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Osmia solitary bees are important pollinators of various crops worldwide. Refrigeration has been widely used to synchronize the emergence time of Osmia species from cocoons with the blooming time of different crops, but the fitness of Osmia after refrigeration remains unknown. Here, the effects of long‐term refrigeration at 0 °C on the vitality, flight ability, and metabolism of Osmia excavata, which is known as the "king of pollination" in China, were studied. The survival rate (>90% before 120 d), weight loss rate (<15% after 170 d), and mean flight speed of O. excavata were not greatly affected after long‐term refrigeration. The content of fats, which have antifreeze and energy storage properties, was not significantly altered in O. excavata before 130 d of refrigeration, which might explain why the survival rates and flight speed of O. excavata remained high after long‐term refrigeration. However, the flight duration and distance decreased significantly (P < 0.05), and both were positively correlated with the reduced trehalose levels in O. excavata (r = [+0.69] – [+0.71]; P < 0.05). Overall, these findings indicate that the pollination potential of O. excavata for various crops with different flowering periods is high after long‐term refrigeration; however, long‐term refrigeration may decrease pollination efficiency. Our findings highlight new research directions that could improve the ecological service function of refrigerated O. excavata. [ABSTRACT FROM AUTHOR]

[Display omitted] • Mg-Co-Ni LDH were homogenously grown on the surface of reduced graphene (Mg-Co-Ni LDH/rG- x). • The Mg-Co-Ni LDH/rG- x was fabricated by a novel ball milling combined ion-exchange method. • The present ball milling combined ion-exchange method is versatile and does not needs extra alkali sources or auxiliary assembly reagents. • The Mg-Co-Ni LDH/rG- x based asymmetric supercapacitor achieve high energy density and superlong cycling stability. As an electrode for energy storage, the inherently poor conductivity of metal hydroxides (MHs) can be improved by in situ growth of MHs on conductive carbon based substrates so that their performances on energy storage could be enhanced to a high level. However, the incompatibility of hydrophilic component (metal hydroxides) and hydrophobic counterpart (carbon based materials) makes it difficult to be accomplished. Herein, we presented a scalable and easy-operated strategy by ball-milling combined with ion-exchange technique to grow Mg-Co-Ni LDH (layered double hydroxides) on reduced graphene, in which ball-milling was utilized to disperse the staring material of magnesium acetate on graphene oxide (GO) to obtain the composite of Mg(Ac) 2 /GO. The composite can be in situ transformed to MgO/reduced grapheme (rG) by following heat treatment. While, the ion-exchange reaction could enables the in situ growth of Mg-Co-Ni LDHs on the reduced graphene. The derived products (denoted as Mg-Co-Ni LDH/rG- x) owns nanosheet morphology, surface area of 59–115 m2/g, homogenous elements distribution. As electrode for supercapacitor, the maximum capacitance of 1204F/g@1.0 A/g was achieved and the corresponding asymmetric supercapacitor device shows a large energy density of 44.3 Wh/kg@800 W/kg. Particularly, a superlong cycling stability with 90.5% capacitance retention of the first cycle was attained after continuous charge/discharge for 20 000 cycles at current density of 5.0 A/g, promising great potential for practical energy storage application. The present strategy is simple and scalable that can be widely applied to the synthesis of various hydroxides/oxides or multi-component hydroxides/oxides on carbon substrates forming a composite structure, thus offers a great potential for broad application areas including catalysis, adsorption, energy storage, etc. [ABSTRACT FROM AUTHOR]

Electrochromic energy storage devices (EESDs) are incorporating electrochromic and energy storage functions, which can visually display energy storage levels in real‐time to promote the next generation of transparent battery development. However, their performances are still limited for practical applications. Herein, a self‐powered EESD based on complex niobium tungsten oxide is designed using aqueous Zn2+ and hybrid Zn2+/Mn+ (Mn+ = Al3+, Mg2+, and K+) electrolytes. The results reveal that the use of Zn2+/Al3+ hybrid electrolyte achieves superior electrochromic performances including a short self‐coloring time, high optical contrast, and excellent cyclic stability. Furthermore, it is also found that the self‐coloring process is accompanied by a high discharged capacity of niobium tungsten oxide, with high optical modulation in the Zn2+/Al3+ hybrid electrolyte. The detailed mechanism on the performances of EESD using various electrolytes is systematically studied. This work provides a simple and effective strategy for an aqueous and self‐powered EESD with high optical contrast and good cycle stability. [ABSTRACT FROM AUTHOR]

