Highly Porous Metal-Organic Framework Entrapped by Cobalt Telluride-Manganese Telluride as an Efficient Bifunctional Electrocatalyst.

The electrochemical conversion of oxygen holds great promise in the development of sustainable energy for various applications, such as water electrolysis, regenerative fuel cells, and rechargeable metal-air batteries. Oxygen electrocatalysts are needed that are both highly efficient and affordable, since they can serve as alternatives to costly precious-metal-based catalysts. This aspect is particularly significant for their practical implementation on a large scale in the future. Herein, highly porous polyhedron-entrapped metal-organic framework (MOF)-assisted CoTe2/MnTe2 heterostructure one-dimensional nanorods were initially synthesized using a simple hydrothermal strategy and then transformed into ZIF-67 followed by tellurization which was used as a bifunctional electrocatalyst for both the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR). The designed MOF CoTe2/MnTe2 nanorod electrocatalyst exhibited superior activity for both OER (η = 220 mV@ 10 mA cm-2) and ORR (E1/2 = 0.81 V vs RHE) and outstanding stability. The exceptional achievement could be primarily credited to the porous structure, interconnected designs, and deliberately created deficiencies that enhanced the electrocatalytic activity for the OER/ORR. This improvement was predominantly due to the enhanced electrochemical surface area and charge transfer inherent in the materials. Therefore, this simple and cost-effective method can be used to produce highly active bifunctional oxygen electrocatalysts.

Synergistic advancements in sewage-driven microbial fuel cells: novel carbon nanotube cathodes and biomass-derived anodes for efficient renewable energy generation and wastewater treatment.

Microbial fuel cells (MFCs) offer a dual solution of generating electrical energy from organic pollutants-laden wastewater while treating it. This study focuses on enhancing MFC performance through innovative electrode design. Three-dimensional (3D) anodes, created from corncobs and mango seeds via controlled graphitization, achieved remarkable power densities. The newly developed electrode configurations were evaluated within sewage wastewater-driven MFCs without the introduction of external microorganisms or prior treatment of the wastewater. At 1,000°C and 1,100°C graphitization temperatures, corncob and mango seed anodes produced 1,963 and 2,171 mW/m2, respectively, nearly 20 times higher than conventional carbon cloth and paper anodes. An advanced cathode composed of an activated carbon-carbon nanotube composite was introduced, rivaling expensive platinum-based cathodes. By optimizing the thermal treatment temperature and carbon nanotube content of the proposed cathode, comparable or superior performance to standard Pt/C commercial cathodes was achieved. Specifically, MFCs assembled with corncob anode with the proposed and standard Pt/C cathodes reached power densities of 1,963.1 and 2,178.6 mW/m2, respectively. Similarly, when utilizing graphitized mango seeds at 1,100°C, power densities of 2,171 and 2,151 mW/m2 were achieved for the new and standard cathodes, respectively. Furthermore, in continuous operation with a flow rate of 2 L/h, impressive chemical oxygen demand (COD) removal rates of 77% and 85% were achieved with corncob and mango seed anodes, respectively. This work highlights the significance of electrode design for enhancing MFC efficiency in electricity generation and wastewater treatment.

Synergistic doping with Ag, CdO, and ZnO to overcome electron-hole recombination in TiO2 photocatalysis for effective water photo splitting reaction.

