranes are difficult to exfoliate due to strong metallic bonding between layers. Here, we fabricate free-standing monatomic-thick Au membranes and nanoribbons framed in bulk crystals using dealloying inside transmission electron microscope. The Au membranes are robust under high energy electron beam. Monatomic-thick nanoribbons with a minimal width of 0.6 nm are observed. First-principles calculations reveal that zigzag-edged nanoribbons are ferromagnetic with magnetic moments ranging 0.38-0.51 μB per unit-cell for a width less than 0.9 nm. In addition, a linear relationship between the bond length and the coordination number of atoms is directly investigated using atomic resolution images of monolayer and bilayer Au membranes. This work provides a pathway for direct fabrication of metal membranes and nanoribbons and to achieve novel physical properties.

Colloidal core-shell semiconductor nanocrystals form an important class of optoelectronic materials, in which the exciton wave functions can be tailored by the atomic configuration of the core, the interfacial layers, and the shell. Here, we provide a trustful 3D characterization at the atomic scale of a free-standing PbSe(core)-CdSe(shell) nanocrystal by combining electron microscopy and discrete tomography. Our results yield unique insights for understanding the process of cation exchange, which is widely employed in the synthesis of core-shell nanocrystals. The study that we present is generally applicable to the broad range of colloidal heteronanocrystals that currently emerge as a new class of materials with technological importance.

The surface energy is a fundamental property of the different facets of a crystal that is crucial to the understanding of various phenomena like surface segregation, roughening, catalytic activity, and the crystal’s equilibrium shape. Such surface phenomena are especially important at the nanoscale, where the large surface area to volume ratios lead to properties that are significantly different from the bulk. In this work, we present the largest database of calculated surface energies for elemental crystals to date. This database contains the surface energies of more than 100 polymorphs of about 70 elements, up to a maximum Miller index of two and three for non-cubic and cubic crystals, respectively. Well-known reconstruction schemes are also accounted for. The database is systematically improvable and has been rigorously validated against previous experimental and computational data where available. We will describe the methodology used in constructing the database, and how it can be accessed for further studies and design of materials.