电解质
复合数
材料科学
电池(电)
铁电性
离子
固态
快离子导体
钠
钠离子电池
纳米技术
光电子学
复合材料
工程物理
电极
化学
工程类
物理
热力学
物理化学
冶金
电介质
法拉第效率
功率(物理)
有机化学
作者
Yumei Wang,Zhongting Wang,Xiaoyu Xu,Jin An Sam Oh,Jianguo Sun,Feng Zheng,Xiao Lu,Chaohe Xu,Binggong Yan,Guangsheng Huang,Li Lü
标识
DOI:10.1007/s40820-024-01474-6
摘要
Abstract Symmetric Na-ion cells using the NASICON-structured electrodes could simplify the manufacturing process, reduce the cost, facilitate the recycling post-process, and thus attractive in the field of large-scale stationary energy storage. However, the long-term cycling performance of such batteries is usually poor. This investigation reveals the unavoidable side reactions between the NASICON-type Na 3 V 2 (PO 4 ) 3 (NVP) anode and the commercial liquid electrolyte, leading to serious capacity fading in the symmetric NVP//NVP cells. To resolve this issue, an all-solid-state composite electrolyte is used to replace the liquid electrolyte so that to overcome the side reaction and achieve high anode/electrolyte interfacial stability. The ferroelectric engineering could further improve the interfacial ion conduction, effectively reducing the electrode/electrolyte interfacial resistances. The NVP//NVP cell using the ferroelectric-engineered composite electrolyte can achieve a capacity retention of 86.4% after 650 cycles. Furthermore, the electrolyte can also be used to match the Prussian-blue cathode Na x Fe y Fe(CN) 6− z ·nH 2 O (NFFCN). Outstanding long-term cycling stability has been obtained in the all-solid-state NVP//NFFCN cell over 9000 cycles at a current density of 500 mA g −1 , with a fading rate as low as 0.005% per cycle.
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