This manuscript is dedicated to a comprehensive exploration of the multifaceted challenge of fast electron-hole recombination in titanium dioxide photocatalysis, with a primary focus on its critical role in advancing the field of water photo splitting. To address this challenge, three prominent approaches-Schottky barriers, Z-scheme systems, and type II heterojunctions-were rigorously investigated for their potential to ameliorate TiO2's photocatalytic performance toward water photo splitting. Three distinct dopants-silver, cadmium oxide, and zinc oxide-were strategically employed. This research also delved into the dynamic interplay between these dopants, analyzing the synergetic effects that arise from binary and tertiary doping configurations. The results concluded that incorporation of Ag, CdO, and ZnO dopants effectively countered the fast electron-hole recombination problem in TiO2 NPs. Ag emerged as a critical contributor at higher temperatures, significantly enhancing photocatalytic performance. The photocatalytic system exhibited a departure from Arrhenius behavior, with an optimal temperature of 40°C. Binary doping systems, particularly those combining CdO and ZnO, demonstrated exceptional photocatalytic activity at lower temperatures. However, the ternary doping configuration involving Ag, CdO, and ZnO proved to be the most promising, surpassing many functional materials. In sum, this study offers valuable insights into how Schottky barriers, Z-scheme systems, and type II heterojunctions, in conjunction with specific dopants, can overcome the electron-hole recombination challenge in TiO2-based photocatalysis. The results underscore the potential of the proposed ternary doping system to revolutionize photocatalytic water splitting for efficient green hydrogen production, significantly advancing the field's understanding and potential for sustainable energy applications.

(Fe-Co-Ni-Zn)-Based Metal-Organic Framework-Derived Electrocatalyst for Zinc-Air Batteries.

Zinc-air batteries (ZABs) have garnered significant interest as a viable substitute for lithium-ion batteries (LIBs), primarily due to their impressive energy density and low cost. However, the efficacy of zinc-air batteries is heavily dependent on electrocatalysts, which play a vital role in enhancing reaction efficiency and stability. This scholarly review article highlights the crucial significance of electrocatalysts in zinc-air batteries and explores the rationale behind employing Fe-Co-Ni-Zn-based metal-organic framework (MOF)-derived hybrid materials as potential electrocatalysts. These MOF-derived electrocatalysts offer advantages such as abundancy, high catalytic activity, tunability, and structural stability. Various synthesis methods and characterization techniques are employed to optimize the properties of MOF-derived electrocatalysts. Such electrocatalysts exhibit excellent catalytic activity, stability, and selectivity, making them suitable for applications in ZABs. Furthermore, they demonstrate notable capabilities in the realm of ZABs, encompassing elevated energy density, efficacy, and prolonged longevity. It is imperative to continue extensively researching and developing this area to propel the advancement of ZAB technology forward and pave the way for its practical implementation across diverse fields.

Marigold Flower-Shaped Metal-Organic Framework Supported Manganese Vanadium Oxide Electrocatalyst for Efficient Oxygen Evolution Reactions in an Alkaline Medium.

The electrochemical oxygen evolution reaction (OER) is a key process in many renewable energy systems. The development of low-cost, long-lasting alternatives to precious-metal catalysts, particularly functional electrocatalysts with high activity for OER processes, is crucial for reducing the operating expense and complexity of renewable energy generating systems. This work describes a concise method for generating marigold flower-like metal-organic frameworks (MOFs) aided manganese vanadium oxide via a hydrothermal procedure for increased OER activity. As synthesized MOF MnV oxide has a higher surface area due to the 3D flower-like structure, which is reinvented with enhanced electrocatalytic active sites. These distinctive structural features result in remarkable catalytic activity for MOF MnV oxide microflowers towards OER with a low overpotential of 310 mV at 50 mA cm-2 and a Tafel slope with only 51.4 mV dec-1 in alkaline conditions. This study provides a concise method for developing an optimized catalytic material with greater morphology and beneficial features for potential energy and environmental applications.

In Vivo and In Vitro Biodistribution of Inulin-Tethered Boron-Doped Amine-Functionalized Carbon Dots.

Carbon dots (CDs) are considered a potential substance for use in biomarker applications due to their exceptional light stability. However, there are several unsolved uncertainties about CD toxicity in vitro and in vivo. In this study, a redesigned derivative of the natural polysaccharide inulin is connected with boron-doped amine-functionalized carbon dots (In@BN-CDs) through carbodiimide coupling to improve the biocompatibility of the nanoformulation. The toxicity and biodistribution of ln@BN-CDs in vivo and in vitro were explored in detail. The In@BN-CDs were tested after a single inhalation dosage of 10, 7, 5, 3, and 1 mg/kg. We explored a dose- and time-dependent technique of collecting blood samples and then centrifuged the blood samples and obtained serum samples, which were then analyzed for fluorescence inspection; findings showed that the fluorescence intensity decreased with time. Similarly, In@BN-CDs were effectively used as in vitro toxicity and fluorescent probes for cellular imaging in living cells due to their biocompatibility and cell membrane accessibility. The biocompatibility and efficacy of In@BN-CDs as fluorescent imaging agents have been demonstrated. The data suggest that the usage of In@BN-CDs in vitro and in vivo should be examined.

