Interconnected Microstructure Research Articles

Recycling single use surgical face mask waste for reinforcing cement-treated/untreated dredged marine sediments: Strength, deformation and micro-mechanisms analysis

To prevent the transmission of airborne infectious diseases (SARS, H1N1, COVID-19, and influenza), the use of disposable surgical face masks has increased dramatically in the past few years. To mitigate the environmental consequences associated with mask waste, implementing circular economy strategies with the reuse of mask waste is a sustainable method. This study explores an innovative way to reuse mask fiber (MF) with dredged sediment waste together as road construction materials. First, the MF was introduced into cement-treated/untreated dredged marine sediment mixtures with different content and lengths. Then, a variety of laboratory tests were carried out to explore the basic physical and chemical characterization of raw materials and the development of mechanical properties of mixtures. In addition, the intrinsic mechanism of MF inclusion on cement-treated sediments was analyzed by scanning electron microscope (SEM) test. The results show that the inclusion of MF significantly improves the unconfined compression strength (UCS) and splitting tensile strength (STS) of both treated and untreated specimens. The highest UCS and STS values are at the condition with an MF content of 0.25%, a length of MF of 2 cm, and a curing time of 28 days. The combined strength increase caused by cement-MF together inclusion is much greater than the strength increase caused by either of them separately. It was also found that the elastic modulus (E50) decreased with the inclusion of MF. Furthermore, the addition of MF changes the brittle behavior of the specimens, which also improves the ductility and residual strength of the specimens. The SEM analysis demonstrates the microstructure of MF and MF-reinforced specimens. The creation of a stable and interconnected microstructure is largely attributed to the bridging impact of MF and the binding effect of hydration products, which significantly improves the mechanical behavior of specimens. The MF-reinforced cement-treated sediment could be an innovative, environmentally friendly, and economical material for road construction.

Interconnected microstructure and flexural behavior of Ti2C-Ti composites with superior Young’s modulus

Interconnected microstructure and flexural behavior of Ti2C-Ti composites with superior Young’s modulus

Double laser two-step process for creating interconnected frame microstructures' superhydrophobic surface with dual scales

Superhydrophobic surfaces have garnered significant attention for their unique wettability and extensive applications across various critical fields. In this paper, a two-step laser processing technique, involving infrared nanosecond laser patterning and ultraviolet picosecond laser surface modification, was employed to fabricate interconnected frame surfaces with dual-scale microstructures on Ti6Al4V substrates. After that, the microstructure surface was chemically modified with 1H,1H,2H,2H-perfluorodecyl trimethoxy-silane to achieve a superhydrophobic surface. An L32 (47) orthogonal experiment was used to analyze the effect of seven main factors (including the structure size, scanning velocity and the fluence, number of scans of infrared nanosecond laser and ultraviolet picosecond laser) on the wettability of the interconnected frame microstructures surface. After optimization, the surface strongly corresponded with the Cassie-Baxter model and demonstrated a water contact angle of 153.22±1.64° and roll-off angle of 4.43±1.70°. The experiments demonstrated that the optimized surface possesses excellent mechanical stability and corrosion resistance. Additionally, the optimized surface exhibits anti-adhesion, effective self-cleaning, and anti-fouling properties, which hold promise for addressing issues of liquid adhesion and dust pollution in industrial machinery.

In-vitro and in-vivo evaluation of angiogenic potential of a novel lithium chloride loaded silk fibroin / alginate 3D porous scaffold with antibacterial activity, for promoting diabetic wound healing

