摘要
Anode-fre Li−S batteries can achieve extremely high energy density and excellent intrinsic safety by circumventing the direct use of metallic Li. However, the actual output performance is largely constrained by sluggish reaction kinetics and severe structural deterioration of Li2S cathode. Here, we report an anchor-encapsulated nanostructure cooperated with alkaline-earth metal sulfides’ catalysis to promote Li2S kinetics and simultaneously stabilize sulfur species. DFT calculations are first implemented to screen out an optimized MgS electrocatalyst, then a synthetic paradigm of metallothermic-sulfidation-carbonization via burning LiMg alloy in CS2 vapor is proposed to in situ construct Li2S-MgS@graphene nanocapsules. Systematic studies reveal its integrated anchor-encapsulated structure and synergistic physicochemical interactions among three key components: robust C−S bonding facilitates fast electron/ion transport and stable interface, compact graphene encapsulation alleviates volume change and electrolyte's erosion, and symbiotic MgS bears excellent electrocatalytic effect on Li2S dissociation, greatly reducing activation barrier. Owing to the improvement on electrical, catalytic and volumetric properties, this cathode design enables promising electrochemical performance. It demonstrates a great potential for anode-free Li−S battery and Li2S-MgS@graphene//Cu cell exhibits 823 mAh g−1 initial specific capacity and 73% capacity retention after 100 cycles. Findings in this work are expected to spark a promising direction for designing high-performing anode-free batteries.
| 源语言 | 英语 |
|---|---|
| 期刊 | Angewandte Chemie - International Edition |
| DOI | |
| 出版状态 | 已接受/待刊 - 2026 |
| 已对外发布 | 是 |
学术指纹
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