钙钛矿(结构)
离子电导率
差示扫描量热法
电解质
氯化物
材料科学
电导率
离子键合
相(物质)
离子
电池(电)
无机化学
化学
分析化学(期刊)
结晶学
物理化学
电极
冶金
有机化学
物理
功率(物理)
热力学
量子力学
作者
Ryo Sakamoto,Nobuaki Shirai,Liwei Zhao,Atsushi Inoishi,Hikarí Sakaebe,Shigeto Okada
出处
期刊:Electrochemistry
[The Electrochemical Society of Japan]
日期:2023-06-07
卷期号:91 (7): 077003-077003
被引量:5
标识
DOI:10.5796/electrochemistry.23-00041
摘要
Perovskite-type CsSnCl3 is an attractive candidate for use as a solid electrolyte in all-solid-state chloride-ion batteries because it exhibits high ionic conductivity. However, perovskite-type CsSnCl3 is metastable at room temperature and easily undergoes a phase transition to a stable phase. Here, we prepared perovskite-type CsSn0.95Mn0.05Cl3, in which the Sn2+ in CsSnCl3 is partly substituted with Mn2+, via a mechanical milling method. Differential scanning calorimetry showed that the perovskite-type CsSn0.95Mn0.05Cl3 is stable to −15 °C. Moreover, it exhibits a high chloride ionic conductivity of 2.0 × 10−4 S cm−1 at 25 °C. We demonstrated the room-temperature operation of an all-solid-state chloride-ion battery with a BiCl3 cathode, an Sn anode, and CsSn0.95Mn0.05Cl3 as the electrolyte. The first discharge capacity of the all-solid-state cell at room temperature was 169 mAh g−1 based on the weight of BiCl3. X-ray diffraction and X-ray photoelectron spectroscopic analyses confirmed that the reaction mechanism of the cell is derived from the redox reaction of BiCl3 and Sn.
科研通智能强力驱动
Strongly Powered by AbleSci AI