Porous Structure Research Articles

Enhanced n-butanol sensing performance of Co3O4/LaFeO3 nanocomposites

Co3O4 and LaFeO3 composites were successfully prepared by sol–gel method and hydrothermal method. The morphology test results showed that Co3O4 nanoparticles uniformly attached to the surface of LaFeO3 nano-bricks. Gas sensing tests results showed that sensors based on Co3O4/LaFeO3 have lower operating temperatures and higher response than those of pure Co3O4 and LaFeO3, and better performance in response/recovery time and selectivity. The sample of Co3O4 and LaFeO3 with molar ratio of 1:1 is the best among all samples, with the response of 54.21 for 100 ppm n-butanol and 6.54 for 1 ppm n-butanol at 150 °C. The heterojunction and porous structure of Co3O4/LaFeO3 composite materials are the main reasons for improving its gas sensing performance.

Cardiac Matrix-Derived Granular Hydrogel Enhances Cell Function in 3D Culture.

Hydrogels derived from decellularized porcine myocardial matrix have demonstrated significant potential as therapeutic delivery platforms for promoting cardiac repair after injury. Our previous study developed a fibrin-enriched cardiac matrix hydrogel to enhance its angiogenic capacities. However, the bulk hydrogel structure may limit their full potential in cell delivery. Recently, granular hydrogels have emerged as a promising class of biomaterials, offering unique features such as a highly interconnected porous structure that facilitates nutrient diffusion and enhances cell viability. Several techniques have been developed for fabricating various types of granular hydrogels, among which extrusion fragmentation is particularly appealing due to its adaptability to many types of hydrogels, low cost, and high scalability. In this study, we first confirmed the effects of the bulk cardiac matrix hydrogel on the viability of encapsulated human umbilical vein endothelial cells and human mesenchymal stem cells. We then tested the feasibility of producing granular hydrogels from both cardiac matrix and fibrin-enriched cardiac matrix through cellular cross-linking of microgels fabricated by extrusion fragmentation. Afterward, we examined the roles of the produced granular hydrogels in the embedded cells and cell spheroids. Our in vitro data demonstrate that cardiac matrix-derived granular hydrogels support optimal viability of encapsulated cells and promote sprouting of human mesenchymal stem cell spheroids. Additionally, granular hydrogel derived from fibrin-enriched cardiac matrix accelerates angiogenic sprouting of embedded human mesenchymal stem cell spheroids. The results obtained from this study lay an important foundation for the future exploration of using cardiac matrix-derived granular hydrogels for cardiac cell therapy.

Synchronous vacuum hot pressing ultra-high performance geopolymer: Ultrafast polymerization and early strength development

To overcome the application bottleneck of geopolymer in high-end industries, this study aims to develop ultra-high performance geopolymer products. By employing Synchronous Vacuum Hot Pressing, we have significantly enhanced the rate of polymerization and mechanical properties of Geopolymer based on Metakaolin-Fly Ash. The influence of Si/Al ratio, alkali equivalent, and molding time on the geopolymerization process, mechanical properties, and microstructure of geopolymers was investigated, while elucidating the underlying mechanisms. The compressive strength of SVHP-MFG reaches 90.92 MPa when the Si/Al ratio is 2, alkali equivalent is 8 %, and molding time is 30 min, owing to increased production of aluminosilicate gels and matrix structure densification. The ongoing reaction of unreacted particles and the subsequent transformation from "alumina-rich gel" to "silica-rich gel" in later stages further enhance the mechanical properties of the material. Additionally, the mean pore diameter of Synchronous vacuum hot pressing of metakaolin-fly ash geopolymer measures below 13.24 nm, thereby significantly enhancing the pore structure of the geopolymer. The synchronous vacuum hot pressing metakaolin fly ash-based geopolymers synthesized in this study represents a novel category of ultra-high performance ceramic-like geopolymers, exhibiting exceptional early strength and early stability. The research aims to promote the application of geopolymer in high-end industry and provide technical and theoretical support for the development of ultra-high performance geopolymer based products.

