Publications by authors named "Xingfeng Lei"

Multiband-compatible stealth materials play an increasingly crucial role in the field of modern military defence because they can enable the targeted objects to dodge advance detection technologies. In this study, chain-like FeO@poly(ethyleneglycol dimethacrylate-co-methacrylic acid) nanocomposites were constructed as precursors through the magnetic field-induced distillation precipitation polymerisation. Then, the liquid-phase seed-mediated growth method, together with subsequent calcination, was applied to introduce SnO shells and remove poly(ethyleneglycol dimethacrylate-co-methacrylic acid) shells, which led to the successful preparation of innovative core-shell FeO@SnO nanochains.

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Gas barrier membranes with impressive moisture permeability are highly demanded in air or nature gas dehumidification. We report a novel approach using polyetheramine oligomers covalently grafted on the carbon nanotubes (CNTs) to engineer liquid-like CNT nanofluids (CNT NFs), which are incorporated into a polyimide matrix to enhance the gas barrier and moisture permeation properties. Benefiting from the featured liquid-like characteristic of CNT NFs, a strong interfacial compatibility between CNTs and the polyimide matrix is achieved, and thus, the resulting membranes exhibit high heat resistance and desirable mechanical strength as well as remarkable fracture toughness, beneficially to withstanding creep, impact, and stress fatigue in separation applications.

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High-performance microwave absorption absorbers play important roles in the fields of radar stealth, electromagnetic protection, and antenna technology. In this work, high aspect-ratio Ag nanowires were decorated with magnetic CoNi nanoparticles via a PVP-induced solvothermal method, and then amorphous Sn(OH)/SnO shells were introduced through an in-situ oxidative hydrolysis method, successfully preparing Ag-CoNi@Sn(OH)/SnO composites. The morphology and ingredient of composites were ascertained by SEM, TEM, XRD, EDX, and XPS.

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Due to strong interlayer interaction and ease of oxidation issues of black phosphorus (BP), the domain size of artificial synthesized few-layer black phosphorus (FL-BP) crystals is often below 10 µm, which extremely limits its further applications in large-area thin-film devices and integrated circuits. Herein, a hydrogen-free electrochemical delamination strategy through weak Lewis acid intercalation enabled exfoliation is developed to produce ultralarge FL-BP single-crystalline domains with high quality. The interaction between the weak Lewis acid tetra-n-butylammonium acetate (CH COOTBA) and P atoms promotes the average domain size of FL-BP crystal up to 77.

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Achieving a desirable combination of good mechanical properties and healing efficiency is a great challenge in the development of self-healing elastomers. Herein, a class of tough and strong self-healing polyacrylate elastomers (denoted as HPs) was developed simply by free-radical copolymerization of n-butyl acrylate (nBA) and tert-butyl acrylate (tBA) and a subsequent hydrolysis reaction rather than direct copolymerization of nBA and acrylic acid (AA). The tiny difference in reactivity between nBA and tBA makes the structural units of the copolymer easy to control.

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The monoclinic-phase 1T' MoTe crystal exhibits inversion symmetry as an anisotropic semi-metal, dictating its interesting quantum transport phenomenon and other novel physical properties. However, large-scale controllable growth of uniform MoTe crystals still remains a great challenge, hindering its further fundamental research and applications for novel devices. Herein, we report a modified growth method for synthesizing few-layer 1T' MoTe crystals with large-scale uniformity with the assistance of molecular sieves.

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Electronic skin (e-skin) mimicking functionalities and mechanical properties of natural skin can find broad applications. We report the first dynamic covalent thermoset-based e-skin, which is connected through robust covalent bonds, rendering the resulting devices good chemical and thermal stability at service condition. By doping the dynamic covalent thermoset with conductive silver nanoparticles, we demonstrate a robust yet rehealable, fully recyclable, and malleable e-skin.

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A novel bovine serum albumin surface-imprinted thermosensitive magnetic composite microsphere was successfully prepared by the surface grafting copolymerization method in the presence of temperature-sensitive monomer N-isopropylacrylamide (NIPAM), functional monomer methacrylic acid (MAA) and cross-linking agent N,N'-methylenebisacrylamide (MBA). The structure and component of the thermosensitive magnetic molecularly imprinted microsphere were investigated by transmission electron microscopy (TEM), Fourier transform infrared (FT-IR), vibrating sample magnetometer (VSM) and thermogravimetric analysis (TGA). The results of thermosensitivity, adsorption capacity, selectivity and reusability showed the formation of a thermosensitivity grafting polymer layer P(NIPAM-MAA-MBA) on the surface of Fe3O4@SiO2 and the good adsorption capacity and specific recognition for template protein.

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BSA/Fe3O4 magnetic composite microspheres with high saturation magnetization and paramagnetic property were prepared via inverse emulsion technology at room temperature, bovine serum albumin (BSA, 60 KD), magnetic nanoparticles (Fe3O4) and glutaraldehyde as macromonomer, inorganic particles and cross-linking agent, respectively. Fourier transform infrared (FTIR), scanning electron microscope (SEM), metalloscope, and particle size analyzer were used to characterize morphology and structure of composite microspheres. Vibrating sample magnetometer (VSM) and thermogravimetric analysis (TGA) were used to test magnetic properties of the synthesized samples, adsorption capacity of microspheres was determined by ultraviolet spectrophotometer (UV).

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