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Cost‐effective synthesis of carbon nanospheres with a desirable mesoporous network for diversified energy storage applications remains a challenge. Herein, a direct templating strategy is developed to fabricate monodispersed N‐doped mesoporous carbon nanospheres (NMCSs) with an average particle size of 100 nm, a pore diameter of 4 nm, and a specific area of 1093 m2 g?1. Hexadecyl trimethyl ammonium bromide and tetraethyl orthosilicate not only play key roles in the evolution of mesopores but also guide the assembly of phenolic resins to generate carbon nanospheres. Benefiting from the high surface area and optimum mesopore structure, NMCSs deliver a large specific capacitance up to 433 F g?1 in 1 m H2SO4. The NMCS electrodes–based symmetric sandwich supercapacitor has an output voltage of 1.4 V in polyvinyl alcohol/H2SO4 gel electrolyte and delivers an energy density of 10.9 Wh kg?1 at a power density of 14014.5 W kg?1. Notably, NMCSs can be directly applied through the mask‐assisted casting technique by a doctor blade to fabricate micro‐supercapacitors. The micro‐supercapacitors exhibit excellent mechanical flexibility, long‐term stability, and reliable power output.  相似文献   

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MXene, an important and increasingly popular category of postgraphene 2D nanomaterials, has been rigorously investigated since early 2011 because of advantages including flexible tunability in element composition, hydrophobicity, metallic nature, unique in‐plane anisotropic structure, high charge‐carrier mobility, tunable band gap, and favorable optical and mechanical properties. To fully exploit these potentials and further expand beyond the existing boundaries, novel functional nanostructures spanning monolayer, multilayer, nanoparticles, and composites have been developed by means of intercalation, delamination, functionalization, hybridization, among others. Undeniably, the cutting‐edge developments and applications of clay‐inspired 2D MXene platform as electrochemical electrode or photo‐electrocatalyst have conferred superior performance and have made significant impact in the field of energy and advanced catalysis. This review provides an overview of the fundamental properties and synthesis routes of pure MXene, functionalized MXene and their hybrids, highlights the state‐of‐the‐art progresses of MXene‐based applications with respect to supercapacitors, batteries, electrocatalysis and photocatalysis, and presents the challenges and prospects in the burgeoning field.  相似文献   

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From graphene oxide wrapped iron oxide particles with etching/reduction process, high‐performance anode and cathode materials of lithium‐ion hybrid supercapacitors are obtained in the same process with different etching conditions, which consist of partially etched crumpled graphene (CG) wrapped spiky iron oxide particles (CG@SF) for a battery‐type anode, and fully etched CG for a capacitive‐type cathode. The CG is formed along the shape of spikily etched particles, resulting in high specific surface area and electrical conductivity, thus the CG‐based cathode exhibits remarkable capacitive performance of 210 F g?1 and excellent rate capabilities. The CG@SF can also be ideal anode materials owing to spiky and porous morphology of the particles and tightly attached crumpled graphene onto the spiky particles, which provides structural stability and low contact resistance during repetitive lithiation/delithiation processes. The CG@SF anode shows a particularly high capacitive performance of 1420 mAh g?1 after 270 cycles, continuously increases capacity beyond the 270th cycle, and also maintains a high capacity of 170 mAh g?1 at extremely high speeds of 100 C. The full‐cell exhibits a higher energy density up to 121 Wh kg?1 and maintains high energy density of 60.1 Wh kg?1 at 18.0 kW kg?1. This system could thus be a practical energy storage system to fill the gap between batteries and supercapacitors.  相似文献   

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The high‐performance electrode materials with tuned surface and interface structure and functionalities are highly demanded for advanced supercapacitors. A novel strategy is presented to conFigure high‐stacking‐density, superior‐roughness nickel manganese layered double hydroxide (LDH) bridged by vertically aligned graphene (VG) with nickel foam (NF) as the conductive collector, yielding the LDH‐NF@VG hybrids for asymmetric supercapacitors. The VG nanosheets provide numerous electron transfer channels for quick redox reactions, and well‐developed open structure for fast mass transport. Moreover, the high‐stacking‐density LDH grown and assembled on VG nanosheets result in a superior hydrophilicity derived from the tuned nano/microstructures, especially microroughness. Such a high stacking density with abundant active sites and superior wettability can be easily accessed by aqueous electrolytes. Benefitting from the above features, the LDH‐NF@VG can deliver a high capacitance of 2920 F g?1 at a current density of 2 A g?1, and the asymmetric supercapacitor with the LDH‐NF@VG as positive electrode and activated carbon as negative electrode can deliver a high energy density of 56.8 Wh kg?1 at a power density of 260 W kg?1, with a high specific capacitance retention rate of 87% even after 10 000 cycles.  相似文献   

