Tracking the Diffusion-Controlled Lithiation Reaction of LiMn2O4 by In Situ TEM

被引:32
作者
Erichsen, Torben [1 ]
Pfeiffer, Bjorn [1 ]
Roddatis, Vladimir [1 ]
Volkert, Cynthia A. [1 ,2 ]
机构
[1] Univ Gottingen, Inst Mat Phys, D-37077 Gottingen, Germany
[2] Univ Gottingen, Int Ctr Adv Studies Energy Convers ICASEC, D-37077 Gottingen, Germany
关键词
lithium manganese oxide spinel; tetragonal Li2Mn2O4; EELS; twinning; defects; interface; lithiation; TRANSMISSION ELECTRON-MICROSCOPY; LITHIUM MANGANESE OXIDE; TRANSITION-METAL OXIDES; PHASE-TRANSFORMATIONS; SPINEL ELECTRODES; ELECTROCHEMICAL LITHIATION; OXIDATION-STATE; CRYSTAL; INSERTION; FRACTURE;
D O I
10.1021/acsaem.0c00380
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
Spinel lithium manganese oxide (LixMn2O4) is used as an active material in battery cathodes. It is a relatively inexpensive and environmentally friendly material but suffers from capacity fade during use. The capacity losses are generally attributed to the formation of the tetragonal phase (x > 1) due to overpotentials at the surfaces of the micrometer-sized particles that are used in commercial electrodes. In this study, we investigate the mechanisms of tetragonal phase formation by performing electrochemical lithiation (discharging) in situ in the transmission electron microscope (TEM) utilizing diffraction and high resolution imaging as well as spectroscopy. We observe a sharp interface between the cubic spinel (x = 1) and the tetragonal phase (x = 2) that moves under lithium diffusion control. The tetragonal phase forms as a complex nanotwinned microstructure, presumably to relieve the stresses due to expansion during lithiation. We propose that the twinned microstructure stabilizes the tetragonal phase, adding to capacity loss upon deep discharge.
引用
收藏
页码:5405 / 5414
页数:10
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