Three-dimensional Porous Network Structure Research Articles

Facile synthesis of an acrylic acid-co-2-acrylamide-2-methylpropanesulfonic acid copolymer / polyvinylpyrrolidone semi-IPN hydrogel with excellent swelling and anti-leakage properties

Water scarcity becomes an increasingly serious problem for humankind due to climate change and population growth, especially the water leakage in arid and semi-arid areas. Hydrogel polymers show increasingly important roles on water resources utilization. A novel hydrogel copolymer, acrylic acid-co-2-acrylamide-2-methylpropanesulfonic acid copolymer / polyvinylpyrrolidone (P(AA-co-AMPS)/PVP) semi-interpenetrating network (semi-IPN) hydrogel, was designed and successfully synthesized via a facile one-pot free radical copolymerization method. The main parameters during the synthesis process were optimized, including relative contents of polymer monomers, cross-linking agent, initiator and neutralization agent. Physical characterizations demonstrate that, P(AA-co-AMPS)/PVP hydrogel shows porous three-dimensional network structure, including a crosslinked network structure in P(AA-co-AMPS) copolymers and their intermolecular hydrogen bonding interactions with linear PVP. The as-synthesized P(AA-co-AMPS)/PVP hydrogel not only can deliver superior water absorbing capability (up to 1689.95 g g−1) and good reswelling performance, but also shows excellent water anti-leakage performance when being composed with red clay, demonstrating its multi-role applications in future sustainable agriculture.

Scleroglucan-Based Foam Incorporating Recycled Rigid Polyurethane Waste for Novel Insulation Material Production

This study details the synthesis and performance evaluation of a novel lightweight thermal and acoustic insulation material, resulting from the combination of a scleroglucan-based hydrogel and recycled rigid polyurethane waste powder. Through a sublimation-driven water-removal process, a porous three-dimensional network structure is formed, showcasing notable thermal and acoustic insulation properties. Experimental data are presented to highlight the material’s performance, including comparisons with commercially available mineral wool and polymeric foams. This material versatility is demonstrated through tunable mechanical, thermal and acoustic characteristics, achieved by strategically adjusting the concentration of the biopolymer and additives. This adaptability positions the material as a promising candidate for different insulation applications. Addressing environmental concerns related to rigid polyurethane waste disposal, the study contributes to the circular economy.

Synthesis and Electrochemical Characterization of Nitrate-Doped Polypyrrole/Ag Nanowire Nanorods as Supercapacitors.

Polypyrrole (PPy)-capped silver nanowire (Ag NW) nanomaterials (core-shell rod-shaped Ag NW@PPy) were synthesized using a one-port suspension polymerization technique. The thickness of the PPy layer on the 50 nm thickness/15 μm length Ag NW was effectively controlled to 10, 40, 50, and 60 nm. Thin films cast from one-dimensional conductive Ag NW@PPy formed a three-dimensional (3D) conductive porous network structure and provided excellent electrochemical performance. The 3D Ag NW@PPy network can significantly reduce the internal resistance of the electrode and maintain structural stability. As a result, a high specific capacitance of 625 F/g at a scan rate of 1 mV/s was obtained from the 3D porous Ag NW@PPy composite film. The cycling performance over a long period exceeding 10,000 cycles was also evaluated. We expect that our core-shell-structured Ag NW@PPy composites and their 3D porous structure network films can be applied as electrochemical materials for the design and manufacturing of supercapacitors and other energy storage devices.

Turning Polysaccharides into Injectable and Rapid Self-Healing Antibacterial Hydrogels for Antibacterial Treatment and Bacterial-Infected Wound Healing.