Direct-through channels of ZIF-8 composite membranes via in-situ PolyBMA sealing: Radical-induced phase transformation and dye removal efficiency

Metal-organic frameworks (MOFs)-based hybrid composite membranes are promising candidates for achieving highly efficient water purification. In this study, a facile, novel pressure-induced filtration method involving in-situ polymerization of butyl methacrylate (BMA) was proposed for sealing ZIF-8 nanoparticles on top of polyethersulfone (PES) ultrafiltration membrane support. The developed (ZIF-8+polyBMA)/PES composite membranes with thin toplayers of <1 μm present attractive water permeance (up to 31 LMH/bar) and good rejection of Congo red (99.2 %) and Methylene blue (99.1 %). The ZIF-8 particles served as direct-through channels with superior separation performance due to their high porosity and tunable pore structure, while the interstices were successfully sealed with polyBMA by in-situ polymerization, as demonstrated by SEM and dye removal experiments. It was found that the morphology of ZIF-8 transformed from a rhombic dodecahedron to two-dimensional hexagonal nanosheets during the fabrication process. We hypothesize that this surprising phenomenon is caused by the reaction of the initiators (Na2S2O5 and K2S2O8) that generate the hydroxyl and sulfate radicals attacking and transforming the Zn-MIM bond network of ZIF-8. However, insights into the structural changes need to be further investigated to understand the mechanism involved.

In-Situ construction of Bulge-like microstructures in sugarcane-based superhydrophobic membranes for efficient separation of water-in-oil emulsions

The separation of oil/water pollution is of great importance to environmental protection. However, the development of superwetting materials for efficient separation of surfactant-stabilized oil/water emulsions still faces challenges. As agricultural waste, sugarcane straw contains many hydrophilic groups and multilayered pore structures, making it suitable for purifying oil/water emulsions by simple chemical modification treatments. Herein, sugarcane-based superhydrophobic membranes (SSMs) were prepared by a facile vacuum impregnation method in hexadecyltrimethoxysilane (HDTMS) solution. The unique bulge-like microstructures were constructed in the intrinsic pores of sugarcane, which significantly increased the roughness and resulted in superhydrophobicity with the water contact angle of 153.5°. More importantly, the bulge-like structure is easy to break the emulsion and thus SSMs offer excellent separation efficiency (> 99 %), suitable fluxes (368 L•m−2•h−1) and strong cycling stability for surfactant-stabilized water-in-oil emulsions. In addition, SSMs can separate oil/water mixtures and directly adsorb oil from water with adsorption rates exceeding 99 %. SSMs have good durability and anti-mold adherence properties, and they do not lose their unique wetting properties even in harsh environments. More importantly, SSMs can be degraded in soil at the end of their life cycle, avoiding secondary pollution for the environment. This simple, in-situ impregnation technique offers a novel way to create green, inexpensive and stable biomass membranes for effective water-in-oil emulsion separation, showing great promise for use in oily wastewater treatment.

Obtaining Highly Efficient Radon Adsorbents by Adjusting the Pore Structure of Bamboo Charcoal with Particle Size Fractionated Activation.

To achieve highly efficient adsorbents for radon (Rn), this study prepared bamboo activated carbon (BAC) using bamboo charcoal as the precursor and KOH and NaOH as activators and employed a method of activation by adjusting the pore structure through particle size fractionation. Under the same activation conditions, KOH was consumed less and showed better Rn adsorption performance than NaOH, and the solid milling method saved more activator dosage compared to the liquid immersion method. After carbonizing the bamboo, the highest Rn adsorption coefficients of the bamboo charcoal activated with particle size fractionation (0.43-0.85, 0.25-0.43, 0.18-0.25, and <0.18 mm) were 8.41 ± 0.05, 10.03 ± 0.24, 9.31 ± 0.01, and 8.15 ± 0.21 L/g, respectively under N2 conditions (at a temperature of 25 °C and humidity of 35%), which were significantly greater than those of bamboo charcoal with overall activation (7.05 ± 0.23 L/g). After optimization, all of the bamboo charcoals with different particle sizes had the highest volume ratio for pores with a diameter of 0.77 nm. BC0.43-0.85K1.25 and BC0.25-0.43K0.75 maintained 95.74 and 92.36%, respectively, of the original adsorption coefficient after 5 cycles of regeneration under nitrogen. As the bamboo charcoal particle size decreased, the optimal mass ratio of alkali/carbon also decreased. This indicates that particle-size-fractionated activation can reduce the raw material and activator waste. The optimized BAC has a significantly higher Rn adsorption coefficient than the currently used coconut shell activated carbon (4.13 ± 0.51 L/g), making it an efficient and economical adsorbent with excellent application value for radon removal.

