Qiang Li, Chenxiang Xie, Xin Jiang, Chuannan Geng, Zhonghao Hu, Huilin Ge, Jiwei Shi, Li Wang, Wei Lv, Quan-Hong Yang
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引用次数: 0
摘要
全固态锂硫电池(ASSLSBs)因其固有的安全性和高能量密度而获得了重要的研究兴趣。然而,它们的实际应用仍然受到硫反应动力学缓慢的限制。虽然催化策略已被证明可以促进硫转化,但其功效从根本上受到缺乏界面连续性的限制。因此,迫切需要通过界面融合来实现这种连续性并构建高效的催化界面。在这项工作中,提出了一种非晶界面融合策略,使用TiS2作为催化“焊料”,使硫、催化剂和固态电解质之间的紧密结合。在与硫和硫化物基固体电解质反应后,TiS2诱导原位形成非晶TiS4和Li-Ti-P-S-Cl界面相。这些非晶相促进了界面的“焊接”,创造了集成的催化界面,增强了Li+的传输和催化效率。结果表明,优化后的ASSLSBs在1℃下循环2000次后的可逆比容量为720 mAh g-1,并且在4.0 mg cm-2的硫负荷下提供了7.05 mAh cm-2的高面容量。这种界面融合策略为高性能asslbs的实际开发提供了一条有希望的途径。
Catalytic Solder Fuses Solid-Solid Interfaces for All-Solid-State Lithium-Sulfur Batteries.
All-solid-state lithium-sulfur batteries (ASSLSBs) have garnered significant research interest due to their inherent safety and high energy density. Nevertheless, their practical applications remain constrained by the sluggish sulfur reaction kinetics. While catalytic strategies have been demonstrated to facilitate sulfur conversion, their efficacy is fundamentally constrained by the lack of interfacial continuity. Thus, there is an urgent need for interfacial fusion to achieve such continuity and construct efficient catalytic interfaces. In this work, an amorphous interfacial fusion strategy using TiS2 as a catalytic "solder", enabling intimate integration among sulfur, the catalyst, and the solid-state electrolyte is proposed. Upon reacting with sulfur and the sulfide-based solid electrolyte, TiS2 induces the in situ formation of amorphous TiS4 and Li-Ti-P-S-Cl interfacial phases. These amorphous phases facilitate interfacial "soldering", creating integrated catalytic interfaces that enhance Li+ transport and catalytic efficiency. As a result, the optimized ASSLSBs show a reversible specific capacity of 720 mAh g-1 after 2000 cycles at 1 C. It also delivers a high areal capacity of 7.05 mAh cm-2 at a sulfur loading of 4.0 mg cm-2. This interfacial fusion strategy offers a promising pathway toward the practical development of high-performance ASSLSBs.
期刊介绍:
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