Carbon Nanofibers-Sheathed Graphite Rod Anode and Hydrophobic Cathode for Improved Performance Industrial Wastewater-Driven Microbial Fuel Cells.

Carbon nanofiber-decorated graphite rods are introduced as effective and low-cost anodes for industrial wastewater-driven microbial fuel cells. Carbon nanofiber deposition on the surface of the graphite rods could be performed by the electrospinning of polyacrylonitrile/N,N-Dimethylformamide solution using the rod as nanofiber collector, which was calcined under inert atmosphere. The experimental results indicated that at 10 min electrospinning time, the proposed graphite anode demonstrates very good performance compared to the commercial anodes. Typically, the generated power density from sugarcane industry wastewater-driven air cathode microbial fuel cells were 13 ± 0.3, 23 ± 0.7, 43 ± 1.3, and 185 ± 7.4 mW/m2 using carbon paper, carbon felt, carbon cloth, and graphite rod coated by 10-min electrospinning time carbon nanofibers anodes, respectively. The distinct performance of the proposed anode came from creating 3D carbon nanofiber layer filled with the biocatalyst. Moreover, to annihilate the internal cell resistance, a membrane-less cell was assembled by utilizing a poly(vinylidene fluoride) electrospun nanofiber layer-coated cathode. This novel strategy inspired a highly hydrophobic layer on the cathode surface, preventing water leakage to avoid utilizing the membrane. However, in both anode and cathode modifications, the electrospinning time should be optimized. The best results were obtained at 5 and 10 min for the cathode and anode, respectively.

CdTiO3-NPs incorporated TiO2 nanostructure photocatalyst for scavenger-free water splitting under visible radiation.

Nanofibrous morphology and the doping technique can overcome the problem of electron/hole fast recombination and improve the activity of titanium oxide-based photocatalysts. In this study, nanoparticulate and nanofibrous forms of CdTiO3-incorporated TiO2 were synthesized with different cadmium contents; the morphology and composition were determined by SEM, TEM, EDX, and XRD techniques. The nanomorphology, cadmium content, and reaction temperature of Cd-doped TiO2 nanostructures were found to be strongly affect the hydrogen production rate. Nanofibrous morphology improves the rate of hydrogen evolution by around 10 folds over the rate for nanoparticles due to electron confinement in 0D nanostructures. The average rates of hydrogen production for samples of 0.5 wt.% Cd are 0.7 and 16.5 ml/gcat.min for nanoparticles and nanofibers, respectively. On the other hand, cadmium doping resulted in increasing the hydrogen production rate from 9.6 to 19.7 ml/gcat.min for pristine and Cd-doped (2 wt%) TiO2 nanofibers, respectively. May be the formation of type I heterostructures between the TiO2 matrix and CdTiO3 nanoparticles is the main reason for the observed enhancement of photocatalytic activity due to the strong suppressing of electron/holes recombination process. Consequently, the proposed photocatalyst could be exploited to produce hydrogen from scavenger-free solution. Varying reaction temperature suggests that hydrogen evolution over the proposed catalyst is incompatible with the Arrhenius equation. In particular, reaction temperature was found to have a negative influence on photocatalytic activity. This work shows the prospects for using CdTiO3 as a co-catalyst in photon-induced water splitting and indicates a substantial enhancement in the rate of hydrogen production upon using the proposed photocatalyst in nanofibrous morphology.

Three-dimensional carbon nanofiber-based anode for high generated current and power from air-cathode micro-sized MFC.

