Environmental problems are among the most pressing issues in the modern world, including the shortage of clean drinking water partially caused by contamination from various industries and the excessive emission of CO₂ primarily from the massive use of fossil fuels. Consequently, it is crucial to develop inexpensive, effective, and environmentally friendly methods for wastewater treatment and CO₂ reduction, turning them into useful feedstocks. This study explores a unique method that addresses both challenges by utilizing ZnO, which is recognized as one of the most active semiconductors for photocatalysis, as well as a cost-effective electrocatalyst for the CO₂ reduction reaction (CO₂RR). Specifically, we investigate the influence of the morphology of various ZnO nanostructures synthesized via different low-cost routes on their photocatalytic properties for degrading the rhodamine-B dye (RhB) and on their electrocatalytic performance for the CO₂RR. Our results show that the ZnO lamella morphology achieves the best performance compared to the nanorod and nanoparticle structures. This outcome is likely attributed to the lamella’s higher aspect ratio, which plays a critical role in determining the structural, optical, and electrical properties of ZnO.

We investigated the spatial phase separation of the two components forming a bosonic mixture distributed in a four-well lattice with a ring geometry. We studied the ground state of this system, described by means of a binary Bose–Hubbard Hamiltonian, by implementing a well-known coherent-state picture which allowed us to find the semi-classical equations determining the distribution of boson components in the ring lattice. Their fully analytic solutions, in the limit of large boson numbers, provide the boson populations at each well as a function of the interspecies interaction and of other significant model parameters, while allowing to reconstruct the non-trivial architecture of the ground-state four-well phase diagram. The comparison with the L-well ($L=2,3$) phase diagrams highlights how increasing the number of wells considerably modifies the phase diagram structure and the transition mechanism from the full-mixing to the full-demixing phase controlled by the interspecies interaction. Despite the fact that the phase diagrams for $L=2,3,4$ share various general properties, we show that, unlike attractive binary mixtures, repulsive mixtures do not feature a transition mechanism which can be extended to an arbitrary lattice of size L.

Electromagnetic temporal boundaries, emerging when the constitutive parameters of a medium undergo abrupt temporal variations, have garnered significant interest for their role in facilitating unconventional wave phenomena and enabling sophisticated field manipulations. A key manifestation is temporal reflection in an unbounded spatial domain, where a sudden temporal discontinuity induces phase‐conjugated backward waves alongside anomalous spin conversion. This study explores distinctive spin‐conversion dynamics at a time‐dependent spatial interface governed by Lorentz‐type dispersion, in which the plasma frequency undergoes rapid modulation over time. The interaction of a circularly polarized wave with a space‐time interface excites electromagnetic signals at the system's natural resonance, allowing precise control over polarization states. The scattered field stems from the combined influence of temporal and spatial boundaries, yielding a superposition of the original incident wave's polarization and its phase‐conjugated counterpart.