Poor Mechanical Durability Research Articles

An Adhesive Hydrogel Technology for Enhanced Cartilage Repair: A Preliminary Proof of Concept.

Knee cartilage has limited natural healing capacity, complicating the development of effective treatment plans. Current non-cell-based therapies (e.g., microfracture) result in poor repair cartilage mechanical properties, low durability, and suboptimal tissue integration. Advanced treatments, such as autologous chondrocyte implantation, face challenges including cell leakage and inhomogeneous distribution. Successful cell therapy relies on prolonged retention of therapeutic biologicals at the implantation site, yet the optimal integration of implanted material into the surrounding healthy tissue remains an unmet need. This study evaluated the effectiveness of a newly developed photo-curable adhesive hydrogel for cartilage repair, focusing on adhesion properties, integration performance, and ability to support tissue regeneration. The proposed hydrogel design exhibited significant adhesion strength, outperforming commercial adhesives such as fibrin-based glues. An in vivo goat model was used to evaluate the hydrogels' adhesion properties and long-term integration into full-thickness cartilage defects over six months. Results showed that cell-free hydrogel-treated defects achieved superior integration with surrounding tissue and enhanced cartilage repair, with notable lateral integration. In vitro results further demonstrated high cell viability, robust matrix production, and successful cell encapsulation within the hydrogel matrix. These findings highlight the potential of adhesive hydrogel formulations to improve the efficacy of cell-based therapies, offering a potentially superior treatment for knee cartilage defects.

Lead-free Polymer Composite Film for Photon Energy Influenced Piezoelectric Nanogenerator based on Photoactive SnS2

Piezoelectric nanogenerators (PENGs) can power microelectronics, which convert weak mechanical vibrations to electrical impulses; however, low output voltage and poor mechanical durability limit PENG use. Thus, we provide photoactive SnS2 nanofillers in a PVDF matrix for piezoelectric nanogenerators (PPENGs). Raman spectroscopy demonstrates improvement of the electroactive β-phase of PVDF due to adding photoactive hexagonal SnS2 nanoparticles with a band gap of 2.4 eV. Sandwiching the PVDF-SnS2 composite between ITO-coated substrates with silver paste contacts fabricated the PPENG. The open-circuit voltage of PPENG is 24.4 V in the dark and 72.9 V under illumination with a short-circuit current of 0.75 μA, showing its outstanding photo responsiveness. The high light absorption of SnS2 and PVDF-SnS2 interfacial polarization caused the improved response. High-performance optoelectronic and energy harvesting applications may employ this photoactive piezoelectric nanogenerator development technique.

Microstructure and radiation shielding characteristics of PVA fiber-reinforced ultra-high performance concrete

The application of nuclear technologies simulates the development of radiation shielding materials. Traditional heavy-weight concrete used for radiation shielding is limited in practical construction due to the poor mechanical properties and durability. This study developed a PVA fiber-reinforced ultra-high performance concrete (UHPFRC) with magnetite as heavy aggregates used for radiation shielding. Due to the scientific skeleton design, UHPFRC exhibits superior mechanical properties, with compressive strength and flexural strength reaching up to 121.9 MPa and 23.2 MPa, respectively. The microstructure of UHPFRC was investigated in detail and the results revealed that the incorporation of PVA fibers refined the pore structure of UHPFRC. The interfacial transition zone between magnetite aggregates and cementitious matrix in UHPFRC was much denser than that in traditional concrete due to the low water to binder ratio. The gamma and neutron radiations shielding capacity of UHPFRC were evaluated by the combination of actual measurement and simulation. By introducing light nuclei and refining the pore structure, the incorporation of PVA fibers improved the neutron radiation shielding capabilities of UHPFRC by 5.1%.