[Display omitted] • Electrochemically active Oxygen doped carbon (O-PCNs) was fabricated by superbase templated method. • The template basicity on the functionalities and the supercapacitor performances of the derived O-PCNs were disclosed. • The O-PCN-20 is rich in porosity, large in surface area (930 m2/g) and high in active oxygen content (11.4 atom%). • · The O-PCN-20 electrode exhibits large capacitance of 375 F/g@1.0 A/g and energy density of 25.7 Wh/kg@900 W/kg. Templating techniques have been widely adopted for the synthesis of porous carbons, such as oxygen-doped porous carbon nanosheets (O-PCNs), but the effect of the surface characteristics of templates on the surface functionality and performance of a derived carbon has not been well studied. Herein, a series of laboratory-made superbases of K/Mg(OH) 2 with different K/Mg ratios were employed as template to fabricate nanocarbon materials. The aim is to find out how the strength of template basicity could influence the surface functionalities and the supercapacitor performances of the derived O-PCNs. The resulting materials are rich in conjugated hydroxyl and carbonyl groups that are electrochemically active owing to the protection of the conjugated hydroxyl group by KOH and the dehydrogenation step catalyzed by magnesium oxide. Systematic investigations revealed that with the increase of basic strength, the content of the derived electrochemically active oxygen species in the forms of conjugated carbonyl (C O) and hydroxyl (C OH) first increases from 8.4 atom% to 11.4 atom% then decreases to 9.25 atom%. Moreover, the microporosity of the O-PCNs stepwise increases with the rise of KOH loading, ascribable to the effect of KOH etching on the carbon skeleton. The O-PCN-20 templated by 20 % K/Mg(OH) 2 is rich in porosity, large in surface area (930 m2/g) and high in active oxygen content (11.4 atom%). With high active surface area and extra Faradaic capacitance, O-PCN-20 exhibited superior supercapacitor performances including large specific capacitance of 375 F/g@1.0 A/g, high rate capability of 81.1 % (from 1.0 A/g to 20 A/g), energy density of 25.7 Wh/kg@900 W/kg and excellent cycling stability with near 100 % capacitance retentions after 10 000 cycles and more than 86.2 % capacitance retention over 20 000 cycles at large current density of 10 A/g, indicating O-PCN-20 has potential to be used as electrode material for energy storage devices. [ABSTRACT FROM AUTHOR]

All-solid-state lithium-metal batteries have been regarded as the next-generation energy storage due to the potential high safety and high energy density. However, for oxide solid electrolytes (SEs), the relatively low ionic conductivities and the growth of lithium dendrite leading to safety issues limit their commercialization. Here, we systematically investigate the influences of external magnetic field on electrochemical performances of oxide SEs. It reveals that the magnetic field can improve ionic conductivity of SEs and the cycle performance in Li symmetric cells. The enhanced performance is because the magnetohydrodynamics effect can promote diffusion in SEs and homogenize distribution of lithium deposition to avoid the propagation of lithium dendrite. This strategy can be extent to other types of SEs or various energy applications. [ABSTRACT FROM AUTHOR]

[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]

[Display omitted] • Expired coffee derived carbons (HCDC) achieves high packing density of 1.81–1.83 cm3/g. • The derived HCDC owns rich nitrogen (4.5 atom%) and oxygenic (12.0 atom%) functionalities. • The HCDC electrode achieves high gravimetric and volumetric capacitance of 312F/g and 567F/cm3. • The HCDC electrode exhibits a high volumetric energy density of 27.8 Wh/L@1820 W/L. Clean production of activated carbon from household expired food provide an alternative way to get value-added product thus benefits waste reutilization and environmental protection. Herein, we fabricated N, O co-doped activated carbons (HCDC) from expired coffee to by a green route of direct water vapor carbonization/activation approach. In our approach, the expired coffee was firstly grinded and then carbonized under water vapor atmosphere. The derived HCDC owns low surface area (172–184 m2/g), large packing density (1.81–1.83 cm3/g), rich redox-active nitrogen (4.5 atom%) and oxygenic (12.0 atom%) functionalities. As electrode for supercapacitor, the HCDC achieves a high gravimetric capacitance of 312F/g at 1.0 A/g (vs 258F/g of commercial AC) and the value can be maintained 223F/g at 20 A/g, showing a high rate capability of 71.5%. Particularly, because of the large packing density, the HCDC exhibits an excellent volumetric supercapacitor performances: ultrahigh volumetric capacitance of 567F/cm3 (vs 165F/cm3 of commercial AC) and large energy density of 27.8 Wh/L@1820 W/L (vs 7.5 Wh/L@576 W/L for commercial AC) and superlong cycling stability with near 100 capacitance retention after continual 30 000 cycles at large current density of 9.0 A/g, suggesting a promising application for practical energy storage devices. [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]