Healing diabetic ulcers with chronic inflammation is a major challenge for researchers and professionals, necessitating new strategies. To rapidly treat diabetic wounds in rat models, we have fabricated a composite scaffold composed of alginate (Alg) and silk fibroin (SF) as a wound dressing that is laden with molecules of lithium chloride (LC). The physicochemical, bioactivity, and biocompatibility properties of Alg-SF-LC scaffolds were investigated in contrast to those of Alg, SF, and Alg-SF ones. Afterward, full-thickness wounds were ulcerated in diabetic rats in order to evaluate the capacity of LC-laden scaffolds to regenerate skin. The characterization findings demonstrated that the composite scaffolds possessed favorable antibacterial properties, cell compatibility, high swelling, controlled degradability, and good uniformity in the interconnected pore microstructure. Additionally, in terms of wound contraction, re-epithelialization, and angiogenesis improvement, LC-laden scaffolds revealed better performance in diabetic wound healing than the other groups. This research indicates that utilizing lithium chloride molecules loaded in biological materials supports the best diabetic ulcer regeneration in vivo, and produces a skin replacement with a cellular structure comparable to native skin.

High-load Ti3C2 MXene cathode through surface modification for degradable aqueous zinc-ion micro-supercapacitors with excellent energy density and anti-self-discharge

Micro Zn-ion supercapacitors (MZSCs) with excellent power density and safety are considered the most promising micro-energy storage devices. However, the energy density per unit area of these devices is insufficient to meet the requirements for portable/wearable electronics. Furthermore, traditional energy storage devices produce a large amount of e-waste, causing serious environmental hazards. To solve these problems, degradable MZSCs are proposed based on high-load surface-modified MXene (O-Ti3C2 MXene) cathodes and Zn/carbon nanotube (CNT) anodes. Owing to the advantages of their three-dimensional interconnected microstructures and abundant oxygen-rich functional groups, the thick O-Ti3C2 MXene electrodes show high rate performances and excellent Zn2+ diffusion kinetics. Therefore, MZSCs exhibit an extremely high energy density (384.90 μWh cm−2 at 0.30 mW cm−2) and power density (6.0 mW cm−2 at 126.84 μWh cm−2) and are degradable. More importantly, because of the strong adsorption capacity of the O-Ti3C2 MXene cathode for SO42− and the redox reaction of Zn/Zn2+ in the Zn/CNT anode, MZSCs have an extremely low self-discharge rate (1.92 mV h−1). This research is expected to provide a promising direction for next-generation, high-performance, anti-self-discharge and degradable devices.

Influence of Graphene Oxide on Mechanical Properties and Durability of Cement Mortar.

The effect of graphene oxide (GO) on the mechanical strengths and durability of cement composites was researched by preparing GO-modified cement mortars. Thermogravimetric analysis (TGA) and nuclear magnetic resonance (29Si MAS-NMR) were performed on the cement paste to evaluate the influence of GO on the hydration process and chain structure of calcium-silicate-hydrate (C-S-H) gels. TGA revealed that the high GO dosage increased the content of C-S-H by 5.46% compared with the control at 28 days. Similarly, 29Si-NMR improved the hydration degree and main chain length (MCL) in GO-modified samples at 28 days. The GO led to increases of 2.54% and 7.01% in the hydration degree and MCL, respectively, compared with the control at 28 days. These findings underscore the multifaceted role of GO in improving the mechanical properties and durability of cement composites. Mechanical strength tests, such as compressive and flexural tests, were conducted on cement mortars. The optimal dosage of GO increased the compressive strength by 9.02% after 28 days. Furthermore, the flexural strength of cement mortars with the combination of GO and superplasticizer (SP) after 28 days increased by 21.86%, compared with reference mortar. The impact of GO proved to be more pronounced and beneficial in the durability tests, suggesting that GO can enhance the microstructure through hydration products to create a dense and interconnected microstructure.

