Study of C-coated LiFe0.33Mn0.67PO4 as positive electrode material for Li-ion batteries

被引:18
|
作者
Perea, A. [1 ]
Castro, L. [2 ]
Aldon, L. [1 ]
Stievano, L. [1 ]
Dedryvere, R. [2 ]
Gonbeau, D. [2 ]
Tran, N. [3 ]
Nuspl, G. [3 ]
Breger, J. [4 ]
Tessier, C. [4 ]
机构
[1] UMR 5253 CNRS UM2 ENSCM UM1 Agregats, Inst Charles Gerhardt Montpellier, F-34095 Montpellier 5, France
[2] Univ Pau, IPREM ECP, F-64053 Pau 9, France
[3] Sud Chem AG, D-85368 Moosburg, Germany
[4] SAFT, F-33074 Bordeaux, France
关键词
Lithium-ion batteries; Olivine; Manganese; XPS; Fe-57; Mossbauer; X-ray absorption spectroscopy; X-RAY-ABSORPTION; RECHARGEABLE LITHIUM BATTERIES; IN-SITU; PHOTOELECTRON-SPECTROSCOPY; CATHODE MATERIAL; MOSSBAUER; LIFEPO4; LIXFEPO4; OPERANDO; VALENCE;
D O I
10.1016/j.jssc.2012.04.016
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Commercial C-LiFe0.33Mn0.67PO4 positive electrode material has been investigated by Fe-57 Mossbauer Spectroscopy (MS), X-ray Photoelectron Spectroscopy (XPS) and X-ray Absorption Spectroscopy (XAS). The combined use of these experimental techniques provides a better understanding of the electro-chemical reaction involved during cycling. Fe-57 MS is very efficient to directly follow oxidation state of Fe in the electrode, and gives surprisingly indirect information on the oxidation state of Mn as observed by XAS and XPS. The electrochemical mechanism is proposed based from in situ and operando investigations using both MS and XAS, and is consistent with XPS surface studies. XPS analysis of the electrodes at the end of charge (4.4 V) reveals enhanced electrode/electrolyte interface reactivity at this high potential. Aging of C-LiFe0.33Mn0.67PO4/Li cells after 50 cycles at 60 degrees C indicates a rather good electrochemical behavior (low capacity fading) of the electrode material. Both Fe-57 MS and XPS (Mn 2p and Fe 2p) clearly show no modification on Fe and Mn oxidation state compared to fresh electrode confirming the good electrochemical performances. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:201 / 209
页数:9
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