Thermal and Electrochemical Interface Compatibility of a Hydroborate Solid Electrolyte with 3 V-Class Cathodes for All-Solid-State Sodium Batteries

被引:8
作者
Asakura, Ryo [1 ,2 ]
Duchene, Leo [1 ]
Payandeh, Seyedhosein [1 ]
Rentsch, Daniel [3 ]
Hagemann, Hans [2 ]
Battaglia, Corsin [1 ]
Remhof, Arndt [1 ]
机构
[1] Empa, Swiss Fed Labs Mat Sci & Technol, Lab Mat Energy Convers, CH-8600 Dubendorf, Switzerland
[2] Univ Geneva, Dept Chim Phys, CH-1211 Geneva 4, Switzerland
[3] Empa, Swiss Fed Labs Mat Sci & Technol, Lab Funct Polymers, CH-8600 Dubendorf, Switzerland
基金
瑞士国家科学基金会;
关键词
all-solid-state battery; solid electrolyte; hydroborate; interface compatibility; thermal stability; ION BATTERIES; 3-DIMENSIONAL AROMATICITY; SUPERIONIC CONDUCTIVITY; NACRO2; CATHODE; STABILITY; LITHIUM; NA; DECOMPOSITION; ALPHA-NAFEO2; PERFORMANCE;
D O I
10.1021/acsami.1c15246
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Thermal stability of solid electrolytes and their compatibility with battery electrodes are key factors to ensure stable cycling and high operational safety of all-solid-state batteries. Here, we study the compatibility of a hydroborate solid electrolyte Na-4(B12H12)(B10H10) with 3 V-class cathode active materials: NaCrO2, NaMnO2, and NaFeO2. Among these layered sodium transition metal oxide cathodes, NaCrO2 shows the highest thermal compatibility in contact with the hydroborate solid electrolyte up to 525 degrees C in the discharged state. Furthermore, the electrolyte remains intact upon the internal thermal decomposition of the charged, that is, desodiated, cathode (Na0.5CrO2) above 250 degrees C, demonstrating the potential for highly safe hydroborate-based all-solid-state batteries with a wide operating temperature range. The experimentally determined onset temperatures of thermal decomposition of Na-4(B12H12)(B10H10) in contact with 3 V-class cathodes surpass those of sulfide and selenide solid electrolytes, exceeding previous thermodynamic calculations. Our results also highlight the need to identify relevant decomposition pathways of hydroborates to enable more valid theoretical predictions.
引用
收藏
页码:55308 / 55317
页数:10
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