Research on Efficient Electromagnetic Shielding Performance and Modulation Mechanism of Aero/Organo/Hydrogels with Gravity-Induced Asymmetric Gradient Structure.

To eliminate electromagnetic pollution, it is a challenging task to develop highly efficient electromagnetic shielding materials that integrate microwave absorption (MA) performance with high shielding capability and achieve tunability in shielding performance. Asymmetrically structured aero/organo/hydrogels with a progressively changing concentration gradient of liquid metal nanoparticles (LMNPs), induced by gravity, are prepared by integrating the conductive fillers Ti3C2Tx MXene and LMNPs into a dual-network structure composed of polyvinyl alcohol and cellulose nanofibers. Benefiting from the unique structure, which facilitates the absorption-reflection-reabsorption process of electromagnetic waves along with conductive fillers and the porous structure, three types of gels demonstrate efficient shielding performance. HPCML achieves a total shielding effectiveness (SET) of up to 86.9dB and a reflection shielding effectiveness (SER) of as low as 2.85dB. Especially, APCML, with an ultra-low reflection coefficient (R) of 6.4%, achieves compatibility between shielding performance and MA properties. The relationship between dispersing media (air, water, and glycerol/water) and the shielding performance of aero/organo/hydrogels is explored, thereby achieving modulation of the shielding performance of the gel system. The work has paved a clear path for integrating absorption and shielding capabilities into a composite material, thereby providing a prototype of a highly efficient shielding material with MA performance.

Porous Monolithic Perovskite Structures for High-Temperature Thermochemical Heat Storage in Concentrated Solar Power (CSP) Plants and Renewable Electrification of Industrial Processes

A novel approach towards thermal energy storage of surplus renewable energy (RE) is introduced via a hybrid thermochemical/sensible heat storage concept implemented with the aid of porous structures made of redox metal oxides, capable of reversible reduction/oxidation upon heating/cooling in direct contact with air, accompanied, respectively, by endothermic/ exothermic heat effects and demonstrating fully reversible dimensional changes under cyclic operation. The proposed modular storage units can be heated during the day to a level exceeding the metal oxide’s reduction onset temperature either by hot air streams from air-operated Concentrated Solar Power (CSP) tower plants or via surplus/cheap RE-electricity from photovoltaics, wind, or other renewable sources (“charging”/energy storage step). When this RE sources become non-available or upon demand, the fully charged system can transfer its energy to a controlled airflow that passes through the porous oxide block and initiates the exothermic oxidation of the reduced metal oxide. Thus, a hot air stream is produced which can be used to provide electricity or exploitable heat for industrial processes. The present work elaborates on the operating principles and the potential application of this concept and reports progress in the preparation and shaping of reticulated porous ceramics (RPCs also known as “ceramic foams”) from CaMnO3-based perovskite compositions and their preliminary testing with respect to cyclic reduction-oxidation.

Study on the rheological properties and compressive strength mechanism of geopolymer cementitious materials for solid waste

The large-scale storage of industrial solid waste can cause serious environmental pollution issues. Utilizing industrial solid waste to produce green cementitious materials is an effective alternative to cement. This study utilizes steel slag (SS) and calcium carbide residue (CCR) as alkaline activators, combining them with blast furnace slag (BFS) and fly ash (FA) to create SCBF cementitious materials. Investigate the flowability, setting time, rheological properties, compressive strength, pore structure, and microscopic morphology of SCBF cementitious materials under different conditions and conduct molecular dynamics simulations. The research findings indicate that with an increase in BFS content, the flow performance of SCBF decreases, setting time shortens, plastic viscosity and yield stress gradually increase, UCS increases, and the proportion of harmful pores inside the samples decreases. When SS:CCR:BFS:FA is at a ratio of 25:25:30:20, with an increase in curing temperature, the UCS of samples shows a trend of first increasing and then decreasing. The proportion of harmful pores follows a pattern of initial decrease followed by an increase. When the curing temperature is 30 °C, the proportion of harmful pores is 0.31 %, reaching a local minimum, and the UCS strength reaches 13.83 MPa. In the raw materials, SiO2 and Al2O3 aggregate with Ca2+ in an alkaline environment to form C-(A)-S-H three-dimensional network gel. The potential energy, kinetic energy, non-bonding energy, and total energy of Tobermorite 14 Å crystals gradually increase with higher curing temperatures, with the most intense molecular motion occurring at 60 °C. The research findings are beneficial for promoting the use of industrial solid waste to manufacture green cementitious materials as substitutes for cement-based materials. They also provide a theoretical basis for the industrial application of high-temperature-cured solid waste cementitious materials.

