Interfacial Electronic Structure Engineering of NiCo2Se4 and NiTe2 Nanorods for Enhanced Hydrogen Evolution Reaction.

Finding the best candidates with outstanding electrocatalytic capabilities for the hydrogen evolution reaction is essential for realizing large-scale hydrogen production through electrolysis. In this study, we synthesized NiCo2Se4 (NCS) and NiTe2 (NT) nanorod arrays using a hydrothermal method. The confirmation of catalyst formation was achieved through X-ray diffraction analysis, electron microscopy imaging, and X-ray photoelectron spectroscopy. Leveraging the plentiful heterointerfaces and synergistic effects arising from the incorporation of bimetallic components, the NCS/NT electrocatalyst demonstrates remarkable efficacy in catalyzing the hydrogen evolution reaction. It achieves a minimal overpotential of 163 mV to attain a current density of 50 mA cm-2, showcasing exceptional catalytic activity. Further exploration has revealed that the engineering of heterogeneous interfaces and the morphology of nanorods not only guarantee the exposure of numerous active sites and expedite electron-mass transfer but also trigger electron modulation. Such modulation serves to fine-tune the adsorptive and adsorptive dynamics of reaction intermediates, culminating in an enhancement of the catalyst's inherent activity. This study illuminates the novel composite electrocatalyst with robust synergy, highlighting the pivotal role of their unique nanostructures in achieving high-efficiency hydrogen production via electrolysis.

Metal-Organic Framework-Derived FeCo2S4/Co3O4 Heterostructure with Enhanced Electrocatalytic Performance for Oxygen Evolution and Hydrogen Evolution Reactions.

Herein, a versatile FeCo2S4/Co3O4 heterostructure consisting of zeolitic imidazolate framework ZIF-derived Co3O4 and FeCo-layered double hydroxide-derived Fe-doped Co sulfide is employed for the all-important alkaline full water splitting process. The heterostructure is prepared by combining pyrolysis and hydrothermal/solvothermal processes. The synthesized heterostructure possesses an electrocatalytically rich interface and renders excellent bifunctional catalytic performance. An overpotential of 139 mV for a standard cathodic current of 10 mA cm-2 with a low Tafel slope of 81 mV dec-1 is recorded for the hydrogen evolution reaction. An overpotential of 210 mV is observed for an anodic current of 20 mA cm-2 with a low Tafel slope of 75 mV dec-1 recorded for the oxygen evolution reaction. The full-symmetric two-electrode cell was capable of generating a current density of 10 mA cm-2 at a cell potential of 1.53 V and a low onset potential of 1.49 V. The symmetric cell architecture exhibits remarkable stability, as a negligible potential increase is observed for continuous water splitting over a 10 h period. With the reported performance, the heterostructure compares well with most of the excellent reported catalysts for alkaline bifunctional catalysts.

Synergetic Role of Nano-/Microscale Structures of the Trifolium Leaf Surface for Self-Cleaning Properties.

Wetting has an essential pertinence to surface applications. The exemplary water-repelling and self-cleaning surfaces in nature have stimulated considerable scientific exploration, given their practical leverage in cleaning window glasses, painted surfaces, fabrics, and solar cells. Here, we explored the three-tier hierarchical surface structure of the Trifolium leaf with distinguished self-cleaning characteristics. The leaf remains fresh, withstands adverse weather, thrives throughout the year, and self-cleans itself against mud or dust. Self-cleaning features are attributed to a three-tier hierarchical synergetic design. The leaf surface is explicated by an optical microscope, a scanning electron microscope, a three-dimensional profilometer, and a water contact angle measuring device. Hierarchical base roughness (i.e., nano-/microscale) comprises a fascinating arrangement, which imparts a superhydrophobic feature to the surface. As a result, the contaminants present on the leaf surface are washed with rolling water droplets. We noticed that self-cleaning is a function of impacting or rolling droplets, and the rolling mechanism is identified as efficient. The self-cleaning phenomenon is studied for contaminations of variable sizes, shapes, and compositions. The contaminations are supplied in both dry and aqueous mixtures. Furthermore, we examined the self-cleaning effect of the Trifolium leaf surface by atmospheric water harvesting. The captured water drops fuse, roll, descend, and wash away the contaminating particles. The diversity of contaminants investigated makes this study applicable to different environmental conditions. And, along with other parallel technologies, this investigation could be useful for crafting sustainable self-cleaning surfaces for regions with acute water scarcity.