Fabrication and characterization of MgF2 anti-reflective films comprising dual-layer prepared by physical vapor deposition technique for optoelectronic applications

Moth eye protuberances, for instance, exhibit highly developed and well-organized nanostructures that allow them to adapt to a wide range of environmental conditions and achieve remarkable antireflective performance, which has inspired and been emulated by scientific advancement. Innovative studies have focused on bioinspired and imitating moth-eye patterns to provide a textured surface in multilayer antireflective coatings (ARC) using nanomaterials, polymers, or composites to eliminate undesired reflection in standard optical components and optoelectronic industrial applications. Multilayer AR systems provide a number of advantages over single-layer designs. Still, their limited applicability is due to obstacles such as mismatched properties at interfaces, high costs, poor mechanical durability, and wetting concerns. Using MgF2 and polytetrafluoroethylene, we develop a technique for fabricating high-performance AR nanostructures on borosilicate crown glass and Fluorine-doped Tin Oxide substrates via the glancing angle deposition technique. By inducing porosity and changing the deposition angle (α) at 550 nm, the refractive index of MgF2 is reduced from 1.38 to 1.14. In agreement with optical modelling predictions, high-performance ARC has been successfully produced on different substrates. Besides this, introducing a thin layer of polytetrafluoroethylene on MgF2 ARC via vapor deposition having a refractive index of 1.21 deposited at α ∼80° results in inducing water-repellent properties in ARC. Hence, our fabricated ARC yields stable AR efficiency with outstanding directional uniformity, durability, and negative temperature stability, having hydrophobic characteristics.

Comparison Study of a Thermal-Driven Microstructure in a High-Ni Cathode for Lithium-Ion Batteries: Critical Calcination Temperature for Polycrystalline and Single-Crystalline Design.

High-Ni layered oxide cathodes are promising candidates for lithium-ion batteries due to their high energy density. However, their cycle stability is compromised by the poor mechanical durability of the particle microstructure. In this study, we investigate the impact of the calcination temperature on microstructural changes, including primary particle growth and pore evolution, using LiNi0.88Mn0.08Co0.04O2 (N884), with an emphasis on the critical calcination temperature for polycrystalline and single-crystal designs in high-Ni cathodes. As the calcination temperature increases, the primary particles undergo a rectangular growth pattern while the pore population decreases. Beyond a certain critical temperature (in this case, 850 °C), a sudden increase in primary particle size and a simultaneous rapid reduction in the pore population are observed. This sudden microstructure evolution leads to poor cycle retention in N884. In contrast, single-crystal particles, free of grain boundaries, synthesized at this critical temperature exhibit superior cycle retention, underscoring the significance of microstructural design over crystalline quality for achieving long-term cyclability. Our study sheds light on the interplay between calcination temperature and microstructural evolution, proposing the critical temperature as a key criterion for single-crystal synthesis.

Janus stainless steel mesh-based membrane with asymmetric wettability for highly efficient gravity-driven oil-water emulsion separation

With the asymmetric wettability of the membrane due to its unique transmission features and functions, the application of oil-water separation achieved rapid development. Nevertheless, their practical application is severely restricted due to poor mechanical durability and low flux in the absence of external pressure. Herein, the Janus ZIF-8/stainless steel mesh/polydopamine (DZIF-8/SSM/PDA) membrane was successfully prepared using electrodeposition, in-situ growth, and shell ligand exchange reaction methods. The Janus membrane surface was created through the combination of 5, 6-dimethylbenzimidazole (DMBIM) modified superhydrophobic nanoparticles ZIF-8 (DZIF), and PDA, exhibiting underwater superoleophobicity (UWOCA 156°), superhydrophobicity (WCA 154°), and excellent anti-oil (light and heavy oil) pollutants ability. By manipulating the molecular repulsion forces on the Janus membrane surface, a stable interfacial hydration layer is created in conjunction with the micro-nano structure. This combination enables the achievement of interfacial demulsification and gravity-driven separation of emulsified oil, according to the Molecular Dynamics (MD) simulation process. The water-in-oil emulsion achieved an oil flux of 601 L m−2 h−1 with a separation efficiency of 99.1 %, while the oil-in-water emulsion demonstrated a water flux of 62 L m−2 h−1 with a separation efficiency of 99.7 %. The Janus DZIF-8/SSM/PDA demonstrated acid and alkali resistance, mechanical stability and reusability, and resistance to E. coli bacteria. Overall, this research anticipates advancing the production of durable asymmetric Janus membranes with superior separation efficiency under gravity, providing a novel solution for oil-water separation.

Ultrathin, Mechanically Durable, and Scalable Polymer-in-Salt Solid Electrolyte for High-Rate Lithium Metal Batteries.