Emulsion template fabricated heterogeneous bilayer gelatin-based scaffolds with sustained-delivery of lycium barbarum glycopeptide for periodontitis treatment

Periodontitis is a chronic inflammatory disease raising the risks of tooth-supporting structures destruction and even tooth loss. The way to reconstruct periodontal bone tissues in inflammatory microenvironment has been long in demand for periodontitis treatment. In this study, the lycium barbarum glycopeptide (LbGP) loaded gelatin-based scaffolds were fabricated for periodontitis treatment. Gelatin microspheres with suitable size were prepared by emulsification and gathered by oxidized sodium alginate to prepare heterogeneous bilayer gelatin-based scaffolds, and then they were loaded with LbGP. The prepared scaffolds possessed interconnected porous microstructures, good degradation properties, sufficient mechanical properties, sustained release behavior and well biocompatibility. In vitro experiments suggested that the LbGP loaded gelatin-based scaffolds could inhibit the expression of inflammatory factors (IL-1β, IL-6, and TNF-α), promote the expression of anti-inflammatory factor (IL-10), and the expression of osteogenic markers (BMP2, Runx2, ALP, and OCN) in PDLSCs under the LPS-stimulated inflammatory microenvironment. Moreover, in rat periodontitis models, the LbGP gelatin-based scaffolds would reduce the alveolar bone resorption of rats, increase the collagen fiber content of periodontal membrane, alleviate local inflammation and improve the expression of osteogenesis-related factors. Therefore, the LbGP loaded gelatin-based scaffolds in this study will provide a potential therapeutic strategy for periodontitis treatment.

The effect of Bletilla striata polysaccharide on the physical and healing properties of curdlan-based hydrogel for wound healing.

Bletilla striata polysaccharide (BSP) was added to curdlan to form a blend hydrogel through a simple heating-cooling procedure to improve the hydrophilicity and healing efficacy of curdlan-based hydrogel used in wound healing. We explored the interplay between BSP and curdlan, studied how BSP concentration affects the physical properties and microstructures of hydrogels, and examined the biocompatibility and healing properties of the blend hydrogel. It was proved that the hydrogel framework was primarily formed by ordered arranged curdlan molecules, with BSP uniformly dispersed and intertwined with curdlan through hydrogen bonding. This effectively improved its hydrophilicity and strengthened the microstructure. Curdlan was found to be compatible with BSP. The blend hydrogel B3Cd3 (containing 1.5% BSP and 1.5% curdlan, w/v) was identified as the optimal formulation based on its higher water adsorption, water retention, thermal stability and interconnected microstructure, and was thus selected for further research. In vitro experiments revealed the highest cell viability of L929 in B3Cd3 extracts compared to those extracts of single-component curdlan hydrogel (Cd). In vivo, animal studies indicated that the B3Cd3 accelerated wound healing compared to the control group by improving re-epithelialization and blood vessel regeneration. On Days 3 and 11, the therapeutic benefits of B3Cd3 exceeded those of the Cd group, and no significant differences were observed in wound healing rates between the B and B3Cd3 groups from Day 7. The study proves that BSP enhances the physical and healing properties, as well as cell proliferation, of the curdlan-based hydrogel. The blend hydrogel B3Cd3, with its exceptional properties, holds potential for future application as a material for non-infected wound healing.

Synthesis and characterisations of clinoptilolite enriched hydroxyapatite nanoceramics by sol-gel route for bone regeneration

Hydroxyapatite (HA) has great bioactive potential in bone tissue engineering (BTE). However, the high crystalline stability of synthetic HA restricts its in-vivo bioresorbability which extends the healing time of bone defects. This study investigates doping HA with biocompatible Clinoptilolite (CLP) mineral rich in silicate and other biomimetic ions (Na+, K+, Ca+2, Mg+2 etc.). Sol-gel-based CLP doped HA nanoceramics are aimed to be exploited as bone filler substitutes with biomimetic morphology, composition, and improved biocompatibility and bioactivity. The pure and CLP (5%, 10% and 20%) doped HA ceramics were synthesised by sol-gel method to provide molecular level interactions of ions and sintered at different temperatures (800 °C, 950 °C, and 1100 °C). Morphological analyses by SEM and S-TEM showed biomimetic nano rod-like HA particles are attached to dispersed CLP sheets. Sintering of composite ceramics led to a cell-friendly interconnected porous microstructure even at 1100 °C, where the pure HA had a compact non-porous structure. The Ca/P ratio of CLP-doped HA samples was lower than the stoichiometric HA which indicates a partial reduction of stability that is supposed to induce bioresorption capacity. Cytotoxicity tests by WST-8 with Saos-2 cell lines showed that CLP addition into HA has significantly improved cell viability. The HA-CLP nanoceramics are expected to promote bone regeneration due to cell-friendly microstructure and biomimetic composition which can be supported by further in-vivo clinical studies.

