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排序方式: 共有350条查询结果,搜索用时 421 毫秒
41.
Spatial Charge Storage within Honeycomb‐Carbon Frameworks for Ultrafast Supercapacitors with High Energy and Power Densities
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Carbon‐based supercapacitors store charge through the adsorption of electrolyte ions onto the carbon surface. Therefore, it would be more attractive for the enhanced charge storage if the locations for storing charge can be extended from carbon surface to space. Here, a novel spatial charge storage mechanism based on counterion effect from Fe(CN)63? ions bridged by oxygen groups and confined into honeycomb‐carbon frameworks is presented, which can provide additionally spatial charge storage for electrical double‐layer capacitances in a negative potential region and pseudocapacitances from Fe(CN)63?/Fe(CN)64? in a positive potential region. More importantly, an ultrafast supercapacitor based on this novelty carbon can be charged/discharged within 0.7 s to deliver both high specific energy of 15 W h kg?1 and ultrahigh specific power of 79.1 kW kg?1 in 1 m Na2SO4 electrolyte, much higher than those of previously reported asymmetric supercapacitors in aqueous electrolytes, as well as excellent cycling stability. These features suggest a new generation of ultrafast asymmetric supercapacitors as novel high‐performance energy storage devices. 相似文献
42.
In Situ TEM Study of Volume Expansion in Porous Carbon Nanofiber/Sulfur Cathodes with Exceptional High‐Rate Performance
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Zheng‐Long Xu Jian‐Qiu Huang Woon Gie Chong Xianying Qin Xiangyu Wang Limin Zhou Jang‐Kyo Kim 《Liver Transplantation》2017,7(9)
Although lithium sulfur batteries (LSBs) have attracted much interest owing to their high energy densities, synthesis of high‐rate cathodes and understanding their volume expansion behavior still remain challenging. Herein, electrospinning is used to prepare porous carbon nanofiber (PCNF) hosts, where both the pore volume and surface area are tailored by optimizing the sacrificial agent content and the activation temperature. Benefiting from the ameliorating functional features of high electrical conductivity, large pore volume, and Li ion permselective micropores, the PCNF/A550/S electrode activated at 550 °C exhibits a high sulfur loading of 71 wt%, a high capacity of 945 mA h g?1 at 1 C, and excellent high‐rate capability. The in situ transmission electron microscope examination reveals that the lithiation product, Li2S, is contained within the electrode with only ≈35% volume expansion and the carbon host remains intact without fracture. In contrast, the PCNF/A750/S electrode with damaged carbon spheres exhibits sulfur sublimation, a larger volume expansion of over 61%, and overflowing of Li2S, a testament to its poor cyclic stability. These findings provide, for the first time, a new insight into the correlation between volume expansion and electrochemical performance of the electrode, offering a potential design strategy to synthesize high‐rate and stable LSB cathodes. 相似文献
43.
In the global transition to a sustainable low‐carbon economy, CO2 capture and storage technology still plays a critical role for deep emission reduction, particularly for the stationary sources in power generation and industry. However, for small and mobile emission sources in transportation, CO2 capture is not suitable and it is more practical to use relatively clean energy, such as natural gas. In these two low‐carbon energy technologies, designing highly selective sorbents is one of the key and most challenging steps. Toward this end, metal‐organic frameworks (MOFs) have received continuously intensive attention in the past decades for their highly porous and diversified structures. In this review, the recent progress in developing MOFs for selective CO2 capture from post‐combustion flue gas and CH4 storage for vehicle applications are summarized. For CO2 capture, several promising strategies being used to improve CO2 adsorption uptake at low pressures are highlighted and compared. In addition, the conventional and novel regeneration techniques for MOFs are also discussed. In the case of CH4 storage, the flexible and rigid MOFs, whose CH4 storage capacity is close to the target set by U.S. Department of Energy are particularly emphasized. Finally, the challenge of using MOFs for CH4 storage is discussed. 相似文献
44.
Nanoparticles Encapsulated in Porous Carbon Matrix Coated on Carbon Fibers: An Ultrastable Cathode for Li‐Ion Batteries
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Rujia Zou Qian Liu Guanjie He Muk Fung Yuen Kaibing Xu Junqing Hu Ivan P. Parkin Chun‐Sing Lee Wenjun Zhang 《Liver Transplantation》2017,7(2)
Nanostructured V2O5 is emerging as a new cathode material for lithium ion batteries for its distinctly high theoretic capacity over the current commercial cathodes. The main challenges associated with nanostructured V2O5 cathodes are structural degradation, instability of the solid‐electrolyte interface layer, and poor electron conductance, which lead to low capacity and rapid decay of cyclic stability. Here, a novel composite structure of V2O5 nanoparticles encapsulated in 3D networked porous carbon matrix coated on carbon fibers (V2O5/3DC‐CFs) is reported that effectively addresses the mentioned problems. Remarkably, the V2O5/3DC‐CF electrode exhibits excellent overall lithium‐storage performance, including high Coulombic efficiency, excellent specific capacity, outstanding cycling stability and rate property. A reversible capacity of ≈183 mA h g?1 is obtained at a high current density of 10 C, and the battery retains 185 mA h g?1 after 5000 cycles, which shows the best cycling stability reported to date among all reported cathodes of lithium ion batteries as per the knowledge. The outstanding overall properties of the V2O5/3DC‐CF composite make it a promising cathode material of lithium ion batteries for the power‐intensive energy storage applications. 相似文献
45.