Great efforts have been devoted to the development of novel and multifunctional wound dressing materials to meet the different needs of wound healing. Herein, we covalently grafted quaternary ammonium groups (QAGs) containing 12-carbon straight-chain alkanes to the dextran polymer skeleton. We then oxidized the resulting product into oxidized quaternized dextran (OQD). The obtained OQD polymer is rich in antibacterial QAGs and aldehyde groups. It can react with glycol chitosan (GC) via the Schiff-base reaction to form a multifunctional GC@OQD hydrogel with good self-healing behavior, hemostasis, injectability, inherent superior antibacterial activity, biocompatibility, and excellent promotion of healing of methicillin-resistant Staphylococcus aureus (MRSA)-infected wounds. The biosafe and nontoxic GC@OQD hydrogel with a three-dimensional porous network structure possesses an excellent swelling rate and water retention capacity. It can be used for hemostasis and treating irregular wounds. The designed GC@OQD hydrogel with inherent antibacterial activity possesses good antibacterial efficacy on both S. aureus (Gram-positive bacteria) and Escherichia coli (Gram-negative bacteria), as well as MRSA bacteria, with antibacterial activity greater than 99%. It can be used for the treatment of wounds infected by MRSA and significantly promotes the healing of wounds. Thus, the multifunctional antibacterial GC@OQD hydrogel has the potential to be applied in clinical practice as a wound dressing.

A cellulose derived nanofibrous nitrogen-doped carbon/TiO2/SnO2/carbon composite anodic material for lithium storage

SnO2 with high theoretical specific capacity is regarded as a desirable anodic material for lithium storage. However, the serious volume variation during discharge/charge cycling and poor conductivity significantly constrain the electrochemical performance. Herein, nanofibrous nitrogen-doped carbon (NC)/TiO2/SnO2/carbon composite was fabricated through layer-by-layer assembly of SnO2 and TiO2-gel layers alternately using cellulosic filter paper as the structural scaffold, followed by deposition of polypyrrole on the surface by chemical polymerization method, and subsequent calcination of the as-obtained matter in inert atmosphere. The achieved composite possesses a typical three-dimensional fibrous porous network structure inherited from the cellulosic substrate, and complete NC nanolayer coating on each nanofiber by adjusting the amount of pyrrole, which can alleviate the volume change and increase the conductivity of SnO2. Furthermore, the interlaced TiO2 multilayer can enhance the cycling stability during cycling, as well as facilitate the lithium-ion transfer through abundant interface. The optimal NC/TiO2/SnO2/carbon composite delivers an initial discharge capacity of 1492.6 mAh g−1 at a current density of 100 mA g−1, and retains a reversible capacity of 680.8 mAh g−1 after 200 discharge/charge cycles. This work provides an efficient strategy for design and construction of metal-oxides/carbon composite anodic materials with hierarchical microstructure that hold great potential in lithium storage.

Cellulose derived fibrous vanadium-sulfide/carbon composite with enhanced lithium storage properties

Vanadium-sulfides are considered as promising anodic materials for lithium-ion batteries (LIBs) due to their unique layered structures and high theoretical capacities. However, the main challenge of vanadium-sulfide as an electrode material is still faced with slow Li-ion diffusion kinetics and inevitable structural damage during charging/discharging processes. Herein, a series of bio-inspired hierarchical fibrous VS4/C composites were designed based on cellulose substance as the scaffold and carbon source via simple hydrothermal method. The resultant fibrous VS4/C composites possessed a three-dimensional porous network structure consisting of carbon fibers coated with VS4 nanosheets. As a consequence, the optimized VS4/C anodic materials exhibit high reversible capacities (953 mAh g−1 at 0.1 A g−1), good rate features (420 mAh g−1 at 2 A g−1), and fast diffusion kinetics. The superior electrochemical properties of the VS4/C composites are mainly attributed to the three-dimensional porous network structures combined with the carbon fibers matrix, which promotes the contact between the electrode and electrolyte, alleviates the structural damage of VS4, as well as facilitates the electron transfer and Li-ion diffusion during the cycling processes.

Adsorption Behavior and Kinetics of 1,4-Dioxane by Carbon Aerogel.