Thermally exfoliated graphene oxide doped microporous bio-nanocomposite hydrogel: A promising substrate for biomedical application

Hydrogels have demonstrated significant promise as flexible/wearable sensors for the diagnosis, monitoring, and delivery of personalized medicine for health issues and deficiencies. To this end, a novel approach was employed towards the development of a hybrid hydrogel nanocomposite-based biosensing substrate. The hierarchical hydrogel matrix derived by using polyaniline (PANI)/polyvinyl-alcohol (PVA) biopolymer-matrix, was reinforced with in-house synthesized thermally exfoliated graphene-oxide (TEGO). Fourier transform infrared spectroscopy (FT-IR) confirmed the interfacial-interactions between hydroxyl groups and functional groups of TEGO, a conducive property for immobilization and catalytic activities. X-ray photoelectron spectroscopy (XPS) investigation of the developed nanocomposite hydrogel demonstrated that the addition of nanofiller facilitated the ordered structure of nanocomposite hydrogel. Further, field emission scanning electron microscopy (FE-SEM) investigations revealed interconnected porous microstructure of the nanocomposites, assisted by nucleating effect of TEGO, a supporting micro-environment for the transportation of biomolecules. Impedance analysis and hall effect studies showed that the nanocomposite hydrogel substrate was highly conductive. In vitro cytocompatibility results demonstrated excellent biocompatibility of the bio-nanocomposite hydrogels. Cyclic-voltammetry analysis indicated a reduction in current on the surface due to long-range shattered conjugated network of TEGO and PANI in presence of functional groups. Overall, this study indicates that developed bio-nanocomposite hydrogel substrates are promising candidates for biomedical applications.

One-step formation of three-dimensional interconnected T-shaped microstructures inside composites by orthogonal bidirectional self-assembly method

ABSTRACT The fillers inside a polymer matrix should typically be self-assembled in both the horizontal and vertical directions to obtain 3-dimentional (3D) percolation pathways, whereby the fields of application can be expanded and the properties of organic-inorganic composite films improved. Conventional dielectrophoresis techniques can typically only drive fillers to self-assemble in only one direction. We have devised a one-step dielectrophoresis-driven approach that effectively induces fillers self-assembly along two orthogonal axes, which results in the formation of 3D interconnected T-shaped iron microstructures (3D-T CIP) inside a polymer matrix. This approach to carbonyl iron powder (CIP) embedded in a polymer matrix results in a linear structure along the thickness direction and a network structure on the top surface of the film. The fillers in the polymer were controlled to achieve orthogonal bidirectional self-assembly using an external alternating current (AC) electric field and a non-contact technique that did not lead to electrical breakdown. The process of 3D-T CIP formation was observed in real time using in situ observation methods with optical microscopy, and the quantity and quality of self-assembly were characterized using statistical and fractal analysis. The process of fillers self-assembly along the direction perpendicular to the electric field was explained by finite element analogue simulations, and the results indicated that the insulating polyethylene terephthalate (PET) film between the electrode and the CIP/prepolymer suspension was the key to the formation of the 3D-T CIP. In contrast to the traditional two-step method of fabricating sandwich-structured film, the fabricated 3D-T CIP film with 3D electrically conductive pathways can be applied as magnetic field sensor.

Porous Microneedles Through Direct Ink Drawing with Nanocomposite Inks for Transdermal Collection of Interstitial Fluid.

