Cathode materials with cross-stack structures for suppressing intergranular cracking and high-performance lithium-ion batteries

被引:12
作者
Chen, Xianglei [1 ]
Li, De [1 ]
Mo, Yan [1 ]
Jia, Xiaobo [1 ]
Jia, Jianfeng [1 ]
Yao, Chao [1 ]
Chen, Daming [1 ]
Chen, Yong [1 ,2 ]
机构
[1] Hainan Univ, Coll Mat & Chem Engn, Hainan Prov Key Lab Res Utilizat Si Zr Ti Resourc, State Key Lab Marine Resource Utilizat South Chin, 58 Renmin Rd, Haikou 570228, Hainan, Peoples R China
[2] Nankai Univ, Minist Educ, Key Lab Adv Energy Mat Chem, Tianjin 300071, Peoples R China
基金
对外科技合作项目(国际科技项目);
关键词
Lithium ion batteries; Concentration-gradient; Cathodes materials; Growth mechanisms; Intergranular cracks; LAYERED OXIDE CATHODES; CONCENTRATION-GRADIENT; HIGH-ENERGY; CORE-SHELL; LONG-LIFE; LINI1/3CO1/3MN1/3O2; ORIGIN;
D O I
10.1016/j.electacta.2017.12.176
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Full concentration-gradient Li[Ni0.6Co0.2Mn0.2] O-2 (FCG622) layered oxide cathodes, consisting of Ni-rich cores and concentration-gradient shells, were synthesized by heterogeneous co-precipitation method. The cross-stack structure of FCG622 appeared different from the polycrystalline aggregates of homogeneous Li[Ni0.6Co0.2Mn0.2]O-2 (H622). The FCG622 showed structural stability and excellent electrochemical performances when compared to H622. The cathode based on this material showed superior rate capability and high voltage performance. The results of charge and discharge testing illustrated that FCG622 could suppress the intergranular cracks delivering initial discharge capacity of 185.2 mAh g(-1) at 1C in the voltage window of 2.8-4.4 V. The corresponding capacity retention after 300 cycles was estimated to 81.1% at 4.4 V. By comparison, the initial discharge capacity of H622 was estimated to only 170.6 mAh g(-1) under the same conditions, with capacity retention of 68.5%. These results suggested that FCG622 had stable morphology, high capacity and superior voltage stability when compared to polycrystalline aggregates. (c) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:513 / 520
页数:8
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