RESUMO
As one of the most important energy storage devices, dielectric capacitors have attracted increasing attention because of their ultrahigh power density, which allows them to play a critical role in many high-power electrical systems. To date, four typical dielectric materials have been widely studied, including ferroelectrics, relaxor ferroelectrics, anti-ferroelectrics, and linear dielectrics. Among these materials, linear dielectric polymers are attractive due to their significant advantages in breakdown strength and efficiency. However, the practical application of linear dielectrics is usually severely hindered by their low energy density, which is caused by their relatively low dielectric constant. This review summarizes some typical studies on linear dielectric polymers and their nanocomposites, including linear dielectric polymer blends, ferroelectric/linear dielectric polymer blends, and linear polymer nanocomposites with various nanofillers. Moreover, through a detailed analysis of this research, we summarize several existing challenges and future perspectives in the research area of linear dielectric polymers, which may propel the development of linear dielectric polymers and realize their practical application.
RESUMO
Resilient and compressible three-dimensional nanomaterials comprising polymers, carbon, and metals have been prepared in diverse forms. However, the creation of thermostable elastic ceramic aerogels remains an enormous challenge. We demonstrate an inâ situ synthesis strategy to develop biomimetic silica nanofibrous (SNF) aerogels with superelasticity by integrating flexible electrospun silica nanofibers and rubber-like Si-O-Si bonding networks. The stable bonding structure among nanofibers is inâ situ constructed along with a fibrous freeze-shaping process. The resultant SNF aerogels exhibit integrated properties of ultralow density (>0.25â mg cm-3 ), temperature-invariant superelasticity up to 1100 °C, and robust fatigue resistance over one million compressions. The ceramic nature also endows the aerogels with fire resistance and ultralow thermal conductivity. The successful synthesis of the SNF aerogels opens new pathways for the design of superelastic ceramic aerogels in a structurally adaptive and scalable form.
RESUMO
The compromise of contradictive parameters, polarization, and breakdown strength, is necessary to achieve a high energy storage performance. The two can be tuned, regardless of material types, by controlling microstructures: amorphous states possess higher breakdown strength, while crystalline states have larger polarization. However, how to achieve a balance of amorphous and crystalline phases requires systematic and quantitative investigations. Herein, the trade-off between polarization and breakdown field is comprehensively evaluated with the evolution of microstructure, i.e., grain size and crystallinity, by phase-field simulations. The results indicate small grain size (≈10-35 nm) with moderate crystallinity (≈60-80%) is more beneficial to maintain relatively high polarization and breakdown field simultaneously, consequently contributing to a high overall energy storage performance. Experimentally, therefore an ultrahigh energy density of 131 J cm-3 is achieved with a high efficiency of 81.6% in the microcrystal-amorphous dual-phase Bi3NdTi4O12 films. This work provides a guidance to substantially enhance dielectric energy storage by a simple and effective microstructure design.
RESUMO
Advanced ceramic aerogel materials with a performance combining sufficient mechanical robustness and splendid high-temperature resistance are urgently needed as thermal insulators in harsh environments. However, the practical applications of ceramic aerogel materials are always limited by poor mechanical performance and degradation under thermal shock. Here, we report the facile creation of lamellar multiarch structured ceramic nanofibrous aerogels that are simultaneously ultrastrong, superelastic, and high temperature resistant by combining ZrO2-Al2O3 nanofibers with Al(H2PO4)3 matrices. The resulting ZrO2-Al2O3 nanofibrous aerogels exhibit the integrated properties of rapid recovery from a strain of 90%, high compression strength of more than 1100 kPa (at a strain of 90%), high fatigue resistance, and temperature-invariant superelasticity. Moreover, the all-ceramic component feature also provides the ceramic nanofibrous aerogels with high-temperature resistance up to 1300 °C and thermal insulation performance with low thermal conductivity (0.0322 W m-1 K-1). These superior performances make the ceramic aerogels ideal for high-temperature thermal insulation materials in extreme conditions.