Interstitial fluid (ISF) is an attractive alternative to regular blood sampling for health checks and disease diagnosis. Porous microneedles (MNs) are well suited for collecting ISF in a minimally invasive manner. However, traditional methods of molding MNs from microfabricated templates involve prohibitive fabrication costs and fixed designs. To overcome these limitations, this study presents a facile and economical additive manufacturing approach to create porous MNs. Compared to traditional layerwise build sequences, direct ink drawing with nanocomposite inks can define sharp MNs with tailored shapes and achieve vastly improved fabrication efficiency. The key to this fabrication strategy is the yield-stress fluid ink that is easily formulated by dispersing silica nanoparticles into the cellulose acetate polymer solution. As-printed MNs are solidified into interconnected porous microstructure inside a coagulation bath of deionized water. The resulting MNs exhibit high mechanical strength and high porosity. This approach also allows porous MNs to be easily integrated on various substrates. In particular, MNs on filter paper substrates are highly flexible to rapidly collect ISF on non-flat skin sites. The extracted ISF is used for quantitative analysis of biomarkers, including glucose, = calcium ions, and calcium ions. Overall, the developments allow facile fabrication of porous MNs for transdermal diagnosis and therapy.

Towards the Clinical Translation of 3D PLGA/β-TCP/Mg Composite Scaffold for Cranial Bone Regeneration.

Recent years have witnessed the rapid development of 3D porous scaffolds with excellent biocompatibility, tunable porosity, and pore interconnectivity, sufficient mechanical strength, controlled biodegradability, and favorable osteogenesis for improved results in cranioplasty. However, clinical translation of these scaffolds has lagged far behind, mainly because of the absence of a series of biological evaluations. Herein, we designed and fabricated a composite 3D porous scaffold composed of poly (lactic-co-glycolic) acid (PLGA), β-tricalcium phosphate (β-TCP), and Mg using the low-temperature deposition manufacturing (LDM) technique. The LDM-engineered scaffolds possessed highly porous and interconnected microstructures with a porosity of 63%. Meanwhile, the scaffolds exhibited mechanical properties close to that of cancellous bone, as confirmed by the compression tests. It was also found that the original composition of scaffolds could be maintained throughout the fabrication process. Particularly, two important biologic evaluations designed for non-active medical devices, i.e., local effects after implantation and subchronic systemic toxicity tests, were conducted to evaluate the local and systemic toxicity of the scaffolds. Additionally, the scaffolds exhibited significant higher mRNA levels of osteogenic genes compared to control scaffolds, as confirmed by an in vitro osteogenic differentiation test of MC3T3-E1 cells. Finally, we demonstrated the improved cranial bone regeneration performance of the scaffolds in a rabbit model. We envision that our investigation could pave the way for translating the LDM-engineered composite scaffolds into clinical products for cranial bone regeneration.

AC Conduction Mechanism and Impedance Analysis of Conventional and Plasma‐Sintered Yttria‐Stabilized ZrO2@Mullite Composite

AbstractThe addition of 8 mol% of Y2O3 to the ZrO2@mullite composites stabilizes the metastable tetragonal phase of ZrO2 in conventional and plasma‐sintered Y2O3‐stabilized ZrO2@mullite composites. A fused, highly dense, and interconnected microstructure is formed in the case of plasma‐sintered Y2O3 stabilized ZrO2@mullite composite. At 1 MHz frequency, the room temperature and tanδ of (10.37 and 2.06) is obtained for the conventional Y2O3 stabilized ZrO2@mullite composite and that of (38.8 and 4.02) is observed for the plasma sintered Y2O3 stabilized ZrO2@mullite composite. The substitution of Y3+ in place of Zr4+ creates sufficiently large oxygen vacancies at the grain boundary regions of these composites endowed mostly with the ZrO2 phase. In conventional Y2O3‐ ZrO2@mullite composites, both dielectric relaxation as well as conductivity relaxation are observed due to the dynamic motion of dipoles and relaxation due to the presence of defect states and porous structures. This leads to higher grain boundary conductivity than the grain conductivity of these composites. Thermally activated conduction mechanisms exhibited in these composite materials are projected from the complex impedance and modulus analysis. The conventional and plasma sintered Y2O3‐ ZrO2@mullite composite has an optical bandgap of 3.26 and 3.58 eV, respectively.

