摘要
Graphical The amorphous titanium dioxide is used to coat eGaSn nanodroplets (eGaSn NDs) to construct the core-shell structure of eGaSn@TiO 2 nanodroplets (eGaSn@TiO 2 NDs). The amorphous TiO 2 shell forms a stable SEI film, alleviates volume expansion, and provides electron/ion transport channels. The resulting eGaSn@TiO 2 NDs exhibit high capacities of 580, 540, 515, 485, 456 and 426 mAh g −1 at 0.1, 0.2, 0.5, 1, 2 and 5 C, respectively. No obvious decay is observed in more than 500 cycles with a capacity of 455 mAh g −1 at 1 C. Gallium-based alloy liquid metal batteries currently face limitations such as volume expansion, unstable solid electrolyte interface (SEI) film and substantial capacity decay. In this study, amorphous titanium dioxide is used to coat eutectic GaSn nanodroplets (eGaSn NDs) to construct the core-shell structure of eGaSn@TiO 2 nanodroplets (eGaSn@TiO 2 NDs). The amorphous TiO 2 shell (~6.5 nm) formed a stable SEI film, alleviated the volume expansion, and provided electron/ion transport channels to achieve excellent cycling performance and high specific capacity. The resulting eGaSn@TiO 2 NDs exhibited high capacities of 580, 540, 515, 485, 456 and 426 mAh g −1 at 0.1, 0.2, 0.5, 1, 2 and 5 C, respectively. No significant decay was observed after more than 500 cycles with a capacity of 455 mAh g −1 at 1 C. In situ X-ray diffraction (in situ XRD) was used to explore the lithiation mechanism of the eGaSn negative electrode during discharge. This study elucidates the design of advanced liquid alloy-based negative electrode materials for high-performance liquid metal batteries (LMBs).
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