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Compared to traditional metal oxides, metal‐organic frameworks exhibit excellent properties, such as a high surface area, significant thermal stability, low density, and excellent electrochemical performance. Here, a simple process is proposed for the fabrication of rod‐like vanadium metal‐organic frameworks (VIV(O)(bdc), bdc = 1,4‐benzenedicarboxylate, or MIL‐47), and the effect of the structure on the electrochemical performance is investigated via a series of electrochemical measurements. The VIV(O)(bdc) electrode exhibits a maximum specific capacitance of 572.1 F g?1 at current densities of 0.5 A g?1. More significantly, aqueous and solid‐state asymmetric supercapacitors are successfully assembled. The solid‐state device shows an excellent energy density of 6.72 mWh cm?3 at a power density of 70.35 mW cm?3. This superior performance confirms that VIV(O)(bdc) electrodes are promising materials for applications in supercapacitors.  相似文献   

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Planar micro‐supercapacitors are attractive for system on chip technologies and surface mount devices due to their large areal capacitance and energy/power density compared to the traditional oxide‐based capacitors. In the present work, a novel material, niobium nanowires, in form of vertically aligned electrodes for application in high performance planar micro‐supercapacitors is introduced. Specific capacitance of up to 1 kF m?2 (100 mF cm?2) with peak energy and power density of 2 kJ m?2 (6.2 MJ m?3 or 1.7 mWh cm?3) and 150 kW m?2 (480 MW m?3 or 480 W cm?3), respectively, is achieved. This remarkable power density, originating from the extremely low equivalent series resistance value of 0.27 Ω (2.49 µΩ m2 or 24.9 mΩ cm2) and large specific capacitance, is among the highest for planar micro‐supercapacitors electrodes made of nanomaterials.  相似文献   

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Flexible and highly efficient energy storage units act as one of the key components in portable electronics. In this work, by planar‐integrated assembly of hierarchical ZnCo2O4 nanowire arrays/carbon fibers electrodes, a new class of flexible all‐solid‐state planar‐integrated fiber supercapacitors are designed and produced via a low‐cost and facile method. The as‐fabricated flexible devices exhibit high‐efficiency, enhanced capacity, long cycle life, and excellent electrical stability. An enhanced distributed‐capacitance effect is experimentally observed for the device. This strategy enables highly flexible new structured supercapacitors with maximum functionality and minimized size, thus making it possible to be readily applied in flexible/portable photoelectronic devices.  相似文献   

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In this study, integrated plaster‐like micro‐supercapacitors based on medical adhesive tapes are fabricated by a simple pencil drawing process combined with a mild solution deposition of MnO2. These solid micro‐supercapacitors not only exhibit excellent stretchability, flexibility, and biocompatibility, but also possess outstanding electrochemical performances, such as exceptional rate capability and cycling stability. Hence they may act as skin‐mountable and thin‐film energy storage devices of high efficiency to power miniaturized and wearable electronic devices.  相似文献   

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Flexible planar micro‐supercapacitors (MSCs) with unique loose and porous nanofiber‐like electrode structures are fabricated by combining electrochemical deposition with inkjet printing. Benefiting from the resulting porous nanofiber‐like structures, the areal capacitance of the inkjet‐printed flexible planar MSCs is obviously enhanced to 46.6 mF cm?2, which is among the highest values ever reported for MSCs. The complicated fabrication process is successfully averted as compared with previously reported best‐performing planar MSCs. Besides excellent electrochemical performance, the resultant MSCs also show superior mechanical flexibility. The as‐fabricated MSCs can be highly bent to 180° 1000 times with the capacitance retention still up to 86.8%. Intriguingly, because of the remarkable patterning capability of inkjet printing, various modular MSCs in serial and in parallel can be directly and facilely inkjet‐printed without using external metal interconnects and tedious procedures. As a consequence, the electrochemical performance can be largely enhanced to better meet the demands of practical applications. Additionally, flexible serial MSCs with exquisite and aesthetic patterns are also inkjet‐printed, showing great potential in fashionable wearable electronics. The results suggest a feasible strategy for the facile and cost‐effective fabrication of high‐performance flexible MSCs via inkjet printing.  相似文献   

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