Ammonia Cracking Catalyzed by Ni Nanoparticles Confined in the Framework of CeO2 Support.

For the extraction of hydrogen from ammonia at low temperatures, we investigated Ni-based catalysts fabricated by the thermal decomposition of RNi5 intermetallics (R = Ce or Y). The interconnected microstructure formed via phase separation between the Ni catalyst and the resulting oxide support was observed to evolve via low-temperature thermal decomposition of RNi5. The resulting Ni/CeO2 nanocomposite exhibited superior catalytic activity of ∼25% at 400 °C for NH3 cracking. The high catalytic activity was attributed to the interlocking of Ni nanoparticles with the CeO2 framework. The growth of Ni nanoparticles was prevented by this interconnected microstructure, in which the Ni nanoparticles incorporated nitrogen owing to the size effect, whereas Ni does not commonly form nitrides. To the best of our knowledge, this is a unique example of a microstructure that enhances catalytic NH3 cracking.

Wood membrane filter for water purification with radial and axial flows

Water availability is an important issue all over the world, and membrane filtration technology is one of the most effective measures for remediation. As a sustainable and renewable biomass material, natural wood has a hierarchical and three-dimensional interconnected microstructure, which provides an alternative for water filter design. Longitudinal filtration could take advantage of the micropores, while the treatment speed is severely limited. This study examined a wood filter in which muddy wastewater can be transported into the microchannels and out of the vertically stacked micropores. The filter takes full advantage of the pores present in the wood without sacrificing the speed of hydraulic flow within the main transport channels, exhibiting excellent performance for mud removal. In this manner, water flux, decolorization, and turbidity are highly dependent on the groove number, groove depth, and thickness of the filter. Due to the reorientation of the water transport pathways, the clogging of micropores could be easily alleviated, thus promoting the filter lifecycle. The design of the cross-flow wood filter can provide an available platform for various wastewater treatment cases with different impurities, displaying an application prospect in the wastewater treatment field.

Morphology and gene expression of sex‐determining region Y‐box 9 and runt‐related transcription factor 2 in centrifugally compressed cell collagen‐combined constructs (C6)

AbstractThe authors previously developed a scaffold‐free tissue‐engineered construct (TEC) from mesenchymal stem cells (MSCs). Although the TEC exhibited even cell distribution and was successfully applied for cartilage repair in animal models, it is unsuitable for relatively large‐scale cartilage defects due to its small size. To solve the problem, the authors recently developed a novel biomaterial, a centrifugally compressed cell‐collagen combined construct (C6) from a mixture of MSCs and atelocollagen, both of which are subjected to centrifugation. The results of the previous study indicated that C6 exhibited high cell viability (70 %) and sufficient cell distribution similar to that of the TEC. In the present study, the morphology and gene expression of C6 were investigated. Histological examination indicated that C6 is six times thicker (approximately 1 mm) than the TEC after a 7‐day culture. The C6 remained unchanged in scale with increased cell density after a 21‐day culture. Scanning electron microscopic observation indicated that C6 exhibited interconnected and porous microstructures, while the TEC had close‐knit microstructures. Reverse transcriptase‐polymerase chain reaction analysis indicated that the expression of sex‐determining region Y‐box 9 and runt‐related transcription factor 2 was significantly higher in C6 than that in TEC.