RESUMO
Silica aerogels are attractive for thermal insulation due to their low thermal conductivity and good heat resistance performance. However, the fabrication of silica aerogels with temperature-invariant superelasticity and ultralow thermal conductivity has remained extremely challenging. Herein, we designed and synthesized a hierarchical cellular structured silica nanofibrous aerogel by using electrospun SiO2 nanofibers (SNFs) and SiO2 nanoparticle aerogels (SNAs) as the matrix and SiO2 sol as the high-temperature nanoglue. This pathway leads to the intrinsically random deposited SNFs assembling into a fibrous cellular structure, and the SNAs are evenly distributed on the fibrous cell wall. The unique hierarchical cellular structure of the ceramic nanofibrous aerogels endows it with integrated performances of the ultralow density of â¼0.2 mg cm-3, negative Poisson's ratio, ultralow thermal conductivity (23.27 mW m-1 K-1), temperature-invariant superelasticity from -196 to 1100 °C, and editable shapes on a large scale. These favorable multifeatures present the aerogels ideal for thermal insulation in industrial, aerospace, and even extreme environmental conditions.
RESUMO
Ultralight aerogels that are both highly resilient and compressible have been fabricated from various materials including polymer, carbon, and metal. However, it has remained a great challenge to realize high elasticity in aerogels solely based on ceramic components. We report a scalable strategy to create superelastic lamellar-structured ceramic nanofibrous aerogels (CNFAs) by combining SiO2 nanofibers with aluminoborosilicate matrices. This approach causes the random-deposited SiO2 nanofibers to assemble into elastic ceramic aerogels with tunable densities and desired shapes on a large scale. The resulting CNFAs exhibit the integrated properties of flyweight densities of >0.15 mg cm-3, rapid recovery from 80% strain, zero Poisson's ratio, and temperature-invariant superelasticity to 1100°C. The integral ceramic nature also provided the CNFAs with robust fire resistance and thermal insulation performance. The successful synthesis of these fascinating materials may provide new insights into the development of ceramics in a lightweight, resilient, and structurally adaptive form.
RESUMO
Constructing nanostructured catalyst-embedded ceramic fibrous membranes would facilitate the remediation or preliminary treatment of dyeing wastewater, however, most of such membranes are brittle with low deformation resistance, thus, restricting their widely applications. Herein, the flexible and hierarchical nanostructured MnO2-immobilized SiO2 nanofibrous membranes (MnO2@SiO2 NFM) were fabricated by combining the electrospinning technique with hydrothermal method. The morphologies of membranes could be regulated from nanowires and nanoflower to mace-like structure via varying concentration of reactants. The resultant MnO2@SiO2 NFM could cooperate with hydrogen peroxide to form a Fenton-like reagent for the degradation of methylene blue (MB). The resultant membrane exhibited prominent catalytic performance towards MB, including high degradation degree of 95% within 40min, fast degradation rate of 0.0865min-1, and excellent reusability in 5 cycles. Moreover, the membranes could be used in a wide pH range of 0 to 14 and the degradation degree reached 76% during dynamic filtration process with a flux of 490,000Lm-2h-1. The successful fabricating of such membrane with extraordinary catalytic performance would provide a platform for preparing high-performance catalysts for remediation of dyeing wastewater.
RESUMO
Functional nanoparticles modified silica nanofibrous materials with good flexibility, a hierarchical mesoporous structure, and excellent durability would have broad applications in efficient removal of contaminants, yet have proven to be enormously challenging to construct. Herein, we reported a strategy for rational design and fabricating flexible, hierarchical mesoporous, and robust ZrO2 nanoparticle-embedded silica nanofibrous membranes (ZrO2/SiO2 NM) for phosphate removal by combining the chitosan dip-coating method with the electrospinning technique. Our approach allows ZrO2 nanoparticles to be in situ firmly and uniformly anchored onto SiO2 nanofibers to drastically enlarge the specific surface area and porosity of membranes. Therefore, the resultant ZrO2/SiO2 NM exhibited a prominent removal efficiency of 85% and excellent adsorption amount of 43.8 mg P g-1 membranes in 30 min toward phosphates. Furthermore, the removal performance toward different types of phosphates revealed that the resultant membranes also could be used to remove phosphates in detergent and fertilizer water samples. More importantly, the membranes with good flexibility could directly be taken out from solution after use without any post-treatment. Such a simple and intriguing approach for fabricating nanofibrous membranes may provide a new platform for constructing membranes with superb phosphate removal performance.