The anode oxygen evolution reaction (OER) is known to largely limit the efficiency of electrolyzers owing to its sluggish kinetics. While crystalline metal oxides are promising as OER catalysts, ...their amorphous phases also show high activities. Efforts to produce amorphous metal oxides have progressed slowly, and how an amorphous structure benefits the catalytic performances remains elusive. Now the first scalable synthesis of amorphous NiFeMo oxide (up to 515 g in one batch) is presented with homogeneous elemental distribution via a facile supersaturated co‐precipitation method. In contrast to its crystalline counterpart, amorphous NiFeMo oxide undergoes a faster surface self‐reconstruction process during OER, forming a metal oxy(hydroxide) active layer with rich oxygen vacancies, leading to superior OER activity (280 mV overpotential at 10 mA cm−2 in 0.1 m KOH). This opens up the potential of fast, facile, and scale‐up production of amorphous metal oxides for high‐performance OER catalysts.
Amorphous NiFeMo oxide (up to 515 g one batch) with homogeneous elemental distribution was synthesized through a facile supersaturated co‐precipitation method. The amorphous NiFeMo oxide undergoes rapid surface self‐reconstruction during OER that forms a metal oxy(hydroxide) active layer with oxygen vacancies, enabling efficient OER catalysis.
SiOx is proposed as one of the most promising anodes for Li‐ion batteries (LIBs) for its advantageous capacity and stable Li uptake/release electrochemistry, yet its practical application is still a ...big challenge. Here encapsulation of SiOx nanoparticles into conductive graphene bubble film via a facile and scalable self‐assembly in solution is shown. The SiOx nanoparticles are closely wrapped in multilayered graphene to reconstruct a flake‐graphite‐like macrostructure, which promises uniform and agglomeration‐free distribution of SiOx in the carbon while ensures a high mechanical strength and a high tap density of the composite. The composites present unprecedented cycling stability and excellent rate capabilities upon Li storage, rendering an opportunity for its anode use in the next‐generation high‐energy LIBs.
SiOx nanoparticles are closely wrapped in multilayered graphene to reconstruct a macrostructure resembling flake graphite, which promises agglomeration‐free distribution of SiOx in the bulk while ensuring a high mechanical strength and a high tap density of the bubble film. By taking the advantages of the graphene network, the composites present unprecedented cycling stability and excellent rate capabilities upon Li storage.
Energy efficient buildings require materials with a low thermal conductivity and a high fire resistance. Traditional organic insulation materials are limited by their poor fire resistance and ...inorganic insulation materials are either brittle or display a high thermal conductivity. Herein we report a mechanically resilient organic/inorganic composite aerogel with a thermal conductivity significantly lower than expanded polystyrene and excellent fire resistance. Co‐polymerization and nanoscale phase separation of the phenol‐formaldehyde‐resin (PFR) and silica generate a binary network with domain sizes below 20 nm. The PFR/SiO2 aerogel can resist a high‐temperature flame without disintegration and prevents the temperature on the non‐exposed side from increasing above the temperature critical for the collapse of reinforced concrete structures.
Fire not starter: Taking advantage of a co‐polymerization strategy an organic–inorganic binary network hybrid aerogel with a nanoscale homogeneity can be prepared. The phenol‐formaldehyde‐resin/SiO2 aerogel is mechanically resilient and has a thermal conductivity significantly lower than expanded polystyrene and excellent fire resistance.
Superelastic carbon aerogels have been widely explored by graphitic carbons and soft carbons. These soft aerogels usually have delicate microstructures with good fatigue resistance but ultralow ...strength. Hard carbon aerogels show great advantages in mechanical strength and structural stability due to the sp3‐C‐induced turbostratic “house‐of‐cards” structure. However, it is still a challenge to fabricate superelastic hard carbon‐based aerogels. Through rational nanofibrous structural design, the traditional rigid phenolic resin can be converted into superelastic hard carbon aerogels. The hard carbon nanofibers and abundant welded junctions endow the hard carbon aerogels with robust and stable mechanical performance, including superelasticity, high strength, extremely fast recovery speed (860 mm s−1), low energy‐loss coefficient (<0.16), long cycle lifespan, and heat/cold‐endurance. These emerging hard carbon nanofiber aerogels hold a great promise in the application of piezoresistive stress sensors with high stability and wide detection range (50 kPa), as well as stretchable or bendable conductors.
A family of hard carbon aerogels with nanofibrous structure templated by various nanofibers is fabricated, displaying robust and stable mechanical performances, including high strength, extremely fast recovery speed (860 mm s−1), and ultralow energy loss coefficient (<0.16). After being compressed for 104 cycles (50% strain), they show only ≈2% plastic deformation and retain ≈93% stress.
As an abundant natural resource, wood has gained great attention for thousands of years, spanning from the primitive construction materials to the modern high‐added‐value engineering materials. The ...unique delicate microstructures and the wonderful properties (e.g., low‐density, high strength and stiffness, good toughness, and environmental sustainability) have made wood a natural source of inspiration that guides researchers to invent various wood‐inspired materials. Herein, as an emerging material system, bioinspired artificial wood, with similar cellular structures and comparable mechanical properties, is discussed in the view of the design concept, fabrication strategy, properties, and possible applications. The present challenges and further research opportunities are also presented for artificial woods to thrive. To achieve the final eco‐friendly artificial wood, more endeavors should be made in biomaterials and biodegradable or recyclable engineering of polymers to gain high mechanical properties and environmental sustainability simultaneously.