This study aims to optimize the fabrication parameters of nickel‑iron phosphate (NiFe-P) electrode to achieve a high areal capacity electrode for supercapattery. The fabrication of binder-free NiFe-P electrode on nickel foam (NF) employs a one-step hydrothermal synthesis method. Further, central composite design (CCD) under the response surface methodology (RSM) is used to optimize the electrode's performance. The factors evaluated are synthesis temperature (60 to 180 °C), time (6 to 24 h), and the molar ratio of precursor solution (1:3, 1:1, 3:1 of Fe: Ni), whereas the response is the areal capacity of NiFe-P electrode at the scan rate of 3 mV/s in a standard three-electrode cell system. The optimal temperature, time, and molar ratio (Fe:Ni) are determined to be 100 °C, 14 h, and 3:1, respectively. The model is confirmed within the confidence interval and prediction as well as comparable with a 10% percentage error between the experimental and predicted specific capacity. The specific capacity of the optimized electrode is 446 C/g at a scan rate of 3 mV/s using cyclic voltammetry (CV) and 413.75 C/g at a current density of 1 A/g in 1 M KOH using a standard three-electrode cell system. Supercapattery is fabricated by combining NiFe-P and activated carbon electrodes (NiFe-P//AC) as positive and negative electrodes, respectively, to evaluate the two-electrode cell system. The results show the maximum power density of NiFe-P//AC supercapattery is 2250 W/kg at an energy density of 45.6 Wh/kg. Furthermore, the NiFe-P//AC supercapattery demonstrated excellent stability and coulombic efficiency by retaining 87.6% and 98.7% of the initial specific capacity values and coulombic efficiency, respectively. • Binder-free NiFe-P electrode was prepared using hydrothermal synthesis. • The fabrication parameters of the electrode were optimized using DOE. • The electrochemical performance of the electrodes was investigated. • Maximum power density of NiFe-P//AC supercapattery is 2250 W/kg at an energy density of 45.6 Wh/kg. • NiFe-P//AC supercapattery retained 87.6% and 98.7% of the initial specific capacity values and coulombic efficiency. [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]

As an industrial material for supercapacitive energy storage, commercial activated carbons (AC) could achieve a satisfactory gravimetric performances by electric double layered capacitance (EDLC) due to their rich microporosity, but the volumetric performances are usually poor resulted from the low packing density. Herein, we presented a strategy to address this tradeoff relationship and to achieve both high gravimetric and volumetric performance by filling the macro/mesoporosity with extra nitrogen doped carbon. The reconstructed activated carbon could inherit most of microporosity from the parent AC, while the macro/mesoporosity of them was greatly decreased, resulting in increase of packing density and the improvement of surface hydrophilicity. Benefited from the increase of packing density and maintenance of microporosity, the resultant activated carbon achieves greatly enhanced energy storage level including three times higher capacitance of 384 F cm−3@ 1.0 A/g (vs 128 F cm−3@ 1.0 A/g for pristine AC), high rate capability of 73.4% (vs 59.2% for pristine AC), larger energy density of 27.5 Wh L−1@ 900 W L−1 (vs 10.0 Wh L−1@747 W L−1). Importantly, the present strategy provides a facile and unique method to process activated carbon, which offers a possibility improving the energy storage level of the commercial activated carbon. [Display omitted] • Commercial activated carbon (AC) was processed by filling the macro/mesoporosity. • The filled AC owns increased packing density and more nitrogen functionalities. • The filled AC achieves greatly enhanced supercapacitor performances. [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]