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A fluorescent and colorimetric poly (acrylamide)-based copolymer probe P(AAm-co-RBNCH) has been designed via free radical polymerization of a commercial acrylamide monomer with a rhodamine-functionalized monomer RBNCH. Metal ion selectivity of RBNCH was investigated by fluorescence and colorimetric spectrophotometry. Upon addition of Fe3+, a visual color change from colorless to red and a large fluorescence enhancement were observed for the ring-opening of the rhodamine spirolactam mechanism. The monomer gives a sensitive method for quantitatively detecting Fe3+ in the linear range of 100–200 μM, with a limit of detection as low as 27 nM and exhibiting high selectivity for Fe3+ over 12 other metal ions. The hydrogel sensor was characterized by FTIR, and the effects of RBNCH amount on gel content and swelling properties were explored. According to the recipe of 1.0 mol% RBNCH to the total monomers, the fabricated hydrogel sensor displayed a good swelling property and reversibility performance and has potential for application in the imaging of Fe3+ level in industrial wastewater. [ABSTRACT FROM AUTHOR]

Supercapacitors, with high energy density, rapid charge–discharge capabilities, and long cycling ability, have gained favor among many researchers. However, the universality of high-performance carbon-based electrodes is often constrained by their complex fabrication methods. In this study, the common industrial materials, zinc gluconate and ammonium chloride, are uniformly mixed and subjected to a one-step carbonization strategy to prepare three-dimensional hierarchical porous carbon materials with high specific surface area and suitable nitrogen doping. The results show that a specific capacitance of 221 F g−1 is achieved at a current density of 1 A g−1. The assembled symmetrical supercapacitor achieves a high energy density of 17 Wh kg−1, and after 50,000 cycles at a current density of 50 A g−1, it retains 82% of its initial capacitance. Moreover, the operating voltage window of the symmetrical device can be easily expanded to 2.5 V when using Et4NBF4 as the electrolyte, resulting in a maximum energy density of up to 153 Wh kg−1, and retaining 85.03% of the initial specific capacitance after 10,000 cycles. This method, using common industrial materials as raw materials, provides ideas for the simple preparation of high-performance carbon materials and also provides a promising method for the large-scale production of highly porous carbons. [ABSTRACT FROM AUTHOR]

Polyamide-imides (PAIs) are highly desired in many applications because of their superior thermal and mechanical properties. In this work, PAI was prepared from an amide-containing diamine and dianhydride by polycondensation and thermal treatment. Both PAI films and aligned electrospun nanofibers (ANFs) were fabricated. FT-IR was used to determine the structure formation of PAI at different annealing temperatures. DSC and TGA were used to evaluate the thermal properties of PAI, while tensile test was applied to evaluate the mechanical properties of PAI films and ANFs. The results indicated that the PAI possessed both outstanding thermal stability and mechanical properties, which provide opportunities for applications in gas separation, high temperature filtration, reinforcement, etc. [ABSTRACT FROM AUTHOR]

Abstract: In this paper, preparation method and actuation properties of an innovative composite membrane composed of thermo‐ and pH‐responsive poly(N‐isopropylacrylamide‐co‐acrylic acid) fibers (average diameter ≈ 905 nm) embedded within a passive thermoplastic polyurethane (TPU) matrix at different angles with degree of alignment as high as 98% are presented. The composite membrane has a gradient of TPU along the thickness. It has the capability of temperature‐ and pH‐dependent direction‐, and size‐controlled actuation in few minutes. The stresses generated at the responsive fiber and nonresponsive matrix provide actuation, whereas the angle at which fibers are embedded in the matrix controls the actuation direction and size. The temperature has no effect on actuation and actuated forms at pH 7 and above, whereas the size of the actuated forms can be controlled by the temperature at lower pH. The membranes are strong enough to reversibly lift and release ≈426 times weight of their own mass (2.47 g metal ring is lifted by a 5.8 mg membrane). Soft actuators are of interest as smart scaffolds, robotics, catalysis, drug release, energy storage, electrodes, and metamaterials. [ABSTRACT FROM AUTHOR]

Tantalum carbide has been widely used as an excellent refractory material. However, there are no reports regarding the continuous tantalum carbide-carbon nanofibers (TaC/CNFs) and their mechanical and electrical properties. In this work, TaC/CNFs were prepared by electrospinning. The morphology and structures of the nanofibers and the distribution of TaC in the nanofibers were investigated by SEM, EDX, TEM, XRD, XPS and Raman spectroscopy. The TaC/CNFs showed excellent thermal stability, mechanical flexibility and conductivity even after folding for 180 cycles. These flexible, refractory and conductive TaC/CNFs could be found potential applications for flexible electronic devices and refractory materials. [ABSTRACT FROM AUTHOR]

Recently, wood‐based composites have absorbed widespread concern in the field of electromagnetic interference (EMI) shielding due to their sustainability and inherent layered porous structure. The channel structure of wood is often used to load highly conductive materials to improve the EMI shielding performance of wood‐based composites. However, there is little research on how to use pure wood to prepare ultrathin EMI shielding materials. Herein, ultrathin veneer is obtained by cutting wood in parallel to the annual rings. Then, carbonized wood film (CWF) is prepared by a simple two‐step compressing and carbonization. The specific EMI shielding effectiveness (SSE/t) of CWF‐1200 with an ultrathin thickness (140 µm) and high electrical conductivity (58 S cm−1) can reach 9861.41 dB cm2 g−1, which is much higher than other reported wood‐based materials. In addition, the zeolitie imidazolate framework‐8 (ZIF‐8) nanocrystals are grown in situ on the surface of the CWF to obtain CWF/ZIF‐8. CWF/ZIF‐8 exhibits an EMI shielding effectiveness (SE) of up to 46 dB and an ultrahigh SSE/t value of 11 330.04 dB cm2 g−1 in X band. In addition, the ultrathin CWF also shows an excellent Joule heating effect. Therefore, the development of ultrathin wood‐based film provides a research basis for wood biomass to replace traditional non‐renewable and expensive electromagnetic (EM) shielding materials. [ABSTRACT FROM AUTHOR]

