A novel microstructure of anode materials for lithium-ion batteries with ternary components, comprising tin (Sn), rice husk-derived silica (SiO 2 ), and bronze-titanium dioxide (TiO 2 (B)), has been developed. The goal of this research is to utilize the nanocomposite design of rice husk-derived SiO 2 and Sn nanoparticles self-assembled on TiO 2 (B) nanorods, Sn–SiO 2 @TiO 2 (B), through simple chemical route methods. Following that, the microstructure and electrochemical performance of as-prepared products were investigated. The major patterns of the X-ray diffraction technique can be precisely indexed as monoclinic TiO 2 (B). The patterns of SiO 2 and Sn were found to be low in intensity since the particles were amorphous and in the nanoscale range, respectively. Small spherical particles, Sn and SiO 2 , attached to TiO 2 (B) nanorods were discovered. Therefore, the influence mechanism of Sn–SiO 2 @TiO 2 (B) fabrication was proposed. The Sn–SiO 2 @TiO 2 (B) anode material performed exceptionally well in terms of electrochemical and battery performance. The as-prepared electrode demonstrated outstanding stability over 500 cycles, with a high discharge capacity of ∼150 mA h g –1 at a fast-charging current of 5000 mA g –1 and a low internal resistance of around 250.0 Ω. The synthesized Sn–SiO 2 @TiO 2 (B) nanocomposites have a distinct structure, the potential for fast charging, safety in use, and good stability, indicating their use as promising and effective anode materials in better power batteries for the next-generation applications.

Novel anode materials for lithium-ion batteries, nanocomposites of Sn (or SnO₂) and SiO₂ with graphene-based sheets (GO, rGO and NrGO), were synthesized by a facile and low-cost technique. The capacity of all composites was relatively high as compared to traditional graphite.

Popped rice carbons (PC) were derived from popped rice by using a facile and low-cost technique. PC was then activated by different kinds of activating agents, such as potassium hydroxide (KOH), zinc chloride (ZnCl2), iron (III) chloride (FeCl3), and magnesium (Mg), in order to increase the number of pores and specific surface area. The phase formation of porous activated carbon (PAC) products after the activation process suggested that all samples showed mainly graphitic, amorphous carbon, or nanocrystalline graphitic carbon. Microstructure observations showed the interconnected macropore in all samples. Moreover, additional micropores and mesopores were also found in all PAC products. The PAC, which was activated by KOH (PAC-KOH), possessed the largest surface area and pore volume. This contributed to excellent electrochemical performance, as evidenced by the highest capacity value (383 mAh g−1 for 150 cycles at a current density of 100 mA g−1). In addition, the preparation used in this work was very simple and cost-effective, as compared to the graphite preparation. Experimental results demonstrated that the PAC architectures from natural popped rice, which were activated by an optimal agent, are promising materials for use as anodes in LIBs.

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