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[Display omitted] • Solvent-free strategy was developed to synthesize porous carbon (MIC x) doped with rich Faradaic active oxygen (5.8–8.2 atom%). • The resultant MICx owns surface area of 326–427 m2/g and large packing density of 1.12–1.28 g/cm3. • The MICx based electrode achieves superior supercapacitor performances with both high gravimetric and volumetric performances. In the selection of carbon-based electrode materials for supercapacitive energy storage, it is hard to get one that is high in both gravimetric and volumetric performance because there is a trade-off between them. In the presented work, microporous carbon materials denoted herein as MIC x were synthesized through catechol polymerization in the presence of molten FeCl 3. As complexing agent, the iron species coordinate with catechol oligomers, functioning as template as well as catalyst in the synthesis of the microporous carbon. The in situ formation of micropores and carbonaceous skeleton is induced by the carbonyl/hydroxyl redox pairs upon catalytic graphitization during carbonization. The derived nanocarbons have high microporosity (70.6 %–79.2 %) and rich oxygenate functionalities (carbonyl: 3.3–4.0 atom% and hydroxyl: 2.5–4.2 atom%). The FeC x materials are high in faradaic activity. For example, the FeC873-based electrode displays excellent supercapacitor performances: capacitance of 440F/g@1.0 A/g (equivalent to 537F/cm3@1.0 A/g) and 289F/g@20 A/g (equivalent to 353F/cm3@20 A/g), large energy density of 25.5 Wh/kg@900 W/kg (equivalent to 31.1 Wh/L@1098 W/L), and good cycling stability (ca.100 % capacitance retention after 20 000 continual charge/discharge cycles). [ABSTRACT FROM AUTHOR]

Three alkaline metal carbonates of MgCO 3 , CaCO 3 and BaCO 3 with different morphology, surface basicity and thermal stability were used as templates to find the template effect towards the morphology, oxygen species as well as supercapacitor performance of the derived nanocarbons. [Display omitted] • Three alkaline carbonates were adopted as catalytic templates for the fabrication of nanocarbons. • Residual oxygen and morphology of nanocarbons are greatly influenced by the nature of templates. • Residual oxygen in final products mainly exists in forms of redox-active carbonyl and hydroxyl. • The derived MgC displays superior surface area and supercapacitor performance. Nanocasting techniques are widely adopted for the fabrication of nanocarbons. However, there is little research on the effect of template nature on the physicochemical properties and performances of the nanocarbons. Herein, we investigated how the morphology, oxygen species as well as supercapacitor performance of the derived nanocarbons were governed by the morphology, surface basicity and thermal stability of MgCO 3 , CaCO 3 and BaCO 3 when the alkaline metal carbonates were used as templates. Using MgCO 3 as catalytic template, the MgC973 produced after carbonization at 973 K has ultrathin nanosheet morphology (∼20 nm), large specific surface area (952 m2/g), and superior supercapacitor performances, showing high capacitance of 421F/g@1.0 A/g (maintaining 306F/g@20 A/g), and large energy density of 31.1 Wh/kg@1000 W/kg. The superiority can be ascribed to the ultrathin morphology and thermal instability of the MgCO 3 template, which upon decomposition generates CO 2 and in situ activates the carbon skeleton. Moreover, the surface alkalinity of templates is conducive to the retention of electrochemically active oxygen, and BaC973 is with oxygen content (9.1 atom%) higher than MgC973 (7.9 atom%) and CaC973 (8.8 atom%). The present work provides insightful ideas for the synthesis of unique carbon materials with specific functionalities through the selection of suitable templates. [ABSTRACT FROM AUTHOR]

