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[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]

Flax fibers, with abundant resources and a low cost, are an excellent precursor of carbon fibers for supercapacitors. At present, they are very attractive for designing electrodes with high electrochemical performance via a simple and green way. Hence, we systemically control the specific surface area and pore structure of flax-based carbon fibers by impregnating them with zinc chloride (ZnCl2) solution. The results show that the dehydration and expansion effects of ZnCl2 affect the microstructure, which is directly related to the specific capacitance. After activation, the optimized electrode exhibited the highest specific capacitance of 105 F g−1 at a current density of 1 A g−1, which has been improved by more than 10 times compared to that of pure-flax based carbon fibers. Moreover, they also show an excellent cycling stability of 98.7% after 10 000 cycles, even at a high current density of 10 A g−1. These results further demonstrate that flax-based electrodes have potential to be applied to some relevant energy storage applications in the future. [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]

High mechanical performance carbon nanofibers are highly required for the carbon nanofiber-reinforced composites, and it is necessary to develop novel precursors for the preparation of carbon nanofibers. In this work, blends of poly(acrylonitrile-butyl acrylate mono-butyl itaconate) (co-PAN) and polyamic acid (PAA) were electrospun into aligned nanofibers and the nanofibers were converted to carbon nanofibers by thermal imidization, pre-oxidation and high-temperature carbonization. FT-IR spectroscopy was applied to monitor the chemical structures of the nanofibers before and after pre-oxidation. Tensile tests were used to characterize the mechanical properties of electrospun carbon nanofibers (ECNFs). The microstructures of ECNFs were investigated by high-resolution TEM and Raman spectroscopy. The results indicated that the ECNFs derived from blend of co-PAN/PAA with molar ratio of 6/4 and with carbonization temperature of 1400 °C possessed the highest tensile strength of 1212 MPa, which could be attributed to the ordered graphitic structures in ECNFs. [ABSTRACT FROM AUTHOR]

Achieving high drug loading capacity and controlling drug delivery are two main challenges related to drug carriers. In this study, polymeric macroporous sponges with very high pore volume and large porosity are introduced as a new-type of drug carrier. Due to the high pore volume (285 and 166 cm³/g for the sponges with densities of 3.5 and 6.0 mg/cm³, respectively), the sponges exhibit very high drug loading capacities with average values of 1870 ± 114 and 2697 ± 73 mg/g in the present study, which is much higher than the meso and microporous drug carriers (<1500 mg/g). In order to control the release profiles, an additional poly(p-xylylene) (PPX) coating was deposited by chemical vapor deposition on the drug loaded sponge. Consequently, Artemisone (ART) release in the aqueous medium could be retarded, depending on the density of the sponge and the thickness of the coating. In future, the new 3D polymeric sponges would be highly beneficial as drug carriers for the programmed release of drugs for treatment of chronic diseases. [ABSTRACT FROM AUTHOR]

Ultralight cellular sponges offer a unique set of properties. We show here that solvent uptake by these sponges results in new gel-like materials, which we term spongy gels. The appearance of the spongy gels is very similar to classic organogels. Usually, organogels are formed by a bottom-up process. In contrast, the spongy gels are formed by a top-down approach that offers numerous advantages for the design of their properties, reproducibility, and stability. The sponges themselves represent the scaffold of a gel that could be filled with a solvent, and thereby form a mechanically stable gel-like material. The spongy gels are independent of a time-consuming or otherwise demanding in situ scaffold formation. As solvent evaporation from gels is a concern for various applications, we also studied solvent evaporation of wetting and non-wetting liquids dispersed in the sponge. [ABSTRACT FROM AUTHOR]

Ultralight cellular sponges offer a unique set of properties. We show here that solvent uptake by these sponges results in new gel-like materials, which we term spongy gels. The appearance of the spongy gels is very similar to classic organogels. Usually, organogels are formed by a bottom-up process. In contrast, the spongy gels are formed by a top-down approach that offers numerous advantages for the design of their properties, reproducibility, and stability. The sponges themselves represent the scaffold of a gel that could be filled with a solvent, and thereby form a mechanically stable gel-like material. The spongy gels are independent of a time-consuming or otherwise demanding in situ scaffold formation. As solvent evaporation from gels is a concern for various applications, we also studied solvent evaporation of wetting and non-wetting liquids dispersed in the sponge. [ABSTRACT FROM AUTHOR]