It is agreed that low mass transfer and poor reaction kinetics are the main reasons behind the low power density of microbial fuel cells (MFCs). Microscale MFCs can introduce a marvelous solution for the mass transfer dilemma. However, the volumetric power density and coulombic efficiency of present microscale MFCs are still limited due to the poor reaction kinetics. The size, shape, chemical properties and material of the electrodes are essential parameters controlling the reaction kinetics. In this study, a 3D carbon nanofiber disk is introduced as an effective anode for a single-chamber air-cathode micro-sized MFC as it improved the reaction kinetics. The proposed electrode was fabricated by a judicious combination of the electrospinning technique and thermal treatment. Owing to the intercalation of the microorganisms in the carbon nanofiber skeleton, compared to many previous reports, high power and current densities of 8.1 Wm-2 and 44.9 Am-2, respectively, were obtained from the 19.6 µL single-chamber air-cathode MFC. However, the thickness of the carbon nanofiber layer has to be optimized by adjusting the electrospinning time. The power density observed from a 10 min electrospinning time-based anode outperformed the 5- and 20 min ones by 1.5 and 2 times, respectively.

Homogeneous Elongation of N-Doped CNTs over Nano-Fibrillated Hollow-Carbon-Nanofiber: Mass and Charge Balance in Asymmetric Supercapacitors Is No Longer Problematic.

The hurdle of fabricating asymmetric supercapacitor (ASC) devices using a faradic cathode and a double layer anode is challenging due to the required large amount of active mass of anodic material compared to that of the cathodic material during mass balancing due to the large difference in capacitance values of the two electrodes. Here, the problem is addressed by engineering a negative electrode that furnishes an ultrahigh capacitance. An in situ developed metal-organic framework (MOF)-based thermal treatment is adopted to grow highly porous N-doped carbon nanotubes (CNTs) containing submerged Co nanoparticles over nano-fibrillated electrospun hollow carbon nanofibers (HCNFs). The optimized CNT@HCNF-1.5 furnishes an ultrahigh capacitance approaching 712 F g-1 with excellent rate capability. The capacitance reported from this work is the highest for any carbonaceous material reported to date. The CNT@HCNF-1.5 is further used to fabricate symmetric supercapacitors (SSCs), as well as ASC devices. Remarkably, both the SSC and ASC devices furnish incredible performances in all aspects of SCs, such as a high energy density, long cycle life, and high rate capability, displaying decent practical applicability. The energy density of the SSC device reaches as high as 20.13 W h kg-1 , whereas that of ASC approaches 87.5 W h kg-1 .

Polypyrrole Nanotunnels with Luminal and Abluminal Layered Double Hydroxide Nanosheets Grown on a Carbon Cloth for Energy Storage Applications.

The structural design of transition metal-based electrode materials with gigantic energy storage capabilities is a crucial task. In this work, we report an assembly of thin layered double hydroxide (LDH) nanosheets arrayed throughout the luminal and abluminal parts of polypyrrole tunnels fastened onto both sides of a carbon cloth as a battery-type energy storage system. Electron microscopy images reveal that the resulting electrode (NiCo-LDH@H-PPy@CC, where H-PPy@CC represents carbon cloth-supported hollow polypyrrole fibers) is constructed by combining luminal and abluminal NiCo-LDH nanosheets onto a long polypyrrole tunnel on a carbon cloth. The primary sample shows an excellent specific capacity of 149.16 mAh g-1 at 1.0 mA cm-2, a remarkable rate capability of 80.45%, and comprehensive cyclic stability (93.4%). The improved performance is mainly attributed to the strategic organization of the electrode materials with superior Brunauer-Emmett-Teller (BET) surface area and conductivity. Moreover, an asymmetric supercapacitor device assembled with NiCo-LDH@H-PPy@CC and vanadium phosphate-incorporated carbon nanofiber (VPO@CNFs900) electrodes contributes a specific energy density of 32.42 Wh kg-1 at 3 mA cm-2 with a specific power density of 359.16 W kg-1. When the current density is increased by 6-fold, the specific power density reaches 1999.89 W kg-1 at a specific energy density of 20.06 Wh kg-1. This is a simple, cost-effective, and convenient synthetic strategy for the synthesis of porous nanosheet arrays assimilated into hollow fiber architectures, which can illuminate the ideal approach for the fabrication of novel materials with an immense potential for energy storage.

