阳极
石墨
离子
电子
电荷(物理)
导电体
溶剂
材料科学
化学物理
化学
物理
复合材料
电极
有机化学
物理化学
核物理学
量子力学
作者
Min Niu,Liwei Dong,Junpei Yue,Yaqiang Li,Yueyao Dong,Shichao Cheng,Sheng Lv,Yuhui Zhu,Zuotao Lei,Jia‐Yan Liang,Sen Xin,Chunhui Yang,Yu‐Guo Guo
标识
DOI:10.1002/anie.202318663
摘要
Abstract Graphite has been serving as the key anode material of rechargeable Li‐ion batteries, yet is difficultly charged within a quarter hour while maintaining stable electrochemistry. In addition to a defective edge structure that prevents fast Li‐ion entry, the high‐rate performance of graphite could be hampered by co‐intercalation and parasitic reduction of solvent molecules at anode/electrolyte interface. Conventional surface modification by pitch‐derived carbon barely isolates the solvent and electrons, and usually lead to inadequate rate capability to meet practical fast‐charge requirements. Here we show that, by applying a MoO x −MoN x layer onto graphite surface, the interface allows fast Li‐ion diffusion yet blocks solvent access and electron leakage. By regulating interfacial mass and charge transfer, the modified graphite anode delivers a reversible capacity of 340.3 mAh g −1 after 4000 cycles at 6 C, showing promises in building 10‐min‐rechargeable batteries with a long operation life.
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