材料科学
循环伏安法
共沉淀
介电谱
X射线光电子能谱
结晶度
电化学
阴极
煅烧
锂(药物)
化学工程
分析化学(期刊)
电极
复合材料
物理化学
有机化学
医学
化学
工程类
内分泌学
催化作用
作者
Chengjie Yin,Hongming Zhou,Zhaohui Yang,Jian Li
标识
DOI:10.1021/acsami.8b02553
摘要
A LiNi0.5Mn1.5O4 cathode material with high surface orientation was prepared via a complexing reaction coupled with the elevated-temperature solid-state method. First, a bimetal–organic framework containing Ni2+ and Mn2+ ions was synthesized via a self-assembly route using pyromellitic acid (PMA) as a dispersant and complexing agent. This step was followed by calcination with lithium acetate using PMA as a structure-directing agent. The resulting LiNi0.5Mn1.5O4 (M-LNMO) cathode material was investigated using X-ray diffraction, transmission and scanning electron microscopies, X-ray photoelectron spectroscopy, energy-dispersive X-ray spectroscopy, cyclic voltammetry, electrochemical impedance spectroscopy, and charge/discharge tests. For comparison, LiNi0.5Mn1.5O4 samples were prepared by coprecipitation and the solid-phase method under the same conditions. M-LNMO was highly crystalline with low impurity, uniform grain size, and a preferred orientation in the (111) and (110) planes. Owing to these advantages, the M-LNMO cathode material exhibited overwhelmingly high cyclic stability and rate capability and M-LNMO delivered a capacity of 145 mAh g–1 at a discharge rate of 0.1C and a discharge capacity retention of 86.6% at 5C after 1000 cycles. Even at an extremely high discharge rate (10C), the specific capacity was 112.7 mAh g–1, and 78.7% of its initial capacity was retained over 500 cycles. The superior electrochemical performance, particularly during a low-rate operation, was conferred by improved crystallinity and the crystal orientation of the particles.
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