Carbon Nanofiber Double Active Layer and Co-Incorporation as New Anode Modification Strategies for Power-Enhanced Microbial Fuel Cells.

Co-doped carbon nanofiber mats can be prepared by the addition of cobalt acetate to the polyacrylonitrile/DMF electrospun solution. Wastewater obtained from food industries was utilized as the anolyte as well as microorganisms as the source in single-chamber batch mode microbial fuel cells. The results indicated that the single Co-free carbon nanofiber mat was not a good anode in the used microbial fuel cells. However, the generated power can be distinctly enhanced by using double active layers of pristine carbon nanofiber mats or a single layer Co-doped carbon nanofiber mat as anodes. Typically, after 24 h batching time, the estimated generated power densities were 10, 92, and 121 mW/m2 for single, double active layers, and Co-doped carbon nanofiber anodes, respectively. For comparison, the performance of the cell was investigated using carbon cloth and carbon paper as anodes, the observed power densities were smaller than the introduced modified anodes at 58 and 62 mW/m2, respectively. Moreover, the COD removal and Columbic efficiency were calculated for the proposed anodes as well as the used commercial ones. The results further confirm the priority of using double active layer or metal-doped carbon nanofiber anodes over the commercial ones. Numerically, the calculated COD removals were 29.16 and 38.95% for carbon paper and carbon cloth while 40.53 and 45.79% COD removals were obtained with double active layer and Co-doped carbon nanofiber anodes, respectively. With a similar trend, the calculated Columbic efficiencies were 26, 42, 52, and 71% for the same sequence.

Ruthenium nanoparticles integrated bimetallic metal-organic framework electrocatalysts for multifunctional electrode materials and practical water electrolysis in seawater.

There is still a significant technical hurdle in the integration of better electrocatalysts with coordinated functional units and morphological integrity that improves reversible electrochemical activity, electrical conductivity, and mass transport capabilities. In this work, ruthenium-integrating porous bimetallic transition metal nanoarrays are efficiently generated from metal-organic framework-covered three-dimensional platforms such as carbon cloth using a simple solution-based deposition technique followed by calcination. Heterostructure ruthenium-cobalt-iron hollow nanoarrays are built to permit exceptionally effective multifunctional activities in reactions including the oxygen evolution reaction, hydrogen evolution reaction, and oxygen reduction reaction. As presumed, the as-synthesized porous nanostructured arrays show remarkable electrochemical performance due to the benefits of copious active reaction sites, and efficient electron and ion transport channels. The oxygen reduction reaction of the porous nanostructured array electrocatalyst has a half-wave potential of 0.875 V vs. reversible hydrogen electrode and can achieve a current density of 10 mA cm-2 at low overpotentials of 220 and 50 mV for the oxygen and hydrogen evolution reactions, respectively, and the needed cell voltage for total water splitting is just 1.49 V at a current density of 10 mA cm-2. The fabricated electrolyzer coupling splits seawater at relatively low cell voltages of 1.54 V at ambient temperature.

Synthesis of lanthanide-doped strontium aluminate nanoparticles encapsulated in polyacrylonitrile nanofibres: photoluminescence properties for anticounterfeiting applications.

Photochromism has been applied as an interesting technique in order to improve the anticounterfeiting of commercial commodities. To build up a mechanically reliable anticounterfeiting nanocomposite, it has been vital to enhance the engineering process of the anticounterfeiting material. In the current study, we developed mechanically reliable and highly photoluminescent lanthanide-doped strontium aluminate nanoparticles (LSAN)/polyacrylonitrile (PAN) hybrid nanofibres successfully fabricated using an electrospinning technique for anticounterfeiting applications. The produced nanocomposite films exhibited ultraviolet-induced photochromic anticounterfeiting properties. To guarantee the transparency of the LSAN-PAN film, LSAN must be immobilized onto the nanoparticle size to allow better dispersion without aggregation in the polyacrylonitrile matrix. The LSAN-PAN nanofibrous film demonstrated absorbance intensity that exhibited at 354 nm and associated with an emission intensity at 424 nm. The produced LSAN-PAN films demonstrated an enhanced hydrophobicity when increasing the ratio of LSAN, without adversely influencing their native appearance and mechanical performance. Upon excitation with ultraviolet light, the translucent nanofibrous substrates exhibited fast and reversible photochromic activity to greenish-yellow without exhaustion. The nanofibrous films exhibited stretchability, transparency, flexibility, and ultraviolet light-induced photochromism at low cost. The current strategy can be considered as an efficient technique towards the development of various anticounterfeiting materials for a better market with economic and social values.