Facile preparation and properties of porous poly(vinyl alcohol)/trehalose/nano-clay hydrogels with high mechanical strength for potential application in bone tissue engineering

Among various biomaterials, hydrogels are considered as the most attractive tissue engineering material due to their resemblances to extracellular matrix. However, due to the poor mechanical properties, poly(vinyl alcohol) hydrogels are restricted to be applied in load-bearing tissue repair and regeneration. In this work, we designed a series of porous biocompatible composite hydrogels with tough mechanical properties for bone tissue engineering, consisting of poly(vinyl alcohol), trehalose and nano-clay. These novelty hydrogels were prepared by a facile one-pot method. Compositions, microscopic structures, and mechanical properties of hydrogels were investigated in detail. The maximum compressive strength, compressive modulus, tensile strength, elastic modulus, and toughness of hydrogels attained about 2.71 MPa, 0.163 MPa, 0.741 MPa, 0.084 MPa, and 0.94 MJ/m3, respectively. These as-prepared hydrogels exhibited the excellent mechanical properties, which were ascribed to the hydrogen bond interactions between molecules and nano-enhancement effect of the nano-clay. Meanwhile, as-prepared hydrogels also exhibited a three-dimensional and interconnected porous microstructure, which facilitated the transport of nutrients to promote cells growth. In addition, the mechanical properties and microscopic structures of hydrogels could be controlled by adjusting the concentrations of trehalose and nano-clay. In vitro cell experiments demonstrated that the hydrogels had good biocompatibility. And hydrogels possessed the excellent ability to induce MC3T3-E1 cells osteogenesis to accelerate bone defects repair. Above illustrated results demonstrated that the potential applications of the hydrogels used as bone tissue engineering materials. Therefore, we anticipated this kind of poly(vinyl alcohol)-based composite hydrogel could develop a new strategy for bone tissue repair.

Facile hydrothermal synthesis of monoclinic VO2/graphene nanowhisker composite for enhanced performance electrode material for energy storage applications

Vanadium dioxide/reduced graphene oxide (VO2/G) nanowhisker composites are synthesized under hydrothermal conditions by a simple method. VO2 nanowhisker and 2D flexible graphene sheets are formed during the formation of VO2/G architecture to build interconnected porous microstructure via hydrogen bonding which allows charging and ion transport in the electrode. The composite electrode shows outstanding electrochemical performances due to the hierarchical network structure and pseudo-capacity contribution from VO2 nanowhiskers. The composite electrode used for electrochemical investigations in the aqueous electrolyte solution of 1 M Na2SO4. Noteworthy is the galvanostatic charge-discharge test which shows that, with a current density of 1 Ag−1, the specific capacitance value of the composite attained a high value of 294.5 Fg−1, which is significantly better than pure vanadium dioxide (VO2), and retains its capacitance at 203 Fg−1 at 10 Ag−1. The specific capacitance remained 96.3 % after 5000 continuous discharge cycles at 0.6 Ag−1 and shows an excellent cycle life for the material. It has also a high power density with a reasonably high-energy density. (i.e) energy density reached 48.07 Wh kg−1 at a power density of 213.6 Wkg−1. The results of the composite electrode were due to synergistic effects of VO2 and graphene, and excellent VO2 redox activity coupled with high electronic graphene sheet conductivity.

An Armour Structure to Suppress the Brittle Failure of Ceramic Coatings.

The brittle failure of ceramic coatings limits their application in many fields. To address this issue, a novel armoured ceramic coating was developed to suppress brittle failure. First, an interconnected frame microstructure was micromachined onto the surface of a mild steel substrate using a nanosecond laser. Subsequently, a polymer-derived ceramic slurry was sprayed and sintered to obtain an armoured ceramic coating. The laser-micromachined burr-like microstructure of the substrate facilitated adhesion between the coating and the substrate. The results of the mechanical properties test showed that the armoured coating could withstand more than 20 cycles of water-cooled thermal shock at 600 °C, and the peeling area of the armoured coating was approximately three times less than that of the unarmoured coating under a normal load of 1471 N. The laboratory and field corrosion test results indicated that at high temperatures, the corrosion resistance of the armoured coating was comparable with that of the unarmoured coating and was approximately 10 times higher than that of the uncoated sample. The proposed method will aid in suppressing the brittle failure of ceramic coatings and broaden their scope of application in different fields.