Fe1-xNix(PO3)2/Ni2P Heterostructure for Boosting Alkaline Oxygen Evolution Reaction in Fresh Water and Real Seawater at High Current Density.

Oxygen evolution reaction (OER) is a limiting reaction for highly efficient water electrolysis. Thus, the development of cost-effective and highly efficient OER catalysts is the key to large-scale water electrolysis for hydrogen production. Herein, by using an interfacial engineering strategy, a unique nanoflower-like Fe1-xNix(PO3)2/Ni2P/NF heterostructure with abundant heterogeneous interfaces is successfully fabricated. The catalyst exhibits excellent OER catalytic activity in alkaline fresh water and alkaline natural seawater at high current densities, which only, respectively, requires overpotentials of 318 and 367 mV to drive 1000 mA cm-2 in fresh water and natural seawater both containing 1 M KOH. Furthermore, Fe1-xNix(PO3)2/Ni2P/NF demonstrates excellent durability, which can basically remain stable for 80 h during the electrocatalytic OER processes, respectively, in alkaline fresh water and natural seawater. This work provides a new construction strategy for designing highly efficient electrocatalysts for OER at high current densities both in alkaline fresh water and in natural seawater.

Leadless pacing using induction technology: impact of pulse shape and geometric factors on pacing efficiency.

AIMS: Leadless pacing can be done by transmitting energy by an alternating magnetic field from a subcutaneous transmitter unit (TU) to an endocardial receiver unit (RU). Safety and energy consumption are key issues that determine the clinical feasibility of this new technique. The aims of the study were (i) to evaluate the stimulation characteristics of the non-rectangular pacing pulses induced by the alternating magnetic field, (ii) to determine the extent and impact of RU movement caused by the beating heart, and (iii) to evaluate the influence of the relative position between TU and RU on pacing efficiency and energy consumption. METHODS AND RESULTS: In the first step pacing efficiency and energy consumption for predefined positions were determined by bench testing. Subsequently, in a goat at five different ventricular sites (three in the right ventricle, two in the left ventricle) pacing thresholds using non-rectangular induction pulses were compared with conventional pulses. Relative position, defined by parallel distance, radial distance, and angulation between TU and RU, were determined in vivo by X-ray and an inclination angle measurement system. Bench testing showed that by magnetic induction for every alignment between TU and RU appropriate pulses can be produced up to a distance of 100 mm. In the animal experiment pacing thresholds were similar for non-rectangular pulses as compared with conventional pulse shapes. In all five positions with distances between 62 and 102 mm effective pacing was obtained in vivo. Variations in distance, displacement and angle caused by the beating heart did not cause loss of capture. At pacing threshold energy consumptions between 0.28 and 5.36 mJ were measured. Major determinants of energy consumption were distance and pacing threshold. CONCLUSION: For any given RU position up to a distance of 100 mm reliable pacing using induction can be obtained. In anatomically crucial distances, up to 60 mm energy consumption is within a reasonable range.

Efficient and rapid adsorption of methylene blue dyes by novel metal-organic frameworks and organic/inorganic hybrid alginate-based dual network gel composites.

To address the limitations of gel-based adsorbents, such as inadequate mechanical strength, low adsorption capacity, and limited reusability, this study presents an innovative approach employing a dual network gel. The dual network consists of calcium alginate (CA) ionic crosslinked organic networks, and vinyl silica-based nanoparticles (VSNP) as crosslinking agents in acrylic acid (AA) free radical polymerization networks (denoted as P (AA-co-VSNP), abbreviated as PAV). After freeze-drying, ultimately yielding an organic/inorganic hybrid dual network gel (referred to as CA/P(AA-co-VSNP), abbreviated as CPAV), enriched with abundant functional groups, thereby enhancing material reusability. To further enhance the adsorption capacity, CPAV undergoes hydrothermal reactions to obtain metal-organic frameworks (MOFs) composite dual network gel adsorbent (UiO-66@CPAV). UiO-66@CPAV exhibited a density of 0.165 g/cm3 and showcased a unique pore structure with nested macropores and mesopores, featuring a uniform distribution of pore holes. Notably, the specific surface area was measured at 96.3 m2/g, and an average pore diameter was 17.9 nm. Most impressively, the actual maximum adsorption capacity reached 841.7 mg/g, and even after 10 cycles of use, the adsorption capacity remained 91.9 % of its initial value. Overall, this research introduced a novel methodology for the development of dual network MOFs@gel adsorbents, showcasing promising advancements in the field.

PVA/sodium alginate multi-network aerogel fibers, incorporated with PEG and ZnO, exhibit enhanced temperature regulation, antibacterial, thermal conductivity, and thermal stability.

This paper presents a novel approach for the fabrication of polyvinyl alcohol (PVA)/sodium alginate (SA) aerogel fibers with a multilayered network structure using wet spinning and freeze-thaw cycling techniques. The multiple cross-linking networks regulate the pore structure, leading to the formation of stable and tunable multilevel pore architectures. PEG and nano-ZnO were successfully loaded onto the PVA/SA modified aerogel fibers (MAFs) using vacuum impregnation. MAFs exhibited excellent thermal stability at 70 °C without leakage after 24 h of heating. Furthermore, MAFs demonstrated excellent temperature regulation performance, with a latent heat of 121.4 J/g, which accounts for approximately 83 % of PEG. After modification, the thermal conductivity of MAFs was significantly improved, and they exhibited excellent antibacterial properties. Therefore, MAFs are expected to be widely used in intelligent temperature-regulating textiles.

One-Step Bulk-Suspension Polymerization of Polyethylene Glycol-Based Copolymer Microspheres for Phase Change Textiles.

The paper presents a feasible strategy through one-step bulk-suspension polymerization, grafting PEG onto an in situ synthesized copolymer. In more detail, PEG was grafted onto a homemade polystyrene/maleic anhydride copolymer (SMA) via bulk-suspension polymerization with poly(vinyl alcohol) as a suspending agent. According to the optimal reaction conditions, the grafting rate of PEG was 56.2% through chemical titration experiments. At the same time, the quantitative relationship between the grafting rate and enthalpy was demonstrated for the first time in a PEG-based solid-solid phase change material (S-SPCM). Morphology observation revealed that the obtained S-SPCM is made up of white microspheres of approximately 100-150 µm. The powdery product polystyrene/maleic anhydride grafted polyethylene glycol (SMA-g-PEG) obtained through bulk-suspension polymerization endowed that the whole product could be used directly as a phase change material without postprocessing. The melting enthalpy and crystallization enthalpy of SMA-g-PEG were 79.3 J/g and 76.9 J/g, respectively. Based on the effective fixed load of PEG, the macrostructure of SMA-g-PEG was almost unchanged at 70 °C compared with the macrostructures at 20 °C, and the latent heat of SMA-g-PEG was decreased slightly after 1000 thermal cycles. Overall, the obtained SMA-g-PEG can be used as a filler in insulation materials and composited with fibers to obtain phase change thermoregulated smart textiles.