Anisotropic etching of rhodium and gold as the onset of nanoparticle formation by cathodic corrosion.

Cathodic corrosion is a phenomenon in which negatively polarized metal electrodes are degraded by cathodic etching and nanoparticle formation. Though these changes are dramatic and sometimes even visible by eye, the exact mechanisms underlying cathodic corrosion are still unclear. This work aims to improve the understanding of cathodic corrosion by studying its onset on rhodium and gold electrodes, which are subjected to various constant cathodic potentials in 10 M NaOH.

Anisotropic etching of platinum electrodes at the onset of cathodic corrosion.

Cathodic corrosion is a process that etches metal electrodes under cathodic polarization. This process is presumed to occur through anionic metallic reaction intermediates, but the exact nature of these intermediates and the onset potential of their formation is unknown. Here we determine the onset potential of cathodic corrosion on platinum electrodes.

Landing and catalytic characterization of individual nanoparticles on electrode surfaces.

We demonstrate a novel and versatile pipet-based approach to study the landing of individual nanoparticles (NPs) on various electrode materials without any need for encapsulation or fabrication of complex substrate electrode structures, providing great flexibility with respect to electrode materials. Because of the small electrode area defined by the pipet dimensions, the background current is low, allowing for the detection of minute current signals with good time resolution. This approach was used to characterize the potential-dependent activity of Au NPs and to measure the catalytic activity of a single NP on a TEM grid, combining electrochemical and physical characterization at the single NP level for the first time.

Cathodic corrosion as a facile and effective method to prepare clean metal alloy nanoparticles.

The cathodic corrosion method described here is a simple, clean, and fast way of synthesizing nanoalloys with high catalytic performance. Using a series of Pt-Rh alloys as an example, we show that this one-step method can convert a bulk alloy electrode into an aqueous suspension of nanoparticles, retaining the composition and crystal lattice structure of the starting alloy. Compared to pure metals, these alloy nanocatalysts are more active toward CO and methanol oxidation and nitrate reduction reactions.