1,4-dioxane is a potential carcinogen in water and is difficult to deal with due to its robust cycloether bond and complete miscibility with water. To remove 1,4-dioxane in an economically viable and environmentally friendly way, a series of carbon aerogels were synthesized as adsorbents for 1,4-dioxane. The experiment results showed that adsorption performances were closely related to the preparation conditions of carbon aerogels, such as the molar ratio, heating rate, pyrolysis temperature and residence time, which were carefully controlled. Scanning electron microscope analysis revealed the presence of a three-dimensional porous network structure in carbon aerogels. Brunauer-Emmett-Teller analysis results demonstrated an increase in specific surface area (673.89 m2/g) and total pore volume after carbonization, with an increase in mesoporous porosity and a decrease in microporosity. When considering each variable individually, the highest specific surface area of prepared carbon aerogels was achieved at a pyrolysis temperature of 800 °C, a holding time of 1 h, and a heating rate of 2 °C/min. Under optimal experimental conditions, the adsorption removal of 1,4-dioxane by carbon aerogels exceeded 95%, following quasi-second-order kinetics and Langmuir isothermal adsorption isotherms, indicating that monolayer adsorption on the surface of carbon aerogels occurred. The maximum adsorption capacity obtained was 67.28 mg/g at a temperature of 318 K, which was attributed to the presence of a large proportion of mesopores and abundant micropores simultaneously in carbon aerogels. Furthermore, with the interference of chlorinated solvents such as trichloroethylene (TCE), the removal efficiency of 1,4-dioxane had no obvious inhibition effect. Regeneration experiments showed that after five continuous cycles, the carbon aerogels still kept a comparable adsorption capacity, which illustrates its potential application in 1,4-dioxane-polluted water purification.

Fabrication of nitrogen-doped reduced graphene oxide/tricobalt tetraoxide composite aerogels with high efficiency, broadband microwave absorption, and good compression recovery performance

The fabrication of advanced graphene-based microwave absorbing materials with thin thickness, wide bandwidth, strong absorption strength, and low filling ratio remains a huge challenge. In this paper, nitrogen-doped reduced graphene oxide/tricobalt tetraoxide (NRGO/Co3O4) composite aerogels were synthesized by a three-step method of solvothermal reaction, high-temperature calcination, and hydrothermal self-assembly. The results showed that the attained NRGO/Co3O4 composite aerogels had a unique three-dimensional porous network structure, extremely low bulk density, and good compression recovery. Furthermore, the effect of the addition amounts of flower-like Co3O4 on the complex dielectric constant and microwave absorption properties of NRGO/Co3O4 composite aerogels was investigated. When the addition amount of Co3O4 was equal to 15 mg, the prepared binary composite aerogel showed the strongest absorption strength of –62.78 dB and a wide absorption bandwidth of 5.5 GHz at a thin thickness of 2.13 mm and a low filling ratio of 15 wt.%. It was worth noting that the maximum absorption bandwidth could reach 6.32 GHz (11.68–18 GHz, spanning the entire Ku-band) at a thickness of 2.24 mm. In addition, the possible microwave absorption mechanism of NRGO/Co3O4 composite aerogels was also proposed. Therefore, this paper will provide a new and simple strategy for preparing RGO-based porous nanocomposites as lightweight, efficient, and broadband microwave absorbers.

Porous Collagen Sponge Loaded with Large Efficacy-Potentiated Exosome-Mimicking Nanovesicles for Diabetic Skin Wound Healing.

Diabetic skin wounds are difficult to heal quickly due to insufficient angiogenesis and prolonged inflammation, which is an urgent clinical problem. To address this clinical problem, it becomes imperative to develop a dressing that can promote revascularization and reduce inflammation during diabetic skin healing. Herein, a multifunctional collagen dressing (CTM) was constructed by loading large efficacy-potentiated exosome-mimicking nanovesicles (L-Meseomes) into a porous collagen sponge with transglutaminase (TGase). L-Meseomes were constructed in previous research with the function of promoting cell proliferation, migration, and angiogenesis and inhibiting inflammation. CTM has a three-dimensional porous network structure with good biocompatibility, swelling properties, and degradability and could release L-Meseome slowly. In vitro experiments showed that CTM could promote the proliferation of fibroblasts and the polarization of macrophages to the anti-inflammatory phenotype. For in vivo experiments, on the 21st day after surgery, the wound healing rates of the control and CTM were 83.026 ± 4.17% and 93.12 ± 2.16%, respectively; the epidermal maturation and dermal differentiation scores in CTM were approximately four times that of the control group, and the skin epidermal thickness of the CTM group was approximately 20 μm, which was closest to that of normal rats. CTM could significantly improve wound healing in diabetic rats by promoting anti-inflammation, angiogenesis, epidermal recovery, and dermal collagen deposition. In summary, the multifunctional collagen dressing CTM could significantly promote the healing of diabetic skin wounds, which provides a new strategy for diabetic wound healing in the clinic.

