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[Display omitted] The flexible and self-healing supercapacitors (SCs) are considered to be promising smart energy storage devices. Nevertheless, the SCs integrated with flexibility, lightweight, pattern editability, self-healing capabilities and desirable electrochemical properties remain a challenge. Herein, an all-in-one self-healing SC fabricated with the free-standing hybrid film (TCMP) composed of the 2,2,6,6-tetramethylpiperidin-1-yloxy-oxidized cellulose nanofibers (TOCNs) carried carbon nanotubes (CNTs), manganese dioxide (MnO 2) and polyaniline (PANI) as the electrode, polyvinyl alcohol/sulfuric acid (PVA/H 2 SO 4) gel as the electrolyte and dynamically cross-linked cellulose nanofibers/PVA/sodium tetraborate decahydrate (CNF/PB) hydrogel as the self-healing electrode matrix is developed. The TCMP film electrodes are fabricated through a facile in-situ polymerization of MnO 2 and PANI in TOCNs-dispersed CNTs composite networks, exhibiting lightweight, high electrical conductivity, flexibility, pattern editability and excellent electrochemical properties. Benefited from the hierarchically porous structure and high mechanical properties of TOCNs, excellent electrical conductivity of CNTs and the desirable synergistic effect of pseudocapacitance induced by MnO 2 and PANI, the assembled SC with an interdigital structure demonstrated a high areal capacitance of 1108 mF cm−2 at 2 mA cm−2, large areal energy density of 153.7 μWh cm−2 at 1101.7 μW cm−2. A satisfactory bending cycle performance (capacitance retention up to 95 % after 200 bending deformations) and self-healing characteristics (∼90 % capacitance retention after 10 cut/repair cycles) are demonstrated for the TCMP-based symmetric SC, delivering a feasible strategy for electrochemical energy storage devices with excellent performance, designable patterns and desirable safe lifespan. [ABSTRACT FROM AUTHOR]

[Display omitted] • Ultra-flexible bimetallic nanowire decorated foams via facile dip-coating method. • An ultra-low filler content of 0.22 vol% for high performances. • Effective microwave absorption of −69.61 dB with ultra-wide absorption bandwidth. • Integrated multi-functional applications in one. Nowadays, functional electronic devices with excellent flexibility and thermal management capability for effective electromagnetic wave absorption are urgently in demand. Herein, a novel and highly flexible silver nanowire (AgNW)/iron nanowire (FeNW) decorated melamine composite foam (AgFe-MF) was prepared via simple dip-coating process. Owing to optimal impedance matching, synergistic dielectric and magnetic losses as well as three-dimensional porous structure, the AgFe-MF with an ultra-low filler content (0.22 vol%) exhibited an outstanding minimum reflection loss of −69.61 dB, and the best effective absorption bandwidth (EAB) could reach up to 6.37 GHz. Importantly, the EAB of long-time working AgFe-MF was enhanced to 7.01 GHz after 1000 compress-release cycles under 40 % strain. Besides, it also featured considerate Joule heating capacity and achieved a saturation temperature of over 85.7 ℃ under 2.6 V voltage. The impressive thermal isolation and long-term stability ensured the safety used as portable heater. Therefore, this work will provide a vital slight for fabricating smart wearable electronic devices with integrated anti-electromagnetic radiation and personalized thermal management performances towards potential thermal and health threats. [ABSTRACT FROM AUTHOR]

[Display omitted] • A facile "chemical blowing" strategy is developed to expand the dense and micron-scale thickness walls into interconnected carbon nanosheets. • Zn(NO 3) 2 is proved to functioned as blowing agent, precursor of template, activator, and nitrogen dopant. • The optimized thick carbon monolith with high-mass loading (∼30 mg cm−2) delivers encouraging capacitive performance in low-temperature. Biomass-derived carbon materials are promising electrode materials for capacitive energy storage. Herein, inspired by the hierarchical structure of natural wood, carbon monoliths built up by interconnected porous carbon nanosheets with enriched vertical channels were obtained via zinc nitrate (Zn(NO 3) 2)-assisted synthesis and served as thick electrodes for capacitive energy storage. Zn(NO 3) 2 is proved to function as expansion agent, activator, dopant, and precursor of the template. The dense and micron-scale thickness walls of wood were expanded by Zn(NO 3) 2 into porous and interconnected nanosheets. The pore volume and specific surface area were increased by more than 430 %. The initial specific capacitance and rate performance of the optimized carbon monolith was approximately three times that of the pristine dense carbon framework. The assembled symmetric supercapacitor possessed a high initial specific capacitance of 4564 mF cm−2 (0–1.7 V) at −40 °C. Impressively, the robust device could be cycled more than 100,000 times with little capacitance attenuation. The assembled zinc-ion hybrid capacitor (0.2–2 V) delivered a large specific capacitance of 4500 mF cm−2 at −40 °C, approximately 74 % of its specific capacitance at 25 °C. Our research paves a new avenue to design thick carbon electrodes with high capacitive performance by multifunctional Zn(NO 3) 2 for low-temperature applications. [ABSTRACT FROM AUTHOR]

