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Room-temperature-operating Na solid-state battery with complex hydride as electrolyte
被引:45
作者:
Murgia, Fabrizio
[1
]
Brighi, Matteo
[1
]
Cerny, Radovan
[1
]
机构:
[1] Univ Geneva, Dept Quantum Matter Phys, Lab Crystallog, Quai Ernest Ansermet 24, CH-1211 Geneva, Switzerland
基金:
瑞士国家科学基金会;
关键词:
Na solid-state battery;
Solid electrolyte;
Complex hydride;
Anion mixing;
In situ EIS;
SODIUM SUPERIONIC CONDUCTION;
LITHIUM;
STABILITY;
CHALLENGES;
ANODES;
D O I:
10.1016/j.elecom.2019.106534
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
All-solid-state sodium batteries are potentially game-changer devices in the transition towards a fossil-fuel-free society. They combine better sustainability, switching from lithium, to the largely available sodium with enhanced safety, replacing the flammable liquid electrolyte by a more thermally stable solid material. Nonetheless, several challenges plague the development of highly performing cells, such as the electrochemical stability of the solid electrolyte vs. both sodium and positive electrode, and the fragile interfacial contact between the components of the cell. On the basis of a Na+ conductor recently developed by our group, Na-4(CB11H12)(2)(B12H12), herein we report its superior performance as solid electrolyte in room-temperature-working batteries. This carbacloso-closohydroborate-based material shows stable Na plating/stripping with limited polarization. Galvanostatic tests in Na parallel to NaCrO2 cells exhibit good electrochemical performance, owing to a specific capacity around 100 mAh g(-1) up to a delivered current density of 24 mA g(-1). These findings represent a step further towards viable Na-based solid-state batteries operating safely while keeping elevate performance even at room temperature.
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