A flexible pH sensor based on polyaniline@oily polyurethane/polypropylene spunbonded nonwoven fabric.

To fabricate a two-electrode flexible pH sensor based on polypropylene spunbonded nonwoven fabric (PP SF), oily polyurethane (OPU) was first coated on the surface of PP SF to obtain OPU/PP SF. Then, silver/silver chloride (Ag/AgCl) paste, used as the reference electrode and conductive carbon (C) paste were transferred to the OPU/PP SF surface through screen printing. Polyaniline (PANI) was deposited on the surface of the C paste to form a sensing working electrode via the electro-chemical deposition method. The results showed that the surface of the obtained PANI@OPU/PP SF flexible pH sensor (3D PANI pH sensor) presented a three-dimensional (3D) porous network structure. The 3D PANI pH sensor had good mechanical properties, an excellent Nernst response (-67.67 mV pH-1) and linearity (R2 = 0.99) in the pH range from 2.00 to 8.00 in the normal state. In the bent state, the 3D PANI pH sensor retained similar sensitivity (-68.87 mV pH-1) and linearity (R2 = 0.99). Moreover, the 3D PANI pH sensor exhibited a short response time (8 s), excellent reversibility (1.20 mV), low temperature drift (-0.0872 mV pH-1 °C-1) and long-term stability (0.83 mV h-1) in the normal state. Furthermore, the 3D PANI pH sensor can be effectively applied for pH monitoring of liquids and fruits with irregular curved surfaces. The error margin is no more than 0.16 compared to a commercial pH meter.

Efficient adsorption of anionic and cationic dyes by PVA/PAA/GO composite hydrogel with three-dimensional porous double network structure

Polyvinyl alcohol (PVA) and polyacrylic acid (PAA) were introduced into graphene oxide (GO) by a water bath method, and PVA/PAA/GO (PPG) with a three-dimensional double network structure was prepared under the action of hydrogen bonding. With the help of a large number of oxygen-containing functional groups and a three-dimensional double network structure in the PPG composite hydrogel, the adsorption performance of anionic and cationic dyes was greatly improved, and the adsorption rates of 100 mg∙L−1 malachite green (MG) and Congo red (CR) within 6 min were 93 % and 55 %, respectively. For comparison, the adsorption rates of MG and CR by graphene hydrogel alone within 30 min were only 10 % and 48 %, respectively. Meanwhile, the free radical polymerization of PAA and PVA also effectively improved the mechanical strength of the graphene hydrogel, and the PPG remained structurally stable under the action of 800 g of gravity. The results of adsorption kinetics showed that the adsorption process of PPG on CR and MG was in accordance with Freundlich adsorption and pseudo-second-order kinetic adsorption. Based on the X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectrometer (FTIR) results, the adsorption performance of PPG mainly originated from physical adsorption, electrostatic attraction, hydrogen bonding and π-π conjugation.

In situ forming of PEG-NH2/dialdehyde starch Schiff-base hydrogels and their application in slow-release urea

In this study, a biodegradable Schiff-base hydrogel urea, possessing substantial water retention and certain slow-release ability was designed and synthesized. Firstly, dialdehyde starch (DAS) and amine-terminated polyethylene glycol (PEG-(NH2)2) were synthesized using potato starch and polyethylene glycol. Then, a novel Schiff-base hydrogel (SH) was prepared through the in-situ reaction between the aldehyde group of DAS and the amino group of PEG-(NH2)2. Three SH based slow-release urea, designated as SHU1, SHU2, and SHU3 and distinguished by varying urea content, were obtained using SH as the substrate. Several characterizations and tests were conducted to determine the structure, thermal properties, morphology, swelling properties, sustainable use, water retention, and biodegradation properties of SH. Additionally, the slow-release behavior of SHU was studied. SEM results revealed that SH possessed a porous three-dimensional network structure, with a maximum water absorption capacity of 4440 % ± 6.23 %. Compared to pure urea, SHU exhibited better slow-release performance after 30 days of release in soil, with SHU1 having a residual nitrogen content of specifically 36.01 ± 0.57 % of the initial nitrogen content. A pot experiment with pakchoi substantiated the water retention and plant growth promotion properties of SHU. This study demonstrated a straightforward method for the preparation of starch-based Schiff-base hydrogels as fertilizer carriers.