[Display omitted] • Construct multi-scale architectures from 0D to 2D with abundant heterostructures. • Enhanced microwave absorption of −67 dB with ultrabroad absorption bandwidth. • Rich heterogeneous interfaces and synergistic multiple loss mechanisms for EWA. Two-dimensional (2D) MXene has attracted vast attention in electromagnetic wave absorption (EWA), but there remains a contradiction between maintaining impedance matching and enhancing dielectric loss. Herein, the multi-scale architectures of ecoflex/2D MXene (Ti 3 C 2 T x)@zero-dimensional CoNi sphere@one-dimensional carbon nanotube composite elastomers were successfully constructed by simple liquid-phase reduction and thermo-curing method. The binding between the hybrids as fillers and ecoflex as a matrix greatly enhanced the EWA capability of the obtained composite elastomer and improved its mechanical properties. Owing to its good impedance matching, abundant heterostructures, and synergistic electrical and magnetic losses, this elastomer exhibited an excellent minimum reflection loss of −67 dB at 9.46 GHz under a thickness of 2.98 mm. In addition, its ultrabroad effective absorption bandwidth reached 6.07 GHz. This achievement will pave the way for the exploitation of multi-dimensional heterostructures as high-performance electromagnetic absorbers with superior EWA ability. [ABSTRACT FROM AUTHOR]

[Display omitted] • Novel wheat-like Ni-coated core–shell silver nanowire using facile one-pot method. • High-efficiency microwave absorption of −61.1 dB with wide absorption bandwidth. • Synergistic effect of unique structure and multiple loss mechanisms for EWA. • Long-term operational stability for three months. Nowadays, developing high-performance electromagnetic functional materials to eliminate the ever-increasing electromagnetic pollution problem is necessary for the complex electromagnetic environment. However, the materials with high electrical conductivity are prone to secondary electromagnetic pollution due to interface impedance mismatching. Herein, the wheat-like electrically conductive and magnetic silver nanowire@nickle (AgNW@Ni) composites were fabricated via a one-pot in-situ growth method. The electromagnetic properties of the composites could be regulated by adjusting different ratios of precursors, resulting in various morphological features of the nanowire as the core with different Ni shell thicknesses. When the Ag and Ni molar ratio was 1:1.1, the AgNW@Ni composite exhibited the optimal minimum reflection loss (RL min) of −61.1 dB with an adequate effective absorption bandwidth (EAB) of 4.06 GHz owing to good impedance matching, abundant heterostructures, and synergistic electrical and magnetic losses. Even after three months, it still maintained an acceptable RL min value of −39.7 dB and similar EAB , demonstrating its long-term operational stability. This unique composite is expected to be applied in more actual electromagnetic protection occasions. [ABSTRACT FROM AUTHOR]

[Display omitted] • Flower-like bimetallic MOF-derived carbon composites. • Regulate structures by adjusting different precursor ratios. • High-efficiency microwave absorption of −56.89 dB with wide bandwidth of 4.7 GHz. • Synergistic effect of unique structure and electromagnetic characteristic for EWA. Recently, high-performance functional composites for electromagnetic wave absorption (EWA) with tunable nano/micro-structures have attracted extensive attention. Herein, the flower-like electrically conductive and magnetic cobalt-nickel@carbon (CoNi@C) composites derived from bimetallic metal-organic frameworks (MOFs) were fabricated via solvothermal method and pyrolysis. By adjusting the ratios of different precursors, different morphological features of composites were formed. When the molar ratio of Co and Ni was 1:2, the CoNi@C composites exhibited the optimal minimum reflection loss (RL min) of −56.89 dB at 6.7 GHz with an effective absorption bandwidth of 4.7 GHz, due to the coordinated dielectric and magnetic loss caused by the electromagnetic properties of each component as well as the interactions between the unique three-dimensional (3D) interfaces of flower-like structures that promoted the absorption and dissipation of composites for microwaves. The composites are expected to become promising candidates as high-efficiency absorbers in the electromagnetic protection field. [ABSTRACT FROM AUTHOR]

