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Synthesis, electrochemistry and transition metal-doping of monoclinic Li4Ti5O12 and Na4Ti5O12
Solid State Ionics ( IF 3.2 ) Pub Date : 2020-06-07 , DOI: 10.1016/j.ssi.2020.115375
Pierre J.P. Naeyaert , Maxim Avdeev , Chris D. Ling

A new candidate Li-ion battery anode material, monoclinic M-Li4Ti5O12, has been prepared for the first time by ion-exchange from monoclinic M-Na4Ti5O12, and found to offer a stable electrochemical performance at rates of C/20 and 2C. The structural and electrochemical effects of transition metal M(III) doping of M-Na4Ti5O12 and Li4Ti5O12 have also been investigated. Doping was found to facilitate the synthesis of the M-Na4Ti5O12 type structure, eliminating the need for strongly reducing conditions; increase the Na-ion content; and improve the stability in atmospheric conditions. Neutron powder diffraction and ex situ X-ray powder diffraction data collected at various points during electrochemical cycling reveal that phase changes in Li4Ti5O12 proceed via a two-phase mechanism, in contrast to M-Na4Ti5O12 which proceeds via a solid-solution mechanism.



中文翻译:

单斜晶Li 4 Ti 5 O 12和Na 4 Ti 5 O 12的合成,电化学和过渡金属掺杂

一个新的候选锂离子电池的阳极材料,单斜晶M-栗4的Ti 5 ø 12,已经通过从单斜晶M-Na离子交换首次制备4的Ti 5 ø 12,并且发现其提供了一个稳定的电化学性能以C / 20和2C的速率。还研究了过渡金属M(III)掺杂M-Na 4 Ti 5 O 12和Li 4 Ti 5 O 12的结构和电化学效应。发现掺杂有助于M-Na 4 Ti 5 O 12的合成类型结构,无需大幅减少条件;增加钠离子含量;并提高了在大气条件下的稳定性。在电化学循环期间在不同点收集的中子衍射和易地X射线粉末衍射数据显示了李该相位的变化4的Ti 5 ö 12经由两相机制进行,而相比之下,M-的Na 4的Ti 5 ø 12,其通过固溶机制进行。

更新日期:2020-06-07
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