Production of photoluminescent transparent poly(methyl methacrylate) for smart windows.

Photochromic and long-lasting photoluminescent transparent, rigid, ultraviolet (UV) protective and superhydrophobic poly(methyl methacrylate) (PMMA) plastic able to switch colour beneath UV irradiation was developed. Photoluminescent transparent PMMA plastic was prepared by the simple polymerization process of methyl methacrylate immobilized with alkaline earth aluminate (AEA) nanoparticles. These colourless PMMA plastic substrates showed a colour switch to greenish underneath UV light as proved using CIELAB screening. The morphology of AEA was evaluated using transmission electron microscopy. Conversely, transparent PMMA samples were evaluated using energy-dispersive X-ray spectra, scanning electron microscope, X-ray fluorescence spectroscopy and for hardness properties. Additionally, the photoluminescence properties were explored by studying excitation and emission spectra. The produced luminescence colourless PMMA plastic substrates displayed excitation band at 370 nm, and three emission peaks at 433, 494 and 513 nm. Photoluminescent PMMA with lower contents of AEA showed fast and reversible photochromism under UV light, while PMMA samples with higher contents of AEA showed long-lasting luminescence such as a flashlight with the ability to replace electric power. The findings showed that the produced photoluminescence colourless PMMA plastic substrates exhibited enhanced UV shielding and superhydrophobicity.

Fabrication, microstructure characterization, and degradation performance of electrospun mats based on poly(3-hydroxybutyrate-co-3 hydroxyvalerate)/polyethylene glycol blend for potential tissue engineering.

There have been strong demands for nanofibrous scaffolds fabricated by electrospinning for various fields due to their various advantages. Electrospun poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) fibre mats were prepared. The effects of processing variables as well as the inclusion of poly(ethylene glycol) (PEG) on the morphologies of generated fibres were investigated using Fourier-transform infrared spectroscopy and scanning electron microscopy. The average fibrous diameter was monitored in the range 400-3000 nm relying on the total content of PEG. The fluorescence cell imaging of electrospun mats was also explored. The results of cell viability demonstrated that skin fibroblast BJ-1 cells showed different adhesions and growth rates for the three kinds of PHBV fibres. Electrospun PHBV mats with low amount of PEG offer a high-quality medium for cell growth. Therefore, those mats exhibited high potential for soft tissue engineering, in particular wound healing.

Effect of Process Control Parameters on the Filtration Performance of PAN-CTAB Nanofiber/Nanonet Web Combined with Meltblown Nonwoven.

Nanofibers have potential applications as filters for particles with diameters <10 µm owing to their large specific surface area, macropores, and controllable geometry or diameter. The filtration efficiency can be increased by creating nanonets (<50 nm) whose diameter is smaller than that of nanofibers. This study investigates the effect of process conditions on the generation of nanonet structures from a polyacrylonitrile (PAN) solution containing cation surfactants; in addition, the filtration performance is analyzed. The applied electrospinning voltage and the electrostatic treatment of meltblown polypropylene (used as a substrate) are the most influential process parameters of nanonet formation. Electrospun polyacrylonitrile-cetylmethylammonium bromide (PAN-CTAB) showed a nanofiber/nanonet structure and improved thermal and mechanical properties compared with those of the electrospun PAN. The pore size distribution and filter efficiency of the PAN nanofiber web and PAN-CTAB nanofiber/nanonet web with meltblown were measured. The resulting PAN-CTAB nanofiber/nanonet air filter showed a high filtration efficiency of 99% and a low pressure drop of 7.7 mmH2O at an air flow rate of 80 L/min. The process control methods for the nanonet structures studied herein provide a new approach for developing functional materials for air-filtration applications.