Carbon-based electrodes are usually poor in volumetric supercapacitor performance in terms of volumetric capacitance (<200 F/cm3) and energy density (usually <10 Wh/L) resulted from low packing density. Herein, we propose a strategy for the preparation of nanocarbon electrodes that are ultrahigh in volumetric supercapacitor performance by creating nanocarbon with high packing density and rich pseudocapacitive nitrogen doping, in which the nitrogen doping is to provide extra capacitance. The derived nanocarbons (ZHNCs) have not only large packing density of 1.14–1.49 g/cm3 and rich nitrogen content (12.3–24.8 atom%), but also homogeneous element distribution. Benefited from the synergetic effect of the above characteristics, the ZHNCs-based electrodes exhibit superior volumetric performances of ultrahigh capacitance of 528 F/cm3 in 1.0 M H 2 SO 4 and 465 F/cm3 in 6.0 M KOH, large energy density of 26.8 Wh/L at 2682 W/L, and impressive cycling stability with about 95% capacitance retention after continual charge/discharge of 20 000 cycles at current density of 20 A/g, indicative of potential applications in the fields of energy storage. [Display omitted] • Nanocarbons (ZHNCs) with high density and rich nitrogen (24.3 atom%) were fabricated. • ZHNCs achieves large gravimetric- (464 F/g) and ultrahigh volumetric capacitances (528 F/cm3). • The ZHNCs based electrode shows a large energy density of 26.8 Wh/L at 2682 W/L. • ZHNCs electrode exhibits superior stability with about 95% capacitance retention after 20 000 cycles. [ABSTRACT FROM AUTHOR]

[Display omitted] • An all-solid-state (ASS) strategy without using any solvents and activators was developed. • The ASS strategy derived carbon owns abundant nitrogen species and large packing density. • The resultant product show superior supercapacitor performances with both high gravimetric and volumetric performances. Template synthesis of porous carbon with rich functionalities by a scalable strategy without using any solvents and activators will be a green and promising route. Herein, we reported an all-solid-state synthesis strategy by mixing glucose and graphitic carbon nitride (g -C 3 N 4) by milling and then undergoing a segmented carbonization in which first at low temperature of 573 K to polymerize sucrose onto g -C 3 N 4 , then at high temperature of 973 K to carbonized the composite to obtain a porous carbon (denoted as GNC) with abundant nitrogen species over 20 atom% and large packing density (0.91–1.25 g cm−3). Due to the features of large packing density and rich electrochemically-active N species, as electrode for supercapacitive energy storage, the developed GNC exhibit a comparable energy storage level with both high gravimetric energy density of 26.8 Wh kg−1@1000 W kg−1 and volumetric energy density of 30.8 Wh L−1@1150 W L−1, suggesting a potentiality in energy storage field. Importantly, the present strategy owns characteristics of ease of operation, green and scalable, which would be a promising synthesis route towards the fabrication of functional carbon utilizing in many fields like sorption & separation, catalysis, energy storage and so on. [ABSTRACT FROM AUTHOR]

[Display omitted] • Co 3 O 4 nanoneedle arrays is grafted on V 2 O 5 nanosheet arrays to form VNSAs/CNNAs. • The VNSAs/CNNAs composite shows a high C s value of 1023 F g−1at 5 mV s−1. • The VNSAs/CNNAs composite can work under a large voltage window of 1.6 V. • The VNSAs/CNNAs composite has a high E d value of 127.3 Wh kg−1 at 400 W kg−1. • The high performance is ascribed to the synergistic effect of V 2 O 5 and Co 3 O 4. In this work, two-dimensional V 2 O 5 nanosheet arrays/one-dimensional Co 3 O 4 nanoneedle arrays (2D VNSAs/1D CNNAs) composite is successfully prepared on nickel foam substrate. A variety of structural characterization techniques (SEM, XRD, EDS, TEM, and XPS) show that the as-prepared composite is V 2 O 5 monocrystal with a layered structure grafting by Co 3 O 4 polycrystal with a 1D needle-like structure. The VNSAs/CNNAs composite is used as supercapacitor electrode material. In a three-electrodes system, it shows high specific capacitance (C s) values (1023 F g−1@5 mV s−1 from CV curve and 826 F g−1@0.5 A/g from GCD curve), a high coulombic efficiency (98.6 %@10 A/g), a good cyclic stability (92.7 % after 6000 cycles), a low charge transfer resistance (2.7 Ω), and a fast ionic diffusion rate (2.01 × 10−8 cm2 s−1). In a two-electrodes system, the assembled VNSAs/CNNAs//VNSAs/CNNAs symmetric supercapacitor has C s values of 445 F g−1@5 mV s−1 and 363 F g−1@0.5 A/g. Its cycle stability and rate capability could reach up to 92.3 % and 90.7 % after 6000 cycels, respectively. It also shows a high energy density (E d) of 127.3 Wh kg−1@400 W kg−1 and can retain 72.2 Wh kg−1@8000 W kg−1. The excellent electrochemical properties indicate that VNSAs/CNNAs composite can greatly increase the E d of supercapacitors. [ABSTRACT FROM AUTHOR]