Artificial woods have emerged as a novel kind of wood‐inspired engineering material with almost exactly the same channel microstructures and similar wall components. The performances of artificial woods depend on both the oriented channel and wall designs. The rational combination of other engineering polymers and channel‐making techniques hold promise to develop more useful artificial woods.
Cellulose aerogels are plagued by intermolecular hydrogen bond‐induced structural plasticity, otherwise rely on chemicals modification to extend service life. Here, we demonstrate a ...petrochemical‐free strategy to fabricate superelastic cellulose aerogels by designing hierarchical structures at multi scales. Oriented channels consolidate the whole architecture. Porous walls of dehydrated cellulose derived from thermal etching not only exhibit decreased rigidity and stickiness, but also guide the microscopic deformation and mitigate localized large strain, preventing structural collapse. The aerogels show exceptional stability, including temperature‐invariant elasticity, fatigue resistance (∼5 % plastic deformation after 105 cycles), high angular recovery speed (1475.4° s−1), outperforming most cellulose‐based aerogels. This benign strategy retains the biosafety of biomass and provides an alternative filter material for health‐related applications, such as face masks and air purification.
A new type of cellulose aerogels with anisotropic and hierarchical porous architecture are developed via a petrochemical‐free method. The aerogels display temperature‐invariant elasticity (∼5 % plastic deformation after 105 compressive cycles at 50 % strain), large‐strain recoverability (folding and twisting), angular recovery speed high up to 1475.4° s−1, and exceptional fatigue resistance.
Soft woods have attracted enormous interest due to their anisotropic cellular microstructure and unique flexibility. The conventional wood-like materials are usually subject to the conflict between ...the superflexibility and robustness. Inspired by the synergistic compositions of soft suberin and rigid lignin of cork wood which has good flexibility and mechanical robustness, an artificial soft wood is reported by freeze-casting the soft-in-rigid (rubber-in-resin) emulsions, where the carboxy nitrile rubber confers softness and rigid melamine resin provides stiffness. The subsequent thermal curing induces micro-scale phase inversion and leads to a continuous soft phase strengthened by interspersed rigid ingredients. The unique configuration ensures crack resistance, structural robustness and superb flexibility, including wide-angle bending, twisting, and stretching abilities in various directions, as well as excellent fatigue resistance and high strength, overwhelming the natural soft wood and most wood-inspired materials. This superflexible artificial soft wood represents a promising substrate for bending-insensitive stress sensors.
Polymer‐derived carbon aerogels can be obtained by direct polymerization of monomers under hypersaline conditions using inorganic salts. This allows for significantly increased mechanical robustness ...and avoiding special drying processes. This concept was realized by conducting the polymerization of phenol–formaldehyde (PF) in the presence of ZnCl2 salt. Afterwards, the simultaneous carbonization and foaming process conveniently converts the PF monolith into a foam‐like carbon aerogel. ZnCl2 plays a key role, serving as dehydration agent, foaming agent, and porogen. The carbon aerogels thus obtained are of very low density (25 mg cm−3), high specific surface area (1340 m2 g−1), and have a large micro‐ and mesopore volume (0.75 cm3 g−1). The carbon aerogels show very promising potential in the separation/extraction of organic pollutants and for energy storage.
Rather salty: Carbon aerogels were obtained upon conducting the polymerization of phenol–formaldehyde (PF) resin under hypersaline conditions, for example, by using ZnCl2. The simultaneous carbonization and foaming process conveniently converts the PF monoliths into foam‐like carbon aerogels.
Continuous porous carbon fibers with uniformly distributed Co3O4 hollow nanoparticles (NPs) have been prepared by direct electrospinning of ZIF-67 NPs followed by a thermal treatment. Benefiting from ...the unique structural and compositional advantages, ES-CNCo3O4 with hierarchical porous structure shows excellent electrochemical performance as an anode material for lithium ion batteries.
Effect of tea polyphenols (TP) on the quality of Chinese steamed bun (CSB) was investigated, while the interaction and action mechanism between TP and vital wheat gluten (VWG, constitutive proteins ...of flour) were further explored. With a low concentration (1%) of TP, CSB showed positive changes in quality, and the hardness of CSB decreased by 33.95%, while its specific volume, springiness, and resilience separately increased by 1.8%, 11.9%, and 5.5%, whereas the higher concentrations of TP (2% and 4%) caused an adverse impact. By observation of scanning electron microscope, VWG formed a fluffier structure with a low concentration of TP, while the structure deteriorated at high concentration of TP. In addition, the secondary and tertiary structures of VWG were both changed by TP. Along with the results of thermodynamic analysis (thermogravimetric and differential scanning calorimetry measurements), TP could induce the structural rearrangement of VWG. Further, a lower amidogen and sulfhydryl contents of VWG were obtained in TP groups, which illustrated that peptide and disulfide bonds of VWG were not possibly interrupted by TP. Instead, hydrophobic residues of VWG were bonded to form a more hydrophilic structure. Moreover, according to molecular docking results, epigallocatechin‐3‐gallate interacted tightly with VWG by hydrogen bonds and hydrophobic actions, and the action sites were mainly at hydrophobic and hydrophilic residues. All results suggested that the VWG structure was affected greatly by TP, and a low dose of TP might be potential to improve the quality of flour products.
Practical Application
The physicochemical properties of gluten show the significant effects on the quality of flour products in food industry. In the present study, a low dose of tea polyphenols exhibited a strengthened effect on gluten, so as to ameliorate the texture of Chinese steamed bun (CSB) due to their tight interactions with gluten, while the color of CSB was changed to brown as tea polyphenols. All results suggested that a low dose of tea polyphenols could be potentially utilized to improve flour quality and enhance gluten strength in food industry.
