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构建具有改善的化学机械稳定性的匹配阴阳极界面用于高能电池。

Constructing Matching Cathode-Anode Interphases with Improved Chemo-mechanical Stability for High-Energy Batteries.

作者信息

Chen Shiming, Zheng Guorui, Yao Xiangming, Xiao Jinlin, Zhao Wenguang, Li Ke, Fang Jianjun, Jiang Zhuonan, Huang Yuxiang, Ji Yuchen, Yang Kai, Yin Zu-Wei, Zhang Meng, Pan Feng, Yang Luyi

机构信息

School of Advanced Materials, Peking University Shenzhen Graduate School, Shenzhen 518055, People's Republic of China.

Institute of Materials Research (IMR), Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, People's Republic of China.

出版信息

ACS Nano. 2024 Feb 27;18(8):6600-6611. doi: 10.1021/acsnano.3c12823. Epub 2024 Feb 14.

DOI:10.1021/acsnano.3c12823
PMID:38353590
Abstract

Coupling Ni-rich layered oxide cathodes with Si-based anodes is one of the most promising strategies to realize high-energy-density Li-ion batteries. However, unstable interfaces on both cathode and anode sides cause continuous parasitic reactions, resulting in structural degradation and capacity fading of full cells. Herein, lithium tetrafluoro(oxalato) phosphate is synthesized and applied as a multifunctional electrolyte additive to mitigate irreversible volume swing of the SiO anode and suppress undesirable interfacial evolution of the LiNiCoMnO (NCM) cathode simultaneously, resulting in improved cycle life. Benefiting from its desirable redox thermodynamics and kinetics, the molecularly tailored additive facilitates matching interphases consisting of LiF, LiPO, and P-containing macromolecular polymer on both the NCM cathode and SiO anode, respectively, modulating interfacial chemo-mechanical stability as well as charge transfer kinetics. More encouragingly, the proposed strategy enables 4.4 V 21700 cylindrical batteries (5 Ah) with excellent cycling stability (92.9% capacity retention after 300 cycles) under practical conditions. The key finding points out a fresh perspective on interfacial optimization for high-energy-density battery systems.

摘要

将富镍层状氧化物阴极与硅基阳极耦合是实现高能量密度锂离子电池最具前景的策略之一。然而,阴极和阳极两侧不稳定的界面会引发持续的寄生反应,导致全电池的结构退化和容量衰减。在此,合成了四氟(草酸根)磷酸锂并将其用作多功能电解质添加剂,以减轻SiO阳极不可逆的体积变化,并同时抑制LiNiCoMnO(NCM)阴极不良的界面演变,从而延长循环寿命。得益于其理想的氧化还原热力学和动力学,这种经过分子定制的添加剂分别促进了在NCM阴极和SiO阳极上由LiF、LiPO和含P大分子聚合物组成的匹配界面相的形成,调节了界面化学机械稳定性以及电荷转移动力学。更令人鼓舞的是,所提出的策略使4.4 V 21700圆柱形电池(5 Ah)在实际条件下具有出色的循环稳定性(300次循环后容量保持率为92.9%)。这一关键发现为高能量密度电池系统的界面优化指出了一个全新的视角。

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