Scientific Highlights

A new incrementally extendable thermodynamic model, CASH+, was developed, aimed at accurately describing equilibrium composition, solubility, and elemental uptake of C-A-S-H gel-like phases at varying chemical conditions in cement systems. Cement is widely used as matrix and backfill for low and intermediate level waste. Calcium-Aluminum-Silicate Hydrates (C-A-S-H) are the most important binding phases in cement. They are also responsible for the initial entrapment of radionuclides via sorption or solid solution formation mechanisms. Therefore, the thermodynamic modelling of C-A-S-H stability, solubility and interaction with radionuclides in cement porewater is crucial for understanding hydration, blending, degradation of cement-based materials and for the performance assessment of cementitious repositories.

Water management is crucial to the successful cold-start in polymer electrolyte fuel cells (PEFCs). The sudden freeze of supercooled water blocks the reactant gas in the cathode and causes rapid voltage failure. In this work, we statistically evaluated the effects of the gas diffusion layer (GDL) substrate, size, saturation, and the coating loads and methods of hydrophobic polymer on the freezing probability of supercooled water by differential scanning calorimetry (DSC).

We report on the first example of quantum coherence between the spins of muons and quadrupolar nuclei. We reveal that these entangled states are highly sensitive to a local charge environment and thus, can be deployed as a functional quantum sensor of that environment. The quantum coherence effect was observed in vanadium intermetallic compounds which adopt the A15 crystal structure, and whose members include all technologically pertinent superconductors. Furthermore ...

Rahel Wallimann, PhD student in the “Nuclide Chemistry Group”, received the first prize (AKB Foundation) of the SAPhW Poster Award at the Swiss Pharma Science Day 2022.

We report an excellent realization of the highly nonclassical incommensurate spin-density wave (SDW) state in the quantum frustrated antiferromagnetic insulator Cs₂CoBr₄. In contrast to the well-known Ising spin chain case, here the SDW is stabilized by virtue of competing planar in-chain anisotropies and frustrated interchain exchange.