The performance of a Ce(III)-4,4′,4″-((1,3,5-triazine-2,4,6-triyl) tris (azanediyl)) tribenzoic acid–organic framework (Ce-H3TATAB-MOFs) for capturing excess fluoride in aqueous solutions and its subsequent defluoridation was investigated in depth. The optimal sorption capacity was obtained with a metal/organic ligand molar ratio of 1:1. The morphological characteristics, crystalline shape, functional groups, and pore structure of the material were analyzed via SEM, XRD, FTIR, XPS, and N2 adsorption–desorption experiments, and the thermodynamics, kinetics, and adsorption mechanism were elucidated. The influence of pH and co-existing ions for defluoridation performance were also sought. The results show that Ce-H3TATAB-MOFs is a mesoporous material with good crystallinity, and that quasi-second kinetic and Langmuir models can describe the sorption kinetics and thermodynamics well, demonstrating that the entire sorption process is a monolayer-governed chemisorption. The Langmuir maximum sorption capacity was 129.7 mg g−1 at 318 K (pH = 4). The adsorption mechanism involves ligand exchange, electrostatic interaction, and surface complexation. The best removal effect was reached at pH 4, and a removal effectiveness of 76.57% was obtained under strongly alkaline conditions (pH 10), indicating that the adsorbent has a wide range of applications. Ionic interference experiments showed that the presence of PO43− and H2PO4− in water have an inhibitory effect on defluoridation, whereas SO42−, Cl−, CO32−, and NO3− are conducive to the adsorption of fluoride due to the ionic effect. [ABSTRACT FROM AUTHOR]

As a common two-dimensional carbon material, graphene has been widely doped into polymers to prepare high-performance dielectric materials. However, the shortcomings of graphene, such as large specific surface area and poor dispersion, limit its further application. Therefore, in this work, to solve the problem regarding the uniform dispersion of graphene in the matrix, in situ polymerization was used to prepare graphene/polyimide films, in which 1,4-diiodobutane was used as a reduction agent to prevent the aggregation of graphene oxide (GO) during imidization. High dielectric constant composite films were obtained by adjusting the ratio of 1,4-diiodobutane in GO. The results show that the resulting graphene/polyimide composite film possessed a dielectric constant of up to 197.5, which was more than 58 times higher than that of the polyimide (PI) film. Furthermore, compared to the pure PI film, the composite films showed better thermal stability and mechanical properties. Thermal performance tests showed that the 1,4-diiodobutane added during the preparation of the composite film was thermally decomposed, and there was no residue. We believe our preparation method can be extended to other high dielectric composite films, which will facilitate their further development and application in high power density energy storage materials. [ABSTRACT FROM AUTHOR]

With the increasing pollution of electromagnetic (EM) radiation, it is necessary to develop low-cost, renewable electromagnetic interference (EMI) shielding materials. Herein, wood-derived carbon (WC) materials for EMI shielding are prepared by one-step carbonization of renewable wood. With the increase in carbonization temperature, the conductivity and EMI performance of WC increase gradually. At the same carbonization temperature, the denser WC has better conductivity and higher EMI performance. In addition, due to the layered superimposed conductive channel structure, the WC in the vertical-section shows better EMI shielding performance than that in the cross-section. After excluding the influence of thickness and density, the specific EMI shielding effectiveness (SSE/t) value can be calculated to further optimize tree species. We further discuss the mechanism of the influence of the microstructure of WC on its EMI shielding properties. In addition, the lightweight WC EMI material also has good hydrophobicity and heat insulation properties, as well as good mechanical properties. [ABSTRACT FROM AUTHOR]

As a new member of the silica-derivative family, modified glass fiber (MGF) has attracted extensive attention because of its excellent properties and potential applications. Surface modification of glass fiber (GF) greatly changes its performance, resulting in a series of changes to its surface structure, wettability, electrical properties, mechanical properties, and stability. This article summarizes the latest research progress in MGF, including the different modification methods, the various properties, and their advanced applications in different fields. Finally, the challenges and possible solutions were provided for future investigations of MGF. [ABSTRACT FROM AUTHOR]

In terms of new-generation energy-storing devices, aqueous zinc-ion batteries (AZIBs) are becoming the prime candidates because of their inexpensive nature, inherent safety, environmental benignity and abundant resources. Nevertheless, due to a restrained selection of cathodes, AZIBs often perform unsatisfactorily under long-life cycling and high-rate conditions. Consequently, we propose a facile evaporation-induced self-assembly technique for preparing V2O3@carbonized dictyophora (V2O3@CD) composites, utilizing economical and easily available biomass dictyophora as carbon sources and NH4VO3 as metal sources. When assembled in AZIBs, the V2O3@CD exhibits a high initial discharge capacity of 281.9 mAh g−1 at 50 mA g−1. The discharge capacity is still up to 151.9 mAh g−1 after 1000 cycles at 1 A g−1, showing excellent long-cycle durability. The extraordinary high electrochemical effectiveness of V2O3@CD could be mainly attributed to the formation of porous carbonized dictyophora frame. The formed porous carbon skeleton can ensure efficient electron transport and prevent V2O3 from losing electrical contact due to volume changes caused by Zn2+ intercalation/deintercalation. The strategy of metal-oxide-filled carbonized biomass material may provide insights into developing high-performance AZIBs and other potential energy storage devices, with a wide application range. [ABSTRACT FROM AUTHOR]

Polyelectrolyte has wide applications in biomedicine, agriculture and soft robotics. However, it is among one of the least understood physical systems because of the complex interplay of electrostatics and polymer nature. In this review, a comprehensive description is presented on experimental and theoretical studies of the activity coefficient, one of the most important thermodynamic properties of polyelectrolyte. Experimental methods to measure the activity coefficient were introduced, including direct potentiometric measurement and indirect methods such as isopiestic measurement and solubility measurement. Next, progress on the various theoretical approaches was presented, ranging from analytical, empirical and simulation methods. Finally, challenges for future development are proposed on this field. [ABSTRACT FROM AUTHOR]