High Na+ Mobility in rGO Wrapped High Aspect Ratio 1D SbSe Nano Structure Renders Better Electrochemical Na+ Battery Performance.

We chose to understand the cyclic instability and rate instability issues in the promising class of Na+ conversion and alloying anodes with Sb2 Se3 as a typical example. We employ a synthetic strategy that ensures efficient rGO (reduced graphene oxide) wrapping over Sb2 Se3 material. By utilization of the minimum weight of additive (5 wt.% of rGO), we achieved a commendable performance with a reversible capacity of 550 mAh g-1 at a specific current of 100 mA g-1 and an impressive rate performance with 100 % capacity retention after high current cycling involving a 2 Ag-1 intermediate current step. The electrochemical galvanostatic intermittent titration technique (GITT) has been employed for the first time to draw a rationale between the enhanced performance and the increased mobility in the rGO wrapped composite (Sb2 Se3 -rGO) compared to bare Sb2 Se3 . GITT analysis reveals higher Na+ diffusion coefficients (approx. 30 fold higher) in the case of Sb2 Se3 -rGO as compared to bare Sb2 Se3 throughout the operating voltage window. For Sb2 Se3 -rGO the diffusion coefficients in the range of 8.0×10-15  cm2 s-1 to 2.2×10-12  cm2 s-1 were observed, while in case of bare Sb2 Se3 the diffusion coefficients in the range of 1.6×10-15  cm2 s-1 to 9.4×10-15  cm2 s-1 were observed.

Surfactant-assisted synthesis of polythiophene/Ni0.5Zn0.5Fe2-xCexO4 ferrite composites: study of structural, dielectric and magnetic properties for EMI-shielding applications.

This work reports the exploitation of nanocrystalline Ni0.5Zn0.5Fe2-xCexO4 ferrite for potential application by designing quasi-spherical shaped polythiophene (PTH) composites via in situ emulsion polymerization. The structural, electronic, dielectric, magnetic, and electromagnetic interference (EMI) shielding properties of PTH/Ni0.5Zn0.5Fe2-xCexO4 composites were investigated. Our results suggest that these properties could be optimized by modulating the concentration of x (composition) in the polymer matrix. Higher values of ε' and ε'' were obtained on composite formation, and could be due to the heterogeneity developed in the material. An enhancement in the value of saturation magnetization (123 emu g-1 for x = 0.04) and Curie temperature was obtained with Ce concentration, which is useful for high density recording purposes. A low value of saturation magnetization was obtained for the PTH/Ni0.5Zn0.5Fe2-xCexO4 composite (36 emu g-1 for x = 0.04). This could be attributed to the non-magnetic nature of the polymer. A total shielding effectiveness (SET = SEA + SER) up to 34 dB (≈99.9% attenuation) was recorded for PTH/Ni0.5Zn0.5Fe2-xCexO4 composites (x = 0.04) in a frequency range of 8.2-12.4 GHz (X-band), which surpasses the shielding criteria of SET > 30 dB for commercial purposes. Such a material with high SE identifies its potential for making electromagnetic shields. The effect of Ce substitution on the microstructure, dielectric, impedance and magnetic properties of PTH/Ni0.5Zn0.5Fe2-xCexO4 ferrite composites was also investigated. X-ray diffraction analysis confirmed cubic spinel phase formation, and the broad reflection peaks indicated the formation of smaller sized particles. The smaller energy band gap (2.53 eV) of the composite indicated that this material could be used for photocatalysis in the visible region. Dielectric and impedance measurements were carried out in a frequency range of 8.2-12.4 GHz. Dielectric properties were improved considerably by the substitution of Ce3+ ions in PTH/Ni0.5Zn0.5Fe2-xCexO4 composites. Impedance spectroscopy was used to study the effect of grain and grain boundaries on the electrical properties of PTH/Ni0.5Zn0.5Fe2-xCexO4 composites. Cole-Cole plots showed the formation of single semi-circles for all samples in the measured frequency range. This showed that the composite material was composed of good conducting grains and poorly conducting grain boundaries.

