RESUMEN
Osmotic energy, often referred to as "blue energy", is the energy generated from the mixing of solutions with different salt concentrations, offering a vast, renewable, and environmentally friendly energy resource. The efficacy of osmotic power production considerably relies on the performance of the transmembrane process, which depends on ionic conductivity and the capability to differentiate between positive and negative ions. Recent advancements have led to the development of membrane materials featuring precisely tailored ion transport nanochannels, enabling high-efficiency osmotic energy harvesting. In this review, ion diffusion in confined nanochannels and the rational design and optimization of membrane architecture are explored. Furthermore, structural optimization of the membrane to mitigate transport resistance and the concentration polarization effect for enhancing osmotic energy harvesting is highlighted. Finally, an outlook on the challenges that lie ahead is provided, and the potential applications of osmotic energy conversion are outlined. This review offers a comprehensive viewpoint on the evolving prospects of osmotic energy conversion.
RESUMEN
Removal of high toxic Cr(VI) with solar plays an important role in improving water pollution, but is facing a dilemma of developing excellent photocatalysts with high conversion efficiency and low cost. Different from traditional nano-structuring, this work focuses on the interfacial hybridization by considering the intrinsic difference in bonding interaction. Herein, we intentionally make some layered black phosphorus (BP) sheets with Van der Waals interaction to bond with ZnO surfaces, in which some additional electron channels can be formed by this multilevel atomic hybridization to accelerate carrier transfer and separation. Compared to the pristine ZnO and BP nanosheets, the light absorption and carrier separation efficiency can be sharply enhanced by this particular electronic structure, which makes the Cr reduction performance enhanced about 7.1 times. Our findings suggest a new insight into accelerating Cr(VI) reduction by designing interfacial atom hybridization.
RESUMEN
While acidic oxygen evolution reaction plays a critical role in electrochemical energy conversion devices, the sluggish reaction kinetics and poor stability in acidic electrolyte challenges materials development. Unlike traditional nano-structuring approaches, this work focuses on the structural symmetry breaking to rearrange spin electron occupation and optimize spin-dependent orbital interaction to alter charge transfer between catalysts and reactants. Herein, we propose an atomic half-disordering strategy in multistage-hybridized BixEr2-xRu2O7 pyrochlores to reconfigure orbital degeneracy and spin-related electron occupation. This strategy involves controlling the bonding interaction of Bi-6s lone pair electrons, in which partial atom rearrangement makes the active sites transform into asymmetric high-spin states from symmetric low-spin states. As a result, the half-disordered BixEr2-xRu2O7 pyrochlores demonstrate an overpotential of ~0.18 V at 10 mA cm-2 accompanied with excellent stability of 100 h in acidic electrolyte. Our findings not only provide a strategy for designing atom-disorder-related catalysts, but also provides a deeper understanding of the spin-related acidic oxygen evolution reaction kinetics.