Construction of a floating photothermal-assisted photocatalytic system with a three-dimensional hollow porous network structure

Solar energy is the inevitable choice to achieve the low-carbon, green, and circular development of society, and photocatalysis technology is one of the shining pearls. To make full use of the solar spectrum and solve the shortcomings of the recovery difficulty of powdery materials and the loss of activity due to the influence of the external environment, it is possible to construct floating materials using melamine sponges to recover photocatalytic materials quickly. At the same time, floating materials can absorb oxygen in the air for the generation of active groups, effectively solving the problem of less O2 in the water. The carbon-based materials have excellent light absorption properties, high thermal conductivity, and excellent photothermal conversion efficiency and are ideal for constructing floating photothermal photocatalytic systems. As an example, we combined a cheap melamine sponge with urea, prepared a hollow porous network structure g-C3N4 (HPNCN) with a high specific surface area by direct thermal shrinkage method, and then attached the CoO to its surface by hydrothermal method to form a heterojunction with a suitable band gap. Various characterization tests verified the photothermal-photocatalytic properties. Among them, 30% CoO/HPNCN has the best photocatalytic degradation effect on tetracycline (TC), and the removal rate is 88.1%. After five cycles, the removal rate is only 5% lower than the initial, indicating that it has good stability and recyclability. We conducted an active ingredient capture experiment, ESR, and LC-MS analysis to clarify the intermediates and reaction mechanism of TC photocatalytic degradation. On this basis, the ECOSAR program and QSAR method were used to analyze the environmental toxicity of TC and its intermediate products. These results provide a broad prospect for the potential application of the floating photothermal-photocatalysis system in antibiotic pollution control and its application in other fields.

Design and properties of alginate/gelatin/cellulose nanocrystals interpenetrating polymer network composite hydrogels based on in situ cross-linking

Alginate (Alg) hydrogels have attracted extensive attention in the biomedical field due to their biocompatibility. However, single Alg hydrogels exhibit weak mechanical strength, poor stability and cell adhesion, which severely restricts their biomedical application. For this reason, we designed alginate/gelatin/cellulose nanocrystals (Alg/G/CNCs) composite hydrogels by combining interpenetrating network (IPN) technology, cellulose nanocrystals (CNCs) reinforcement and in situ cross-linking method to improve the functional defects of Alg hydrogels. The structure and properties of the resultant Alg/G/CNCs composite hydrogels were comprehensively evaluated by FT-IR, TGA, XRD, swelling and degradability measurements, and cytocompatibility experiments. Alg/G/CNCs composite hydrogels with regular three-dimensional porous network (3D) structures was successfully fabricated through the ionic cross-linking of alginate and the covalent cross-linking of gelatin, followed by the reinforcement of colloidal cellulose nanocrystals (CNCs) that were prepared by sulfuric acid hydrolysis of microcrystalline cellulose (MCC). The addition of CNCs could generate interaction force with the polymer in the IPN matrix, which was able to regulate the physicochemical properties of the composite hydrogel to a certain extent. Moreover, with the increase of gelatin (G) content, the compressive strength of Alg/G/CNCs composite hydrogels gradually increased, while the swelling property decreased gradually. Meanwhile, Alg/G/CNCs composite hydrogels exhibited good cell adhesion, proliferation and differentiation properties. In particular, Alg/0.5G/CNCs composite hydrogels displayed the best cell proliferation effect, while Alg/2G/CNCs composite hydrogels revealedthe most significant cell differentiation effect. Therefore, Alg/G/CNCs composite hydrogels could exhibit good mechanical properties and biocompatibility, which possessed great application potential in the field of tissue engineering.

