固态
锂(药物)
快离子导体
材料科学
电解质
固溶体
化学工程
无机化学
化学
电极
物理化学
冶金
医学
工程类
内分泌学
作者
Deliang Xu,Mengyuan Jin,Zilong Su,Ran Liu,Manyu Xiang,Wanggang Fang,Liqing He,Renbing Wu,Y. P. Guo
标识
DOI:10.1002/advs.202510193
摘要
Abstract Hydroborate‐based solid electrolytes (SEs), distinguished by their eco‐friendliness and non‐flammability have emerged as a research hotspot in energy storage research. Despite these advantages, their widespread adoption is constrained by insufficient ionic conductivity and poor high‐voltage compatibility. To overcome this challenge, a novel hydroborate SEs, 400‐0.6Li 2 B 12 H 12 ‐0.4LiI (denoted as 400‐0.6B 12 ‐0.4I), is engineered through a facile synthesis strategy combining high‐temperature processing (400 °C, 2 h, in Ar) and LiI doping. 400‐0.6B 12 ‐0.4I exhibits an outstanding ionic conductivity up to 0.75 mS cm −1 at 25 °C, which is the highest level among the reported inorganic Li 2 B 12 H 12 ‐based SEs so far. It also improves the cycling stability against lithium metal anodes, limits dendrite growth with a high critical current density of 5.0 mA cm −2 , which enables the Li symmetrical cells to cycle over 1000 h at 25 °C with only 10 mV of overpotential. Moreover, it cycles well in cells using lithium anodes and various high voltage (>4 V vs Li + /Li) cathodes materials such as LiCoO 2 , NCM811, and LiMn 2 O 4 . The proposed 400‐0.6B 12 ‐0.4I SEs offer valuable guidance for designing next‐generation lithium‐ion solid electrolytes with superior ionic conductivity, enhanced interfacial stability, and exceptional electrode compatibility.
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