Ni, Mo Co-doped Lithium Manganate with Significantly Enhanced Discharge Capacity and Cycling Stability

被引:38
作者
Chen, Meifeng
Chen, Peng
Yang, Fan
Song, Huiyu
Liao, Shijun [1 ]
机构
[1] S China Univ Technol, Sch Chem & Chem Engn, Key Lab Fuel Cell Technol Guangdong Prov, Guangzhou 510641, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Lithium manganate; solid-state; co-doping; lithium-ion batteries; cycling stability; IMPROVED ELECTROCHEMICAL PERFORMANCE; LIMN2O4 CATHODE MATERIALS; POLYMER PRECURSOR METHOD; LI(MMN11/6)O-4 M; ENERGY-STORAGE; ION BATTERIES; SPINEL; TEMPERATURE; OXIDE; LINIXMN2-XO4;
D O I
10.1016/j.electacta.2016.04.148
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Ni, Mo co-doped LiMn2O4 cathode materials for lithium-ion batteries were prepared using a high-temperature solid-state method. The materials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and electrochemical impedance spectroscopy. The original material's performance was significantly enhanced by co-doping. The sample with optimal composition, LiNi0.03Mo0.01Mn1.96O4, had a discharge capacity at 1C of 114 mAhg(-1), which was 8.6% higher than that of undoped LiMn2O4. Importantly, this doped material exhibited significantly improved stability: after 300 charge-discharge cycles at 1C, its capacity retention was 91.2%, whereas the capacity retention of the undoped LiMn2O4 was only 61.9% after 300 cycles. SEM images and XRD patterns showed no obvious morphological changes in the co-doped material after cycling, implying that it had high structural stability. We suggest that this material's significantly improved electrochemical performance was probably caused by reduced Mn3+ dissolution and decreased Li+ intercalation and de-intercalation resistances. (c) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:356 / 365
页数:10
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