介观物理学
材料科学
电解质
离子键合
快离子导体
渗透(认知心理学)
化学物理
导电体
电导率
离子电导率
纳米技术
离子
电极
物理化学
复合材料
凝聚态物理
神经科学
物理
生物
化学
量子力学
作者
Cheng Ma,Yongqiang Cheng,Kai Chen,Juchuan Li,Bobby G. Sumpter,Ce‐Wen Nan,Karren L. More,Nancy J. Dudney,Miaofang Chi
标识
DOI:10.1002/aenm.201600053
摘要
Li‐ion‐conducting solid electrolytes can simultaneously overcome two grand challenges for Li‐ion batteries: the severe safety concerns that limit the large‐scale application and the poor electrolyte stability that forbids the use of high‐voltage cathodes. Nevertheless, the ionic conductivity of solid electrolytes is typically low, compromising the battery performances. Precisely determining the ionic transport mechanism(s) is a prerequisite for the rational design of highly conductive solid electrolytes. For decades, the research on this subject has primarily focused on the atomic and microscopic scales, where the main features of interest are unit cells and microstructures, respectively. Here, it is shown that the largely overlooked mesoscopic scale lying between these extremes could be the key to fast ionic conduction. In a prototype system, (Li 0.33 La 0.56 )TiO 3 , a mesoscopic framework is revealed for the first time by state‐of‐the‐art scanning transmission electron microscopy. Corroborated by theoretical calculations and impedance measurements, it is demonstrated that such a unique configuration maximizes the number of percolation directions and thus most effectively improves the ionic conductivity. This discovery reconciles the long‐standing structure–property inconsistency in (Li 0.33 La 0.56 )TiO 3 and also identifies mesoscopic ordering as a promising general strategy for optimizing Li + conduction.
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