Saffanah Khuder Mahmood Md Zuki Abu Bakar Zakaria Intan Shameha Binti Abdul Razak Loqman Mohamed Yusof Alhaji Zubair Jaji Isa Tijani Nahidah Ibrahim Hammadi 《Biochemistry and Biophysics Reports》2017
The demands for applicable tissue-engineered scaffolds that can be used to repair load-bearing segmental bone defects (SBDs) is vital and in increasing demand. In this study, seven different combinations of 3 dimensional (3D) novel nanocomposite porous structured scaffolds were fabricated to rebuild SBDs using an extraordinary blend of cockle shells (CaCo3) nanoparticles (CCN), gelatin, dextran and dextrin to structure an ideal bone scaffold with adequate degradation rate using the Freeze Drying Method (FDM) and labeled as 5211, 5400, 6211, 6300, 7101, 7200 and 8100. The micron sized cockle shells powder obtained (75 µm) was made into nanoparticles using mechano-chemical, top-down method of nanoparticles synthesis with the presence of the surfactant BS-12 (dodecyl dimethyl bataine). The phase purity and crystallographic structures, the chemical functionality and the thermal characterization of the scaffolds’ powder were recognized using X-Ray Diffractometer (XRD), Fourier transform infrared (FTIR) spectrophotometer and Differential Scanning Calorimetry (DSC) respectively. Characterizations of the scaffolds were assessed by Scanning Electron Microscopy (SEM), Degradation Manner, Water Absorption Test, Swelling Test, Mechanical Test and Porosity Test. Top-down method produced cockle shell nanoparticles having averagely range 37.8±3–55.2±9 nm in size, which were determined using Transmission Electron Microscope (TEM). A mainly aragonite form of calcium carbonate was identified in both XRD and FTIR for all scaffolds, while the melting (Tm) and transition (Tg) temperatures were identified using DSC with the range of Tm 62.4–75.5 °C and of Tg 230.6–232.5 °C. The newly prepared scaffolds were with the following characteristics: (i) good biocompatibility and biodegradability, (ii) appropriate surface chemistry and (iii) highly porous, with interconnected pore network. Engineering analyses showed that scaffold 5211 possessed 3D interconnected homogenous porous structure with a porosity of about 49%, pore sizes ranging from 8.97 to 337 µm, mechanical strength 20.3 MPa, Young's Modulus 271±63 MPa and enzymatic degradation rate 22.7 within 14 days. 相似文献
46.
Andrew J.Parsons Ifty Ahmed Papia Haque Ben Fitzpatrick Muhammad I.K.Niazi Gavin S.Walker Chris D.Rudd 《仿生工程学报(英文版)》2009,6(4):318-323
We investigate high-modulus degradable materials intended to replace metals in biomedical applications.These are typicallycomposites comprising a polylactide(PLA)matrix reinforced with phosphate glass fibres,which provide reinforcementsimilar to E-glass but are entirely degradable in water to produce,principally,calcium phosphate.We have made compositesusing a variety of fibre architectures,from non-woven random mats to unidirectional fibre tapes.Flexural properties in theregion of 30 GPa modulus and 350 MPa strength have been achieved-directly comparable to quoted values for human corticalbone.In collaboration with other groups we have begun to consider the development of foamed systems with structures mimickingcancellous bone and this has shown significant promise.The fibres in these foamed structures provide improved creepresistance and reinforcement of the pore walls.To date the materials have exhibited excellent cellular responses in vitro andfurther studies are due to include consideration of the surface character of the materials and the influence of this on cell interaction,both with the composites and the glass fibres themselves,which show promise as a standalone porous scaffold. 相似文献
47.
The effect of temperature on the adsorption of a simple mixture (Ar/Kr) in disordered porous materials is investigated by means of molecular simulation. In the larger mesopores of porous silica glasses, capillary condensation occurs upon decreasing the temperature. At temperatures above the capillary condensation temperature, Kr is preferentially adsorbed at the pore surface and Ar adsorption occurs in regions of low Kr density. For temperatures below the capillary condensation temperature, Ar density surprisingly increases as temperature increases, the behaviour that is consistent with an over-solubility effect. In contrast, in the disordered sub-nanoporous carbon, filling of the pores occurs in a reversible and continuous way upon decreasing the temperature, owing to the small size and amorphous shape of the pores. These results show that the crossover between capillary condensation and continuous reversible filling observed for pure fluids in pores also exists for mixtures. We also show that the Kr selectivity exhibits a minimum in the disordered porous silica that is located at the capillary condensation temperature. In contrast, in the disordered porous carbon where no capillary condensation occurs, the selectivity decreases monotonically with increasing the temperature. These results shed light on low-temperature adsorption of mixtures confined in porous materials and provide a guide to design efficient phase separation processes. 相似文献
48.
One‐Step Template‐Free Synthesis of Highly Porous Boron Nitride Microsponges for Hydrogen Storage
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Highly porous, sponge‐like boron nitride materials, namely microsponges (BNMSs), with ultrahigh surface areas up to 1900 m2 g‐1, are prepared by a facile, one‐step, template‐free reaction of boric acid and dicyanamide. Detailed analysis confirms the increase of the interlayer (0002) distances compared to standard graphitic BN and reveals special dislocation structures in the BNMSs. The resulting textural parameters such as the Brunauer‐Emmett‐Teller (BET) specific surface areas and pore volumes are easily tunable over a wide range by adjusting the synthesis temperature or composition of the precursors. It is demonstrated that these microporous materials (with pore widths of 1.0 nm) display comparatively high and reversible H2 sorption capacities from 1.65 to 2.57 wt% at 1 MPa and –196 °C on a material basis. 相似文献
49.
Solar Cells: Triple‐Layer Structured Composite Separator Membranes with Dual Pore Structures and Improved Interfacial Contact for Sustainable Dye‐Sensitized Solar Cells (Adv. Energy Mater. 13/2014)
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50.