We have demonstrated the synthesis of γ-Fe2O3 nano-particles through a facile and novel calcination process in the air. There is no pH regulation, gas atmosphere, additive, centrifugation or other complicated procedures during the preparing process. A detailed formation process of the nano-particles is proposed, and DMF as a polar solvent may slower the reaction process of calcination. The structures, morphologies, and magnetic properties of γ-Fe2O3 nano-particles were investigated systematically, and the pure γ-Fe2O3 nano-particles obtained at 200 °C display uniform morphology good magnetic property. The saturation magnetization of obtained pure γ-Fe2O3 is about 74 emu/g, which is comparable with bulk material (76 emu/g) and larger than other results. In addition, the photocatalytic activity for degradation of methylene blue is also studied, which shows proper photocatalytic activity.

The micrometer-sized H-Nb2O5 could achieve fast lithium-ion storage by engineering its planar defects.

Ba(FeTa)O/poly(vinylidene fluoride) (BFT/PVDF) flexible nanocomposite films are fabricated by tape casting using dopamine (DA)-modified BFT nanopowders and PVDF as a matrix polymer. After a surface modification of installing a DA layer with a thickness of 5 nm, the interfacial couple interaction between BFT and PVDF is enhanced, resulting in less hole defects at the interface. Then the dielectric constant (ε'), loss tangent (tan δ), and AC conductivity of nanocomposite films are reduced. Meanwhile, the value of the reduced dielectric constant (Δε') and the strength of interfacial polarization (k) are introduced to illustrate the effect of DA on the dielectric behavior of nanocomposite films. Δε' can be used to calculate the magnitude of interfacial polarization, and the strength of the dielectric constant contributed by the interface can be expressed as k. Most importantly, the energy-storage density and energy-storage efficiency of nanocomposite films with a small BFT@DA filler content of 1 vol % at a low electric field of 150 MV/m are enhanced by about 15% and 120%, respectively, after DA modification. The high energy-storage density of 1.81 J/cm is obtained in the sample. This value is much larger than the reported polymer-based nanocomposite films. In addition, the outstanding cycle and bending stability of the nanocomposite films make it a promising candidate for future flexible portable energy devices.

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Width-controlled M-type hexagonal SrFe12O19 nanoribbons were synthesized for the first time via polyvinylpyrrolidone (PVP) sol assisted electrospinning followed by heat treatment in air, and their chemical composition, microstructure and magnetic performance were investigated. Results demonstrated that as-obtained SrFe12O19 nanoribbons were well-crystallized with high purity. Each nanoribbon was self-assembled by abundant single-domain SrFe12O19 nanoparticles and was consecutive on structure and uniform on width. PVP in the spinning solution played a significant influence on the microstructure features of SrFe12O19 nanoribbons. With PVP concentration increasing, the ribbon-width was increased but the particle-size was reduced, which distributed on a same ribbon were more intensive, and then the ribbon-surface became flat. The room temperature magnetic performance investigation revealed that considerable large saturation magnetization (Ms) and coercivity (Hc) were obtained for all SrFe12O19 nanoribbons, and they increased with the ribbon-width broadening. The highest Ms of 67.9 emu·g−1 and Hc of 7.31 kOe were concurrently acquired for SrFe12O19 nanoribbons with the maximum ribbon-width. Finally, the Stoner-Wohlfarth curling model was suggested to dominate the magnetization reverse of SrFe12O19 nanoribbons. It is deeply expected that this work is capable of opening up a new insights into the architectural design of 1D magnetic materials and their further utilization.

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Fe‐N‐C single‐atom catalysts (SACs) are emerging as a promising class of electrocatalysts for the oxygen reduction reaction (ORR) to replace Pt‐based catalysts. However, due to the limited loading of Fe for SACs and the inaccessibility of internal active sites, only a small portion of the sites near the external surface are able to contribute to the ORR activity. Here, this work reports a metal–organic framework‐derived Fe‐N‐C SAC with a hierarchically porous and concave nanoarchitecture prepared through a facile but effective strategy, which exhibits superior electrocatalytic ORR activity with a half‐wave potential of 0.926 V (vs RHE) in alkaline media and 0.8 V (vs RHE) in acidic media while maintaining excellent stability. The superior ORR activity of the as‐designed catalyst stems from the unique architecture, where the hierarchically porous architecture contains micropores as Fe SAC anchoring sites, meso‐/macro‐pores as accessible channels, and concave shell for increasing external surface area. The unique architecture has dramatically enhanced the utilization of previously blocked internal active sites, as confirmed by a high turnover frequency of 3.37 s−1 and operando X‐ray absorption spectroscopy analysis with a distinct shift of adsorption edge.