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Capacity degradation mechanism and improvement actions for 4 V-class all-solid-state lithium-metal polymer batteries

机译:4 V类全固态锂金属电池的容量降解机理及改进作用

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Owing to high safety and considerable energy density, rechargeable all-solid-state lithium-metal polymer batteries (ASSLPBs) with organic-inorganic composite solid-state electrolytes (CSSEs) have been recognized as one of the most promising battery systems. However, 4 V or above-class ASSLPBs still suffer serious capacity degradation arising from the complex interface issues between the electrode and electrolyte. Herein, for the first time, we find the oxidation decomposition of TFSI- anion and further interaction with PEO polymer matrix in the LiNi0.8Co0.1Mn0.1LiO2 (NCM811)/CSSEs (PEO-LiTFSI-LAGP)/Li cell, which cause continuous damage to the interfacial stability and persistent capacity degradation. Increasing the ratio of LAGP filler in CSSEs membrane and employing PEO-LiBOB electrolyte in composite cathode were demonstrated effective. As a consequence, the ASSLPBs show high reversibility, and high capacity retention up to 88% (3.0-4.2 V) and 78% (3.0-4.3 V) after 100 cycles with the charge/discharge current density of 30 mA g(-1) (35 degrees C). The understanding on capacity degradation mechanism, along with the positive improvement strategies validly boosts the development and promising application of 4 V-class ASSLPBs.
机译:由于具有高安全性和相当大的能量密度,具有有机 - 无机复合固态电解质(CSSES)的可充电全固态锂金属聚合物电池(ASSLPBS)被认为是最有前途的电池系统之一。然而,4 V或上面的ASSLPBS仍然遭受来自电极和电解质之间的复杂界面问题产生的严重容量劣化。在此,我们首次发现TFSi-阴离子的氧化分解和与LINI0.8CO0.1MN0.1LIO2(NCM811)/ CSSES(PEO-LITFSI-LAGP)/锂细胞的PEO聚合物基质的进一步相互作用,这导致对界面稳定性和持续产能降解的持续损坏。提高CSSES膜中LAGP填料的比例并在复合阴极中使用PEO-LiboB电解质进行了有效。因此,ASSLPBS在100次循环后显示出高可逆性,高容量潴留高达88%(3.0-4.2 v)和78%(3.0-4.3 v),电荷/放电电流密度为30 mA g(-1 )(35℃)。对能力退化机制的理解以及积极的改善策略有效地提高了4 V类AsslPBS的开发和有前途申请。

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