材料科学
阴极
氧化物
纳米技术
化学工程
复合材料
冶金
物理化学
工程类
化学
作者
Yilong Chen,Minye Yang,Yuanlong Zhu,Jianhua Yin,Li Li,Jiyuan Xue,Baodan Zhang,Haiyan Luo,Kang Zhang,Zixin Wu,Yuan Tian,Juping Xu,Wen Yin,Qingsong Wang,Niu Liu,Yang Sun,Maolin Yang,Yongfu Qiu,Xin Sun,Yu Qiao
标识
DOI:10.1002/adma.202509827
摘要
Abstract To improve the energy density of Li‐ion batteries, conventional sacrificial prelithiation agents (Li 5 FeO 4 , Li 2 O and Li 2 CO 3 , etc.) are introduced to compensate for active lithium loss, but they undergo serious volumetric shrinkage during decomposition, generating voids that compromise electrode architecture integrity and deteriorate electrochemical performance. Herein, the typical Li‐rich layered oxide cathode is converted into Li‐rich disordered rocksalt oxide (LRDO) prelithiation agent, achieving 330 mAh g −1 charge capacity and retaining 130 mAh g −1 reversible capacity (contributing 200 mAh g −1 irreversible prelithiation capacity). Compared with the layered structure, the cation‐disordered structure in LRDO tunes the local oxygen environment, completely activating oxygen‐related anionic oxidation activity at lower potential (<4.5 V). Moreover, coupled with a fluorinated electrolyte additive, the nucleophilic oxygen species released during de‐lithiation of LRDO are synergistically utilized, constructing a gradient cathode‐electrolyte interphase architecture with enhanced interfacial stability during the cell formation process. Most importantly, the phase‐transition‐free nature of LRDO during prelithiation completely eradicates volume shrinkage, effectively preventing electrode architecture degradation. Furthermore, a long‐life graphite||LiFePO 4 pouch cell with high discharge capacity of 150.02 mAh (7.59% higher than without prelithiation) are achieved, maintaining 91.33% capacity after 1800 cycles.
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