A novel synthesis of Porous Fe4N/carbon hollow microspheres for thin and efficient electromagnetic wave absorbers.

Modulating the structure and morphology is essential in fabricating high-performance electromagnetic absorbing materials. Herein, we obtained porous Fe3O4/carbon hollow microspheres and porous Fe4N/carbon hollow microspheres derived from Fe-glycerol hollow microspheres. Through structure and morphology analysis, we proved the existence of porous and hollow features. By comparison, it can be found that the porous Fe4N/carbon hollow microspheres have electromagnetic wave absorption performance superior to that of porous Fe3O4/carbon hollow microspheres. The reflection loss value of porous Fe4N/carbon hollow microspheres reaches -42.2 dB at a matching thickness of merely 1.4 mm, and its effective absorbing bandwidth approaches 4.5 GHz, whereas the reflection loss of porous Fe3O4/carbon hollow microspheres in the 2-18 GHz range is over -10 dB. Reasons for the better electromagnetic wave absorption performance are revealed to be that the magnetic Fe4N has higher complex permittivity and complex permeability, and the porous hollow microspherical structure increases the multiple scattering and reflection of electromagnetic waves. Meanwhile, the impedance matching and attenuation constant are optimized together through the synergy of dielectric and magnetic loss. This research can provide instructive findings for thin-thickness electromagnetic wave absorbing materials based on Fe4N with an appropriate microstructure.

Li-N Interaction Induced Deep Eutectic Gel Polymer Electrolyte for High Performance Lithium-Metal Batteries.

As emerging eutectic mixtures, deep eutectic electrolytes (DEEs) show unique properties for Li-metal batteries (LMBs). However, the limited choice and inferior electrode compatibility hinder their further development in LMBs. Herein, we report a new 1,2-dimethylimidazole (DMIm)-based deep eutectic gel polymer electrolyte induced by Li-N interaction. We demonstrate that incorporating electron-withdrawing polyvinylidene difluoride (PVDF) polymer into the DMIm-based DEE changes the coordination environment of Li+ ions, leading to a high transference number of Li+ ions (0.65) and superior interface stability between the electrolyte and Li anode. The deep eutectic gel polymer electrolyte exhibits excellent non-flammability, high ionic conductivity (1.67 mS cm-1 at 30 °C), and high oxidation voltage (up to 4.35 V vs. Li/Li+ ). The Li||LFP cell based on the newly developed deep eutectic gel polymer electrolyte can achieve superior long-term cycling stability at a wide range of rates.

Equipment-free photothermal effect promoted self-healing and self-recovery of hydrogels.

The self-healing and self-recovery of the hydrogel materials can be promoted under sunlight without the assistance of electrical equipment by adding a light-to-heat conversion substance during the synthetic process, which will greatly extend the service life of the hydrogels even for the elastomer materials in the off-grid areas.

Fabrication of shape-tunable macroparticles by seeded polymerization of styrene using non-cross-linked starch-based seed.

Nonspherical colloidal particles with various geometries and different compositions have attracted tremendous attention and been widely researched. The preparation of polymer colloidal particles with controlled shapes by seeded polymerization is recognized as the most promising technique owing to the precise control of various morphologies and using non-cross-linked seed particles are of particular interest. Seeds particles derived from natural biopolymers are seldom applied. Hence, non-cross-linked starch-based seed could be used to fabricate the anisotropic particles by soap-free seed polymerization. Non-cross-linked starch-based seed particles were prepared by a nanoprecipitation method. Starch/polystyrene composite colloidal particles with shape-tunable were fabricated by soap-free seeded polymerization using starch-based seed. The effect of the polymerization time, monomer feed ratio and seed type were investigated. The seed particles with a single- or multi-hole structure were obtained after swelling with styrene. The resulting particles including golf-like, raspberry-like, octahedron-like and snowman-like structures, was fabricated on the polymerization process. This study firstly reports that the morphology of composite particles from golf-like to snowman-like at high monomer feed ratio using starch-based seed. At low monomer feed ratio, raspberry-like particles were obtained by surface nucleation increasing process. In addition, seed type also effect the morphology of composite particles.

Interfacial Activity of Starch-Based Nanoparticles at the Oil-Water Interface.

Understanding the interfacial activity of polysaccharide nanoparticles adsorbed at oil-water interfaces is essential and important for the application of these nanoparticles as Pickering stabilizers. The interfacial properties of starch-based nanospheres (SNPs) at the interface of an n-hexane-water system were investigated by monitoring the interfacial tension at different bulk concentrations. The three-phase contact angle (θ) and the adsorption energy (ΔE) increased with increasing size and degree of substitution with octenyl succinic groups (OSA) in the particles. Compared with the OSA-modified starch (OSA-S) macromolecule, the SNPs effectively reduced the interfacial tension of the n-hexane-water system at a relatively higher concentration. These results and the method reported herein are useful for selecting and preparing polysaccharide nanoparticles as Pickering stabilizers for oil-water emulsions.

Tough, rapid-recovery composite hydrogels fabricated via synergistic core-shell microgel covalent bonding and Fe3+ coordination cross-linking.

We developed tough, rapid-recovery composite hydrogels that are fabricated via core-shell microgel covalent bonding and Fe3+ dynamic metal coordination cross-linking. First, core-shell microgels are used as cross-linking agents and initiators to prepare homogeneous hydrogel networks with rapid recovery in the absence of an organic cross-linking agent. The toughness and recoverability of the composite hydrogels can be improved by adding the dynamic reversibility of ionic cross-linking. Owing to the synergistic effect of microgel covalent bonding, Fe3+ coordination cross-linking, and H-bond cross-linking, the multi-cross-linked composite hydrogels exhibit excellent toughness and a fast recovery rate. These characteristics demonstrate that the dynamic reversibility of the ionic cross-linking can significantly improve the toughness and recoverability of the hydrogels. In addition, the core-shell microgels play a key role in toughening the hydrogels and accelerating their recovery by transferring stress to grafted polymer chains and homogenizing the hydrogel network.