[Display omitted] • Ternary metal oxide electrodes are prepared by a feasible green hydrothermal method. • Nanografting effectively increases active interfaces with interpenetrating channels. • These electrodes demonstrate an improved specific capacitance of 788F g−1. • The symmetrical supercapacitors show an energy density of 138 W h kg−1 at 450 W kg−1. • The steadiness of these supercapacitors is retained at 93.5 % after 5000 cycles. Supercapacitors with improved specific capacitance, long cycling life, high power density and energy density are fabricated to close the gap between traditional and emerging energy storage. We develop interactive ternary metal oxides nano-ribbon electrodes used to assemble symmetric supercapacitor. The well-aligned vanadium oxide ribbon arrays act as the matrix, growing from nickel oxide/nickel substrate and then being grafted by manganese oxide nanoparticles. These tri-metallic oxides are formed in a cost-effective and green hydrothermal chemistry. The electrodes composed of ribbon arrays retain their crystallographic structure during charging and discharging processes, enabling steadiness at 83.6 % after 10,000 cycles. These as-prepared electrodes demonstrate a specific capacitance of 788 F g−1 at 5 mV s−1. The symmetrical supercapacitors are assembled using triple component electrodes, achieving a high energy density of 138 W h kg−1 at a power density of 450 W kg−1. These binderless single-cell devices are reported with a simplified design showing 10–20 times higher energy density in comparison with reported results of the V 2 O 5 -MnO 2 system. The nanografting results in reactive interfaces with interpenetrating channels for efficient ion transport and electron conduction. The advances to design nanostructured supercapacitor materials are based on these heterojunction arrays to enhance their supercapacitive performances. [ABSTRACT FROM AUTHOR]

V 2 O 5 nanobelt arrays (VNBAs) is fabricated on Ni foam by using an easy hydrothermal route and then NiO nanosheet arrays (NNSAs) is grown on VNBAs by using a simple chemical bath deposition approach to form VNBAs/NNSAs composite. It is found that the monocrystalline VNBAs with a lamellar structure is uniformly distributed on nickel foam and the polystalline NNSAs with a close packed structure is closely covered on the VNBAs. CV, GCD, EIS and CA electrochemical techniques are used to test the supercapacitive properties of the VNBAs/NNSAs composite. The single electrode displays a high specific capacity of 875 F g−1, a good cycling stability of 96.1%, a small charge transfer resistance of 1.32 Ω and a rapid ion diffusivity of 2.5 × 10−8 cm2 s−1. The symmetric supercapacitor combined by the VNBAs/NNSAs displays a large energy density of 120.1 W h kg−1 at 400 W kg−1 and it retains 68.3 W h kg−1 at 8000 W kg−1. The VNBAs/NNSAs composite with high electrochemical performance is a potential supercapacitor electrode material. [Display omitted] • The V 2 O 5 nanobelt arrays (VNBAs) is successfully prepared on a nickel foam. • The NiO nanosheet arrays (NNSAs) is compounded on the VNBAs to form a hierarchy. • The VNBAs/NNSAs shows a high specific capacitance of 875 F g−1 at 5 mV s−1. • The VNBAs/NNSAs has an energy density of 120.1 W h kg−1 at 400 W kg−1. • The high performance of the VNBAs/NNSAs are ascribed to its synergistic effect. [ABSTRACT FROM AUTHOR]

