Unraveling transition metal dissolution of Li1.04Ni1/3Co1/3Mn1/3O2 (NCM 111) in lithium ion full cells by using the total reflection X-ray fluorescence technique

被引:172
作者
Evertz, Marco [1 ]
Horsthemke, Fabian [1 ]
Kasnatscheew, Johannes [1 ]
Boerner, Markus [1 ]
Winter, Martin [1 ]
Nowak, Sascha [1 ]
机构
[1] Univ Munster, Inst Phys Chem, MEET Battery Res Ctr, Corrensstr 46, D-48149 Munster, Germany
关键词
TXRF; NCM degradation; Lithium-ion battery; Transition metal dissolution; Sample pretreatment; SOLID-ELECTROLYTE-INTERPHASE; AGING MECHANISMS; MASS-SPECTROMETRY; CATHODE MATERIAL; GRAPHITE ANODES; LI BATTERIES; MANGANESE; DEGRADATION; PRODUCTS; PERFORMANCE;
D O I
10.1016/j.jpowsour.2016.08.099
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
In this work we investigated the transition metal dissolution of the layered cathode material Li1.04Ni1/ 3Co1/3Mn1/3O2 in dependence on the cycle number and cut-off cell voltage during charge by using the total reflection X-ray fluorescence technique for the elemental analysis of the specific lithium ion battery degradation products. We could show that with ongoing cycling transition metal dissolution from the cathode increased over time. However, it was less pronounced at 4.3 V compared to elevated charge cut-off voltages of 4.6 V. After a maximum of 100 cycles, we detected an overall transition metal loss of 0.2 wt parts per thousand in relation to the whole cathode active material for cells cycled to 4.3 V. At an increased charge cut-off voltage of 4.6 V, 4.5 wt parts per thousand transition metal loss in relation to the whole cathode active material could be detected. The corresponding transition metal dissolution induced capacity loss at the cathode could thus be attributed to 1.2 mAh g(-1). Compared to the overall capacity loss of 80 mAh g(-1) of the complete cell after 100 galvanostatic charge/discharge cycles the value is quite low. Hence, the overall full cell capacity fade cannot be assigned exclusively to the transition metal dissolution induced cathode fading. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:364 / 371
页数:8
相关论文
共 47 条
[1]   Evidence of Transition-Metal Accumulation on Aged Graphite Anodes by SIMS [J].
Abraham, D. P. ;
Spila, T. ;
Furczon, M. M. ;
Sammann, E. .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2008, 11 (12) :A226-A228
[2]   Lithium Ion Battery Anode Aging Mechanisms [J].
Agubra, Victor ;
Fergus, Jeffrey .
MATERIALS, 2013, 6 (04) :1310-1325
[3]   Main aging mechanisms in Li ion batteries [J].
Broussely, M ;
Biensan, P ;
Bonhomme, F ;
Blanchard, P ;
Herreyre, S ;
Nechev, K ;
Staniewicz, RJ .
JOURNAL OF POWER SOURCES, 2005, 146 (1-2) :90-96
[4]   Solvation of M3+ lanthanide cations in room-temperature ionic liquids.: A molecular dynamics investigation [J].
Chaumont, A ;
Wipff, G .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2003, 5 (16) :3481-3488
[5]   Effect of Manganese Contamination on the Solid-Electrolyte-Interphase Properties in Li-Ion Batteries [J].
Delacourt, C. ;
Kwong, A. ;
Liu, X. ;
Qiao, R. ;
Yang, W. L. ;
Lu, P. ;
Harris, S. J. ;
Srinivasan, V. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2013, 160 (08) :A1099-A1107
[6]   Development of a method for direct elemental analysis of lithium ion battery degradation products by means of total reflection X-ray fluorescence [J].
Evertz, Marco ;
Luerenbaum, Constantin ;
Vortmann, Britta ;
Winter, Martin ;
Nowak, Sascha .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 2015, 112 :34-39
[7]   Correlation Between Oxygen Vacancy, Microstrain, and Cation Distribution in Lithium-Excess Layered Oxides During the First Electrochemical Cycle [J].
Fell, Christopher R. ;
Qian, Danna ;
Carroll, Kyler J. ;
Chi, Miaofang ;
Jones, Jacob L. ;
Meng, Ying Shirley .
CHEMISTRY OF MATERIALS, 2013, 25 (09) :1621-1629
[8]  
Friesen A., 2015, ECS Transactions, V69, P89, DOI 10.1149/06918.0089ecst
[9]   Deciphering the multi-step degradation mechanisms of carbonate-based electrolyte in Li batteries [J].
Gachot, Gregory ;
Grugeon, Sylvie ;
Armand, Michel ;
Pilard, Serge ;
Guenot, Pierre ;
Tarascon, Jean-Marie ;
Laruelle, Stephane .
JOURNAL OF POWER SOURCES, 2008, 178 (01) :409-421
[10]   The influence of different conducting salts on the metal dissolution and capacity fading of NCM cathode material [J].
Gallus, Dennis Roman ;
Schmitz, Rene ;
Wagner, Ralf ;
Hoffmann, Bjoern ;
Nowak, Sascha ;
Cekic-Laskovic, Isidora ;
Schmitz, Raphael Wilhelm ;
Winter, Martin .
ELECTROCHIMICA ACTA, 2014, 134 :393-398