This study reports on gold nanoparticles (AuNPs) immobilized in a sponge made of short electrospun fibers (Au-sponge), which show surprisingly high reaction rates at extremely low gold amount. Au-sponges are made by freeze-drying of dispersions of short electrospun fibers with preimmobilization of AuNPs. The resulting Au-sponges show very low densities around 7 mg cm−3 corresponding to a pore volume of about 150 mL g−1, but low surface area and very low amount of AuNPs in the range of 0.29-3.56 wt%. In general, catalysts with immobilized AuNPs show much low reaction rates compared to systems with dispersed AuNPs. By contrast, the Au-sponge catalyst with immobilized AuNPs is discerned here as an extremely efficient catalyst even superior to other systems with dispersed AuNPs. The fidelity of the Au-sponges after reactions is good enough for manifold use and thereby provides a sustainable catalyst design as well. [ABSTRACT FROM AUTHOR]

Achieving a simple and mild preparation method to obtain high performance carbon-based flax fiber electrode for supercapacitor has become particularly important but still challenges. Hence, the excellent electrochemical performance of electrode was constructed by impregnation-heat treatment with ethylenediamine tetraacetic acid disodium zinc (EDTANa 2 Zn) and zinc nitrate (ZnNO 3) as activators. The results show that the decomposed zinc oxide (ZnO) of EDTANa 2 Zn leads to the prominently hierarchical porous structure and abundant nitrogen-doping, which provides more active storage sites for electrolyte. Likewise, the as-prepared electrode by EDTANa 2 Zn treatment exhibits the specific capacitance of 292 F g−1 at the current density of 0.5 A g−1, and keeps up with the capacitance retention of 102 % even after a 10, 000 long-cycles at the high current density of 10 A g−1. Significantly, the suitable zinc salt assisted preparation of high performance flax fiber carbon-based electrode provides a novel idea for future electrochemical energy storage. [Display omitted] • The obtained electrode was constructed by EDTANa 2 Zn and zinc nitrate. • The 950-EA electrode exhibits the specific capacitance of 292 F g−1–0.5 A g−1 • The 950-EA electrode keeps up with the capacitance retention of 102 % after 10,000 cycles. [ABSTRACT FROM AUTHOR]

Mechanically strong electrospun nanofibers at high temperature are highly desired in the aerospace industry, high temperature filtration and fire protection clothing. In the present work, highly tough poly(imide-co-benzoxazole) (PI-co-PBO) nanofiber belts with excellent thermal stability, mechanical properties and thermomechanical properties were produced from the highly viscous methoxy-containing polyamic acid (MeO-PAA) solution by electrospinning followed by thermal rearrangement. The chemical structures of the polymer nanofibers and the corresponding thermal rearrangement were confirmed by 1H-NMR, FT-IR and TGA. The mechanical properties and thermomechanical properties were characterized by a tensile test and thermomechanical analysis (TMA). The aligned nanofiber belts heat-treated at 450 °C (ANF-450) had the highest tensile strength of 559 MPa, a modulus of 11.2 GPa and a toughness of 12.0 J g−1, respectively, which were much higher than those of the pure PBO films made by thermal rearrangement. The TMA test showed that the ANF-450 exhibited a high tensile strength retention of 90% and a modulus retention of 94% at a high temperature of 200 °C. These excellent thermomechanical properties make electrospun PI-co-PBO nanofibers promising candidates in high temperature areas. [ABSTRACT FROM AUTHOR]

Ultralight polymer sponges are prepared by freeze-drying of dispersions of short electrospun fibers. In contrast to many other highly porous materials, these sponges show extremely low densities (<3 mg cm−3) in combination with low specific surface areas. The resulting hierarchical pore structure of the sponges gives basis for soft and reversibly compressible materials and to hydrophobic behavior in combination with excellent uptake for hydrophobic liquids. Owing to their large porosity, cell culturing is successful after hydrophilic modification of the sponges. [ABSTRACT FROM AUTHOR]

High mechanical performance materials at high temperature are highly desired for the materials used in high temperature industries. This study reports the aligned electrospun polyimide nanofiber belt (A-PI-NFB) fabricated from the electrospinning followed with imidization. The A-PI-NFB showed increased mechanical and thermal mechanical properties as increasing the imidization temperature. At room temperature, the A-PI-NFB imidized at 450 °C (A-PI-NFB-450) had the highest tensile strength (689 MPa) and E modulus (13.2 GPa). The thermomechanical analysis (TMA) and dynamic mechanical analysis (DMA) showed that A-PI-NFB-450 possessed 80% tensile strength and 90% modulus when heated at 300 and 350 °C in N 2 , respectively. These excellent properties made A-PI-NFB good candidates for use in high temperature filtration, protective clothes etc. [ABSTRACT FROM AUTHOR]

