阳极
材料科学
电解质
阴极
电化学
锂(药物)
快离子导体
工作(物理)
离子电导率
储能
金属锂
离子键合
固态
纳米技术
离子
工程物理
机械工程
热力学
电气工程
电极
功率(物理)
医学
内分泌学
化学
物理
物理化学
量子力学
工程类
作者
Grayson Deysher,Phillip Ridley,So‐Yeon Ham,Jean‐Marie Doux,Yu‐Ting Chen,Erik A. Wu,Darren H. S. Tan,Ashley Cronk,Jihyun Jang,Ying Shirley Meng
标识
DOI:10.1016/j.mtphys.2022.100679
摘要
All-solid-state batteries (ASSBs) have been promoted as a highly promising energy storage technology due to the prospects of improved safety and a wider operating temperature range compared to their conventional liquid electrolyte-based counterparts. While solid electrolytes with ionic conductivities comparable to liquid electrolytes have been discovered, fabricating solid-state full cells with high areal capacities that can cycle at reasonable current densities remains a principal challenge. To overcome these challenges, a quantitative and in-depth understanding of the phenomena governing ionic and electronic transport limitations within the cathode composite, in addition to mechanical aspects arising from significant volume changes associated with Li metal anodes (including anode-less cell designs) are needed. Such understanding can be obtained from proper electrochemical measurements described herein. In this review we seek to highlight solutions to these existing challenges and several directions for future work are proposed.
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