Mineralized Biopolymers-Based Scaffold Encapsulating with Dual Drugs for Alveolar Ridge Preservation.

Mineralization of scaffolds is essential for alveolar ridge preservation and bone tissue engineering, enhancing the mechanical strength and bioactivity of scaffolds, and promoting better integration with natural bone tissue. While the in situ mineralization method using concentrated SBF solutions is promising, there is limited comprehensive research on its effects. In this study, it is demonstrate that soaking gelatin/alginate scaffolds (GAS) in fivefold concentrated SBF significantly reduces the mineralization time to 3-7 days but also leads to considerable degradation and loss of the scaffold's original microstructure. The ratio of gelatin to alginate is optimized to improve the properties of GAS. The optimized GAS sample, when soaked in concentrated SBF to form GAS/HAp, exhibited hydroxyapatite (HAp) crystal formation starting from day 3, with mature hexagonal crystals forming by day 7. However, this process also caused significant decomposition and deformation of the scaffold's pore structure. Additionally, the biocompatibility of GAS and GAS/HAp is evaluated through in vitro, in ovo, haemolysis, and anti-ROS assays. The findings highlight the impact of SBF5× on the mineralization of GAS, laying the groundwork for further research in alveolar ridge preservation and bone tissue engineering.

Solar-Adaptive Cooling Blocks Composed of Recycled Fabric.

Radiative cooling technologies have had a significant impact on advancing carbon neutrality efforts by significantly improving the passive cooling efficiency. The tandem of conduction and radiation enables solar-adaptive radiative cooling through the insulating effect of materials along with solar absorption, which affects the thermal state of materials and enhances radiative thermal transfer from the surface under solar irradiation. This enhancement is achieved by utilizing the porous polymeric structure of materials, which facilitates improved conduction pathways along with solar reflectance, while maintaining the effective emission of thermal radiation. In this particular scenario, blocks, which were made of recycled fibers, offer a great opportunity as solar-adaptive cooling materials, enabling their easy deployment for cooling applications. Herein, we have fabricated a porous block using fiber wastes that combines strong solar reflectance (92%) at the 1 μm region and high thermal infrared emittance (∼75%) at the 10 μm region. The combination of effective solar reflection and thermal infrared emission allows the fiber block to achieve a high cooling performance of approximately 68 W/m2 under solar irradiation. In addition, the fiber block works effectively for insulation during the night, thereby enhancing its heat retention capabilities. The economic and environmental advantages of the fiber block make it a cost-competitive and sustainable choice for near-market cooling technologies. This design is anticipated to expand the practical application range of passive cooling.

Experimental study on repairing rat abdominal wall defect with chitosan hydrogel/polypropylene mesh composite