Coconut shell waste-derived graphene oxide composite with neodymium oxide (Nd2O3) for advanced applications

This paper reports the synthesis and physical properties of graphene oxide/neodymium oxide (GO/Nd2O3) composites. The GO/Nd2O3 composite was prepared by a simple Sonochemical Method, and graphene oxide was synthesized by a modified hummers method. The synthesized composites were characterized by using X-Ray Diffraction (XRD), Fourier Transform Infra-Red (FT-IR), Scanning Electron Microscopy-Energy Dispersive X-ray (SEM-EDX), Raman Spectroscopy, and UV–Vis Spectroscopy. The XRD data confirmed that the GO/Nd2O3 composite had a hexagonal phase structure and showed that the more Nd2O3 nanoparticles were added to GO, the more the crystallinity index increased. The FT-IR spectra showed six types of bonds of functional groups of the GO/Nd2O3 composite, namely the hydroxyl (-OH), carbonyl (C]O), (C]C), (C–O–H), (C–O–C), and the absorption band at 678 cm−1 shows REOs (Nd2O3). Raman spectroscopic analysis showed that the intensity of the ratio of ID/IG was (∼0.85) with the size of sp2 graphitic area of ∼22.6 nm. The addition of Nd2O3 particles to GO did not affect the intensity ratio of ID/IG and was almost the same for the GO and GO/Nd2O3 composite. SEM results show that the composite has a porous three-dimensional carbon network structure. The optical properties were analyzed using UV–Visible spectroscopy. The results of Urbach Energy showed that the GO/Nd2O3 composite is a semiconductor material with an Urbach Energy value of 0.050–0.063 eV, showing the potential application of GO/Nd2O3 composites in electronic devices.

Synthesis of nitrogen-doped reduced graphene oxide/magnesium ferrite/polyaniline composite aerogel as a lightweight, broadband and efficient microwave absorber

The fabrication of graphene-based microwave absorbing materials with low density, small filling ratio, broad bandwidth and strong absorption remains a huge challenge. In this work, nitrogen-doped reduced graphene oxide/magnesium ferrite/polyaniline (NRGO/MgFe2O4/PANI) composite aerogel was synthesized by a three-step method of solvothermal reaction, in situ chemical oxidation polymerization and hydrothermal self-assembly. The results showed that the obtained aerogels had a unique three-dimensional (3D) porous network structure and low bulk density (11.1–13.0 mg cm−3). It was worth noting that in the NRGO/MgFe2O4/PANI ternary composite aerogel, MgFe2O4 coated with a thin PANI layer was anchored on the surface of NRGO sheets. Furthermore, the NRGO/MgFe2O4/PANI ternary composite aerogel showed much better microwave absorbing capacity compared with pure NRGO aerogel and NRGO/MgFe2O4 binary composite aerogel. When the filling ratio was as low as 11.5 wt.%, the obtained ternary composite aerogel exhibited the maximum effective absorption bandwidth of 7.0 GHz at a matching thickness of 2.1 mm, and the minimum reflection loss of -42.9 dB at a thickness of 3.57 mm. Additionally, the probable microwave dissipation mechanism was also elucidated. It was believed that this study would pave the way for the construction of 3D graphene-based composites as lightweight, broadband and efficient microwave absorbents.

N/O/P ternary-doped coal-based hierarchical porous carbon networks for high lithium-ion storage performance

Constructing porous structure and surface modification are effective ways to enhance the Li-ion storage performance of commercial graphite anode for lithium-ion batteries (LIBs). Herein, nitrogen, oxygen and phosphorus ternary-doped coal-based hierarchical porous carbon networks (N/O/P-CCNs) were prepared through liquid oxidation combined with self-assembly method. The N/O/P-CCNs have a three-dimensional porous carbon network structure formed by cross-linking carbon nanosheets with an appropriate specific surface area (321 m2 g−1) and distribution of micro-, meso- and macropore, while the surfaces of carbon nanosheets are doped with nitrogen, oxygen and phosphorus. Due to unique hierarchical porous structure and the synergistic effect of ternary doping, the N/O/P-CCNs anode exhibits excellent Li-ion storage properties with initial reversible capacity of 1079 mAh g−1, which is much higher than that of coal-based graphite anode (382 mAh g−1). Besides, the N/O/P-CCNs anode also has superior rate capability (336 and 275 mAh g−1 at 1.0 and 2.0 A g−1) and cycle stability with a high capacity retention (near 100 % after 100 cycles). The excellent electrochemical performance is not only related to the hierarchical pore structure that can provide efficient channels for lithium-ion transport, but also to the ternary-doping of nitrogen, oxygen and phosphorus that can provide more active sites for lithium-ion storage and enhance conductivity. This work provides a novel and effective design strategy for developing high-performance anode materials for LIBs.

