Aligned MoOx /MoS2 Core-Shell Nanotubular Structures with a High Density of Reactive Sites Based on Self-Ordered Anodic Molybdenum Oxide Nanotubes.

The present work demonstrates the self-organized formation of anodic molybdenum oxide nanotube arrays. The amorphous tubes can be crystallized to MoO2 or MoO3 and be converted fully or partially into molybdenum sulfide. Vertically aligned MoOx /MoS2 nanotubes can be formed when, under optimized conditions, defined MoS2 sheets form in a layer by layer arrangement that provide a high density of reactive stacking misalignments (defects). These core-shell nanotube arrays consist of a conductive suboxide core and a functional high defect density MoS2 coating. Such structures are highly promising for applications in electrocatalysis (hydrogen evolution) or ion insertion devices.

Accurate tuning of ordered nanotubular platinum electrodes by galvanic plating.

Platinum nanotubes are created by galvanic deposition inside porous templates. The effects of the electrolyte's ion concentration and pH, of the applied potential and of the deposition duration on the morphology of the tubes are investigated systematically. The system provides a model electrode platform with accurately tunable geometry for the fundamental investigation of electrochemical transformations. For slow electrochemical reactions, we observe a linear increase of the galvanic current with the length of the nanotubes, and therefore with the specific surface area of the electrode. In contrast to this, inherently fast electrochemical transformations are diffusion-limited and give rise to the same current density independently of the geometry. These results delineate a strategy for optimizing the performance of electrochemical energy conversion devices systematically via nanostructuring the electrode surfaces.