Polymer-in-salt solid-state electrolytes (PIS SSEs) are emerging for high room-temperature ionic conductivity and facile handling, but suffer from poor mechanical durability and large thickness. Here, Al2O3-coated PE (PE/AO) separators are proposed as robust and large-scale substrates to trim the thickness of PIS SSEs without compromising mechanical durability. Various characterizations unravel that introducing Al2O3 coating on PE separators efficiently improves the wettability, thermal stability, and Li-dendrite resistance of PIS SSEs. The resulting PE/AO@PIS demonstrates ultra-small thickness (25µm), exceptional mechanical durability (55.1MPa), high decomposition temperature (330°C), and favorable ionic conductivity (0.12 mS cm-1 at 25°C). Consequently, the symmetrical Li cells remain stable at 0.1mA cm-2 for 3000 h, without Li dendrite formation. Besides, the LiFePO4|Li full cells showcase excellent rate capability (131.0 mAh g-1 at 10C) and cyclability (93.6% capacity retention at 2C after 400 cycles), and high-mass-loading performance (7.5mg cm-2). Moreover, the PE/AO@PIS can also pair with nickel-rich layered oxides (NCM811 and NCM9055), showing a remarkable specific capacity of 165.3 and 175.4 mAh g-1 at 0.2C after 100 cycles, respectively. This work presents an effective large-scale preparation approach for mechanically durable and ultrathin PIS SSEs, driving their practical applications for next-generation solid-state Li-metal batteries.

Self-assembly of modified cellulose nanocrystals on flexible fabric via hydrophobic force induction for versatile applications

Over the years, there has been a proliferation of superhydrophobic fabrics constructed by self-assembly techniques. However, most of these suffer from poor mechanical durability and chemical stability, while the complexity of the process severely limits their practical application in textiles with special functionalities. In this study, We have built a self-assembly coating with many advantages such as large specific surface area, ultra-fast, high particle utilization, and dense and homogeneous alignment of particles. We modified cellulose nanocrystals (m-CNCs) using a variety of hydrophobic monomers, and the modified cellulose nanocrystals were suspended in a solution of isopropanol-containing end-hydroxy polysiloxane (MSDS) and hydrogen-containing polysiloxane (PHMS). The silicone system was used to treat a cotton fabric to obtain a superhydrophobic fabric by hydrophobically inducing modified cellulose nanocrystals to self-assemble on the fibre surface. Unlike many previous studies, owing to the m-CNC particles being chemically bonded between the multilayer nanostructure and the fabric, the coating had excellent mechanical durability and remained superhydrophobic after abrasion by sandpaper or peeling with tape. In addition, the nanostructure of the coating surface trapped air in the surface pores, preventing the penetration of H+, Na+, Cl−, and OH− in liquids; thus, the fabric remained hydrophobic both under extreme solution conditions and after soaping cycle tests, showing excellent stability and cycling ability. At the same time, the breaking strength of the fabric is improved after finishing, and the wearability is almost unchanged. Coated fabrics have good potential in the fields of self-cleaning, anti-staining, oil absorption, and oil–water separation.

The Interconnecting Process and Sensing Performance of Stretchable Hybrid Electronic Yarn for Body Temperature Monitoring.

Flexible and stretchable electronic yarn containing electronic components (i.e., hybrid electronic yarn) are essential for manufacturing smart textile garments or fabrics. Due to their low stretchability and easy interconnection fracture, previously reported hybrid electronic sensing yarns have poor mechanical durability and washability. In order to address this issue, a stretchable hybrid electronic yarn for body temperature monitoring was designed and prepared using a spandex filament as the core yarn and a thin enameled copper wire connected with a thermal resistor as the wrapping fiber. The temperature sensing performance of different hybrid electronic yarn samples was evaluated using the following three types of interconnection methods: conductive adhesive bonding, melt soldering, and hot pressure bonding. The optimal interconnection method with good sensing performance was determined. Furthermore, in order to improve the mechanical durability of the hybrid electronic yarn made using the optimal interconnection method, the interconnection area was encapsulated with polymers, and the effect of polymer materials and structures on the temperature-sensing properties was evaluated. The results show that traditional wrapping combined with hot pressing interconnection followed by tube encapsulating technology is beneficial for achieving high stretchability and good temperature-sensing performance of hybrid electronic yarn.

