Reversible ion exchange and structural stability of garnet-type Nb-doped Li7La3Zr2O12 in water for applications in lithium batteries

被引:109
作者
Liu, Cai [1 ]
Rui, Kun [1 ]
Shen, Chen [1 ]
Badding, Michael E. [2 ]
Zhang, Gaoxiao [1 ]
Wen, Zhaoyin [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, CAS Key Lab Mat Energy Convers, Shanghai 200050, Peoples R China
[2] Corning Inc, Corning, NY 14831 USA
基金
中国国家自然科学基金;
关键词
Solid electrolyte; Garnet-type oxide; Structural stability; H+/Li+ ion exchange; TRANSPORT-PROPERTIES; CONDUCTIVITY; OXIDE; LI+; ELECTROLYTE; PEROVSKITE; PHASES; PROBE;
D O I
10.1016/j.jpowsour.2015.02.050
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
H+/Li+ ion exchange and structural stability of the high ionic conductivity Nb-doped Zr-garnet Li6.75La3Nb0.25Zr1.75O12 (LLNZO) are investigated in this study. Relationships between ion exchange and Li-population per unit cell, which are necessary to establish the practical framework of garnet electrolytes, are deduced for garnet oxides within ion-exchange process. H+/Li+ ion exchange of cubic LLNZO powder is performed continuously in distilled water and products with various exchange levels are obtained via this simple method. FTIR spectra show the evolution of H-O bonding through the ion-exchange process. A maximum of 74.8% exchange of Li+ by H+ was found, consistent with a preferential replacement of octahedrally coordinated Li. The cubic garnet phase is maintained throughout all levels of proton exchange observed. The formation of garnet-type solid solution of Li6.75-xHx-La3Nb0.25Zr1.75O12 is indicated by well-resolved lattice fringes as well as the linear evolution of crystal lattice parameters with the ion exchange level. The reverse ion exchange of H+ by Li+ is successfully achieved in Li+ containing aqueous solutions, demonstrating its high structural stability and good compatibility for promising applications in lithium batteries. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:286 / 293
页数:8
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