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Semiconductor-based composites are potential anodes for Li-ion batteries, owing to their high theoretical capacity and low cost. However, low stability induced by large volumetric change in cycling restricts the applications of such composites. Here, a hierarchical SnO2@Ni6MnO8 composite comprising Ni6MnO8 nanoflakes growing on the surface of a three-dimensional (3D) SnO2 is developed by a hydrothermal synthesis method, achieving good electrochemical performance as a Li-ion battery anode. The composite provides spaces to buffer volume expansion, its hierarchical profile benefits the fast transport of Li+ ions and electrons, and the Ni6MnO8 coating on SnO2 improves conductivity. Compared to SnO2, the Ni6MnO8 coating significantly enhances the discharge capacity and stability. The SnO2@Ni6MnO8 anode displays 1030 mAh g−1 at 0.1 A g−1 and exhibits 800 mAh g−1 under 0.5 A g−1, along with high Coulombic efficiency of 95%. Furthermore, stable rate performance can be achieved, indicating promising applications. [ABSTRACT FROM AUTHOR]

A composite composing of TiO2 nanoparticles load on biomass rice husk (RH) is developed by directly growing TiO2 nanoparticles on RH. The in-situ growth of the nanocrystals on RH is achieved by a low-cost and one-step homogeneous precipitation. Rapid hydrolysis proceeds at 90 °C by using ammonium fluotitanate and urea to facilitate the selective growth of TiO2. The method provides an easy access to the TiO2-RH composite with a strong interaction between TiO2 nanoparticles and the underlying RH. The structure and composition of TiO2-RH are characterized by using X-ray diffraction, X-ray photoelectron spectroscopy, Fourier-transform infrared spectroscopy, and UV-vis absorption spectroscopy. TiO2 nanoparticles-RH exhibits a good photocatalytic degradation of methyl orange. The results show that 92% of methyl orange (20 mg L−1) can be degraded within three hours in visible light. The catalytic activity of the composite is not reduced after 6 cycles, and it still reaches 81% after 6 cycles. The enhanced performance is ascribed to the suitable particle size the good dispersibility. It is expected that the high photocatalytical performance and the cost-effective composite presented here will inspire the development of other high-performance photocatalysts. [ABSTRACT FROM AUTHOR]

Magnesium batteries have been considered promising candidates for next‐generation energy storage systems owing to their high energy density, good safety without dendrite formation, and low cost of magnesium resources. However, high‐performance cathodes with stable capacity, good conductivity, and fast ions transport are needed, since many conventional cathodes possess a low performance and poor preparation controllability. Herein, a liquid‐driven coaxial flow focusing (LDCFF) approach for preparing a novel microcapsule system with controllable size, high loading, and stable magnesium‐storage performance is presented. Taking the MoS2‐infilled microcapsule as a case study, the magnesium battery cathode based on the microcapsules displays a capacity of 100 mAh g−1 after 100 cycles. High capacity retention is achieved at both low and high temperatures of −10, ‒5, and 45 °C, and a stable rate‐performance is also obtained. The influences of the liquid flow rates on the size and shell thickness of the microcapsules are investigated; and electron and ion diffusion properties are also studied by first‐principle calculations. The presented LDCFF method is quite general, and the high performance of the microcapsules enables them to find broad applications for making emerging energy‐storage materials and secondary battery systems. [ABSTRACT FROM AUTHOR]