A review of the mechanical properties and durability of basalt fiber recycled concrete

Basalt fiber (BF) is an emerging environmentally-friendly fiber. Adding basalt fiber can improve the deficient recycled concrete's poor mechanical properties and durability. By reviewing nearly 120 related papers, the effects of variables such as BF content and length (0–1.5%, 9–18 mm), recycled aggregate substitution rate (0–100%), and cement mix ratio (w/b, 0.25–0.45) on the mechanical and durability properties of basalt fiber-reinforced recycled concrete (BFRAC) were discussed. Due to the presence of vulnerable interfacial transition zones, the mechanical properties of recycled concrete (RAC) continuously deteriorate over time. However, by adding an appropriate amount of basalt fiber, it is possible to improve these structural defects by forming a network structure that enhances cracking resistance within the matrix and improves interface bonding strength among other benefits. Consequently, this significantly improves the overall mechanical properties of RAC. Additionally, while incorporating recycled aggregate (RA) may reduce compressive strength initially, this deficiency can be mitigated through the proper inclusion of fibers in RAC mixtures. Optimal compressive strength for RAC is achieved with a replacement ratio between 25–50% and a fiber content ranging from 0.2–0.3%. Furthermore, properly incorporating fibers into RAC greatly enhances splitting tensile strength and flexural strength as well; specifically achieving optimal splitting tensile strength with a replacement ratio between 40%− 50%, a fiber content at 0.3%, and utilizing fibers with lengths measuring approximately 12 mm long. The primary cause for poor frost resistance in RAC lies within numerous micro-cracks and pores present in RA aggregates which lead to high water absorption rates ultimately reaching critical water saturation points resulting in freeze-thaw damage occurrences during exposure to freezing conditions. When exposed to sulfate attack, RAC undergoes a chemical reaction with sulfate ions present in the concrete, leading to the formation of numerous expansion products that negatively impact concrete performance. Progressive dehydration of hydration products under high-temperature conditions leads to a porous structure within the concrete matrix. Incorporating fibers can impede microcrack expansion during freeze-thaw, sulfate attack, and high-temperature environments, thus enhancing the erosion resistance of RAC. Compared to conventional concrete, interfacial bonding in RAC is less tight and more vulnerable to damage in complex environments. Current research on RAC suggests that the mechanism behind its damage under complex freeze-thaw load coupling environments remains unclear. It is recommended that future studies combine large-scale component tests with computational simulations to address this issue.

Additive construction using enhanced earthen-based composites: Improvement of the mechanical strength and water durability using chitosan and agave fibers

3D printing has emerged as a revolutionary technology with potential applications in the construction industry. However, the prevalent use of ordinary cement in most 3D printing formulations results in significant greenhouse gas emissions during 3D printing construction. In contrast, earthen-based composites are an eco-friendly alternative for building materials. However, as a construction material, earth presents poor mechanical strength and low durability against water erosion. This study aims to obtain earthen-based composites with suitable mechanical and durability properties to investigate their extrudability and buildability in tests. It also explores the effects of incorporating short sisal fibers (l/d ratio = 138.7) and chitosan (DD = 91%, Mw = 598 kDa) to improve strength and water durability in earthen-based composites for 3D printing purposes. Chitosan is a natural macromolecule derived from a waste product from the food industry, whereas sisal fibers are obtained from the Agave sisalana plant. The change in compressive strength was analyzed through uniaxial compression. Water durability was evaluated by measuring the water contact angle, total and capillary water absorption, and accelerated erosion tests. The results indicate that the use of 3.0% (w/v) aqueous solution of chitosan and 1.0% (w/w) of sisal fibers have an important effect on the hardening and water durability properties of earthen-based composites. This study suggests that these materials could serve as natural additives to enhance the mechanical properties and water durability of new eco-friendly construction materials for 3D printing. In conclusion, this study demonstrates that appropriate formulations with natural and eco-friendly additives can lead to stabilized earthen-based composites with suitable printing, mechanical and durability properties for 3D printing applications in construction materials.

