Well-ordered spherical LiNixCo(1-2x)MnxO2 cathode materials synthesized from cobolt concentration-gradient precursors

被引:57
作者
Huang, Zhenlei [1 ]
Gao, Jian [1 ]
He, Xiangming [1 ]
Li, Jianjun [1 ]
Jiang, Changyin [1 ]
机构
[1] Tsinghua Univ, Inst Nucl & New Energy Technol, Beijing 100084, Peoples R China
关键词
Lithium-ion batteries; Cathode materials; NMC materials; Concentration-gradient; Ordered; LITHIUM-ION BATTERIES; ELECTROCHEMICAL PROPERTIES; LINI0.8CO0.2O2; LICOO2;
D O I
10.1016/j.jpowsour.2011.10.143
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Spherical NixCo(1-2x)Mnx(OH)(2) (x = 0.333, 0.4, 0.416, 0.45) precursors with Co concentration-gradient were prepared by co-precipitation from sulfate solutions using NaOH and NH4OH as precipitation and complexing agents. Then, well-ordered spherical LiNixCo(1-2x)MnxO2 was synthesized by sintering the mixture of as-prepared precursor and Li2CO3 at 950 degrees C for 16h in air. EDXS results indicated that the concentration of cobalt decreased gradually inside out of the spherical precursor particle, and it was uniform in spherical LiNixCo(1-2x)MnxO2, particle obtained by sintering with Li2CO3. According to Rietveld refinement of XRD patterns, the LiNixCo(1-2x)MnxO2 synthesized from Co gradient precursor showed lower degree of cation disorder than that prepared from conventional precursor. The well-ordered LiNixCo(1-2x)MnxO2 from Co gradient precursor delivered much better high-rate capability than conventional one. The decrease of cation disorder of LiNixCo(1-2x)MnxO2 is attributed to the cobalt-rich in core of the precursor particles. Both abundant Co3+ and Li+ can restrain cation mixing effectively. Since Li+ needs long time to reach core during calcining, cobalt-rich in core of the precursor particle is very important for restraining cation mixing. Concentration-gradient precursor is helpful to prepare well-ordered LiNixCo(1-2x)MnxO2 with good high-rate capability, and the total content of expensive and toxic cobalt does not need to be increased. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:284 / 290
页数:7
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