Yuhang Lou, Zedong Lin, Jialong Shen, Junpeng Sun, Nan Wang, Zhihao Chen, Rong Huang, Xianhong Rui, Xiaojun Wu, Hai Yang, Yan Yu
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Herein, an innovative “all-in-one” modification strategy is developed, simultaneously regulating the surface, interface, and bulk via an in-situ gas–solid interface phosphating reaction to create P-doped Li<sub>1.2</sub>Mn<sub>0.54</sub>Ni<sub>0.13</sub>Co<sub>0.13</sub>O<sub>2</sub>@Spinel@Li<sub>3</sub>PO<sub>4</sub>. Specifically, Li<sub>3</sub>PO<sub>4</sub> surface coating layer shields particles from electrolyte corrosion and enhances Li<sup>+</sup> diffusion; in-situ constructed spinel interfacial layer reduces phase distortion and suppresses the lattice strain; the strong P─O bond derived from P-doping stabilizes the lattice oxygen frame and inhibits the release of O<sub>2</sub>, thereby improving the reversibility of oxygen redox reaction. As a result, the phosphatized LRMO demonstrates an exceptional capacity retention of 82.1% at 1C after 300 cycles (compared to 50.8% for LRMO), an outstanding rate capability of 170.5 mAh g<sup>−1</sup> at 5C (vs 98.9 mAh g<sup>−1</sup> for LRMO), along with excellent voltage maintenance and thermostability. 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引用次数: 0
摘要
富锂锰基层状氧化物(LRMOs)被认为是克服高能量密度瓶颈的主要正极材料。然而,它们面临着巨大的挑战,包括电压衰减、循环稳定性差、速率性能差,主要是由于不可逆的氧释放、过渡金属溶解和缓慢的运输动力学。此外,传统的单一修改策略不能充分解决这些问题。本文开发了一种创新的“一体化”改性策略,通过原位气固界面磷化反应同时调节表面、界面和体积,以制备p掺杂Li1.2Mn0.54Ni0.13Co0.13O2@Spinel@Li3PO4。具体来说,Li3PO4表面涂层保护颗粒免受电解质腐蚀,增强Li+扩散;原位构建尖晶石界面层减少了相畸变,抑制了晶格应变;P掺杂形成的强P─O键稳定了晶格氧框架,抑制了O2的释放,从而提高了氧氧化还原反应的可逆性。结果,经过300次循环后,磷酸化的LRMO在1C下的容量保持率为82.1%(相比之下,LRMO为50.8%),在5C下具有170.5 mAh g - 1的出色倍率容量(相比之下,LRMO为98.9 mAh g - 1),以及出色的电压维护和热稳定性。显然,这种“一体化”的改进策略为高能量密度锂离子电池提供了一种新方法。
Simultaneous Regulating the Surface, Interface, and Bulk via Phosphating Modification for High-Performance Li-Rich Layered Oxides Cathodes
Li-rich Mn-based layered oxides (LRMOs) are regarded as the leading cathode materials to overcome the bottleneck of higher energy density. Nevertheless, they encounter significant challenges, including voltage decay, poor cycle stability, and inferior rate performance, primarily due to irreversible oxygen release, transition metal dissolution, and sluggish transport kinetics. Moreover, traditionally single modification strategies do not adequately address these issues. Herein, an innovative “all-in-one” modification strategy is developed, simultaneously regulating the surface, interface, and bulk via an in-situ gas–solid interface phosphating reaction to create P-doped Li1.2Mn0.54Ni0.13Co0.13O2@Spinel@Li3PO4. Specifically, Li3PO4 surface coating layer shields particles from electrolyte corrosion and enhances Li+ diffusion; in-situ constructed spinel interfacial layer reduces phase distortion and suppresses the lattice strain; the strong P─O bond derived from P-doping stabilizes the lattice oxygen frame and inhibits the release of O2, thereby improving the reversibility of oxygen redox reaction. As a result, the phosphatized LRMO demonstrates an exceptional capacity retention of 82.1% at 1C after 300 cycles (compared to 50.8% for LRMO), an outstanding rate capability of 170.5 mAh g−1 at 5C (vs 98.9 mAh g−1 for LRMO), along with excellent voltage maintenance and thermostability. Clearly, this “all-in-one” modification strategy offers a novel approach for high-energy-density lithium-ion batteries.
期刊介绍:
Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.