Xiaoxia Ma

Confining radical polymerization to liquid–liquid interfaces remains a formidable challenge due to the inherent tendency of monomers to diffuse into the bulk phase. Here, we report a poor-solvent-regulated strategy that drives oligomer enrichment at the oil–water interface, enabling confined radical polymerization within Pickering emulsions. This approach synergistically integrates photoinitiated polymerization with MPS-modified aluminum nanoparticles to construct a robust organic–inorganic hybrid shell, which is further densified by interfacial contraction upon solvent evaporation. Applied to hygroscopic ammonium dinitramide (ADN), this strategy yields a conformal coating that reduces the 24 h moisture uptake by up to 56% and significantly enhances combustion intensity. This solvent-mediated interfacial engineering provides a general platform for the precise synthesis of functional core–shell materials, as demonstrated by its successful extension to various polymerizable units, interfacial nanoparticles, and inner-phase solutes.

The composites of expanded graphite (EG) and magnetic particles have good electromagnetic wave attenuation properties in the centimeter band, which is valuable in the field of radar wave interference. In this paper, a novel preparation method of Ni–Zn ferrite intercalated EG (NZF/EG) is provided in order to promote the insertion of Ni–Zn ferrite particles (NZF) into the interlayers of EG. The NZF/EG composite is in situ prepared via thermal treatment of Ni–Zn ferrite precursor intercalated graphite (NZFP/GICs) at 900 °C, where NZFP/GICs is obtained through chemical coprecipitation. The morphology and phase characterization demonstrate the successful cation intercalation and NZF generation in the interlayers of EG. Furthermore, the molecular dynamics simulation shows that the magnetic particles in the EG layers tend to disperse on the EG layers rather than aggregate into larger clusters under the synergy of van der Waals forces, repulsive force, and dragging force. The radar wave attenuation mechanism and performance of NZF/EG with different NZF ratios are analyzed and discussed in the range of 2–18 GHz. The NZF/EG with the NZF ratio at 0.5 shows the best radar wave attenuation ability due to the fact that the dielectric property of the graphite layers is well retained while the area of the heterogeneous interface is increased. Therefore, the as-prepared NZF/EG composites have potential application value in attenuating radar centimeter waves.

Energetic materials, including explosives, pyrotechnics, and propellants, are widely used in mining, demolition, automobile airbags, fireworks, ordnance, and space technology. Nanoenergetic materials (nEMs) have a high reaction rate and high energy density, which are both adjustable to a large extent. Structural control over nEMs to achieve improved performance and multifunctionality leads to a fascinating research area, namely, nanostructured energetic materials. Among them, core–shell structured nEMs have gained considerable attention due to their improved material properties and combined multiple functionalities. Various nEMs with core–shell structures have been developed through diverse synthesis routes, among which core–shell structured nEMs associated with explosives and metastable intermolecular composites (MICs) are extensively studied due to their good tunability and wide applications, as well as excellent energetic (e.g., enhanced heat release and combustion) and/or mechanical properties. Herein, the preparation methods and fundamental properties of the abovementioned kinds of core–shell structured nEMs are summarized and the reasons behind the satisfactory performance clarified, based on which suggestions regarding possible future research directions are proposed.

Integrating energetic materials with a microelectromechanical system (MEMS) to achieve miniaturized integrated smart energetic microchips is promising. The potential applications include actuation in lab-on-a-chip devices, ignition in automobile airbags, propulsion and attitude control of micro-/nano-satellites, and miniaturized electro-explosive devices. In this work, a new type of MEMS-compatible energetic arrays was in situ realized on a copper substrate, which comprised a new energetic coordination polymer (ECP; Cu_1.5C₂N₈O₂·H₂O) with tunable nanostructures and a nano-aluminum (nano-Al) covering layer. The composition, morphology, and energetic characteristics of the energetic arrays can be easily tuned by adjusting the reaction time. The maximum heat release of 1850.2 J/g in thermal analysis and the intense flame in open burning experiment proved its excellent exothermic and combustion performance. A closed-bomb experiment further revealed that the [email protected] energetic arrays supported on Cu(OH)₂ nanorods had a peak pressure (5.5 MPa) and a pressure duration (0.5 s) more than twice those of nanoscale Al/CuO powder because of the introduction of gas elements (e.g., C, H, and N). A preliminary impulse experiment was also conducted through the torsion pendulum method. The displacement of the torsion pendulum in the micrometer scale proved the potential application of the energetic arrays in micropropulsion systems. Overall, this work can serve as a reference for the synthesis and applications of ECPs.