No abstract

Increasing the performance of seawater electrolyser and enabling direct natural seawater feed by asymmetric electrolyte flow scheme.

The combination of fiber Bragg grating inscription with femtosecond laser sources and the usage of the Talbot interferometer setup not only gives access to the fabrication of Bragg gratings in new types of materials but also allows, at the same time, to keep the high flexibility of an interferometric setup in choosing the Bragg grating wavelength. Since the spatial and temporal coherence properties of the femtosecond laser source differ strongly from those of conventional laser sources, specific limits and tolerances in the interferometric setup have to be considered. Such limits are investigated on the basis of an analytical ray tracing model. The results are applied to tolerance measurements of fiber Bragg grating reflections recorded with a DUV sub-picosecond laser source at 262 nm. Additionally we demonstrate the wavelength versatility of the two-beam interferometer setup for femtosecond inscription over a 40 nm wavelength band. Inscription experiments in Al/Yb doped silica glasses are demonstrated as a prove for the access to non-photosensitive fibers.

We experimentally realize a Fabry-Perot-type optical microresonator near the cesium D2 line wavelength based on a tapered optical fiber, equipped with two fiber Bragg gratings that enclose a subwavelength diameter waist. Owing to the very low taper losses, the finesse of the resonator reaches F=86 while the on-resonance transmission is T=11%. The characteristics of our resonator fulfill the requirements of nonlinear optics and cavity quantum electrodynamics in the strong coupling regime. These characteristics, combined with the demonstrated ease of use and advantageous mode geometry, open a realm of applications.

Electrochemical CO2 reduction is a potential approach to convert CO2 into valuable chemicals using electricity as feedstock. Abundant and affordable catalyst materials are needed to upscale this process in a sustainable manner. Nickel‐nitrogen‐doped carbon (Ni‐N‐C) is an efficient catalyst for CO2 reduction to CO, and the single‐site Ni−Nx motif is believed to be the active site. However, critical metrics for its catalytic activity, such as active site density and intrinsic turnover frequency, so far lack systematic discussion. In this work, we prepared a set of covalent organic framework (COF)‐derived Ni‐N‐C catalysts, for which the Ni−Nx content could be adjusted by the pyrolysis temperature. The combination of high‐angle annular dark‐field scanning transmission electron microscopy and extended X‐ray absorption fine structure evidenced the presence of Ni single‐sites, and quantitative X‐ray photoemission addressed the relation between active site density and turnover frequency.