To investigate the improvement effects and mechanisms of composite chitosan (CS) hydrogel on traditional polypropylene (PP) mesh for repairing abdominal wall defects. CS hydrogel was prepared via physical cross-linking and then combined with PP mesh to create a CS hydrogel/PP mesh composite. The internal structure and hydrophilicity of the composite were characterized using macroscopic observation, upright metallographic microscope, scanning electron microscopy, and water contact angle measurements. The performance of the composite (experimental group) in resisting cell adhesion and supporting cell infiltration was assessed through fibroblast (NIH-3T3) infiltration experiments and human umbilical vein endothelial cells (HUVECs) tube formation assays, and simple cells were used as control group. Finally, a bilateral abdominal wall defect model (1.5 cm×1.0 cm) was established in 18 Sprague Dawley rats aged 8-10 weeks, with the composite used on one side (experimental group) and PP mesh on the other side (control group). The effects on promoting wound healing, preventing adhesion, angiogenesis, and anti-inflammation were investigated through macroscopic observation, histological staining (HE and Masson staining), and immunohistochemical staining (CD31, CD68). The composite appeared as a pale yellow, transparent solid with a thickness of 2-3 mm, with the PP mesh securely encapsulated within the hydrogel. Scanning electron microscopy revealed that the hydrogel contained interconnected pores measuring 100-300 μm, forming a porous structure. Contact angle measurements indicated that CS hydrogel exhibited good hydrophilicity, while PP mesh was highly hydrophobic. In vitro cell culture experiments showed that DAPI staining indicated fewer positive cells in the experimental group after 1 day of culture, while the cells in control group covered the entire well plate. After 3 days of culture, the cells in experimental group were spherical and displayed uneven fluorescence, suggesting that the material could reduce cell adhesion while supporting cell infiltration. HUVECs tube formation experiments demonstrated an increase in cell numbers in experimental group with a trend towards tube formation, while cells in control group were sparsely distributed and showed no migration. In the rat abdominal wall defect repair experiment, results showed that after 1 week post-surgery, the experimental group had tissue and blood vessels infiltrating, and by 4 weeks, the integrity was well restored with significant regeneration of muscle and blood vessels, while the control group exhibited adhesions and incomplete healing. HE staining results indicated weaker cell infiltration in the experimental group, with cell density significantly higher than that of the control group at 2 and 4 weeks post-surgery ( P<0.05). Masson staining revealed that collagen fibers in the experimental group were arranged neatly, with significantly increased collagen content at 2 weeks post-surgery ( P<0.05), while collagen content was similar in both groups at 4 weeks ( P>0.05). Immunohistochemical staining showed that CD31-positive cells were evenly distributed between muscle layers in the experimental group, whereas the control group exhibited notable defects. At 2 weeks after operation, the CD31-positive cell ratio was significantly higher than that in the control group ( P<0.05); at 2 and 4 weeks after operation, the CD68-positive cell ratio in the experimental group was significantly lower than that in the control group ( P<0.05). CS hydrogel has a positive effect on preventing adhesions and promoting wound healing, exhibiting anti-inflammatory and pro-angiogenic properties during the healing process. This provides a promising strategy to address challenges related to abdominal adhesions and reconstruction.

Eco-friendly remedies for soil contamination: manufacturing and analysis of nanobiochar using sugarcane bagasse and olive mill waste.

Soil degradation poses a significant challenge to Egypt's agriculture, making resource optimization essential. Nanobiochar presents a promising solution for pollutant removal; however, its low yields may hinder commercialization. This study investigates the production of biochar from sugarcane bagasse and olive mill waste, focusing on its composition, morphology, and effectiveness in soil immobilization. Advanced techniques like SEM, TEM, and FTIR were used to characterize the nanobiochar, highlighting its potential as a sustainable solution to soil contamination. The study revealed that ZnCl2 treatment significantly lowers pH, while KOH modification raises it. Surface morphology analysis showed that SCB biochar exhibited a highly porous structure, while OMW biochar had less porous edges and irregular oval-shaped pores. The effects of biochar activation on the availability of heavy metals like Ni, Pb, and Mo (in mg.Kg-1) were also examined. Ni concentrations decreased from 1.27mg.Kg-1 in untreated biochar (NA) to 0.78mg.Kg-1 in KOH-treated biochar (KA) and 0.67mg.Kg-1 in ZnCl2-treated biochar (ZnA). Pb levels dropped from 7.7mg.Kg-1 in NA to 5.2mg.Kg-1 in KA and slightly to 4.74mg.Kg-1 in ZnA. Mo showed a similar trend, with the highest concentration in NA at 1.21mg.Kg-1, followed by 0.88mg.Kg-1 in KA and 0.75mg.Kg-1 in ZnA. Overall, OMW nanobiochar demonstrated a greener, more sustainable solution to soil contamination compared to SCB nanobiochar.