Self-supporting electrode materials with the advantages of a simple operation process and the avoidance of the use any binders are promising candidates for supercapacitors. In this work, carbon-based self-supporting electrode materials with nanosheets grown on Al foil were prepared by combining hydrothermal reaction and the one-step chemical vapor deposition method. The effect of the concentration of the reaction solution on the structures as well as the electrochemical performance of the prepared samples were studied. With the increase in concentration, the nanosheets of the samples became dense and compact. The CNS-120 obtained from a 120 mmol zinc nitrate aqueous solution exhibited excellent electrochemical performance. The CNS-120 displayed the highest areal capacitance of 6.82 mF cm−2 at the current density of 0.01 mA cm−2. Moreover, the CNS-120 exhibited outstanding rate performance with an areal capacitance of 3.07 mF cm−2 at 2 mA cm−2 and good cyclic stability with a capacitance retention of 96.35% after 5000 cycles. Besides, the CNS-120 possessed an energy density of 5.9 μWh cm−2 at a power density of 25 μW cm−2 and still achieved 0.3 μWh cm−2 at 4204 μW cm−2. This work provides simple methods to prepared carbon-based self-supporting materials with low-cost Al foil and demonstrates their potential for realistic application of supercapacitors. [ABSTRACT FROM AUTHOR]

Highlights: The crystal facets featured with facet-dependent physical and chemical properties can exhibit varied electrocatalytic activity toward hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) attributed to their anisotropy. The highly active exposed crystal facets enable increased mass activity of active sites, lower reaction energy barriers, and enhanced catalytic reaction rates for HER and OER. The formation mechanism and control strategy of the crystal facet, significant contributions as well as challenges and perspectives of facet-engineered catalysts for HER and OER are provided. The electrocatalytic water splitting technology can generate high-purity hydrogen without emitting carbon dioxide, which is in favor of relieving environmental pollution and energy crisis and achieving carbon neutrality. Electrocatalysts can effectively reduce the reaction energy barrier and increase the reaction efficiency. Facet engineering is considered as a promising strategy in controlling the ratio of desired crystal planes on the surface. Owing to the anisotropy, crystal planes with different orientations usually feature facet-dependent physical and chemical properties, leading to differences in the adsorption energies of oxygen or hydrogen intermediates, and thus exhibit varied electrocatalytic activity toward hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). In this review, a brief introduction of the basic concepts, fundamental understanding of the reaction mechanisms as well as key evaluating parameters for both HER and OER are provided. The formation mechanisms of the crystal facets are comprehensively overviewed aiming to give scientific theory guides to realize dominant crystal planes. Subsequently, three strategies of selective capping agent, selective etching agent, and coordination modulation to tune crystal planes are comprehensively summarized. Then, we present an overview of significant contributions of facet-engineered catalysts toward HER, OER, and overall water splitting. In particular, we highlight that density functional theory calculations play an indispensable role in unveiling the structure–activity correlation between the crystal plane and catalytic activity. Finally, the remaining challenges in facet-engineered catalysts for HER and OER are provided and future prospects for designing advanced facet-engineered electrocatalysts are discussed. [ABSTRACT FROM AUTHOR]

In order to reduce the dependence on fossil energy products, natural fiber/polymer hybrid composites have been increasingly researched. The high price of the quartz optical fibers and glass optical fibers has greatly inspired researchers to engage in the research on polymer optical fibers. Herein, transparent fibers based on plant fibers were innovatively prepared for the first time by delignification and impregnating epoxy diluted with acetone. The epoxy improved the thermal stability of the fiber without deteriorating its mechanical properties, and also endowed the fiber with the property of transparency. The tensile strength of transparent fibers of three diameters were 34.5, 58.6 and 100.3 MPa, respectively and the corresponding Young's modulus reached 1.1, 1.7 and 2.3 GPa, respectively. In addition, the light-conducting properties of transparent fibers were displayed with a green laser and the fibers displayed good light transmission along the fiber growth direction. Transparent fibers are expected to be used in optical fibers because of their high thermal stability, good mechanical properties and light-conducting properties. • Using acetone as diluent skillfully solves the difficulty of epoxy impregnation in rattan fiber. • Transparent fibers based on natural cellulosic fibers were successfully prepared for the first time. • The composite fibers possessed high thermal stability, good mechanical properties and light-conducting properties. • The transparent composite fibers have the potential to be used as the core material of optical fibers. [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]

The occurrence of fluoride contamination in drinking water has gained substantial concern owing to its serious threat to human health. Traditional adsorbents have shortcomings such as low adsorption capacity and poor selectivity, so it is urgent to develop new adsorbents with high adsorption capacity, renewable and no secondary pollution. In this work, magnetic electrospun La-Mn-Fe tri-metal oxide nanofibers (LMF NFs) for fluoride recovery were developed via electrospinning and heat treatment, and its defluoridation property was evaluated in batch trials. Modern analytical tools (SEM, BET, XRD, FTIR) were adopted to characterize the properties of the optimized adsorbent, i.e., LMF11 NFs with a La:Mn molar ratio of 1:1. The surface area calculated via BET method and pHpzc assessed using pH drift method of LMF11 NFs were 55.81 m2 g−1 and 6.47, respectively. The results indicated that the adsorption amount was highly dependent on the pH of the solution, and reached the highest value at pH = 3. The kinetic behavior of defluoridation on LMF11 NFs was dominated by the PSO model with the highest fitted determination coefficients of 0.9999. Compared with the other three isotherm models, the Langmuir model described defluoridation characteristics well with larger correlation coefficients of 0.9997, 0.9990, 0.9987 and 0.9976 at 15 °C, 25 °C, 35 °C and 45 °C, respectively. The optimized LMF11 NFs exhibited superior monolayer defluoridation capacities for 173.30–199.60 mg F−/g at pH 3 at 15–45 °C according to the Langmuir isotherm model. A thermodynamic study proved that the defluoridation by LMF11 NFs is a spontaneous, endothermic along with entropy increase process. In addition, the LMF11 NFs still showed high defluoridation performance after three reused cycles. These findings unveil that the synthesized LMF11 NFs adsorbent is a good adsorbent for fluoride remediation from wastewater owing to its low cost, high defluoridation performance and easy operation. [ABSTRACT FROM AUTHOR]

Recently, the sustainable utilization of waste resources has become a low-cost and effective strategy to design high-performance functional materials to solve the increasingly serious environmental pollution problem. Herein, the flexible and highly stretchable polyurethane (PU) composite foams assisted by one-dimensional carbon nanotubes (CNTs) and zero-dimensional Fe3O4 were fabricated using waste tire rubbers (WTRs) as reinforcements during a simple self-foaming process. The collaborative introduction of conductive CNTs, magnetic Fe3O4, and WTRs with three-dimensional cross-linked structures enabled the construction of an efficient electronic transmission path and heterointerfaces inside the composite foam. The resulting composite foam possessed a desired minimum reflection loss (RLmin) of −47.43 dB, and also exhibited superior mechanical properties with a tensile strength of >3 MPa and multiple tensile deformation recovery abilities. In addition, increasing the temperature could significantly improve the electromagnetic wave absorption performance of the composite foam. This comprehensive composite foam derived from WTRs has shown a promising development potential for using waste materials to relieve electromagnetic pollution. [ABSTRACT FROM AUTHOR]