Fabrication of recyclable and biodegradable PBAT vitrimer via construction of highly dynamic cross-linked network

The emergence of biodegradable materials has not satisfactorily addressed the issue of plastic waste management, owing to their high cost and poor mechanical performance and durability that impair their potential to replace traditional plastics. In this study, a dynamic cross-linked network with robust remoldability was fabricated in PBAT. Transesterification catalysts were employed to catalyze the reaction of β-hydroxyl groups produced from the branching reaction of polyester end groups and epoxy branching agents with the abundant ester groups of PBAT to produce biodegradable PBAT vitrimers. Swelling experiments, DMA tests and stress relaxation experiments confirmed the presence of the dynamic cross-linking structure, while rheological analysis demonstrated that the highly catalyst-loaded PBAT vitrimer dynamic cross-linked network could achieve chain relaxation by exchanging bonds quickly at physical entanglement and chemical cross-linking points. Multiple recycling experiments further demonstrated that the robust dynamic cross-linked network of PBAT vitrimers possessed both strong stress relaxation ability and remoldability, thus conferring excellent recyclability to PBAT. Upon recycling 4 times, the elongation at break of the PBAT vitrimer remained at 93.46 % (with a tensile strength retention of 85.99 %), whereas the raw PBAT could only maintain an elongation at break of 28.01 % (with a tensile strength retention of 56.09 %). TGA and hydrolysis experiments revealed that PBAT vitrimers exhibited better degradation performance relative to raw PBAT. PBAT vitrimers, featuring excellent mechanical performance and durability, can be recycled several times in easily recyclable settings, thus reducing production costs, and finally biodegrade after disposal, thereby serving as a viable replacement for traditional plastics. This straightforward and practicable approach provides a solution for plastic waste management.

Thin alumina-coated polyoxometalates on gold-titania half-shell array photoanode for sustainable plasmonic water oxidation

In solar water splitting, the poor chemical and mechanical durability of photoanode materials under oxidative environments has been raised as a crucial issue. Despite promising water oxidation activity, the stable immobilization of polyoxometalates (POMs) onto photoanodes is very challenging. Here we report sustainable photoelectrochemical water oxidation through the deposition of catalytic POMs onto a plasmonic Au/TiO2 photoanode, followed by the atomic layer deposition of a thin Al2O3 layer. Vacuum deposition techniques were used with polystyrene nanospheres as sacrificial templates to fabricate an Au/TiO2 half-shell array as a photoanode with strong plasmonic absorption and excellent stability in aqueous media. The thin Al2O3 layer serves as a protective layer for [Co4(H2O)2(PW9O34)2]10- (Co4POMs) attached to Au/TiO2 half-shells functionalized with cysteamines. The Al2O3 layer increased the photocurrent and delayed current attenuation by preventing the dissociation of Co4POMs from the surface during the water oxidation. A thicker Al2O3 layer exhibited a higher protection effect but reduced the catalytic activity of Co4POMs in the early stage of water oxidation due to the limited exposure of Co4POMs to electrolytes. Furthermore, regardless of the POMs, the Al2O3 layer also passivated the TiO2 surface, improving electron transfer through the POMs/Au half-shell structure. This work suggests that the catalyst/plasmonic photoelectrode with a thin protection layer is a promising alternative to conventional semiconductor-based photoelectrodes for sustainable and efficient water oxidation.

Scalable fabrication of a robust asymmetric superwetting Janus mesh by facile spray-coating for oil–water emulsions separation

Janus membrane with asymmetric wettability are emerging separation materials for the purification of emulsified oil–water mixtures, however, their poor mechanical durability and low-flux without external pressure severely limit their practical application. Herein, a robust superwetting Janus mesh demonstrating a high water contact angle (WCA) difference up to 157° was developed by simply spraying on the stainless steel mesh (SSM), via the superhydrophobic fluorocarbon resin/polyvinylidene fluoride/1H, 1H, 2H, 2H-perfluorodecyltrichlorosilane modified titanium dioxide@carboxylated CNTs (FEVE/PVDF/F-TiO2@CNTs) layer and a superhydrophilic layer consisting epoxy resin/ethylene imine polymer/sodium perfluorooctanoate modified bentonite (EP/PEI/F-Bentonite). By carefully adjusting the surface polar-nonpolar molecule repulsion based on the two oppositely bond energy side and incorporating nano/microstructures to form a stable interfacial oiling/hydration layer, the robust Janus mesh achieved interface demulsification and gravity separation of emulsified oil–water mixtures. The prepared Janus SSM exhibited excellent gravity-driven separation performance, achieving a flux up to 1508.6 L m−2h−1 for water-in-oil (W/O) emulsions, and 843.1 L m−2h−1 for oil-in-water (O/W) emulsions. Additionally, it exhibited high separation efficiency with water rejection above 99.9 % and oil rejection above 99.7 %. Moreover, the prepared Janus mesh with fine uniform nano/microstructures and functionalized groups demonstrated notable reusability and mechanochemical stability after 10 cycles of O/W and W/O emulsion filtration, 100 cycles of sandpaper abrasion, and strong acid/alkali immersion for 7 d. Overall, this study expected to facilitate the fabrication of a robust asymmetric superwetting Janus mesh with enhanced separation properties for highly efficient oily wastewater treatment.

