利用相间分层技术实现稳定的零钠过量固态电池

IF 42.9 Q1 ELECTROCHEMISTRY
Ruixiao Wang , Wuliang Feng , Xuan Yu , Qinhao Shi , Peiyao Wang , Yiming Liu , Jiujun Zhang , Yufeng Zhao
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引用次数: 0

摘要

零钠过量固态电池(ZSBs)有望克服钠离子电池能量密度低的缺点,但固态电解质与集流器之间的界面问题仍然是其实际应用的瓶颈。本文报道了一种通过MgF2修饰层与Na金属之间的转化反应实现人工界面自调节分层的方法。由于Al-Mg和Al-NaF之间的巨大吸附能差,亲钠的Mg集中在底部,是Na的亲核种子,而亲钠的NaF集中在顶部,为Na枝晶提供了高的热力学稳定性和副反应抑制。结果表明,以Na3V2(PO4)3为阴极构建的ZSBs具有254.4 Wh kg−1的能量密度(基于电极和电解质的总质量计算),350次循环后容量保持率为82.7%。本工作为实现高性能稳定的ZSBs提供了一条可行的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Stable zero-sodium-excess solid-state batteries enabled by interphase stratification

Stable zero-sodium-excess solid-state batteries enabled by interphase stratification
Zero-sodium-excess solid-state batteries (ZSBs) are promising to overcome the disadvantage of low energy density for Na-ion batteries, but the interfacial issues between the solid-state electrolytes and current collectors remain bottlenecks for their practical applications. Herein, we report a self-regulated stratification of the artificial interphase through the conversion reaction between MgF2 modification layer and Na metal. Ascribed to the huge adsorption energy difference between Al–Mg and Al–NaF, the sodiophilic Mg concentrated at the bottom side and served as the nucleophilic seed for Na, while sodiophobic NaF on the top side provided high thermodynamic stability for Na dendrite and side reaction suppressions. Consequently, the as constructed ZSBs with Na3V2(PO4)3 cathode exhibited prominent energy density of 254.4 ​Wh kg−1 (calculated based on the total mass of electrode and electrolyte) with a capacity retention of 82.7% over 350 cycles. This work paves a feasible way to achieve high performance and stable ZSBs.
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CiteScore
33.70
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