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外延镁尖晶石薄膜的相位控制电化学活性

Phase-Controlled Electrochemical Activity of Epitaxial Mg-Spinel Thin Films.

作者信息

Feng Zhenxing, Chen Xiao, Qiao Liang, Lipson Albert L, Fister Timothy T, Zeng Li, Kim Chunjoong, Yi Tanghong, Sa Niya, Proffit Danielle L, Burrell Anthony K, Cabana Jordi, Ingram Brian J, Biegalski Michael D, Bedzyk Michael J, Fenter Paul

机构信息

Center for Nanophase Materials Science, Oak Ridge National Laboratory , Oak Ridge, Tennessee 37831, United States.

Department of Chemistry, University of Illinois at Chicago , Chicago, Illinois 60607, United States.

出版信息

ACS Appl Mater Interfaces. 2015 Dec 30;7(51):28438-43. doi: 10.1021/acsami.5b09346. Epub 2015 Dec 18.

Abstract

We report an approach to control the reversible electrochemical activity (i.e., extraction/insertion) of Mg(2+) in a cathode host through the use of phase-pure epitaxially stabilized thin film structures. The epitaxially stabilized MgMn2O4 (MMO) thin films in the distinct tetragonal and cubic phases are shown to exhibit dramatically different properties (in a nonaqueous electrolyte, Mg(TFSI)2 in propylene carbonate): tetragonal MMO shows negligible activity while the cubic MMO (normally found as polymorph at high temperature or high pressure) exhibits reversible Mg(2+) activity with associated changes in film structure and Mn oxidation state. These results demonstrate a novel strategy for identifying the factors that control multivalent cation mobility in next-generation battery materials.

摘要

我们报道了一种通过使用相纯外延稳定薄膜结构来控制阴极主体中Mg(2+)的可逆电化学活性(即提取/插入)的方法。结果表明,处于不同四方相和立方相的外延稳定MgMn2O4(MMO)薄膜表现出截然不同的性质(在非水电解质碳酸丙烯酯中的Mg(TFSI)2中):四方相MMO的活性可忽略不计,而立方相MMO(通常在高温或高压下以多晶型物形式存在)表现出可逆的Mg(2+)活性,并伴随着薄膜结构和Mn氧化态的相关变化。这些结果证明了一种用于识别控制下一代电池材料中多价阳离子迁移率的因素的新策略。

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