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富镍层状微球阴极:锂/镍无序化与电化学性能

Nickel-rich layered microspheres cathodes: lithium/nickel disordering and electrochemical performance.

作者信息

Fu Chaochao, Li Guangshe, Luo Dong, Li Qi, Fan Jianming, Li Liping

机构信息

Key Lab of Optoelectronic Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, and ‡State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, University of Chinese Academy of Sciences , Fuzhou 350002, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2014 Sep 24;6(18):15822-31. doi: 10.1021/am5030726. Epub 2014 Sep 9.

Abstract

Nickel-rich layered metal oxide materials are prospective cathode materials for lithium ion batteries due to the relatively higher capacity and lower cost than LiCoO2. Nevertheless, the disordered arrangement of Li(+)/Ni(2+) in local regions of these materials and its impact on electrochemistry performance are not well understood, especially for LiNi(1-x-y)Co(x)Mn(y)O2 (1-x-y > 0.5) cathodes, which challenge one's ability in finding more superior cathode materials for advanced lithium-ion batteries. In this work, Ni-Co-Mn-based spherical precursors were first obtained by a solvothermal method through handily utilizing the redox reaction of nitrate and ethanol. Subsequent sintering of the precursors with given amount of lithium source (Li-excess of 5, 10, and 15 mol %) yields LiNi0.7Co0.15Mn0.15O2 microspheres with different extents of Li(+)/Ni(2+) disordering. With the determination of the amounts of Li(+) ions in transition metal layer and Ni(2+) ions in Li layer using structural refinement, the impact of Li(+)/Ni(2+) ions disordering on the crystal structure, valence state of nickel ions, and electrochemical performance were investigated in detailed. It is clearly demonstrated that with increasing the amount of lithium source, lattice parameters (a and c) and interslab space thickness of unit cell decrease, and more Li(+) ions incorporated into the 3a site of transition metal layer which leads to an increase of Ni(3+) content in LiNi0.7Co0.15Mn0.15O2 as confirmed by X-ray photoelectron spectroscopy and a redox titration. Moreover, the electrochemical performance for as-prepared LiNi0.7Co0.15Mn0.15O2 microspheres exhibited a trend of deterioration due to the changes of crystal structure from Li(+)/Ni(2+) mixing. The preparation method and the impacts of Li(+)/Ni(2+) ions disordering reported herein for the nickel-rich layered LiNi0.7Co0.15Mn0.15O2 microspheres may provide hints for obtaining a broad class of nickel-rich layered metal oxide microspheres with superior electrochemical performance.

摘要

富镍层状金属氧化物材料因其比LiCoO₂具有相对更高的容量和更低的成本,是锂离子电池很有前景的正极材料。然而,这些材料局部区域中Li(⁺)/Ni(²⁺)的无序排列及其对电化学性能的影响尚未得到充分理解,特别是对于LiNi(1 - x - y)Co(x)Mn(y)O₂(1 - x - y > 0.5)正极而言,这对寻找更优质的先进锂离子电池正极材料的能力构成了挑战。在这项工作中,首先通过溶剂热法巧妙利用硝酸盐和乙醇的氧化还原反应获得了Ni - Co - Mn基球形前驱体。随后将前驱体与给定数量的锂源(锂过量5、10和15 mol%)进行烧结,得到具有不同程度Li(⁺)/Ni(²⁺)无序的LiNi0.7Co0.15Mn0.15O₂微球。通过结构精修确定过渡金属层中Li(⁺)离子的数量和锂层中Ni(²⁺)离子的数量,详细研究了Li(⁺)/Ni(²⁺)离子无序对晶体结构、镍离子价态和电化学性能的影响。结果清楚地表明,随着锂源量的增加,晶格参数(a和c)和晶胞层间空间厚度减小,更多的Li(⁺)离子掺入过渡金属层的3a位点,这导致LiNi0.7Co0.15Mn0.15O₂中Ni(³⁺)含量增加,这通过X射线光电子能谱和氧化还原滴定得到证实。此外,由于Li(⁺)/Ni(²⁺)混合导致晶体结构变化,所制备的LiNi0.7Co0.15Mn0.15O₂微球的电化学性能呈现出恶化的趋势。本文报道的富镍层状LiNi0.7Co0.15Mn0.15O₂微球的制备方法以及Li(⁺)/Ni(²⁺)离子无序的影响,可能为获得具有优异电化学性能的一类广泛的富镍层状金属氧化物微球提供线索。

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