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用于先进锂金属电池的超长寿命原位构建多功能复合阳极

In Situ-Constructed Multifunctional Composite Anode with Ultralong-Life Toward Advanced Lithium-Metal Batteries.

作者信息

Cao Liang, Chu Mingjing, Li Yue, Xu Xin, Qiu Yawen, Dai Yue, Sun Chencheng, Huang Zhi-Xiong, Wu Xing-Long, Geng Hongbo

机构信息

School of Materials Engineering, Changshu Institute of Technology, Changshu, Jiangsu, 215500, P. R. China.

Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin, 300071, P. R. China.

出版信息

Adv Mater. 2024 Oct;36(41):e2406034. doi: 10.1002/adma.202406034. Epub 2024 Aug 17.

DOI:10.1002/adma.202406034
PMID:39152937
Abstract

Metallic lithium is the most competitive anode material for next-generation high-energy batteries. Nevertheless, the extensive volume expansion and uncontrolled Li dendrite growth of lithium metal not only cause potential safety hazards but also lead to low Coulombic efficiency and inferior cycling lifespan for Li metal batteries. Herein, a multifunctional dendrite-free composite anode (Li/SnS) is proposed through an in situ melt-infusion strategy. In this configuration, the 3D cross-linked porous LiS/LiSn framework facilitates the rapid penetration of electrolytes and accommodates the volume expansion during the repeated Liplating process. Meanwhile, the lithiophilic LiS phases with a low Li transport barrier ensure preferential Li deposition, effectively avoiding uneven electron distribution. Moreover, the LiSn electron conductors with appropriate Li bonding ability guarantee rapid charge transport and mass transfer. Most importantly, the steady multifunctional skeleton with sufficient inner interfaces (LiS/LiSn) in the whole electrode, not only realizes the redistribution of the localized free electron, contributing to the decomposition of Li clusters, but also induces a planar deposition model, thus restraining the generation of Li dendrites. Consequently, an unprecedented cyclability of over 6 500 h under an ultrahigh areal capacity of 10 mAh cm and a current rate of 20 mA cm is achieved for the prepared LiS/LiSn composite anode. Moreover, the assembled Li/SnS||LiFePO (LFP) pouch full-cells also demonstrate remarkable rate capability and a convincing cycling lifespan of more than 2 000 cycles at 2 C.

摘要

金属锂是下一代高能电池中最具竞争力的负极材料。然而,锂金属广泛的体积膨胀和不受控制的锂枝晶生长不仅会造成潜在的安全隐患,还会导致锂金属电池的库仑效率低下和循环寿命较差。在此,通过原位熔体注入策略提出了一种多功能无枝晶复合负极(Li/SnS)。在这种结构中,三维交联多孔LiS/LiSn框架促进了电解质的快速渗透,并在反复锂电镀过程中容纳体积膨胀。同时,具有低锂传输势垒的亲锂LiS相确保了优先锂沉积,有效避免了电子分布不均。此外,具有适当锂键合能力的LiSn电子导体保证了快速的电荷传输和质量传输。最重要的是,整个电极中具有足够内部界面(LiS/LiSn)的稳定多功能骨架不仅实现了局部自由电子的重新分布,有助于锂簇的分解,还诱导了平面沉积模型,从而抑制了锂枝晶的产生。因此,所制备的LiS/LiSn复合负极在10 mA cm的超高面积容量和20 mA cm的电流速率下实现了超过6500 h的前所未有的循环稳定性。此外,组装的Li/SnS||LiFePO(LFP)软包全电池在2 C下也表现出显著的倍率性能和超过2000次循环的令人信服的循环寿命。

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