Synthesis of Li1.33Mn1.67O4 spinels with different morphologies and their ion adsorptivities after delithiation

被引:100
作者
Yang, XJ
Kanoh, H
Tang, WP
Ooi, K
机构
[1] Shikoku Natl Ind Res Inst, Takamatsu, Kagawa 7610395, Japan
[2] Res Inst Solvothermal Technol, Takamatsu, Kagawa 7610301, Japan
关键词
D O I
10.1039/b000219o
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
From different precursors, including gamma-, beta-MnO2, hollandite, and H+-form birnessite manganese oxides, well-crystallized Li1.33Mn1.67O4 spinels were synthesized at 400 degrees C by using LiNO3 as a flux. Alkali metal ion adsorptivities of the spinels after delithiation were investigated. SEM observation showed that each spinel obtained preserved the morphology of its precursor. The lack of morphology change, and the time-dependence of the lithium insertion into the precursors, illustrate that the formation of the spinel is a topotactic template reaction. None of the delithiated spinels preserved the original ion-exchange sites in their precursors but all showed nearly the same high affinity for Li+, while the amount of uniform acidic sites increased and the steric hindrance during lithiation decreased in the order of spinels obtained from birnessite, hollandite, and gamma-, beta-MnO2. This is probably because birnessite has more (buffer) space for the accommodation of ions in its layered structure than other precursors with a tunnel structure and some part of the space remains after structural transformation to the spinel.
引用
收藏
页码:1903 / 1909
页数:7
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