Electrical conductivity and reaction with lithium of LiFe1-yMnyPO4 olivine-type cathode materials

被引:131
作者
Molenda, J. [1 ]
Qjczyk, W. [1 ]
Marzec, J. [1 ]
机构
[1] AGH Univ Sci & Technol, Fac Mat Sci & Ceram, PL-30059 Krakow, Poland
关键词
phospho-olivines; LiF1-yMnyPO4; intecalation; two-phase electrode reaction; cyclic voltammetry; EIS;
D O I
10.1016/j.jpowsour.2007.06.238
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
Structural, electrical and electrochemical properties of Mn-substituted phospho-olivines LiFe1-yMnyPO4 were investigated and compared to those of LiFePO4. Rietvield refined XRD patterns taken in the course of delithiation process showed apparent difference between phase compositions of these cathode materials upon lithium extraction. Contrary to the LiFePO4 and LiMnPO4 compositions for which a two-phase mechanism of electrochemical lithium extraction/insertion is observed, in case of Mn-substituted LiF1-yMnyPO4 samples a single-phase mechanism of deintercalation was observed in the studied range of lithium concentration. Electrochemical characterization of the cathode materials were performed in Li/Li+/LixFe1-yMnyPO4-type cells for y = 0.0, 0.25, 0.55, 0.75 and 1.0 compositions. Voltammery studies showed low reversibility of the lithium extraction process in the high-voltage "manganese" range, while in the "iron" range the reversibility of lithium extraction is high. Impedance measurements of the LiFe1-yMnyPO4 cathode materials, which enabled separation of the ionic and electronic components of their entire electrical conductivity, showed distinct influence of Mn content on the electronic part of conductivity. EIS measurements performed at different states of cell charge revealed that the charge-transfer impedance in LixFe1-yMnyPO4 is much lower than that of LixFePO4. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:689 / 694
页数:6
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