[Display omitted] • Flower-like bimetallic MOF-derived carbon composites. • Regulate structures by adjusting different precursor ratios. • High-efficiency microwave absorption of −56.89 dB with wide bandwidth of 4.7 GHz. • Synergistic effect of unique structure and electromagnetic characteristic for EWA. Recently, high-performance functional composites for electromagnetic wave absorption (EWA) with tunable nano/micro-structures have attracted extensive attention. Herein, the flower-like electrically conductive and magnetic cobalt-nickel@carbon (CoNi@C) composites derived from bimetallic metal-organic frameworks (MOFs) were fabricated via solvothermal method and pyrolysis. By adjusting the ratios of different precursors, different morphological features of composites were formed. When the molar ratio of Co and Ni was 1:2, the CoNi@C composites exhibited the optimal minimum reflection loss (RL min) of −56.89 dB at 6.7 GHz with an effective absorption bandwidth of 4.7 GHz, due to the coordinated dielectric and magnetic loss caused by the electromagnetic properties of each component as well as the interactions between the unique three-dimensional (3D) interfaces of flower-like structures that promoted the absorption and dissipation of composites for microwaves. The composites are expected to become promising candidates as high-efficiency absorbers in the electromagnetic protection field. [ABSTRACT FROM AUTHOR]

[Display omitted] Designing intertwined porous structure is highly desirable to improve the electrochemical performance of carbon materials for supercapacitor. In this contribution, three-dimensional (3D) carbonized polyimide/cellulose (CPC) composite is fabricated via a facile "one-step" carbonization, in which cellulose as cross-linked agent is capable of modulating the molecular structure of polyamic acid, thus ensuring the formation of intertwined porous networks in the obtained carbon skeleton. Benefitting from the high specific surface area (951 m2 g−1) and uniformly distributed pores, the optimized CPC-5 electrode exhibits an outstanding specific capacitance of 300F g−1 in 6.0 M KOH electrolyte. More impressively, the CPC-5 based symmetrical supercapacitor affords a high energy density of 22.6 Wh kg−1 at power density of 800 W kg−1, as well as an exceptional capacitance retention of 91.4% after 10,000 cycles. This work affords an effective strategy to yield a promising polyimide derived carbon material for high-performance supercapacitors. [ABSTRACT FROM AUTHOR]

[Display omitted] • Nitrogen, sulfur co-doped PCG composite has been fabricated via a facile co-pyrolysis method. • Pollen-derived carbon with inherited charge-transfer structure can serve as as effective "porous spacer". • The optimized PCG-0.5 electrode exhibits excellent specific capacitance, rate performance and stability. • The symmetrical PCG-0.5//PCG-0.5 device displays a remarkable energy density in neutral medium. • The "sphere-in-layer" interconnection and heteroatoms doping may be the key factors for high performance. Rational design of electrode with hierarchical charge-transfer structure and good electronic conductivity is important to achieve high specific capacitance and energy density for supercapacitor, but it still remains a challenge. Herein, a nitrogen, sulfur co-doped pollen-derived carbon/graphene (PCG) composite with interconnected "sphere-in-layer" structure was fabricated, in which hierarchically pollen-derived carbon microspheres can serve as "porous spacers" to prevent the agglomeration of graphene nanosheets. The optimized PCG composite prepared with 0.5 wt% of graphene oxide (PCG-0.5) exhibited high specific capacitance (420 F g−1 at 1 A g−1), rate performance (280 F g−1 at 20 A g−1), and excellent cycling stability with 94% of capacitance retention after 10,000 cycles. The symmetrical device delivered a remarkable energy density of 31.3 Wh kg−1 in neutral medium. Moreover, density functional theory calculation revealed that PCG electrode possessed the accelerated charge transfer and enhanced electronic conductivity, thus ensuring a remarkable electrochemical performance. This work may afford an effective strategy for the development of biomass-derived carbon electrodes with novel charge-transfer structure toward supercapacitor applications. [ABSTRACT FROM AUTHOR]

Graphical abstract The preparation of superhydrophobic and superoleophilic PI-based nanofibrous membrane for oil-water separation. Abstract Marine pollution and industrial wastewater have caused serious environmental pollution, thereby resulting into an alarming damage to public health in the past decades, hence the high demand for, cost effective, energy-efficient oil-water separation technologies for the removal of oil contaminants from such water. Herein, we report a facile method to fabricate superhydrophobic/superoleophilic membrane by immersing a polyimide (PI)-based nanofibrous membrane into a water/ethanol/ammonia/dopamine mixture, followed by modification with 1H, 1H, 2H, 2H-perfluorodecanethiol (PFDT). The PI-based membrane exhibited water contact angle (WCA) above 153°, while the oil contact angle (OCA) approached 0°, thereby promoting an outstanding chemical stability which sustained its superhydrophobicity when immersed in aqueous solutions at different pH values. Additionally, the PI-based membrane possesses ultrahigh flux, high separation efficiency and good reusability in oil-water separation. The aforementioned properties, as well as the easily scale-up preparation process ensure that this promising as-fabricated membrane can be applied for practical environmental applications including treatment of oily wastewater and oil spillage clean-up. [ABSTRACT FROM AUTHOR]