The heavy metal copper is a serious hazard to human health and the environment. It is challenging to develop a highly efficient adsorbent that is easy to prepare, low cost, having large adsorption capacity, and non-polluting to the environment. Herein, an aminated electrospun polyacrylonitrile (PAN) staple fiber was prepared by grafting diethylenetriamine (DETA) after a hydrothermal reaction. DETA possessed numerous amino functional groups, thus providing more adsorption sites and higher adsorption capacity for copper ions (Cu2+). The Cu2+ adsorption behavior of the aminated fiber conformed to the pseudo-second-order kinetic model. It not only possessed high adsorption activity in the pH range of 3.0–6.0 and could reach a high saturated adsorption capacity of 349.65 mg g−1 at high Cu2+ concentrations but also had the ability to reduce the concentration below 1 mg L−1 at low Cu2+ concentrations with a small amount of adsorbent (0.5 mg). After 5 adsorption–desorption experiments, the removal efficiency of Cu2+ was maintained at more than 90%. This aminated PAN fiber is expected to become a candidate material for dealing with Cu2+ pollution. [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]

Abstract: This work highlights the usage of short electrospun fibers for the first time for the preparation of homogeneous polymer nanofiber/polymer composites and the improvement in mechanical properties by an order to magnitude compared to as-electrospun long and continuous nanofibers. Dispersions of short electrospun nanofibers can be processed by liquid processing techniques resulting in nanofiber nonwovens similar to electrospun nonwovens but is independent from the demands of the electrospinning process is one of the emphasis of this work. The re-formation of electrospun fiber nonwovens by dispersion casting of short electrospun polyimide (PI) nanofibers and the preparation of homogeneous polymer/polymer nanofiber composite films were selected as representative examples for showing the versatility of short electrospun fibers. The self-reinforced PI/PI-short nanofiber composite films were obtained from mixtures of short electrospun PI nanofibers and polyamic acid after imidization. Significant improvement of 53% and 87% in mechanical properties like tensile strength and modulus, respectively in comparison to the neat PI film was observed by using just 2wt% of short fibers. Parallel experiments were also carried out with long and continuous electrospun PI fibers and amazingly a huge difference was observed. The amount of continuously long fibers required for achieving almost the same strength was much higher i.e. 38wt% in comparison to the 2wt% required of short fibers. [Copyright &y& Elsevier]

In recent years, single‐atom catalysts (SACs) have become the most active part of the catalytic field due to their excellent catalytic activity. Among them, Ru SACs exhibit excellent performance in many catalytic applications due to their high atomic utilization efficiency, catalytic activity and selectivity, and relatively low cost. In order to understand the structure–performance relationship and potential catalytic mechanism of Ru SACs, this review summarizes the research progress of Ru SACs in the fields of electrocatalytic water splitting, fuel cells, nitrogen reduction, and nitrate reduction in recent years. The catalytic process of Ru single atom in different synthesis methods and modification strategies is summarized. Finally, some opportunities and challenges for the future development of Ru SACs are prospected. [ABSTRACT FROM AUTHOR]

Electrospinning is an effective and versatile method to prepare continuous polymer nanofibers and nonwovens that exhibit excellent properties such as high molecular orientation, high porosity and large specific surface area. Benefitting from these outstanding and intriguing features, electrospun nanofibers have been employed as a promising candidate for the fabrication of food packaging materials. Actually, the electrospun nanofibers used in food packaging must possess biocompatibility and low toxicity. In addition, in order to maintain the quality of food and extend its shelf life, food packaging materials also need to have certain functionality. Herein, in this timely review, functional materials produced from electrospinning toward food packaging are highlighted. At first, various strategies for the preparation of polymer electrospun fiber are introduced, then the characteristics of different packaging films and their successful applications in food packaging are summarized, including degradable materials, superhydrophobic materials, edible materials, antibacterial materials and high barrier materials. Finally, the future perspective and key challenges of polymer electrospun nanofibers for food packaging are also discussed. Hopefully, this review would provide a fundamental insight into the development of electrospun functional materials with high performance for food packaging. [ABSTRACT FROM AUTHOR]

