材料科学
阳极
锂(药物)
钛
纳米片
氧烷
介孔材料
离子
分析化学(期刊)
纳米技术
电极
物理化学
化学
冶金
物理
有机化学
催化作用
内分泌学
医学
量子力学
生物化学
色谱法
光谱学
作者
Hsien‐Chieh Chiu,Jigang Zhou,Lin Gu,Joel W. Reid,Xia Lu,Raynald Gauvin,Karim Zaghib,George P. Demopoulos
出处
期刊:Meeting abstracts
日期:2015-04-29
卷期号:MA2015-01 (2): 352-352
标识
DOI:10.1149/ma2015-01/2/352
摘要
Mesoporous Li deficient Li 4 Ti 5 O 12 nanosheets with major [110] preferred orientation were prepared by a novel low T (<100 °C) aqueous synthesis process. Surface relaxation due to nanosize effect in the near surface region and 10 % deficiency of lithium were found to lead to local chemical bond length extension that influences the electronic structure and Li storage capacity. Thus the lithiated material over the potential range from 1 to 2.5 V vs. Li/Li + reaches the following over-stoichiometrical composition: Li 7.92 Ti 5 O 12 . As determined by XANES the excess Li-ion storage is the result of preferential crystal orientation along the (110) and (111), facets. During lithiation, it was further determined the charge compensation to occur primarily by oxygen, rather than by titanium. Finally, both the oxygen and titanium in the near surface region exhibit different electronic structure from bulk. Those results point to the importance of surface reconstruction and relaxation in accommodating excess Li storage. As a consequence, the newly prepared Li 4 Ti 5 O 12 nanosheets exhibit superior Li-ion storage performance exceeding by far most of the alternatively prepared LTO anode materials.
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