Azolla Pinnata: Sustainable Floating Oil Cleaner of Water Bodies.

Various plant-based materials effectively absorb oil contaminants at the water/air interface. These materials showcase unparalleled efficiency in purging oil contaminants, encompassing rivers, lakes, and boundless oceans, positioning them as integral components of environmental restoration endeavors. In addition, they are biodegradable, readily available, and eco-friendly, thus making them a preferable choice over traditional oil cleaning materials. This study explores the phenomenal properties of the floating Azolla fern (Azolla pinnata), focusing on its unique hierarchical leaf surface design at both the microscale and nanoscale levels. These intricate structures endow the fern with exceptional characteristics, including superhydrophobicity, high water adhesion, and remarkable oil or organic solvent absorption capabilities. Azolla's leaf surface exhibits a rare combination of dual wettability, where hydrophilic spots on a superhydrophobic base enable the pinning of water droplets, even when positioned upside-down. This extraordinary property, known as the parahydrophobic state, is rare in floating plants, akin to the renowned Salvinia molesta, setting Azolla apart as a natural wonder. Submerged in water, Azolla leaves excel at absorbing light oils at the air-water interface, demonstrating a notable ability to extract high-density organic solvents. Moreover, Azolla's rapid growth, doubling in the area every 4-5 days, especially in flowing waters, positions it as a sustainable alternative to traditional synthetic oil-cleaning materials with long-term environmental repercussions. This scientific lead could pave the way for more environmentally friendly approaches to mitigate the negative impacts of oil spills and promote a cleaner water ecosystem.

Multiscale Janus Surface Structure of Trifolium Leaf with Atmospheric Water Harvesting and Dual Wettability Features.

Numerous fascinating hierarchical surfaces from nature, including cactus spines, rice leaves, Namib desert beetle, spider silks, and pitcher plants, have been thoroughly investigated to emulate and architect superior surfaces for capturing sustainable, clean, and safe freshwater from the atmosphere. Hitherto, the adaxial side of biological surfaces has been meticulously investigated for wettability and atmospheric water harvesting (AWH) applications. However, the abaxial face has not yet attracted much scientific scrutiny. Here, we revealed the multifunctional Janus surface traits of Trifolium pratense (i.e., red clover) leaf with extrusive atmospheric water fishing ability on both adaxial and abaxial faces. Water harvesting is performed by conical outgrowths (microhairs). The individual hair's intriguing topography comprises asymmetric shape and surface roughness, which plays synergetic roles in water deposition and directional transport. The water collection quantity on the leaf surface is a function of hair density, which varies significantly on two sides. Noticeably, instead of gravitational pull, the hairs perform water reaping competence under the collective impact of surface energy and Laplace pressure gradients. Consequently, both straight-up and upside-down water harvesting are presented. Furthermore, the leaf surface exhibits dual water wettability features. The upper side manifests the water-repelling and water roll-off phenomenon. In contrast, the lower surface displays a water-retaining/or pinning effect. Optical microscopy, scanning electronic microscopy, real-time optical visualization, and contact angle analysis were employed to characterize the natural and template specimens. The dorsiventral asymmetry of the Trifolium leaf examined in this work could be helpful for a plethora of applications, such as scalable AWH, rainwater collection, self-cleaning, and adhesive fixtures.