Materials with outstanding mechanical properties and excellent dielectric properties are increasingly favored in the microelectronics industry. The application of polyimide (PI) in the field of microelectronics is limited because of the fact that PI with excellent mechanical properties does not have special features in the dielectric properties. In this work, PI composite films with high dielectric properties and excellent mechanical properties are fabricated by in-situ reduction of fluorinated graphene (FG) in polyamide acid (PAA) composites. The dielectric permittivity of pure PI is 3.47 and the maximum energy storage density is 0.664 J/cm3 at 100 Hz, while the dielectric permittivity of the PI composite films reaches 235.74 under the same conditions, a 68-times increase compared to the pure PI, and the maximum energy storage density is 5.651, a 9-times increase compared to the pure PI films. This method not only solves the problem of the aggregation of the filler particles in the PI matrix and maintains the intrinsic excellent mechanical properties of the PI, but also significantly improves the dielectric properties of the PI. [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]

Superior strong and tough structural materials are highly desirable in engineering applications. However, it remains a big challenge to combine these two mutually exclusive mechanical properties into one body. In the work, an ultrastrong and tough cellulosic material was fabricated by a two-step process of delignification and water molecule-induced hydrogen bonding under compression. The strong and tough cellulosic material showed enhanced tensile strength (352 MPa vs. 56 MPa for natural wood) and toughness (4.1 MJ m−3 vs. 0.42 MJ m−3 for natural wood). The mechanical behaviors of ultrastrong and tough bulk material in a tensile state were simulated by finite element analysis (FEA) using mechanical parameters measured in the experiment. FEA results showed that the tensile strength and toughness gradually simultaneously improved with the increase in moisture content, demonstrating that water molecules played an active role in fabricating strong and tough materials, by plasticizing and forming hydrogen bonding among cellulose nanofibrils. [ABSTRACT FROM AUTHOR]

[Display omitted] • Near-infrared (NIR) fluorescent nanomaterials are highly-promising in the quest for a next-generation of food toxicity sensors. • Exploiting NIR photoluminescence for food security assessment is effective in detecting inorganic and organic contaminants. • Perspectives and challenges concerning the use of NIR photoluminescence for food safety detection are discussed. Acknowledged by the World Health Organisation (WHO), over 200 diseases ranging from mild to fatal are linked to the consumption of food products subjected to physical, chemical, or biological contamination. Nevertheless, conventional methods commonly used for the identification of health hazards in foodstuffs have problems coping with the sensitivity requirements imposed by latest-hour regulations in the field. Additionally, their use and availability is wildly limited by aspects such as instrument dimension, prohibitive costs, detection complexity and required operational knowledge. This review provides an overview of recent efforts that have focused on the assesment of food contamination based on near infrared (NIR) photoluminescent sensors. Important endeavors that have targeted the precise detection of various inorganic and organic contaminants, including hydrogen sulfide, cyanide anions, mycotoxins, antibiotic residues, etc., are presented and relevant challenges that lie en route as stumbling blocks for such sensors to reach the next level of maturity and to become more available, are systematically discussed and enunciated. Ingenious food contamination sensors that rely on conventional or up-conversion photoluminescence in the NIR region represent an emerging topic. To date, such sensors have been demonstrated as promising detection candidates, possessing important advantages such as: high efficiency, facile implementation, and convenient flexibility, thereby promising significant contributions to expand the current state of the art in food security. [ABSTRACT FROM AUTHOR]

Reductive homocoupling transformations mediated by bases and TMSCN have been used as a strategy for synthesis of 1,2‐disubstituted ethanones. This protocol provides a method for synthesizing functionalized ethanones from aldehydes in one pot without transition metals. [ABSTRACT FROM AUTHOR]

High dielectric permittivity, good mechanical properties, and excellent thermal stability are highly desired for the dielectric materials used in the embedded capacitors and energy-storage devices. This study reports polyimide (PI)/barium titanate (BaTiO3) nanocomposites fabricated from electrospun PI/BaTiO3 hybrid nanofibers. The PI/BaTiO3 nanocomposites were investigated using Fourier transform infrared spectroscopy, scanning electron microscope, transmission electron microscope, thermal gravimetric analysis, an electromechanical testing machine, a LCR meter and an electric breakdown strength tester. The results showed that BaTiO3 fillers were uniformly dispersed up to 50 vol% in PI matrix. The dielectric permittivity of the composite (50 vol% BaTiO3) was 29.66 with a dielectric loss of 0.009 at 1 kHz and room temperature. The dielectric permittivity showed a very small dependence on temperature (up to 150°C) and frequency (100 Hz-100 kHz). The nanocomposites also showed high thermal stability and good mechanical properties. The PI/BaTiO3 nanocomposites will be a promising candidate for uses in embedded capacitors, especially in high temperature circumstance. POLYM. COMPOS., 37:794-801, 2016. © 2014 Society of Plastics Engineers [ABSTRACT FROM AUTHOR]

Titanium carbides are well-known for their outstanding mechanical and thermal stabilities. However, the studies on the mechanical properties and the conductivity of titanium carbide–carbon nanofibers (TiC/CNF) are missing. This work prepared TiC/CNF by electrospinning and highlighted the high modulus of single TiC/CNF, the flexibility and the excellent electrical conductivity of TiC/CNF felt even under 100 bending cycles. This flexible TiC/CNF felt with distinguished mechanical and electrical properties are promising to apply in titanium matrix composites (TMC), efficient catalyst scaffolds and electronic devices. [ABSTRACT FROM AUTHOR]

Crosslinked poly(ST- co -DVB- co -NaSS) latex nanoparticles (LNPs) with average particle size were used as template to prepare porous carbonized electrospun nanofibers (CENFs) with pore size about 10 nm on the surface and inside by electrospinning and carbonization. The porous CENFs without and with MWCNTs exhibited high specific surface area of 505 and 535 m 2 /g and high mesoporosity percentage of 80% and 84% respectively. The porous CENFs as electrode materials for electrochemical capacitors in 1 M H 2 SO 4 showed a specific capacitance of 235 F/g while the addition of MWCNTs led to an increase to 262 F/g. These free-standing and binder-free mesoporous CENFs with outstanding capacitance could be good candidates as electrode materials for supercapacitors. [ABSTRACT FROM AUTHOR]

