This research demonstrates enhanced lithium-ion diffusion in a microsphere composite, suggesting significant improvements in battery performance.
Tin dioxide (SnO₂) has emerged as a promising anode for lithium‐ion batteries (LIBs) due to its high theoretical capacity and natural abundance. However, it suffers from severe volume expansion during lithiation/delithiation processes and limited rate capability. To address these challenges, this work rationally designed an urchin‐like‐graphitized carbon (GC)‐SnO₂ microsphere composite (denoted for GC‐SnO 2 ) through hydrothermal synthesis followed by controlled annealing. The hierarchical architecture consists of hollow SnO 2 nanospheres encapsulated within branched graphitized carbon protrusions, forming a hierarchically porous network. This structural design enables three key advantages: (1) accelerated Li + diffusion through interconnected channels, (2) stress buffering via spiny carbon branches to mitigate SnO 2 pulverization, and (3) enhanced conductivity through conformal GC coating. Benefiting from these synergistic features, the GC‐SnO 2 anode exhibits outstanding cyclability, maintaining 765 mA h g −1 after 100 cycles at 0.2 A g −1 . Notably, it achieves 538 mA h g −1 at 2 A g −1 over 1000 cycles, surpassing bare SnO 2 (89 mA h g −1 ) and exceeding the performance of most reported SnO 2 ‐based anodes. This work provides an effective strategy for designing stress‐tolerant oxide/carbon composites toward high‐energy‐density LIBs.
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Tang et al. (2025) studied this question.
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