4.8 Article

Synchronous Tailoring Surface Structure and Chemical Composition of Li-Rich-Layered Oxide for High-Energy Lithium-Ion Batteries

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 28, 期 37, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201803392

关键词

electrochemical performance; Li-rich-layered oxide cathode materials; lithium-ion batteries; phase-gradient outer layers; poor nickel surfaces

资金

  1. National Natural Science Foundation of China [21703191]
  2. Project of Innovation Team of the Ministry of Education [IRT_17R90]
  3. Hunan Provincial Natural Scientific Foundation of China [2017JJ3297]
  4. China Postdoctoral Science Foundation [2015M570682]
  5. Hunan Provincial Education Office Foundation of China [16C1534]
  6. Scientific Research Fund of Xiangtan University [16XZX20, 15XZX21]
  7. Hunan Provincial excellent doctor degree dissertation [YB2016B025]

向作者/读者索取更多资源

Li-rich-layered oxide is considered to be one of the most promising cathode materials for high-energy lithium ion batteries. However, it suffers from poor rate capability, capacity loss, and voltage decay upon cycling that limits its utilization in practical applications. Surface properties of Li-rich-layered oxide play a critical role in the function of batteries. Herein, a novel and successful strategy for synchronous tailoring surface structure and chemical composition of Li-rich-layered oxide is proposed. Poor nickel content on the surface of carbonate precursor is initially prepared by a facile treatment of NH3 center dot H2O, which can retain at a certain low amount on the surface in the final lithiated Li-rich-layered oxide after a solid-phase reaction process. Moreover, a phase-gradient outer layer with layered-coexisting phase-spinel structure toward to the outside surface is self-induced and formed synchronously based on poor nickel surface of the precursor. Electrochemical tests reveal this unique surface enables excellent cycling stability, improved rate capability, and slight voltage decay of cathodes. The finding here sheds light on a universal principle both for masterly tailoring surface structure and chemical composition at the same time for improving electrochemical performance of electrode materials.

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