卤化物
分离器(采油)
硫化物
电解质
介电谱
材料科学
阴极
快离子导体
储能
化学工程
离子电导率
电导率
氧化物
电化学
化学
无机化学
冶金
电极
物理化学
功率(物理)
物理
量子力学
工程类
热力学
作者
Laura E. Goodwin,Maya Ziegler,Paul Till,Nazia S. Nazer,Philipp Adelhelm,Wolfgang G. Zeier,Felix H. Richter,Jürgen Janek
标识
DOI:10.1021/acsami.4c01652
摘要
Sodium all-solid-state batteries may become a novel storage technology overcoming the safety and energy density issues of (liquid-based) sodium ion batteries at low cost and good resource availability. However, compared to liquid electrolyte cells, contact issues and capacity losses due to interface reactions leading to high cell resistance are still a problem in solid-state batteries. In particular, sulfide-based electrolytes, which show very high ionic conductivity and good malleability, exhibit degradation reactions at the interface with electrode materials and carbon additives. A new group of solid electrolytes, i.e., sodium halides, shows wider potential windows and better stability at typical cathode potentials. A detailed investigation of the interface reactions of Na3SbS4 and Na2.4Er0.4Zr0.6Cl6 as catholytes in cathodes and their cycling performance in full cells is performed. X-ray spectroscopy, time-of-flight spectrometry, and impedance spectroscopy are used to study the interface of each catholyte with a transition metal oxide cathode active material. In addition, impedance measurements were used to study the separator electrolyte Na3SbS4 with the catholyte Na2.4Er0.4Zr0.6Cl6. In conclusion, cathodes with Na2.4Er0.4Zr0.6Cl6 show a higher stability at low C-rates, resulting in lower interfacial resistance and improved cycling performance.
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