Conductive hydrogels have emerged as excellent candidate materials for designing and fabricating flexible wearable sensors. However, there are still critical challenges in preparing high-performance, strongly adhesive, and biocompatible hydrogels through robust and green strategies. A central issue is the lack of an efficient, environmentally friendly and adaptable catalytic system for hydrogel construction. Herein, a series of natural polyphenol/Fe3+ nanodots (PPL/Fe3+ NDs) has been developed as nanoreactors to catalyze the self-gelation of vinyl monomers. The NDs could provide confined spaces for electron transfer, achieving an exceptionally high catalytic efficiency. Remarkably, they were effective in promoting the polymerization of vinyl monomers to form hydrogels even at the Fe content as low as 0.13 μg mL−1. The resulting hydrogels exhibited outstanding mechanical properties, excellent adhesive capacity, stable ultraviolet (UV)-shielding ability, and feasible electrical conductivity. These advantages allow the hydrogel as a flexible wearable sensor to monitor various human motions. It is believed that these natural polyphenolic NDs could open up new possibilities for the advancement of conductive hydrogels and contribute to the design and implementation of human–machine interaction devices. [ABSTRACT FROM AUTHOR]

Coaxial electrospinning is an attractive technology to produce core/sheath and hollow fibers. However, until now, the relatively low productivity has limited its broad applications. In this work, coaxial electrospinning with air‐blowing‐assistance is applied to improve the productivity of core/sheath and hollow fibers. Different core and shell materials are used for this electrospinning. The flow rate and air‐blowing rate during electrospinning are optimized. SEM and TEM are used to confirm the core/sheath and hollow structure of fibers. The results show that air‐blowing‐assisted electrospinning technology can be successfully applied for the large‐scale production of core/sheath and hollow fibers which open the path to new applications of this promising class of materials. [ABSTRACT FROM AUTHOR]

Recently, there has been a growing demand for ultra‐thin carbonized wood films (CWF) with high shielding efficiency (SE) to replace non‐renewable alternatives. Researchers aim to enhance electromagnetic (EM) wave absorption and improve electromagnetic interference (EMI) SE in CWF materials to reduce secondary pollution from reflected EM waves. In this work, the carbonized wood composite film (CWF/EP/Co) with a thickness of 120 µm through the process of hot‐pressing and carbonizing wood soaked in a mixed solution of water‐borne epoxy (EP) and Co/Zn‐MOF (ZIF‐67/8) is obtained. The CWF/EP/Co film exhibits excellent conductivity (105 S cm−1) and demonstrates an excellent EMI SE (73 dB) at a 200 µm thickness. Remarkably, the specific EMI shielding effectiveness (SSE/t) of CWF/EP/Co films reached 15833.3 dB·cm2·g−1 in the X‐band, making it the highest reported value among all wood‐derived EMI shielding materials. CWF/EP/Co films have a high absorption coefficient (A) of 0.4, indicating their effectiveness in absorbing EM waves. Furthermore, the EMI shielding effect of the large‐scale wallpaper (170 mm×170 mm) is confirmed by finite element analysis. Additionally, the CWF/EP/Co film exhibits good mechanical properties and effective Joule heating performance. This shielding film shows promise in applications such as buildings and smart homes, providing EMI shielding and warming effects. [ABSTRACT FROM AUTHOR]

Electrospun polyimide (PI) nanofiber nonwovens with excellent mechanical and thermal performance are highly required in many applications. The addition of phosphorus-containing compounds could be used as plasticizer to achieve this purpose. Herein, different amounts of trace diphenyl phosphate (DPhP) as plasticizer are added into the PI's precursor for electrospinning. After imidization, phosphorous-containing electrospun PI nonwovens (PI-PX) are produced. The results indicate that the addition of DPhP significantly enhanced the thermal and mechanical properties of PI-PX. PI-P0.6 (0.6 wt% DPhP) shows a T5% of 510 °C in air and 561 °C in Ar, 29 °C and 40 °C higher than those of pure PI. PI-P0.6 also shows the highest tensile strength/modulus/toughness of 44 MPa/2.0 GPa/8.5 MPa, 208 MPa/9.7 GPa/40.7 MPa, and 123 MPa/3.3 GPa/25.1 MPa, respectively, when applying different thickness determinations. In addition, PI-P0.6 also exhibited much higher puncture strength than other Li-ion battery separators. Such PI-PX composite nonwovens would be good candidates for various applications, especially for Li-ion battery separators. [ABSTRACT FROM AUTHOR]