A hierarchical host microstructure enables regulated inner Li deposition for stable Li metal electrodes

Dendritic lithium (Li) deposition is a critical issue hindering the development of next-generation high-energy-density Li metal batteries (LMBs). Confining Li deposition within a three-dimensional host is a general strategy to suppress the volume expansion of the Li electrode. However, precise control of continuous Li growth in the pore space of the host is rarely investigated, which is a crucial issue to enable a high utilization ratio of the hosted Li for practical LMBs. Herein, a novel hierarchical host structure possessing a multifunctional secondary porous structure to regulate the continuous Li growth with high uniformity and reversibility is proposed. The secondary porous structure consisting of carbon nanotubes, nickel and Li2O-enriched solid electrolyte interphase is in-situ generated via lithiation reaction of a modified nickel foam scaffold, exhibiting high lithiophilicity, fast Li+ transportation and charge transfer. The LMB utilizing Li metal electrodes hosted by this rational structure achieved a stable cycling over 300 cycles with a practical LiFePO4 positive electrode (~2.5 mAh cm-2) at 0.5C/0.5C in the voltage window of 2.5-4.4 V. This work provides a novel approach to designing the host microstructure for constructing more stable Li metal electrode in practical LMBs.

Cyano-modified molecular cage silica gel stationary phase: Multi-functional chromatographic performance by high-performance liquid chromatography

This study successfully prepared different loading levels of cyano-functionalized RCC3 molecular cage silica gel stationary phase (RCC3-CN@SiO2) through aldehyde-amine condensation reaction and subsequent modification strategies. Fourier transform infrared spectroscopy, thermogravimetric analysis, nitrogen adsorption-desorption, and scanning electron microscopy confirmed the successful synthesis of RCC3-CN@SiO2 chromatographic stationary phase. The research demonstrates that due to hydrophobic/hydrophilic interactions, π-π interactions, hydrogen bonding, and size-selective porous structure, the stationary phase effectively separates moderately polar and weakly polar compounds in reversed-phase liquid chromatography (RPLC) mode, exhibiting hydrophobic selectivity comparable to the commercial DaisoC18-RP columns. Additionally, the tertiary amine and cyanogen groups on the molecular cage surface enhance the interaction with polar compounds, successfully separating nucleosides, sulfonamides, amino acids, and sugars in hydrophilic interaction chromatography (HILIC) mode. Further applications in the separation analysis of acidic drugs, alkaline drugs, cinnamic acid natural products, and chiral compounds demonstrate the multifunctional chromatographic capabilities for diverse compound types. Compared to Unitary Diol commercial columns, the prepared stationary phase showed significant advantages in wide polarity range separation performance. Moreover, through nucleoside compound separation mode switching analysis, RCC3-CN@SiO2 stationary phase further validates its favorable performance in both RPLC and HILIC modes, demonstrating extensive potential applications in the field of analytical chemistry. Importantly, the stationary phase exhibits efficient separation of nucleoside compounds in pure water systems, aligning with the principles of green analysis.

Synergistic Effects of Polypropylene Fibers and Silica Fume on Structural Lightweight Concrete: Analysis of Workability, Thermal Conductivity, and Strength Properties

Structural lightweight concrete (SLWC) is crucial for reducing building weight, reducing structural loads, and enhancing energy efficiency through lower thermal conductivity. This study explores the effects of incorporating silica fume (SF), micro-polypropylene (micro-PP), and macro-PP fibers on the workability, thermal properties, and strength of SLWC. SF was added to all mixtures, substituting 10% of the Portland cement (PC), except for the control mixture. Macro-PP fibers were introduced alone or in combination with micro-PP fibers at volumetric ratios of 0.3% and 0.6%. The study evaluated various parameters, including slump, Vebe time, density, water absorption (WA), ultrasonic pulse velocity (UPV), thermal conductivity coefficients (k), compressive strength (CS), and splitting tensile strength (STS) across six different SLWC formulations. The results indicate that while SF negatively impacted the workability of SLWC mortars, it improved CS and STS due to the formation of calcium silicate hydrate (C-S-H) gels from SF’s high pozzolanic activity. Additionally, using micro-PP fibers in combination with macro-PP fibers rather than solely macro-PP fibers enhanced the workability, CS, and STS of the SLWC samples. Although SF had a minor effect on reducing thermal conductivity, the use of macro-PP fibers alone was more effective for improving thermal properties by creating a more porous structure compared to the hybrid use of micro-PP fibers. Moreover, increasing the ratio of micro- and macro-PP fibers from 0.3% to 0.6% resulted in lower CS values but a significant increase in STS values.

