Structural transformation of Na2Mn2(SO4)3 alluaudite into orthorhombic Li2Mn2(SO4)3 induced after lithium intercalation

被引:2
|
作者
Marinova, D. [1 ]
Veselinov, K. [1 ]
Kalapsazova, M. [1 ]
Zhecheva, E. [1 ]
Stoyanova, R. [1 ]
机构
[1] Bulgarian Acad Sci, Inst Gen & Inorgan Chem, Acad G Bonchev,str,bld 11, Sofia 1113, Bulgaria
关键词
Na2Mn2(SO4)(3 )alluaudite; OrthorhombicLi(2)Mn(2)(SO4)(3); Lithium intercalation; Ionic liquid-based electrolytes; ELECTROCHEMICAL PROPERTIES; SODIUM INTERCALATION; SULFATE; INSERTION; PHASE; MN; FE; CO;
D O I
10.1016/j.matpr.2022.02.559
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Double sulfate salts of sodium and manganese, Na2Mn2(SO4)(3), with an alluaudite-type of structure has been shown to intercalate Li+ ions reversibly, but the mechanism is still unclear. This study aims to exam-ine the structure transformation of the alluaudite sodium manganese sulfate Na2Mn2(SO4)(3) after Li+ intercalation by means of ex-situ transmission electron microscopy. We demonstrate that lithium inter-calation into alluaudite Na2Mn2(SO4)(3) proceeds at a nano-scale and leads to a formation of orthorhombic phase Li2Mn2(SO4)(3). Although the alluaudite and orthorhombic structures possess common Mn2O10 enti-ties, they are completely different. Because of the nano-structure, in-situ generated phase Li2Mn2(SO4)(3) displays better capacity in comparison with the phase obtained before the electrochemical experiment. The orthorhombic Li2Mn2(SO4)(3) is obtained by freeze-drying method, followed by thermal treatment at 500 C. The revised electrochemical property shows that orthorhombic Li2Mn2(SO4)(3) is able to intercalate reversible at least 1 mol of Li only in the case when electrolyte based on ionic liquid is used. Copyright (C) 2022 Elsevier Ltd. All rights reserved.
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页码:1260 / 1264
页数:5
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