Due to the rapid development of intelligent technology and the pursuit of green environmental protection, responsive materials with single response and actuation can no longer meet the requirements of modern technology for intelligence, diversification, and environmental friendliness. Therefore, intelligent responsive materials have received much attention. In recent years, with the development of new materials and technologies, cellulose materials have become increasingly used as responsive materials due to their advantages of sustainability and renewability. This review summarizes the relevant research on cellulose-based intelligent responsive materials in recent years. According to the stimuli responses, they are divided into temperature-, light-, electrical-, magnetic-, and humidity-responsive types. The response mechanism, application status, and development trend of cellulose-based intelligent responsive materials are summarized. Finally, the future perspectives on the preparation and applications of cellulose-based intelligent responsive materials are presented for future research directions. [ABSTRACT FROM AUTHOR]

The shortage of freshwater resources has become a major obstacle threatening human development, and directly utilizing solar energy by solar evaporators is emerging as a promising method to produce freshwater from the seawater. Compared to many synthetic polymer‐based evaporators, cellulose‐based evaporators are expected to offer more interesting features benefiting from the renewable feature and abundant reserves of cellulose‐contained naturally occurring materials. First, according to the different fabrication methods, cellulose‐based solar evaporators can be divided into two types, i.e., top‐down utilization (wood‐based) and bottom‐up assembled (cellulose composite‐based), respectively. The different fabrication schemes also bring their own unique advantages, such as the bimodal porous structure of wood‐based evaporators and the artificial interconnection microporous network of cellulose composite‐based evaporators. Subsequently, this review further summarizes the most recent advances and highlights of those cellulose‐based solar evaporators, by focusing on their structural regulation strategies (e.g., drilled channel array, asymmetric wettability structure, delignification, 2D waterway, etc.) and evaporation performance improvements (e.g., salt resistance, high evaporation rate, etc.). Finally, the challenges in this field and potential solutions are also discussed, which are anticipated to provide new opportunities toward the future development of cellulose and other kinds of biomass‐based evaporators. [ABSTRACT FROM AUTHOR]

Compared with traditional metal materials, carbon-based materials have the advantages of low density, high conductivity, good chemical stability, etc., and can be used as reliable alternative materials in various fields. Among them, the carbon fiber conductive network constructed by electrospinning technology has the advantages of high porosity, high specific surface area and rich heterogeneous interface. In order to further improve the conductivity and mechanical properties of pure carbon fiber films, tantalum carbide (TaC) nanoparticles were selected as conductive fillers. The crystallization degree, electrical and mechanical properties of electrospun TaC/C nanofibers at different temperatures were investigated. As the carbonization temperature increases, the crystallization degree and electrical conductivity of the sample also increases, while the growth trend of electrical conductivity is markedly slowed. The best mechanical properties of 12.39 MPa was achieved when the carbonization temperature was 1200 °C. Finally, through comprehensive analysis and comparison, it can be concluded that a carbonization temperature of 1200 °C is the optimum. [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]

[Display omitted] The interfacial solar desalination has been considered a promising method to address the worldwide water crisis without sophisticated infrastructures and additional energy consumption. Although various advanced solar evaporators have been developed, their practical applications are still restricted by the unsustainable materials and the difficulty of precise customization for structure to escort high solar-thermal efficiency. To address these issues, we employed two kinds of naturally occurring molecules, tannic acid and iron (III), to construct a low-cost, highly efficient and durable interfacial solar evaporator by three-dimensional (3D) printing. Based on a rational structural design, a robust and 3D-printed evaporator with conical array surface structure was developed, which could promote the light harvesting capacity significantly via the multiple reflections and anti-reflection effects on the surface. By optimizing the height of the conical arrays, the 3D-printed evaporator with tall-cone structure could achieve a high evaporation rate of 1.96 kg m–2 h−1 under one sun illumination, with a photothermal conversion efficiency of 94.4%. Moreover, this evaporator was also proved to possess excellent desalination performance, recycle stability, anti-salt property, underwater oil resistance, as well as adsorption capacity of organic dye contaminants for multipurpose water purification applications. It was believed that this study could provide a new strategy to fabricate low-cost, structural regulated solar evaporators for alleviating the dilemma of global water scarcity using abundant naturally occurring building blocks. [ABSTRACT FROM AUTHOR]

