电化学
纳米晶材料
材料科学
阳离子聚合
氧化物
锰
阴极
氧化还原
化学
无机化学
化学工程
电极
冶金
纳米技术
物理化学
高分子化学
工程类
作者
Xiao Tan,Rui Li,Chao-Ming Xie,Qiang Shen
标识
DOI:10.1016/j.jpowsour.2017.11.004
摘要
Lithium-rich manganese(IV) oxide Li2MnO3 has hardly any activity as the cathode active substance of lithium-ion batteries (LIBs) but its reversible capacity can be greatly improved by introducing oxygen deficiencies. After the solid-state heat treatment of nanocrystalline Li2MnO3 by sodium borohydride (NaBH4), the resulting Li2MnO3-δ crystallites comparatively acquire distinguishable appearances in color and shape and slight differences in surface composition and lattice structure. As a LIB cathode within the potential range of 2.5–4.7 V, at 20 mA g−1 pristine Li2MnO3 gives the specific discharge capacities of 3.3, 5.0 and 7.4 mAh·g−1 in the 1st, 10th and 100th cycles, while the derivative Li2MnO3-δ delivers the relatively high values of 64.8, 103.8 and 140.2 mAh·g−1 in the 1st, 10th and 120th cycles, respectively. Aside from the similar phenomenon of gradual electrochemical activation, substituting Li2MnO3-δ for Li2MnO3 means the great enhancements of charge-transfer ability and electrochemical performances. Especially, the cationic-anionic redox mechanisms of Li2MnO3 and Li2MnO3-δ are similar to each other, suggesting a possible solution to prepare high-performance xLi2MnO3-δ·(1-x)LiMO2 solid solutions for application purposes.
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