Temperature-controlled in situ synthesized carbon nanotube-protected vanadium phosphate particle-anchored electrospun carbon nanofibers for high energy density symmetric supercapacitors.

Designing a novel composite material with hierarchical nanostructures as a negative electrode material with high capacitance and outstanding stability is challenging. To this end, we synthesized carbon nanotubes (CNTs)-protected vanadium phosphate (VPO) nanoparticles trapped within an electrospun carbon matrix (CNTs@VPO@CNFs) for potential use in energy storage applications. Temperature was found to be the major controlling factor for the fabrication of composites with CNT decoration. CNTs@VPO@CNFs exhibited the highest capacitance of 576.1F g-1 at a current density of 0.66 A g-1 among other corresponding electrode materials. Furthermore, this electrode exhibited outstanding stability of up to 99% after 5000 cycles, which was attributed to the coating of core-forming VPO@CNFs by the CNTs as the sheath material. Interestingly, the as-fabricated material worked in a wide potential range from -1.2 to 0.6, thereby providing the opportunity to assemble a symmetric supercapacitor device (SSCD). The SSCD showed an exceptionally high energy density of 69.1 W h kg-1 at a power density of 3.2 kW h and ~ 90% stability after 5000 cycles. Thus, this work presents a strategy for fabricating a new composite as a negative electrode material that can be used in a symmetrical supercapacitor device with an ultrahigh energy density.

Integrating the Essence of a Metal-Organic Framework with Electrospinning: A New Approach for Making a Metal Nanoparticle Confined N-Doped Carbon Nanotubes/Porous Carbon Nanofibrous Membrane for Energy Storage and Conversion.

The fabrication of an economic and efficient multifunctional advanced nanomaterial with a rational composition and configuration by a facile methodology is a crucial challenge. Herein, we are the first to report the growth of Co nanoparticle-integrated nitrogen-doped carbon nanotubes (N-CNTs) on porous carbon nanofibers by simply heating in the situ-developed metal-organic framework (MOF)-based electrospun nanofibrous membrane with no need for an external supply of any additional precursors and reducing gases. The long and entangled N-CNTs originating from highly porous and graphitic carbon nanofibers offer good flexibility, large surface area, high porosity, high conductivity, the homogeneous incorporation of heteroatoms and metallic constituents, and an abundant exposure of active nanocatalytic sites. The as-developed nanoassembly demonstrates attractive characteristics for electrocatalytic hydrogen and oxygen evolution reactions and electrochemical energy storage. This strategy of integrating the essence of an MOF with electrospinning offers a new, direct, and cost-effective approach for making N-doped CNT-based multifunctional membranes.

Fabrication of Nonmetal-Modulated Dual Metal-Organic Platform for Overall Water Splitting and Rechargeable Zinc-Air Batteries.

The fast development of portable water-splitting devices has led to a great deal of work on rechargeable metal-air batteries or solar cells; however, the lack of affordable multifunctional electrocatalysts still hampers their widespread applications. Herein, a well-aligned ternary metal (oxy)hydroxide nanostructure is a sacrificial pseudomorphic transformation template of an integrated metal-organic network on the carbon cloth (CC) surface, that is, the Fe-doped metal-organic framework (MOF) ZnNiCoSe@CC nanosheet network, exhibiting powerful and efficient multifunctional electrocatalysts such as the oxygen reduction reaction, oxygen evolution reaction, and hydrogen evolution reaction in alkaline media combined with desirable electrode kinetics. As a proof-of-concept observational study, the nanostructured Fe-doped MOF ZnNiCoSe@CC could be used as air-cathode materials in the rechargeable metal-air battery. The fabricated device delivered higher open-circuit voltage, higher capacity, and peak power density, excellent discharge-charge performance, and long cycle life. Thus, our research creates a unique perspective on the development of highly portable air electrodes with a favorable electrocatalytic application of overall water-splitting reaction.