法拉第效率
电化学
兴奋剂
材料科学
阴极
电极
离子
六方晶系
化学工程
分析化学(期刊)
化学
光电子学
结晶学
物理化学
有机化学
色谱法
工程类
作者
Zuguang Yang,Xiao-Dong Guo,Wei Xiang,Weibo Hua,Jun Zhang,Fengrong He,Kai Wang,Yao Xiao,Ben-He Zhong
标识
DOI:10.1016/j.jallcom.2016.11.245
摘要
K-doped LiNi0.5Co0.2Mn0.3O2 is successfully synthesized by introducing larger K ions into the Li slabs of the layered material through a substitution of Li source method. Structural and morphological characterizations reveal that the substitution of K ions on the Li site could enlarge the Li layer spacing and decrease the degree of Li+/Ni2+ cation mixing in the hexagonal layered LiNi0.5Co0.2Mn0.3O2. Compared with the LiNi0.5Co0.2Mn0.3O2, the K-doped Li0.97K0.03Ni0.5Co0.2Mn0.3O2 electrode material demonstrates larger reversible discharge capacity (176.5 mAh g−1), higher initial coulombic efficiency (88.45%), and greatly improved rate capability (123.4 mAh g−1, 5 C). The Li0.97K0.03Ni0.5Co0.2Mn0.3O2 electrode also exhibits excellent cycle stability with capacity retention of 93.17% and 86.42% in cell tests at 25 °C and 55 °C after 100 cycles at 1 C. The improved electrochemical performances of Li0.97K0.03Ni0.5Co0.2Mn0.3O2 are attributed to the enlarged interlayer space of O–Li–O, the decreased degree of cation mixing and enhanced structural stability induced by the potassium substitution.
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