SiO is a promising anode material for next-generation lithium-ion batteries (LIBs) with high-energy density. However, the passivation of silicon oxide in SiO remains challenging to reduce its irreversible reactions and volume expansion during cycling. In this work, a scalable approach is proposed to synthesize calcium silicate/nanosilicon composites (pSi@CaO) by transforming the SiO₂ in disproportionate SiO into calcium silicate at 1000 ℃. The bulk-distributed calcium silicate in pSi@CaO can effectively inhibit nanosilicon expansion and enhance ionic transfer. The optimized pSi@20%CaO anode demonstrates a low electrode expansion of 12.3% upon lithiation and 7.6% upon lithiation after 50 cycles. It also exhibits excellent electrochemical stability, delivering a specific capacity of 808 mAh g⁻¹ at 50 mA g⁻¹ with an initial Columbic efficiency of 72% and maintaining 82% capacity after 500 cycles at 1 A g⁻¹. The feasible CaO passivation strategy proposed in this work is expected to promote practical applications of Si-based anodes in high-performance LIBs.

Tantalum (Ta) doped Li₇La₃Zr₂O₁₂ (Ta-LLZO) ceramics were prepared via conventional solid-state reaction. LiOH was used as a lithium source and a sintering additive for ceramics. The effect of LiOH on the microstructure and ionic conductivity of Ta-LLZO ceramics was investigated. The results show that LiOH as a lithium source can promote the formation of cubic Ta-LLZO，and LiOH as a sintering additive can effectively improve the densification of ceramics. The dense cubic garnet Ta-LLZO ceramics were obtained by sintering at 1200 ℃ for 5 h. When the amount of the sintering additive is 6% (in mass fraction), the ionic conductivity of ceramics reaches 6.23×10^–4 S·cm^–1. It is indicated that Li₇La₃Zr₂O₁₂ prepared via solid-state reaction has a great potential in the application of all-solid-state lithium ion batteries.