Robust PVA/GO@MOF membrane with fast photothermal self-cleaning property for oily wastewater purification

The poor mechanical durability and weak fouling resistance of oil/water separation membranes severely restrict their applications in industry. Herein, a robust PVA/GO@MOF membrane with fast photothermal self-cleaning capability was developed through facile chemical crosslinking and suction-filtration strategies. Attributed to the powerful underwater superoleophobicity, the PVA/GO@MOF membrane exhibited extraordinary anti-oil adhesion even for high-viscosity crude oil and continuous crude oil emulsion purification capability with stable flux (1020 L m−2 h−1 bar−1) and exceptional efficiency (> 99.3%) even after 60 min. Most importantly, in comparison to reported photocatalytic self-cleaning oil/water separation membranes, the PVA/GO@MOF membrane can degrade organic contaminants more rapidly with a higher degradation rate (99.9%) in 50 min due to the superior photothermal conversion capacity. The synergistic photothermal and photocatalytic effects significantly enhanced photodegradation efficiency, which created opportunities for in-depth treatment of complex oily wastewater. Besides, the obtained membrane displayed excellent chemical and mechanical durability with underwater oil contact angle (UWOCA) above 150° even in harsh environments, such as corrosive solutions, UV irradiation, ultrasound treatment, abrasion experiment and bending test. Therefore, the developed PVA/GO@MOF membrane with robust durability and fast photocatalytic self-cleaning property is highly expected to purify oily wastewater and degrade organic pollutants.

Preparation of a Wear-Resistant, Superhydrophobic SiO2/Polymethyl Methacrylate Composite Coating on Aluminum Surface Processed with Nanosecond Laser.

Superhydrophobic coatings are limited by complex preparation processes and poor mechanical durability in practical applications. In this study, a mechanically robust superhydrophobic composite coating was applied to an aluminum surface that underwent processing with a nanosecond laser (referred to as a superhydrophobic aluminum surface). It exhibits a high water contact angle (WCA) of 158.81°, a low sliding angle (SA) of less than 5°, and excellent self-cleaning ability. The wear test shows its durability, and the corrosion test shows its excellent corrosion resistance. This study provides a framework for the preparation of robust superhydrophobic surfaces that may have potential applications in many fields.

Optimization strategies of microencapsulated phase change materials for thermal energy storage

Phase change materials (PCMs) have attracted much attention for their ability to store and release sizeable latent heat via the isothermal phase transition process. However, pure PCMs have the disadvantages of leakage and low thermal conductivity. Encapsulation technology has become a research hotspot, which can play an active role in improving these problems. Although the heat storage performance of microencapsulated phase change materials (MEPCMs) is better than that of pure PCMs, the disadvantages of high supercooling, poor mechanical durability still needs to be improved. There are some reviews on the encapsulation of PCMs or the practical application of MEPCMs. Still, few reviews focus integrally on thermal storage performance optimization strategies and the preparation of MEPCMs. We introduce the encapsulation methods of PCMs including physical, chemical, and physical-chemical methods, and present the advantages and disadvantages of these methods. Increasing thermal conductivity, reducing supercooling, and enhancing mechanical durability are vital to improve the performance of MEPCMs. These measures include modifying the shell materials, changing the core-shell structure and core-shell ratio, adding nucleating agents, etc. We hope that this review will serve as a useful guide and contribute to the preparation and performance optimization of MEPCMs.