Size regulation of polydopamine nanoparticles (PDA NPs) is vital to melanin‐inspired materials. The general strategy usually focuses on tuning of the reaction parameters which could affect the dopamine (DA) monomer polymerization process, such as pH, temperature, monomer concentration, etc. The reaction between boronic acids and catechols to form boronic esters has been widely applied in many fields, but little attention has been paid in the size regulation of PDA NPs. Here, it is speculated that the fine size regulation of PDA NPs can be directly achieved by using boronic acids and Lewis base molecules. It is found that these issues could indeed significantly affect the stability of the boronic esters formed by boronic acids and DA, which may further inhibit the monomer polymerization kinetics and tune the particle size of the resulting PDA NPs. It is also found that the several intrinsic properties of PDA NPs such as the free radical scavenging ability, UV spectral absorption, photothermal behavior, and structural color all change with the particle size. It is believed that this work can provide new opportunities for fabricating melanin‐inspired PDA NPs with well controlled size and properties. [ABSTRACT FROM AUTHOR]

Heavy metal ions in industrial sewage constitute a serious threat to human health. Nanocellulose-based adsorbents are emerging as an environmentally friendly material platform for heavy metal ion removal based on their unique properties, which include high specific surface area, excellent mechanical properties, and biocompatibility. In this review, we cover the most recent works on nanocellulose-based adsorbents for heavy metal ion removal and present an in-depth discussion of the modification technologies for nanocellulose in the process of assembling high-performance heavy ion adsorbents. By introducing functional groups, such as amino, carboxyl, aldehyde, and thiol, the assembled nanocellulose-based adsorbents both remove single heavy metal ions and can selectively adsorb multiple heavy ions in water. Finally, the remaining challenges of nanocellulose-based adsorbents are pointed out. We anticipate that this review will provide indispensable guidance on the application of nanocellulose-based adsorbents for the removal of heavy metal ions. [ABSTRACT FROM AUTHOR]

Stimulus-responsive hydrogels are an important member of smart materials owing to their reversibility, soft/wet properties, and biocompatibility, which have a wide range of applications in the field of intelligent actuations. However, poor mechanical property and complicated fabrication process limit their further applications. Herein, we report a light-responsive tissue paper/hydrogel composite actuator which was developed by combining inkjet-printed tissue paper with poly(N-isopropylacrylamide) (PNIPAM) hydrogel through simple in situ polymerization. Due to the high strength of natural tissue paper and the strong interaction within the interface of the bilayer structure, the mechanical property of the composite actuator was highly enhanced, reaching 1.2 MPa of tensile strength. Furthermore, the light-responsive actuation of remote manipulation can be achieved because of the stamping graphite with high efficiency of photothermal conversion. Most importantly, we also made a few remotely controlled biomimetic actuating devices based on the near-infrared (NIR) light response of this composite actuator. This work provides a simple strategy for the construction of biomimetic anisotropic actuators and will inspire the exploration of new intelligent materials. [ABSTRACT FROM AUTHOR]

In this study, ZnO nanoparticles were prepared by a hydrothermal method with varying the reaction times, material ratios and reaction temperatures. The samples were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray Diffraction (XRD) and Fourier infrared spectroscopy (FTIR). It was shown that the material ratio significantly affected the structure and morphology of the synthesized ZnO nanoparticles, and then the uneven nano-octahedral structure, uniform nano-octahedral structure, nano-tubular structure, and nano-sheet structure could be obtained successively. The synthesized ZnO nanoparticles as mordant were used for the dyeing of silk fabrics with different natural dyes (tea polyphenols and hematoxylin). Moreover, they could improve the dyeing properties and fastness (wash and light) on silk fabrics to a certain extent. [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]

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]

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]

Highlights: [•] Heat-resistant electrospun PBO nanofibers were prepared from precursor OH-PAA. [•] The obtained PBO nanofibers are thermally stable up to 643°C. [•] The obtained PBO nanofibers have excellent mechanical properties. [•] PBO nanofibers have retention of tensile strength and modulus over 80% at 350°C. [•] Such heat-resistant PBO nanofibers could be used in high temperature fields. [ABSTRACT FROM AUTHOR]

[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]

Chain-spherical V 2 O 5 /C composites were prepared by using dandelion fibers as bio-templates through a simple vacuum-assisted immersion method, and their microstructure and electromagnetic wave (EMW) absorption properties were investigated. Results indicated that the EMW absorption performance of dandelion fibers is effectively improved by introducing V 2 O 5 and constructing chain-spherical structure. Notably, the minimum reflection loss (RL min) of V 2 O 5 /C composites with a thickness of 2.35 mm is reached −34.05 dB at 17.52 GHz, and the maximum effective absorption bandwidth (EAB) of the composites is up to 7.52 GHz at 2.85 mm. The improvement in EMW absorption performance is mainly ascribed to the synergistic effects of the increased multiple reflections and scattering, enhanced polarization loss and conduction loss, and impedance matching characteristics. The chain-spherical V 2 O 5 /C composites exhibit great potential as promising candidates for high-performance EMW absorbers. • The V 2 O 5 /C composites with a chain-spherical structure are facilely prepared. • The synergy effect of multiple loss mechanisms enhances microwave absorption. • The RL min of −34.05 dB and the widest EAB of 7.52 GHz are achieved. [ABSTRACT FROM AUTHOR]