Manipulating Pt-skin of porous network Pt-Cu alloy nanospheres toward efficient oxygen reduction

Designing Pt-skin on the catalyst surface is critical to developing efficient and stable electrocatalysts toward oxygen reduction reaction (ORR) in proton exchange membrane fuel cells. In this paper, an acidic reductant is proposed to synchronously manipulate in-situ growth of Pt-skin on the surface of alloyed Pt-Cu nanospheres (PtCuNSs) by a facile one-pot synthesis in an aqueous solution. Ascorbic acid can create a Pt-skin of three atomic layers to make the typical PtCu-alloy@Pt-skin core/shell nanostructure rather than the uniform alloys generated by using alkaline reductants. Surfactant as soft-template can make the alloyed PtCuNSs with a three-dimensional porous network structure. Multiple characterizations of XRD, XPS and XAFS are used to confirm Pt-alloying with Cu and formation of core/shell structure of such a catalyst. This PtCuNSs/C exhibits a half-wave potential of 0.913 V (vs. RHE), with mass activity and specific activity about 3.5 and 6.4 times higher than those of Pt/C, respectively. Fuel cell tests verify the excellent activity of PtCuNSs/C catalyst with a maximum power density of about 1.2 W cm−2. Moreover, this catalyst shows excellent stability, achieving a long-term operation of 40,000 cycles. Furthermore, theoretical calculations reveal the enhancement effect of characteristic PtCu-alloy@Pt-skin nanostructure on both catalytic ORR activity and stability.

Magnetic NiFe2O4@FeNi3 core-shell nanospheres derived from FeNi-LDH precursor anchoring on rGO nanosheets for enhanced electromagnetic wave absorption

Graphene has been extensively utilized in the domain of electromagnetic wave (EMW) absorption materials because of its excellent electrical conductivity. However, the inferior impedance matching performance and the single loss mechanism vastly restrict the application. Hence, it's an effective strategy to solve these issues by introducing magnetic components. Notably, layer double hydroxide (LDH) is an appropriate template to obtain magnetic component materials. Considering that ferromagnetic metals such as Fe, Co, Ni, and their corresponding metal oxides are usually treated as magnetic components which are promising candidates for EMW absorption materials. Therefore, in this work, a FeNi-layered double hydroxide-reduced graphene oxide (FeNi-LDH-rGO) aerogel was synthesized through a series of processes such as electrostatic self-assembly, hydrothermal, freeze-drying, and annealing. The magnetic NiFe2O4@FeNi3 core-shell nanospheres were obtained from FeNi-LDH precursor, anchoring on rGO nanosheets after the annealing treatment. Furthermore, the effects of different mass ratios of LDH to GO as well as different annealing temperatures of LDH-rGO aerogel on the EMW absorption property and impedance matching performance were explored. As a consequence, the fabricated ultralight 600LDH-rGO 2:1 aerogel shows a broad effective absorption bandwidth (EAB) of 7.04 GHz at a thickness of 2.3 mm with a low filling content of only 6 wt% and a low density of 4.4 mg/cm3. In conclusion, the synthetic LDH-rGO aerogels offer an effective strategy for preparing EMW absorption materials that own three-dimensional porous network structure and unique magnetic NiFe2O4@FeNi3 core-shell structure nanospheres.

Construction of three-dimensional mesh porous Mo2C/carbon composites by chitosan salting-out for efficient microwave absorption

Constructing conductive network and adjusting impedance matching are effective ways to enhance the microwave absorption capacity of absorbers. However, the experimental procedures for preparing three-dimensional porous network are complex and often involve the use of hazardous agents. We proposed a simple and safe strategy to prepare porous three-dimensional network Mo2C/C composites. The salting-out method can change the aggregation state of chitosan macromolecules and make the free chitosan molecules form a porous three-dimensional network structure autonomously. In addition, the plus-charged amino on chitosan is able to attract minus-charged molybdate ions, which makes the surface of the 3D structured chitosan precursor covered with molybdenum-containing species. The result shows that the porous mesh structure and the heterogeneous interfaces combine to achieve excellent absorption performance of Mo2C/C with effective absorption bandwidth of 5.04 GHz at 1.8 mm. This work demonstrates that salting-out method broadens the idea of porous three-dimensional network electromagnetic wave absorbing materials.