Inspired by creatures, abundant stimulus-responsive hydrogel actuators with diverse functionalities have been manufactured for applications in soft robotics. However, constructing a shape memory and self-sensing bilayer hydrogel actuator with high mechanical strength and strong interfacial bonding still remains a challenge. Herein, a novel bilayer hydrogel with a stimulus-responsive TEMPO-oxidized cellulose nanofibers/poly(N-isopropylacrylamide) (TOCN/PNIPAM) layer and a non-responsive TOCN/polyacrylamide (TOCN/PAM) layer is proposed as a thermosensitive actuator. TOCNs as a nano-reinforced phase provide a high mechanical strength and endow the hydrogel actuator with a strong interfacial bonding. Due to the incorporation of TOCNs, the TOCN/PNIPAM hydrogel exhibits a high compressive strength (~89.2 kPa), elongation at break (~170.7 %) and tensile strength (~24.0 kPa). The prepared PNIPAM/TOCN/PAM hydrogel actuator performs the roles of an encapsulation, jack, temperature-controlled fluid valve and temperature-control manipulator. The incorporation of Fe3+ further endows the bilayer hydrogel actuator with a synergistic performance of shape memory and temperature-driven, which can be used as a temperature-responsive switch to detect ambient temperature. The PNIPAM/TOCN/PAM-Fe3+ conductive hydrogel can be assembled into a flexible sensor and generate sensing signals when driven by temperature changes to achieve real-time feedback. This research may lead to new insights into the design and manufacturing of intelligent flexible soft robots. [Display omitted] [ABSTRACT FROM AUTHOR]

As a convenient photothermal material, polydopamine (PDA) has been widely utilized in wood-based evaporators. However, the loading conditions of polydopamine on biomass bulk materials have not been systematically studied. In this paper, the suitable reaction conditions of polydopamine were studied with rattan as the substrate, and a reference for the improvement of the loading conditions was proposed. The polydopamine-loaded rattan-based evaporator (PDA-R) prepared on this basis exhibits excellent working stability due to the unique large-scale hierarchical porous structure of rattan. In addition to excellent salt resistance and cycle performance (evaporation rate decays by 5.1% after 30 cycles), the larger-aperture channel (200–450 μm) also brings better adaptability to salinity changes than polydopamine-loaded basswood-based evaporator (PDA-BW) (the attenuation coefficient of PDA-R is 6.2%, while the attenuation coefficient of PDA-BW is 16.3%). All of these indicate the broad prospects of polydopamine-loaded rattan-based evaporator as a multi-effect treatment scheme of brine. [Display omitted] • Loading conditions of polydopamine on biomass block material is systematic studied. • PDA-R has excellent salt resistance and cycling performance in high salinity brines. • PDA-R has great adaptability to salinity changes. • The effect of uniformly dense pore size of the substrate on salinity adaptability of evaporator is explored. [ABSTRACT FROM AUTHOR]

Nowadays, high-performance electromagnetic wave (EMW) absorption materials derived from low-cost biomass materials have attracted widespread attention. Herein, a novel biomass‑carbon with porous array structures derived from waste soybean dregs is prepared by a hydrothermal method combined with heat treatment using formaldehyde and KOH as activators. The as-prepared biomass‑carbon with significantly enhanced specific surface area can possess more charge transmission paths, increased multiple reflections and scattering, multiple loss modes, and improved impedance matching, leading to the improvement of EMW absorption performances. The obtained single-component biomass‑carbon without any functional fillers exhibits an effective EMW absorption capability with a wide absorption bandwidth of 4.8 GHz at a thickness of 3.5 mm. This study will provide a valuable approach for the preparation of biomass‑carbon based EMW absorption materials with controllable porous structures by the activation process. [Display omitted] • High-performance single-component biomass carbon derived from soybean dregs • Unique porous array structures formed through an activation process. • Effective EMW absorption capability with a wide absorption bandwidth of 4.8 GHz. [ABSTRACT FROM AUTHOR]

Multichannel-porous carbon derived from wood can serve as a conductive substrate for fast charge transfer and ion diffusion, supporting the high-theory capacitance of pseudocapacitive materials. Herein, NiCo2O4 nanosheets, which are hierarchically porous, anchored on the surface of carbonized wood via electrodeposition for free-binder high-performance supercapacitor electrode materials, were proposed. Benefiting from the effectively alleviated NiCo2O4 nanosheets accumulation and sufficient active surface area for redox reaction, a N-doped wood-derived porous carbon-NiCo2O4 nanosheet hybrid material (NCNS–NCW) electrode exhibited a specific electric capacity of 1730 F g−1 at 1 A g−1 in 1 mol L−1 KOH and splendid electrochemical firmness with 80% capacitance retention after cycles. Furthermore, an all-wood-based asymmetric supercapacitor based on NCNS–NCW//NCW was assembled and a high energy density of 56.1 Wh kg−1 at a watt density of 349 W kg−1 was achieved. Due to the great electrochemical performance of NCNS–NCW, we expect it to be used as an electrode material with great promise for energy storage equipment. [ABSTRACT FROM AUTHOR]

It is an effective way to develop basswood (Tilia americana, hardwood)-derived thick carbon electrode for high energy density supercapacitors. The wood-derived anisotropic structural carbon electrodes have different transfer kinetics of the electrolyte, which will significantly affect the electrochemical performance especially at high current density. Therefore, the relationship between the sectional wood-derived electrodes and the electrochemical performance of supercapacitors were systematically studied. The results show that the high specific surface area (542 m2 g−1) of cross-sectional wood-derived carbon contributes to the excellent electrochemical performance (specific/area capacitance ~ 3040 mF cm−2/118 F g−1 at 1 mA cm−2, cycle stability ~ 82.2% after 10,000 cycles at 50 mA cm−2, and capacitive contribution of 76.64% at 5 mV s−1), which is attributed to the hierarchical porous structure and easily allows electrolytes to enter the interior even at high current density. This work provides a fundamental understanding of the dynamic behaviors of electrolyte at different wood sections, and it is expected to be extended to other wood species and wood-like structures for energy storage applications. [ABSTRACT FROM AUTHOR]