The development of robust and bioinspired adhesives with excellent performances including fast gel time, low cost, good adhesion strength and stability, and excellent solvent and temperature resistance against harsh environment is urgent for practical applications. In this paper, kinds of natural polyphenolic adhesives have been successfully fabricated via the multiple polyphenol-diisocyanate cross-linking (PDC) reactions between natural polyphenols (extracts) and diisocyanate molecules. Under heating, as-prepared adhesives could effectively adhere onto a wide range of substrates (i.e. PTFE, PET, PMMA, Al, Cu, paper, glass, wood) through hierarchical interactions. Moreover, these adhesives exhibited great adhesion stability against complex solvents and low-temperature environments, whose adhesion strength could remain unchanged after soaking solvents after 30 days, which was conducive to their potential applications in industry and chemical fields, including petroleum, wood, metal, glass, plastics, and rubber adhesion. We believed that this work would provide new strategies towards the preparation of robust adhesives with excellent resistant against various solvents and low temperature for many fields by using naturally occurring building blocks. Natural polyphenolic adhesives were successfully fabricated via the multiple polyphenol-diisocyanate cross-linking (PDC) reactions between natural polyphenols (extracts) and diisocyanate molecules. Under heating, as-prepared adhesives could effectively adhere to a wide range of substrates (i.e. PTFE, PET, PMMA, Al, Cu, paper, glass, wood) through hierarchical interactions. Moreover, these adhesives exhibited great adhesion stability against complex solvents and low-temperature environments, and the adhesion strength could even remain unchanged after soaking solvents after 30 days. [Display omitted] • Natural polyphenolic adhesives were successfully fabricated. • As-prepared adhesives could effectively adhere to various substrates. • These adhesives exhibited great solvents and low-temperature resistance. [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]

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]

[Display omitted] • This review focuses on recent development of carbon dots/porous materials composites. • Preparation, structures, and properties of carbon dots/porous materials composites are discussed. • Challenges and future development of carbon dots/porous materials composites are described. Carbon dots (CDs), an emerging fluorescent carbon nanomaterial, have attracted great attention in recent year due to their features such as unique optical property, good biocompatibility and low cost and easy synthesis. When CDs are integrated with porous materials, it not only compensates for the shortcomings of monocomponent CDs in applications, but also produces new functionalities through synergistic interactions to extend new applications. At present, CDs have been assembled with various porous materials such as zeolites, carbonaceous porous materials, porous graphitic carbon nitride (g-C 3 N 4), mesoporous SiO 2 , porous metallic compounds and metal-organic frameworks (MOFs), which exhibit excellent performance and a wide range of applications. Therefore, recent research advances in CDs/porous materials composites should be presented to facilitate further development of the field. In this article, the preparation methods, porous structures, and properties of CDs/porous materials composites are classified and presented. Then, the applications of CDs/porous materials composites in optics, biomedicine, sensing, electrochemistry, and photocatalysis are also discussed. Finally, current challenges and future directions are briefly discussed to facilitate the next development of CDs/porous materials composites. [ABSTRACT FROM AUTHOR]

[Display omitted] • This review focuses on recent development of carbon dots/porous materials composites. • Preparation, structures, and properties of carbon dots/porous materials composites are discussed. • Challenges and future development of carbon dots/porous materials composites are described. Carbon dots (CDs), an emerging fluorescent carbon nanomaterial, have attracted great attention in recent year due to their features such as unique optical property, good biocompatibility and low cost and easy synthesis. When CDs are integrated with porous materials, it not only compensates for the shortcomings of monocomponent CDs in applications, but also produces new functionalities through synergistic interactions to extend new applications. At present, CDs have been assembled with various porous materials such as zeolites, carbonaceous porous materials, porous graphitic carbon nitride (g-C 3 N 4), mesoporous SiO 2 , porous metallic compounds and metal-organic frameworks (MOFs), which exhibit excellent performance and a wide range of applications. Therefore, recent research advances in CDs/porous materials composites should be presented to facilitate further development of the field. In this article, the preparation methods, porous structures, and properties of CDs/porous materials composites are classified and presented. Then, the applications of CDs/porous materials composites in optics, biomedicine, sensing, electrochemistry, and photocatalysis are also discussed. Finally, current challenges and future directions are briefly discussed to facilitate the next development of CDs/porous materials composites. [ABSTRACT FROM AUTHOR]

