The Data Portal "Chromosome Numbers of the Flora of Germany": Progress After Five Years, Recent Developments, and Future Strategies.

Chromosome numbers and information on ploidy level are of great importance for better understanding of plant evolution and taxonomy but also for species identification. Technical developments in flow cytometry dramatically improved the measurement of genome size and triggered a renewed interest in chromosome numbers. Web-based portals make these kind of data accessible for a wide audience in both academia and citizen science.

Dissolution of platinum: limits for the deployment of electrochemical energy conversion?

Platinum stability: Dissolution of Pt, which is one major degradation mechanism in, for example, hydrogen/air fuel cells, was monitored under potentiodynamic and potentiostatic conditions. The highly sensitive and time-resolving dissolution monitoring enables the distinction between anodic and cathodic dissolution processes during potential transient and chronoamperometric experiments, and the precise quantification of the amount of dissolved Pt.

Development and integration of a LabVIEW-based modular architecture for automated execution of electrochemical catalyst testing.

This paper describes a system for performing electrochemical catalyst testing where all hardware components are controlled simultaneously using a single LabVIEW-based software application. The software that we developed can be operated in both manual mode for exploratory investigations and automatic mode for routine measurements, by using predefined execution procedures. The latter enables the execution of high-throughput or combinatorial investigations, which decrease substantially the time and cost for catalyst testing.

Near-surface ion distribution and buffer effects during electrochemical reactions.

The near-surface ion distribution at the solid-liquid interface during the Hydrogen Oxidation Reaction (HOR)/Hydrogen Evolution Reaction (HER) on a rotating platinum disc electrode is demonstrated in this work. The relation between reaction rate, mass transport and the resulting surface pH-value is used to theoretically predict cyclic voltammetry behaviour using only thermodynamic and diffusion data obtained from the literature, which were confirmed by experimental measurements. The effect of buffer addition on the current signal, the surface pH and the ion distribution is quantitatively described by analytical solutions and the fragility of the surface pH during reactions that form or consume H(+) in near-neutral unbuffered solutions or poorly buffered media is highlighted.