Improving cycle life of layered lithium transition metal oxide (LiMO2) based positive electrodes for Li ion batteries by smart selection of the electrochemical charge conditions

被引:67
作者
Kasnatscheew, Johannes [1 ,2 ]
Evertz, Marco [2 ]
Streipert, Benjamin [2 ]
Wagner, Ralf [2 ]
Nowak, Sascha [2 ]
Laskovic, Isidora Cekic [1 ,2 ]
Winter, Martin [1 ,2 ]
机构
[1] Forschungszentrum Julich, IEK 12, Helmholtz Inst Munster HI MS, Corrensstr 46, D-48149 Munster, Germany
[2] Univ Munster, Inst Phys Chem, MEET Battery Res Ctr, Corrensstr 46, D-48149 Munster, Germany
关键词
Li ion batteries; Positive electrodes; Capacity fade characteristics; Cycle life; Formation cycles; Improvement strategies; PLANE SURFACE-AREA; ANODE PERFORMANCE; BASAL-PLANE;
D O I
10.1016/j.jpowsour.2017.05.092
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
Increasing the specific energy of a lithium ion battery and maintaining its cycle life is a predominant goal and major challenge for electrochemical energy storage applications. Focusing on the positive electrode as the specific energy bottleneck, cycle life characteristics of promising layered oxide type active materials (LiMO2) has been thoroughly investigated. Comparing the variety of LiMO2 compositions, it could be shown that the "Ni-rich" (Ni >= 60% for M in LiMO2) electrodes expectably revealed best performance compromises between specific energy and cycle life at 20 degrees C, but only LiNi0.6Mn0.2Co0.2O2 (NMC622) could also maintain sufficient cycle performance at elevated temperatures. Focusing on NMC622, it could be demonstrated that the applied electrochemical conditions ( charge capacity, delithiation amount) in the formation cycles significantly influence the subsequent cycling performance. Moreover, the insignificant transition metal dissolution, demonstrated by means of total X-ray fluorescence (TXRF) technique, and unchanged lithiation degree in the discharged state, determined by the measurement of the Li+ content by means of the inductively coupled plasma optical emission spectroscopy (ICP-OES) technique, pointed to a delithiation (charge) hindrance capacity fade mechanism. Considering these insights, thoughtful modifications of the electrochemical charge conditions could significantly prolong the cycle life. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:458 / 467
页数:10
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