Biomass-derived heteroatom doped porous carbon is a hot electrode material for supercapacitors. Herein, nitrogen and oxygen co-doped porous carbon sheets are prepared by one-step carbonization-activation of hybrids of soybean protein isolate and zinc chloride (ZnCl2). The effect of the mass ratio between the activator and carbon precursor on the microstructure as well as the electrochemical performance of the materials is investigated. The activated samples show enhanced specific surface area, preferably up to 1034.33 m2 g−1, which is dominated by micropores and mesopores. More interestingly, ZnCl2 incorporation can improve the doping rate of nitrogen and oxygen elements from 4.5 at% to 6.37 at%, and 12.89 at% to 13.58 at%, respectively. Ultimately, the porous carbon sheets exhibit good capacitive performance in 6 M KOH electrolyte, and the specific capacitance could reach 210.47 F g−1 in a three-electrode system. In a two-electrode system, a capacitance retention of 93.02% can be achieved after 10 000 cycles at 20 A g−1. In addition, the optimized sample shows a maximum energy density of 16.27 W h kg−1 and a maximum power density of 8.44 kW kg−1. This work indicates that the soybean protein-derived porous carbon sheets are promising electrode materials for supercapacitors. [ABSTRACT FROM AUTHOR]

Constructing lightweight and porous adsorbents which can effectively remove dye contaminants is of great significance in the field of the sewage treatment. In this work, anisotropic cellulose nanofibril (CNF) composite sponges assisted by rectorites are fabricated through directional freeze-drying. The resulted composite sponge exhibits the superior saturated adsorption capacity and removal efficiency of 120.0 mg/g and 96.1% for methylene blue (MB), respectively, which is better than the pure CNF sponge and rectorite powders. This is attributed to the strong electrostatic interaction between CNFs and MB, and good cation exchange property of rectorites inside the three-dimensional (3D) highly porous composite sponge. The MB adsorption process of the composite sponge fits to the pseudo-second-order kinetic model and the Langmuir isotherm model well, which is affected by both boundary layer and intraparticle diffusion, resulting in a theoretical maximum adsorption capacity of 214.6 mg/g. Moreover, it also possesses a selective adsorption capacity for anionic and cationic dyes, which is expected to realize the separation treatment of different dyes according to actual application requirements. [Display omitted] • Anisotropic CNF/rectorite composite sponge by directional freeze-drying. • Superior MB adsorption capacity and removal rate of 120.0 mg/g and 96.1%. • Selective adsorption and separation capacity for anionic and cationic dyes. • Detailed evaluation of the adsorption behavior and mechanism. [ABSTRACT FROM AUTHOR]

A three-phase nanocomposite with outstanding dielectric properties was prepared via electrospinning and hot-pressing, by which multi-walled carbon nanotubes (MWCNTs) were homogeneously dispersed in polyimide (PI) matrix and separated by the BaTiO 3 particles (BTPs). The fairly enhanced dielectric properties were due to synergistic enhancing of the ferroelectric ceramic filler BTPs and conductive filler MWCNTs. The investigation shows that the dielectric permittivity of the as-fabricated three-phase nanocomposites with 40 vol% BTPs and 10 vol% MWCNTs loads is as high as 1061.98 at 100 Hz with a lower dielectric loss of 0.23, and the corresponding energy storage density is 4.773 J/cm 3 , 11 times that of the pure polyimide. The three-phase nanocomposites with enhanced dielectric properties also show excellent thermal properties and will be attractive in application in modern microelectronics. [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]

Abstract: Copolymers, poly(acrylonitrile-co-monobutylitaconate-co-n-butylacrylate) (copolyacrylonitrile, co-PANs) with different content of monobutyl itaconate (MBI) were synthesized by free radical polymerization and then electrospun into aligned nanofibers. After thermal treatments of stabilization, carbonization, and graphitization, the resulting aligned co-PAN nanofibers were converted to aligned electrospun carbon nanofiber bundles (ECNFB) with diameters of approximately 200nm. FT-IR technique was applied to investigate the stabilization process of co-PAN nanofibers, while XRD, TEM and tensile tester were used to characterize the microstructures and mechanical properties of the ECNFB. The measured results revealed that MBI was a fairly useful comonomer for preparing high performance PAN-based CNFs by improving the stabilization of co-PAN nanofibers and by promoting the formation of ordered graphite crystals in the ECNFB. When the content of MBI unit in co-PAN was 5wt%, the aligned ECNFB exhibited a tensile strength of up to 1.8GPa and a Young׳s modulus of up to 97.0GPa, which is 86% and 67% higher than those of the ECNFB previously reported in our group respectively. [Copyright &y& Elsevier]

[Display omitted] • A novel 3D COF (SPB-HHTP-DBF) is synthesized, as the first introduction of spiroborate structures into environmental engineering. • Major cationic dyes including methylene blue (MB), crystal violet (CV), and malachite green (MG) removal of 99% within 10 min. • Highly selective separation of cationic dyes from mixed anionic/cationic dye solutions, advanced adsorption capacity and reliable cycling stability. Covalent organic frameworks (COFs) are undergoing a period of rapid development of novel structures and diverse functions. Ionic COFs have been applied in environmental engineering due to their porous, robust and charged skeleton, making it necessary to expand the family of ionic frameworks. Based on an in-situ functionalization strategy, we report a new 3D anionic COF constructed by the linker 2,3,6,7,10,11-hexahydroxytriphenylene (HHTP), linkage spiroborate (SPB) and counter cation [ n -Bu 2 NH 2 ]+ (DBA). Anionic spiroborate centers are distributed in a 4-fold interpenetrated network of srs topology, constituting a stable crystalline structure. The framework has been used for adsorption of charged dyes and present rapid cationic dyes removal(over 99 % within 10 min), effective adsorption capacities for methylene blue (MB), crystal violet (CV), and malachite green (MG) (maximum values of 892 mg g−1, 1632 mg g−1 and 457 mg g−1, respectively), impressive molecular sieving selectivity (little absorption of anionic dyes) and good recycle performance (no removal loss for at least 5 cycles). In addition, the adsorption behaviors of isotherm and kinetic are discussed. This study not only reveals a new strategy for constructing ionic 3D COFs, but also contributes to their development for environmental engineering related applications. [ABSTRACT FROM AUTHOR]