Reinforced integrated membrane electrode assembly based on ionomer wet-binding and ePTFE reinforcement strategy for proton exchange membrane fuel cells

Optimizing the structure of the membrane electrode assembly (MEA) is an effective strategy for improving the performance and durability of proton exchange membrane fuel cells. To prepare reinforced integrated MEAs, in this study, a wet ionomer solution coating with expanded polytetrafluoroethylene (ePTFE) reinforcement was deposited on a cathode gas diffusion electrode (GDE) surface and then wet-binding with the anode GDE. Reinforced integrated MEAs with different layers of ePTFE were prepared and their performance and mechanical durability were compared. The peak power densities of MEAs with single- and double-layer ePTFE reinforcements are 1.26 and 1.19 W cm−2, respectively, which are higher than that of conventional catalyst-coated membrane (CCM)-type MEA (1.04 W cm−2). The common defects in the direct membrane deposition-type MEA, including poor gas barrier ability and mechanical durability of the MEA, are essentially eliminated. The reinforced integrated MEAs have lower degradation than CCM-type MEA in humidity cycling conditions due to the restrictive effect of the ePTFE reinforcement in PEM and the supporting effect of the GDEs on both sides of the PEM. In addition, the double layers of the ePTFE reinforcement endow the MEAs with higher stability and further alleviated the mechanical degradation. The strategy of ionomer wet-binding and multilayered reinforcement provides a novel approach for fabricating MEAs with high performance and mechanical durability.

Pellet Production from Pruning and Alternative Forest Biomass: A Review of the Most Recent Research Findings.

Typically, coniferous sawdust from debarked stems is used to make pellets. Given the high lignin content, which ensures strong binding and high calorific values, this feedstock provides the best quality available. However, finding alternative feedstocks for pellet production is crucial if small-scale pellet production is to be developed and used to support the economy and energy independence of rural communities. These communities have to be able to create pellets devoid of additives and without biomass pre-processing so that the feedstock price remains low. The features of pellets made from other sources of forest biomass, such as different types of waste, broadleaf species, and pruning biomass, have attracted some attention in this context. This review sought to provide an overview of the most recent (2019-2023) knowledge on the subject and to bring into consideration potential feedstocks for the growth of small-scale pellet production. Findings from the literature show that poor bulk density and mechanical durability are the most frequent issues when making pellets from different feedstocks. All of the tested alternative biomass typologies have these shortcomings, which are also a result of the use of low-performance pelletizers in small-scale production, preventing the achievement of adequate mechanical qualities. Pellets made from pruning biomass, coniferous residues, and wood from short-rotation coppice plants all have significant flaws in terms of ash content and, in some cases, nitrogen, sulfur, and chlorine content as well. All things considered, research suggests that broadleaf wood from beech and oak trees, collected through routine forest management activities, makes the best feasible feedstock for small-scale pellet production. Despite having poor mechanical qualities, these feedstocks can provide pellets with a low ash level. High ash content is a significant disadvantage when considering pellet manufacture and use on a small scale since it can significantly raise maintenance costs, compromising the supply chain's ability to operate cost-effectively. Pellets with low bulk density and low mechanical durability can be successfully used in a small-scale supply chain with the advantages of reducing travel distance from the production site and storage time.

Self-Assembling Ultrathin MXene/Cellulose Nanofiber/MXene Composite Film for High-Performance Electromagnetic Interference Shielding

Ti3C2T[Formula: see text] MXene films exhibited good electromagnetic interference (EMI) shielding performance. However, the poor mechanical property and durability of Ti3C2T[Formula: see text] MXene films limited their commercial application. Herein, the ultrathin flexible conductive MXene/cellulose nanofiber (CNF)/MXene composite films with “sandwich” structure were successfully prepared by a simple vacuum-assisted filtration process. The addition of CNF can shield more electromagnetic microwaves (EMWs) via multiple reflections in the inner space and enhance the mechanical property of composite films by effectively welding the loosely MXene together. The composite film exhibited excellent EMI shielding effectiveness (up to 54.68 dB) at an ultrathin thickness (about 76 [Formula: see text]m) as well as high electrical conductivity (up to 1610.51 S/m), which was mainly attributed to the hierarchical lamellar “sandwich” structure, where CNF was bonded to Ti3C2T[Formula: see text] MXene. The prepared flexible conductive composite films with brilliant EMI shielding effectiveness and good mechanical property possessed promising potential in various fields such as electromagnetic wave protection, weaponry and wearable electronics.