Designing energy storage devices from thick carbon electrodes with high areal/volumetric energy density via a simple and green way is very attractive but still challenging. Cellulose, as an excellent precursor for thick carbon electrodes with abundant sources and low cost, is usually activated by a chemical activator and pyrolysis route to achieve high electrochemical performance. However, there are still some problems to be addressed, such as the harsh activation conditions, easy collapse of porous structures, and the high cost. Herein, a 3D self‐supporting thick carbon electrode derived from wood‐based cellulose is proposed for high areal and volumetric energy density of supercapacitor from a mild, simple, and green enzymolysis treatment. Benefiting from the high specific surface area (1418 m2 g−1) and abundant active sites on the surface of wood‐derived hierarchically porous structures and enzymolysis‐induced micropores and mesopores, the assembled symmetry supercapacitor from the thick carbon electrode can realize the high areal/volumetric energy density of 0.21 mWh cm−2/0.99 mWh cm−3 with excellent stability of 86.58% after 15 000 long‐term cycles at 20 mA cm−2. Significantly, the simple and universal strategy to design material with high specific surface area, provides a new research idea for realizing multi‐functional application. [ABSTRACT FROM AUTHOR]

Flexible bioelectronics have attracted increasing research interests due to their wide range of potential applications in human motion detection, personal healthcare monitoring, and medical diagnosis. Recently, design and fabrication strategies integrated with mussel‐inspired polydopamine (PDA) have demonstrated many appealing properties, which meet the structural and functional requirements of high‐performance flexible bioelectronics. The inherent multiple reactive sites and hierarchical interactions within PDA can promote the total electrochemical activities, self‐healing, surface activation, and biocompatibility of the composite system. This review paper strives to provide a comprehensive overview on this emerging area, including the fabrication methodology, the structural and functional contributions of PDA on the whole composites, and various applications of PDA‐based flexible bioelectronics. The current challenges and future outlook in this field are also extensively discussed at the end. This paper aims to serve as a guideline in this emerging area and provide new inspirations toward next‐generation integrated multifunctional flexible PDA bioelectronics with a broad range of healthcare applications. [ABSTRACT FROM AUTHOR]

Carbon nanotubes microspheres (CNTsM) with porous skeleton and net structure were successfully prepared by a facile method of ultrasonic atomization combined with heat treatment. Dielectric characteristics and electromagnetic wave (EMW) absorption properties within the frequency range of 2–18 GHz of CNTsM were studied. Owing to increased multiple reflection/scattering, enhanced interfacial polarization and optimized impedance matching, an excellent EMW absorption performance is therefore obtained for CNTsM. The maximum reflection loss (RL) reaches −35 dB at the thickness of 4.6 mm, and a wide effective absorption bandwidth (EAB, RL < −10dB) of 4.4 GHz is achieved with a thickness of 1.5 mm. CNTsM can be regarded as a brand-new competitive candidate for EMW absorption materials. [ABSTRACT FROM AUTHOR]

Nanocellulose, as a nanoscale polymer material, has garnered significant attention worldwide due to its numerous advantages including excellent biocompatibility, thermal stability, non-toxicity, large specific surface area, and good hydrophilicity. Various methods can be employed for the preparation of nanocellulose. Traditional approaches such as mechanical, chemical, and biological methods possess their own distinct characteristics and limitations. However, with the growing deterioration of our living environment, several green and environmentally friendly preparation techniques have emerged. These novel approaches adopt eco-friendly technologies or employ green reagents to achieve environmental sustainability. Simultaneously, there is a current research focus on optimizing traditional nanocellulose preparation methods while addressing their inherent drawbacks. The combination of mechanical and chemical methods compensates for the limitations associated with using either method alone. Nanocellulose is widely used in wound dressings owing to its exceptional properties, which can accelerate the wound healing process and reduce patient discomfort. In this paper, the principle, advantages and disadvantages of each preparation method of nanocellulose and the research findings in recent years are introduced Moreover, this review provides an overview of the utilization of nanocellulose in wound dressing applications. Finally, the prospective trends in its development alongside corresponding preparation techniques are discussed. [ABSTRACT FROM AUTHOR]