自来水
阴极
压实
螯合作用
草酸盐
多孔性
材料科学
金属氢氧化物
氢氧化物
化学工程
纳米技术
化学
分析化学(期刊)
无机化学
复合材料
物理化学
色谱法
工程类
环境工程
出处
期刊:Meeting abstracts
日期:2016-06-10
卷期号:MA2016-03 (2): 125-125
标识
DOI:10.1149/ma2016-03/2/125
摘要
A significant drawback for Li-rich layered materials is the low tap and compaction density in contrast to layered LiMO 2 [1]. Thus, improving tap density is an important issue for Li-rich layered materials. In our work, some efforts are contributed to addressing the issue. On one hand, a new pre-heat treatment procedure of carbonate precursors firstly using N 2 and then O 2 is adopted to separate processes of CO 2 emission and O 2 absorption, which presumably can reduce porosity of materials and then result in an improved tap density. The remarkably improved tap density of metal oxide (2.20 g cm –1 ) and cathode material (2.20 g cm –1 ) is observed with the procedure. However, it is at a cost of capacity. On the other hand, the dual chelating agents, ammonia and oxalate, which have a synergistic action on chelating transition-metal ion, are successfully introduced to prepare high tap density hydroxide precursors (1.67 g cm –3 ) and Li-rich cathode (2.28 g cm –3 ) with atomic level uniformity of elemental distribution. From Fig.1 (b) and (c), it is obviously found that the two-steps procedure is indeed beneficial for obtaining the dense morphology with less pores, resulting in a higher tap density. From Fig.2, with the function of the dual chelating agents, the spherical secondary particles with dense morphology, which are closely aggregated from nano-sized primary particles, are demonstrated to be obtained. References [1] P.Oh, S. Myeong, W. Cho, M.-J. Lee, M. Ko, H.Y. Jeong, J. Cho, Nano Lett. 14 (2014) 5965−5972. Figure 1
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