Metal–organic frameworks (MOFs) with porous structures
are
beneficial for electrochemical energy storage. Herein, the in-situ
growth of the S-doped Ni-MOF nanosheet (S-NMN) on the surfaces of
nickel foams was prepared via a facile solvothermal process. Owing
to the rich active sites, small transport barrier, and excellent mechanical
stability, the fabricated S-NMN-2 electrode displays a high specific
capacity (1952 mF cm–2 at 1 mA cm–2), satisfactory rate performance, and remarkable cyclic stability.
For practical application, the assembled S-NMN-2//AC device achieves
a high energy density of 0.189 mWh cm–2 at the power
density of 1.600 mW cm–2 with prominent cycling
stability (93.27% capacity retention after 4000 cycles). The facile
strategy of etching nickel foam demonstrates a new idea for developing
high-performance supercapacitor materials.
In recent years, Schiff base-related conjugated systems have received extensive attention, but little research has been done in the field of electromagnetic materials. In this work, an organic conjugated system based on polypyrrole/hydrazone Schiff base (PPy/HSB) composites was constructed via a Schiff base synthetic route and their electromagnetic behavior was investigated. The electromagnetic response of PPy/HSB complexes demonstrates fine electromagnetic absorption performance. When the filler loading is 30 wt% in a paraffin matrix, an absorption peak of −43.1 dB was achieved and its effective absorption bandwidth (EAB) was located in the range of 10.88−18.0 GHz. The electromagnetic response behavior of PPy/HSB complexes is explained by models involving electronic structure, multi-polarization and conductive network. The mechanisms of PPy/HSB complexes formation and HSB crystallization are also discussed through the compatibility of PPy/HSB and the structure of HSB. Moreover, the morphology transformation of HSB in the PPy/HSB systems has been studied. This study opens the exploration of organic–dielectric conjugated systems in the field of electromagnetic materials, and significantly broadens the application range of organic–dielectric–dielectric composites.
The moderation of the dielectric properties of polymer composites and their environmental stability need to be considered comprehensively in the design of microwave-absorbing materials. In this work, polypyrrole/polystyrene (PPy/PS) composited particles were synthesized through a facile in situ bulk polymerization procedure. The PS component can be modulated conveniently by controlling the polymerization time. FTIR and Raman analyses disclosed that the PS component was immobilized in PPy via covalent bonds. The electromagnetic characterization results indicated that the dielectric properties and, thus, the microwave absorption could be controlled when the styrene polymerization was prolonged from 6 h (PPy-6) to 19 h (PPy-19). The composite PPy-19 displayed an optimal reflection loss of −51.7 dB with a matching thickness of 3.16 mm, and the effective absorption bandwidth (EAB) even reached 5.8 GHz at 2.4 mm. The PS component endowed PPy/PS composites with more robust environmental stability than homogeneous PPy. After being exposed to air for 365 days and hydrothermally treated at 100 °C for 12 h, PPy-19 still exhibited a reflection loss superior to −20 dB. The present work provides a new insight into the adjustment of the electromagnetic properties of PPy composites to fabricate high-performance microwave absorbers with superior environmental stability.
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