Analysis of thermal performance and irreversibility of double-diffusive buoyancy-driven nano-suspension subject to local thermal non-equilibrium model

In fact, local thermal equilibrium (LTE) would be unsuitable when it comes to nuclear reactors, electronic equipment, space devices, geothermal engineering, and high-conductivity foams, due to prominent temperature discrepancy between the two constituents (solid and nanofluid) in porous material. Local thermal non-equilibrium (LTNE) situation may be considered in above real world applications. In view of above relevance, the effects of LTNE model on double-diffusive natural convection (DDNC) within a fluid-saturated porous container loaded with the TiO2-H2O nanofluid and emplacing four cooling and hot channels in Forchheimer-Brinkman-extended Darcy medium have been investigated in the present study. The momentum, heat and mass equations are solved by finite element method. Irreversibility in the two constituents (nanofluid and solid) of the porous structure has been analyzed. The significant outcomes are that fluid circulations enhance due to rise in porosity of the medium. Fluid friction entropy EnFF,T ameliorates significantly by 1514.16 % and 872.97 % with increase in Rayleigh number and porosity of the medium. It is clear that Nuloc,nf,Nuave,nf, Nuloc,s&Nuave,s enhance significantly with rise of buoyancy and thermal conductivity ratio, interstitial solid/fluid heat transfer coefficient.

Nano Silicon Integrated Hard Carbon from Conjugated Microporous Polymer for High‐Efficient Lithium Storage

AbstractIt is a significant issue to develop silicon/carbon composite anode with high‐capacity and long cycling stability for lithium‐ion batteries. However, the huge volume expansion of silicon during lithiation leads to severe pulverization of silicon, resulting in serious capacity fading over cycles. Herein, nano silicon integrated hard carbon (20Si@HC, 20 wt% nano silicon) is prepared by pyrolyzing nano silicon in‐situ coated a conjugated microporous polymer (CMP). CMP‐derived hard carbon coating features developed porous structure, which not only deliver a high lithium storage capacity, but also provide enough space for the volume expansion of nano silicon. When evaluated as an anode for lithium‐ion batteries, the 20Si@HC delivers an impressive 1037 mAh g−1 at 0.1 A g−1 and a capacity retention ratio of 72.07% for 100 cycles at 0.6 A g−1, providing some reference for designing high‐capacity silicon/carbon composites.

Dynamic Behavior and Energy Absorption of Typical Porous Materials under Impacts.

Porous materials are known for their excellent energy absorption capability and, thus, are widely used in anti-impact applications. However, how the pore shape and size impact the failure mechanism and overall behavior of the porous materials under impact loading is still unclear or limitedly touched. Instead of using homogeneous solids for the porous material model, pores with various shapes and sizes were implanted in a solid to establish the porous materials that have true porous structures, which permits exploration of the local failure mechanism. The results revealed that differently shaped holes have two different dominant deformation modes. And due to their different local stress distributions, they enter the plastic phase earlier and, thus, have higher specific energy absorption. Meanwhile, the model changes from hardening to a quasi-zero stiffness model as the hole size increases. The application of this work can be extended into the field of impact resistance.

NiMOF-Derived MoSe2/NiSe Hollow Nanoflower Structures as Electrocatalysts for Hydrogen Evolution Reaction in Alkaline Medium.

Metal-organic frameworks (MOFs) are crystalline porous materials for storage and energy conversion applications with three-dimensional pore structure, high porosity, and specific surface area, which are widely utilized in electrocatalysis. Herein, MoSe2/NiSe composites were synthesized by selenization reaction using NiMOF as the precursor. The composites were hollow nanoflower structures with a synergistic effect between MoSe2 and NiSe to promote rapid electron transfer, which exhibited good hydrogen evolution reaction performance in an alkaline medium. At a current density of 10 mA/cm2, the HER overpotential reaches 80 mV, the Tafel slope is 33.86 mV/dec, and the material has good stability, with polarization curves remaining essentially unchanged after 3000 cycles. These results indicate that the method has a promising application in the preparation of efficient and sustainable catalysts for hydrogen production in alkaline medium.