[Display omitted] • V 2 O 5 nanobelt arrays@RuO 2 nanosheet arrays (VNBs@RNSs) is prepared on a nickel foam. • The VNBs@RNSs electrode shows a specific capacitance of 971F g−1 at 5 mV s−1. • The VNBs@RNSs supercapacitor has an energy density of 174.2 W h kg−1 at 450 W kg−1. • The cyclic steadiness of the supercapacitor is retained at 80.4% after 10,000 cycles. • The high performance of VNBs@RNSs is ascribed to their synergistic effect. V 2 O 5 nanobelt arrays (VNBs) are directly synthesized on porous nickel as the primary structure, and then the VNBs are completely covered by RuO 2 nanosheets (RNSs) as the secondary structure to create a core–shell heterojunction. The as-prepared VNBs@RNSs core–shell heterojunction is systematically researched through SEM, EDS, XRD, XPS and TEM, and the growth process is investigated in detail by sampling at different time. The VNBs@RNSs has a superb specific capacitive value of 971F g−1 at a voltage scanning speed of 5 mV s−1, a better cyclic steadiness of 80.4 % after recycling 10,000 times, a small charge transferring resistance value of 1.8 Ω and a fast effective diffusion coefficient of 1.01 × 10−8 cm2 s−1 calculated by CV, GCD, AC impedance and CA electrochemical techniques in a three-electrode testing system. A symmetrical electrochemical capacitor assembled by the as-prepared VNBs@RNSs electrode material has a superior energy density of 174.2 W h kg−1 at a power density of 450 W kg−1 and still retains 95.9 W h kg−1 at 9000 W kg−1 in a two-electrode testing system. The improved supercapacitive performance makes the VNBs@RNSs as a superior electrode material for supercapacitor. [ABSTRACT FROM AUTHOR]

[Display omitted] • V 2 O 5 nanobelt arrays@RuO 2 nanosheet arrays (VNBs@RNSs) is prepared on a nickel foam. • The VNBs@RNSs electrode shows a specific capacitance of 971F g−1 at 5 mV s−1. • The VNBs@RNSs supercapacitor has an energy density of 174.2 W h kg−1 at 450 W kg−1. • The cyclic steadiness of the supercapacitor is retained at 80.4% after 10,000 cycles. • The high performance of VNBs@RNSs is ascribed to their synergistic effect. V 2 O 5 nanobelt arrays (VNBs) are directly synthesized on porous nickel as the primary structure, and then the VNBs are completely covered by RuO 2 nanosheets (RNSs) as the secondary structure to create a core–shell heterojunction. The as-prepared VNBs@RNSs core–shell heterojunction is systematically researched through SEM, EDS, XRD, XPS and TEM, and the growth process is investigated in detail by sampling at different time. The VNBs@RNSs has a superb specific capacitive value of 971F g−1 at a voltage scanning speed of 5 mV s−1, a better cyclic steadiness of 80.4 % after recycling 10,000 times, a small charge transferring resistance value of 1.8 Ω and a fast effective diffusion coefficient of 1.01 × 10−8 cm2 s−1 calculated by CV, GCD, AC impedance and CA electrochemical techniques in a three-electrode testing system. A symmetrical electrochemical capacitor assembled by the as-prepared VNBs@RNSs electrode material has a superior energy density of 174.2 W h kg−1 at a power density of 450 W kg−1 and still retains 95.9 W h kg−1 at 9000 W kg−1 in a two-electrode testing system. The improved supercapacitive performance makes the VNBs@RNSs as a superior electrode material for supercapacitor. [ABSTRACT FROM AUTHOR]