阳极
成核
化学
复合数
锂(药物)
枝晶(数学)
过电位
纤维
化学工程
扩散
电池(电)
金属
纳米技术
复合材料
材料科学
电化学
电极
医学
有机化学
物理化学
内分泌学
功率(物理)
几何学
数学
物理
量子力学
工程类
热力学
作者
Caihong Wu,Piao Qing,Haifeng Huang,W PAN,Shaozhen Huang,Libao Chen,Mei Lin,Zhibin Wu
标识
DOI:10.1021/acs.inorgchem.4c03719
摘要
Lithium metal anodes generally suffer from uncontrolled dendrite growth and large volume change, while traditional skeletons such as Li13In3 and Li22Sn5 are too heavy and discontinuous to offer highly efficient structural supportability for composite Li anodes. In this work, lightweight and stable fiber-clustered skeletons, which are composed of LiB fibers and jointed Li22Si5 nanoparticles, can be obtained by smelting SiB6 powder and Li ingots. In addition to serving as both ionic and electronic conductors for composite Li anodes, the stable skeletons reduced volumetric fluctuation by offering uniform, heterogeneous, and continuous architectures while suppressing lithium dendrites with low nucleation overpotential and diffusion energy barrier. As a result, the Li–SiB6|Li–SiB6 symmetrical cells achieve an ultralong lifespan over 2000 h cycling at 1 mA cm–2 and 1 mA h cm–2. Eventually, the Li–SiB6|LiFePO4 full cells exhibit a long-term cyclability of 400 cycles with a high-capacity retention of 94.5% at 2 C, and the Li–SiB6|LiCoO2 pouch cells exhibit an impressive 85% capacity retention after 350 cycles. This work develops a new strategy to strengthen the stability of fibrous skeletons and minimize volume changes for dendrite-free Li metal anodes.
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