High-performance porous polyimide (PI) monoliths, including PI aerogels, sponges, and foams, have become one of the hotspots in both researching and applications due to their superior properties such as high porosity, outstanding mechanical and thermal stability, low dielectric constant and thermal conductivity. Up to now, various fabricating methods and applicating situations for PI porous monolith materials have been reported. From the viewpoint of molecular chemistry, porous structure construction, as well as the functional modification, the property optimization and adjustment are feasible, endowing PI monoliths with promising potential for different practical applications (e.g. sensors, low-k materials, thermal management, energy field and utilization, absorption and filtration, photonic utilization, etc.). In this review, the recent progress of porous PI monoliths was summarized in detail based on the fabrication methods, functional modifications, as well as multi-functional applications. Besides, the future perspectives of this field were also provided for reference. Apart from presenting an overview of progress made in the field of PI porous monoliths, this review could also be meaningful for those researching topics which have similarity within. [ABSTRACT FROM AUTHOR]

An alternative magnetic field (AMF)-induced electrospun fibrous thermoresponsive composite actuator showing penetrable remote-control ability with fast response is shown here for the first time. The built-in heater of magnetothermal Fe3O4 nanoparticles in the actuator and the porous structure of the fibrous layer contribute to a fast actuation with a curvature of 0.4 mm−1 in 2 s. The higher loading amount of the Fe3O4 nanoparticles and higher magnetic field strength result in a faster actuation. Interestingly, the composite actuator showed a similar actuation even when it was covered by a piece of Polytetrafluoroethylene (PTFE) film, which shows a penetrable remote-control ability. [ABSTRACT FROM AUTHOR]

Amidst the burgeoning interest in multifunctional superhydrophobic wood-based composites (SWBCs) for their varied applications and the need for improved environmental resilience, recent efforts focus on enhancing their utility by integrating features such as mechanical and chemical stability, self-healing capabilities, flame resistance, and antimicrobial properties. Research indicates that various external conditions can influence the wettability and additional characteristics of SWBCs. This comprehensive review outlines three critical factors affecting SWBCs' performance: synthesis methods, wood taxonomy, and chemical agents. It further provides a detailed overview of SWBCs' specific attributes, including essential qualities for diverse applications and the limitations posed by different contexts. Additionally, it elaborates on performance evaluation techniques, offering a foundational framework for SWBCs' practical application. This work aims to serve as an important resource for future research and development in SWBC engineering. [Display omitted] • Preparation mechanism of superhydrophobic wood-based composites. • Factors affecting superhydrophobic wood-based composites. • Methods for evaluating superhydrophobic wood-based composites properties. • Challenges and directions for future development to achieve industrialization are presented. [ABSTRACT FROM AUTHOR]

Developing high-performance microwave absorption (MA) materials becomes an urgent concern in the field of electromagnetic protection. Constructing porous framework is an efficient approach to MA owing to the abilities of adjusting impedance matching and providing more reflection and scattering paths for electromagnetic waves. Herein, a cellulose nanofibril (CNF)/honeycomb-like carbon-shell encapsulated FeCoNi@C/carbon nanotube (CNT) composite aerogel was fabricated via a facile freeze-drying method. The super-lightweight composites showed a distinctive gradient structure for reflection and scattering inside aerogel pores, micrometer small pores, and nano-fillers on the pore walls. The composite aerogel showed an ideal minimum reflection loss (RL min) of −43.6 dB and remarkable adjustable effective absorption bandwidth (EAB) of 12.18 GHz due to good impedance matching, unique gradient porous structure, and synergies of multiple loss mechanisms. Therefore, this work will provide a viable strategy to improve the MA capability of absorbers by taking full advantage of constructing gradient reflection and scattering porous structure. [Display omitted] [ABSTRACT FROM AUTHOR]

[Display omitted] • Two basic design strategies for 3D COFs: high valency and functionalization. • 3D COFs: building blocks, topology, linkage, and PSM strategy. • Applications in adsorption and separation, catalysis, stimulus response, conduction and energy storage. • The challenges and opportunities are proposed for future research. Covalent organic frameworks (COFs) are a class of porous crystalline organic materials. The dynamic chemistry of covalent bonding and the applications of COFs have made great progress already. Three-dimensional (3D) COFs have attracted much attention in recent years because of their more diverse spatial structures and interconnected pore properties. High valency and functionalization are two key strategies of 3D COFs design, including the development of building blocks, topology, linkage and post synthetic modification strategy. As a result, the diversity of COF spatial structures is significantly extending and various applications in energy, environment, biology and chemical catalysis are developing. In this review, we summarized the recent articles about 3D COFs in the field of framework design, function development and applications, and put forward the critical strategies and comment, the future perspectives of the field are also prospected. [ABSTRACT FROM AUTHOR]

[Display omitted] Self-supporting tree skeleton and densely stackable phenolic resin are cleverly coupled together by a "rebar-concrete" structure. The thick electrode as a master of space utilization has extremely high areal and volumetric energy density. This work confirms the effective coupling of the self-supporting skeleton and powder materials, providing novel ideas for the preparation of thick electrodes with high mass loading. • A "rebar-concrete" structure is proposed to facilitate the high space utilization of thick electrodes. • The areal capacitance of the thick electrode reaches an astonishing 11F cm−2. • The assembled SSC device delivers competitive areal energy density of 0.63 mWh cm−2. The thick electrode design with high packing density of active materials can increase the capacity in a limited space. However, the key challenge is still to develop a system with high space utilization and ensure electron/ion transport in thick electrode. This work proposes an interesting "rebar-concrete" structure, which successfully prepared wood/phenolic resin-derived thick electrode with high space utilization by in-situ polymerization of phenolic resin (concrete) in the wood (rebar) channel. The electrode exhibits an excellent three-dimensional interconnected hierarchical pore structure due to the uniform activation of in-situ anchored KOH particles. The mass loading (35 mg cm−2) and areal capacitance (11F cm−2) of the obtained composite electrode are increased to 446 % and 1257 % of the original balsa wood, respectively. The assembled symmetric supercapacitor (SSC) exhibits a high energy density of 0.63 mWh cm−2 (3.91 mWh cm−3) and an excellent cycle stability (95 % retention after 50 000 cycles), showing good practicability in lighting LEDs or driving a fan. This strategy achieves effective coupling of self-supporting skeleton and powder materials, providing more insights and possibilities for the preparation of high energy density thick electrodes. [ABSTRACT FROM AUTHOR]

