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Collecting fog water is crucial for dry areas since natural moisture and fog are significant sources of freshwater. Sustainable and energy-efficient water collection systems can take a page out of the cactus’s playbook by mimicking its native fog gathering process. Inspired by the unique geometric structure of the cactus spine, we fabricated a bioinspired artificial fog collector consisting of cactus spines featuring barbs of different sizes and angles on the surfaces for water collection and a series of microcavities within microchannels inspired by Nepenthes Alata on the bottom to facilitate water flowing to the reservoir. However, replicating the actual shape of the cactus spine using conventional manufacturing techniques is challenging, and research in this area has faced a limitation in enhancing water-collecting efficiency. Here, we turned to 3D printing technology (vat photopolymerization) to create bio-mimetic fog collectors with a variety of geometric shapes that would allow for the most effective conveyance and gathering of water. Various barb sizes, angles between each barb in a single array, spine and barb arrangements, and quantity of barbs were tested experimentally and numeric analysis was carried out to measure the volume of water collected and optimize the mass rate. The result shows that optimal fog collection is with a mass flow rate of 0.7433 g/min, with Li = 900 μm, θ = 45°, ϕ = 90°, Nb = 2, and Ns = 5. This study presents a sustainable and ecologically sound method for efficiently collecting humid air, which is expected to be advantageous for the advancement of future-oriented fog-collection, water-transportation, and separation technologies. 

Abstract Semiconductor excitations can hybridize with cavity photons to form exciton-polaritons (EPs) with remarkable properties, including light-like energy flow combined with matter-like interactions. To fully harness these properties, EPs must retain ballistic, coherent transport despite matter-mediated interactions with lattice phonons. Here we develop a nonlinear momentum-resolved optical approach that directly images EPs in real space on femtosecond scales in a range of polaritonic architectures. We focus our analysis on EP propagation in layered halide perovskite microcavities. We reveal that EP–phonon interactions lead to a large renormalization of EP velocities at high excitonic fractions at room temperature. Despite these strong EP–phonon interactions, ballistic transport is maintained for up to half-exciton EPs, in agreement with quantum simulations of dynamic disorder shielding through light-matter hybridization. Above 50% excitonic character, rapid decoherence leads to diffusive transport. Our work provides a general framework to precisely balance EP coherence, velocity, and nonlinear interactions. 

Solid polymer electrolytes (SPEs) are one of the most promising solutions to the safety issues of lithium batteries. Understanding the morphology and dynamic effects on the ion transport properties of SPEs would be essential for future SPE design. In this article, using poly(ethylene oxide) (PEO) as an example, we focus on morphology control in semicrystalline SPEs. We show that the effect of semicrystallinity can be quantitatively separated into volume, structure and dynamic effects. We further demonstrate that morphological control plays an important role in ion transport control in semicrystalline SPE systems. 

Crystallization is incommensurate with nanoscale curved space due to the lack of three dimensional translational symmetry of the latter. Herein, we report the formation of single-crystal-like, nanosized polyethylene (PE) capsules using a miniemulsion solution crystallization method. The miniemulsion was formed at elevated temperatures using PE organic solution as the oil phase and sodium dodecyl sulfate as the surfactant. Subsequently, cooling the system stepwisely for controlled crystallization led to the formation of hollow, nanosized PE crystalline capsules, which are named as crystalsomes since they mimic the classical self-assembled structures such as liposome, polymersome and colloidosome. We show that the formation of the nanosized PE crystalsomes is driven by controlled crystallization at the curved liquid/liquid interface of the miniemulson droplet. The morphology, structure and mechanical properties of the PE crystalsomes were characterized using scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and atomic force spectroscopy. Electron diffraction showed the single-crystal-like nature of the crystalsomes. The incommensurateness between the nanocurved interface and the crystalline packing led to reduced crystallinity and crystallite size of the PE crystalsome, as observed from the X-ray diffraction measurements. Moreover, directly quenching the emulsion below the spinodal line led to the formation of hierarchical porous PE crystalsomes due to the coupling of the PE crystallization and liquid/liquid phase separation. We anticipate that this unique crystalsome represents a new type of nanostructure that might be used as nanodrug carriers and ultrasound contrast agents.