Magneto-Seebeck tunneling on the atomic scale.

The tunneling of spin-polarized electrons across a magnetic tunnel junction driven by a temperature gradient is a fundamental process for the thermal control of electron spin transport. We experimentally investigated the atomic-scale details of this magneto-Seebeck tunneling by placing a magnetic probe tip in close proximity to a magnetic sample at cryogenic temperature, with a vacuum as the tunneling barrier. Heating the tip and measuring the thermopower of the junction while scanning across the spin texture of the sample lead to spin-resolved Seebeck coefficients that can be mapped at atomic-scale lateral resolution. We propose a spin detector for spintronics applications that is driven solely by waste heat, using magneto-Seebeck tunneling to convert spin information into a voltage that can be used for further data processing.

Electrochemical stability of elemental metal nanoparticles.

The corrosion behavior of nanometer-scale solids is important in applications ranging from sensing to catalysis. Here we present a general thermodynamic analysis of this for the case of elemental metals and use the analysis to demonstrate the construction of a particle-size-dependent potential-pH diagram for the case of platinum. We discuss the data set required for the construction of such diagrams in general and describe how some parameters are accessible via experiment while others can only be reliably determined from first-principles-based electronic structure calculations. In the case of Pt, our analysis predicts that particles of diameter less than approximately 4 nm dissolve via the direct electrochemical dissolution pathway, Pt --> Pt(2+) + 2e(-), while larger particles form an oxide. As an extension of previously published work by our group, electrochemical scanning tunneling microscopy is used to examine the stability of individual Pt-black particles with diameters ranging from 1 to 10 nm. Our experimental results confirm the thermodynamic predictions, suggesting that our analysis provides a general framework for the assessment of the electrochemical stability of nanoscale elemental metals.

Superhard nanobuttons: constraining crystal plasticity and dealing with extrinsic effects at the nanoscale.

The compressive plastic strength of nanosized single-crystal metallic pillars is known to depend on their diameter D. Herein, the role of pillar height h is analyzed instead, and the suppression of the generalized crystal plasticity below a critical value h(CR) is observed. Novel in situ compression tests on regular pillars as well as nanobuttons, that is, pillars with h < h(CR), show that the latter are much harder, withstanding stresses >2 GPa. A statistical model that holds for both pillars and buttons is formulated. Owing to their superhard nature, the nanobuttons examined here underline with unprecedented resolution the extrinsic effects-often overlooked-that naturally arise during testing when the Saint-Venant assumption ceases to be accurate. The bias related to such effects is identified in the test data and removed when possible. Finally, continuous hardening is observed to occur under increasing stress level, in analogy to reports on nanoparticles. From a metrological standpoint the results expose some difficulties in nanoscale testing related to current methodology and technology. The implications of the analysis of extrinsic effects go beyond nanobuttons and extend to nano-/microelectromechanical system design and nanomechanics in general.

Electrochemical stability of nanometer-scale Pt particles in acidic environments.

Understanding and controlling the electrochemical stability or corrosion behavior of nanometer-scale solids is vitally important in a variety of applications such as nanoscale electronics, sensing, and catalysis. For many applications, the increased surface to volume ratio achieved by particle size reduction leads to lower materials cost and higher efficiency, but there are questions as to whether the intrinsic stability of materials also decreases with particle size. An important example of this relates to the stability of Pt catalysts in, for example, proton exchange fuel cells. In this Article, we use electrochemical scanning tunneling microscopy to, for the first time, directly examine the stability of individual Pt nanoparticles as a function of applied potential. We combine this experimental study with ab initio computations to determine the stability, passivation, and dissolution behavior of Pt as a function of particle size and potential. Both approaches clearly show that smaller Pt particles dissolve well below the bulk dissolution potential and through a different mechanism. Pt dissolution from a nanoparticle occurs by direct electro-oxidation of Pt to soluble Pt(2+) cations, unlike bulk Pt, which dissolves from the oxide. These results have important implications for understanding the stability of Pt and Pt alloy catalysts in fuel cell architectures, and for the stability of nanoparticles in general.

Direct observation of bifunctional electrocatalysis during CO oxidation at Ru(theta=0.37)/Pt{111} surfaces via surface stress measurements.

The surface stress response during the electrooxidation of CO at Pt{111}, Ru{0001}, and Ru(theta=0.37)/Pt{111} textured electrodes was studied in 0.1 M HClO(4) electrolytes. The surface stress signal resolves for the first time the adsorption of OH(-) at the CO-covered Ru{0001} surface prior to significant CO oxidation, a phenomenon that is not discernible in the voltammetry. The surface stress signal shows that significant tensile surface stress occurs upon oxidation of the adsorbed CO and occurs at nearly the same potential on Ru{0001} and Ru/Pt{111} surfaces. These observations demonstrate that the mechanism of bifunctionality is the OH(ads) provided to the Pt surface sites via Ru sites.