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Rational manipulation of hollow structure with uniform heterojunctions is evolving as an effective approach to meet the lightweight and high‐performance microwave absorption for metal‐organic frameworks (MOFs) derived absorbers. Herein, a new and controlled synergistic protecting‐etching strategy is proposed to construct shelled ZIF‐67 rhombic dodecahedral cages using tannic acid under theoretical guidance, then hollow Co@N‐doped carbon nanocages with uniform heterojunctions and hierarchical micro‐meso‐macropores are obtained via a pyrolysis process, which addresses the shortcomings of using sacrificing templates or corrosive agents. The outer Co@N‐doped carbon shell, composed of highly dispersive core‐shell heterojunctions, possesses micro‐mesopores while the inner hollow macroporous cavity endows the absorbers with lightweight characteristics. Accordingly, the maximum reflection loss is −60.6 dB at 2.4 mm and the absorption bandwidth reaches 5.1 GHz at 1.9 mm with 10 wt% filler loading, exhibiting superior specific reflection loss compared with the vast majority of previous MOFs derived absorbers. Furthermore, this synergistic protecting‐etching strategy provides inspiration for precisely creating a hollow void inside other MOFs crystals and broadens the desirable candidates for lightweight and high‐efficient microwave absorbers.

Hybrid nanocomposites with enhanced microwave absorption properties have been designed by growing CuS nanoflakes on magnetically decorated graphene, and the effect of special nanostructures on microwave absorption properties has been investigated. The structure of the nanocomposites was characterized by Fourier transform infrared spectra (FTIR), X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscope (FESEM), transmission electron microscope (TEM), N2 adsorption-desorption, and vibrating sample magnetometer (VSM). The influence of cetyltrimethylammonium bromide (CTAB) on the morphology of CuS nanoflakes was also investigated. A possible formation process of the nanocomposites and the mechanism of microwave absorption were explained in detail. As an absorber, the nanocomposites with a filler loading of 20 wt % exhibited enhanced microwave absorption properties due to the special nanostructures, extra void space, and synergistic effect. The maximum reflection loss can reach -54.5 dB at 11.4 GHz, and the absorption bandwidths exceeding -10 dB are 4.5 GHz with a thickness of 2.5 mm, which can be adjusted by the thickness. The results indicate that the hybrid nanocomposites with enhanced microwave absorption properties and lightweight have a promising future in decreasing electromagnetic wave irradiation.

Hierarchical structures of graphene@Fe3O4@SiO2@NiO nanosheets were prepared by combining the versatile sol-gel process with a hydrothermal reaction. Graphene@Fe3O4 composites were first synthesized by the reduction reaction between FeCl3 and diethylene glycol (DEG) in the presence of GO. Then, graphene@Fe3O4 was coated with SiO2 to obtain graphene@Fe3O4@SiO2. Finally, NiO nanosheets were grown perpendicularly on the surface of graphene@Fe3O4@SiO2 and graphene@Fe3O4@SiO2@NiO nanosheet hierarchical structures were formed. Moreover, the microwave absorption properties of both graphene@Fe3O4 and graphene@Fe3O4@SiO2@NiO nanosheets were investigated between 2 and 18 GHz microwave frequency bands. The electromagnetic data demonstrate that graphene@Fe3O4@SiO2@NiO nanosheet hierarchical structures exhibit significantly enhanced microwave absorption properties compared with graphene@Fe3O4, which probably originate from the unique hierarchical structure with a large surface area and high porosity.

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As an effective method, heteroatom doping is widely used to improve the electrochemical performance of carbon materials. However, the influence of oxygen-containing functional groups in carbon materials is often neglected. Therefore, we use buckwheat hulls as the precursor to prepare oxygen-doped hard carbon by simple carbonization. The buckwheat hull at a pyrolysis temperature of 1100 °C has the highest reversible capacity of 400 mA h g–1 at 50 mA g–1, and the capacity can maintain 96% of the initial capacity after 3000 cycles at 2A g–1. These results confirm that the natural pore structure and proper interlayer spacing of the BPC-1100 contribute to the transport and insertion of sodium ions. In addition, the first principle proves that the role of oxygen atoms cannot be ignored in the storage of sodium ions. In particular, the improvement of the CO bond is helpful to improve the adsorption capacity of hard carbon to sodium ions and enhance the reversible capacitance.

The ternary composites of poly(3,4-ethylenedioxythiophene)-reduced graphene oxide-Co3O4 (PEDOT-RGO-Co3O4) were synthesized and the electromagnetic absorption property of the composites was investigated. The structure of the composites was characterized with Fourier-transform infrared spectra, X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, and transmission electron microscope. The electromagnetic parameters indicate the enhanced electromagnetic absorption property of the composites was attributed to the better impedance matching. On the basis of the above characterization, an electromagnetic complementary theory was proposed to explain the impedance matching. It can be found that the maximum reflection loss of PEDOT-RGO-Co3O4 can reach -51.1 dB at 10.7 GHz, and the bandwidth exceeding -10 dB is 3.1 GHz with absorber thickness of 2.0 mm. Therefore, the PEDOT-RGO-Co3O4 composites, with such excellent electromagnetic absorption properties and wide absorption bandwidth, can be used as a new kind of candidate for microwave absorbing materials.