Nowadays, electromagnetic pollution caused by the development of communication technology and electronic equipment has become an urgent problem to be solved. It is an effective solution to design high-performance electromagnetic wave absorption (EWA) materials with wide-band and powerful absorption characteristics for electromagnetic protection. In this work, a multi-scale MXene/carbon nanotube@Fe 3 O 4 composite material with a heterogeneous structure was synthesized by a solvothermal method, and the high/low-frequency EWA operating bands were adjusted by component regulation. The composite material performed excellent EWA performances based on the synergistic effect of polarization loss, conductive and magnetic loss, and three-dimensional heterointerfaces. Its minimum reflection loss reached − 59.95 dB with an effective absorption bandwidth of 4.7 GHz (13.3–18 GHz), which basically covered the Ku band. Therefore, this feasible scheme is expected to provide an effective strategy for controlling military and civil electromagnetic pollution. [Display omitted] • A facile preparation method of MXene-based multiscale composites was proposed. • Military/civil EWA operating frequency bands were adjusted by component regulation. • A superior RL min value of − 59.95 dB was obtained based on complex loss mechanisms. [ABSTRACT FROM AUTHOR]

The Review summarized and analyzed the modification strategies and application directions of ZIF-67 in photocatalysis. [Display omitted] • An introduction to the structure and properties of ZIF-67 is provided. • The synthetic pathways of ZIF-67 and its derivatives are summarized. • The regulation mechanism and improvement strategy of photocatalytic performance are discussed. • Pioneering and interdisciplinary application in the field of photocatalysis based on ZIF-67. • Application prospects and challenges of ZIF-67 in photocatalysis. Cobalt-based zeolitic imidazolate frameworks (Co-ZIF) have attracted intensive interest in multivariate applications because of their high specific surface area and presence of great active sites. At present, most of the reviews on ZIF-67 focus on electrocatalysis and degradation. This review mainly discusses the application of ZIF-67 and its derivatives in photocatalysis to fill the gap in this field. The structural properties of ZIF-67 and the preparation methods of ZIF-67-derived materials are firstly introduced. Subsequently, we summarize the strategies to improve the photocatalytic performance of ZIF-67, such as ion doping, construction of heterojunctions, and solution etching. Thirdly, the recent applications of ZIF-67 and its derivatives in photocatalysis, such as CO 2 reduction, H 2 production, degradation, and antibacterial are discussed. Finally, the Review summarizes the current development status of ZIF-67 in photocatalysis and provides an outlook on its future development trend and development constraints. [ABSTRACT FROM AUTHOR]

With the rapid development of the Internet of Things, nanogenerator as a green energy collection technology has attracted great attention in various fields. Specifically, the natural renewable nanocellulose as a raw material can significantly improve the environmental friendliness of the nanocellulose-based nanogenerators, which also makes the nanocellulose based nanogenerators expected to further develop in areas such as wearable devices and sensor networks. This paper mainly reports the application of nanocellulose in nanogenerator, focusing on the sensor. The types, sources and preparation methods of nanocellulose are briefly introduced. At the same time, the special structure of nanocellulose highlights the advantages of nanocellulose in nanogenerators. Then, the application of nanocellulose-based nanogenerators in sensors is introduced. Finally, the future development prospects and shortcomings of this nanogenerator are discussed. [ABSTRACT FROM AUTHOR]

Herein, we used a one-pot method to fabricate a novel MOF-on-MOF adsorbent, namely MOF(Zr)-on-MOF(Ce). The adsorbent demonstrated a high maximum fluoride-ions capture capacity of 164.47 mg g−1. The morphology, elemental distribution, pore size distribution, and thermal stability were studied using SEM-EDS, XRD, BET, and TGA. The influence of the temperature, solution pH, fluoride concentration, and coexisting ions was explored using intermittent experiments. The results suggested that MOF(Zr)-on-MOF(Ce) had a fast capture rate for fluoride. MOF(Zr)-on-MOF(Ce) maintained an excellent fluoride removal performance over a wide pH range with an initial fluoride concentration of 20 mg L−1. The optimal effect was obtained at a pH of 4, but a high removal efficiency of 94% was maintained even at a pH of 9. Interference experiments showed that only the PO 4 3– had an adverse inhibition influence. The field experiments demonstrated that MOF(Zr)-on-MOF(Ce) can keep the safety threshold levels of fluoride in drinking water. The Langmuir and pseudo-second order kinetic models were well fitted for the defluoridation process, demonstrating that the adsorption of fluoride ions on MOF(Zr)-on-MOF(Ce) was dominated by monolayer chemisorption. With the further characterization and kinetic thermodynamic studies indicates that the removal mechanism involves ion exchange, electrostatic interactions and complexation effect. [Display omitted] • A novel MOF(Zr)-on-MOF(Ce) adsorbent were fabricated via one-pot methods for defluorination. • The maximum adsorption capacity of MOF(Zr)-on-MOF(Ce) was 164.47 mg g–1 for F ions. • The adsorbent had an excellent defluoridation performance with a wide pH range. • The mechanisms are ion-exchange, electrostatic interaction and complexation effect. [ABSTRACT FROM AUTHOR]

La–Mn bimetal oxide nanofibers, used as an adsorbent for the defluoridation of water, were synthesized by an electrospinning and heat treatment technology. The La–Mn bimetal oxide nanofiber adsorbent with a specific surface area of 35.064 m2 g−1 displayed a good defluoridation performance. Both the adsorption kinetics and equilibrium for fluoride (F−) uptake onto La–Mn bimetal oxide nanofibers were investigated. The kinetic studies established that the adsorption attained equilibrium at about 90 min, and the PSO kinetic model was ideal for the kinetic data under 20 and 50 mg L−1. The Langmuir maximum F− uptake was computed to be 189.39 mg g−1 at 308 K and pH 3. A thermodynamic study affirmed a feasible, endothermic, spontaneous and entropy driven process of F− adsorption towards La–Mn bimetal oxide nanofibers at the studied temperature range. Except for the competitive adsorption of PO43− and F−, the presence of NO3−, CO32−, Cl− and SO42− had little effect on fluoride removal. The La–Mn bimetal oxide adsorbent exhibited a good reusability. [ABSTRACT FROM AUTHOR]