Quantitative lithium mapping of lithium-ion battery cathode using laser- induced breakdown spectroscopy

被引:31
|
作者
Imashuku, Susumu [1 ]
Taguchi, Hiroyuki [1 ]
Kawamata, Toru [2 ]
Fujieda, Shun [2 ]
Kashiwakura, Shunsuke [1 ]
Suzuki, Shigeru [2 ]
Wagatsuma, Kazuaki [1 ]
机构
[1] Tohoku Univ, Inst Mat Res, Aoba Ku, 2-1-1 Katahira, Sendai, Miyagi 9808577, Japan
[2] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, Aoba Ku, Sendai, Miyagi 9808577, Japan
关键词
Lithium distribution; Laser-induced breakdown spectroscopy; Cathode; Lithium fluoride; X-ray absorption spectroscopy; X-RAY-ABSORPTION; COMPOSITE ELECTRODE; STATE; NANOSCALE; LIFEPO4; LICOO2; CHARGE; VISUALIZATION; INTERCALATION; DEGRADATION;
D O I
10.1016/j.jpowsour.2018.07.088
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
A method to obtain the quantitative lithium distribution of a lithium-ion battery cathode using laser-induced breakdown spectroscopy (LIBS) measurements is proposed. We perform LIBS measurements in a reduced argon atmosphere of 1000 Pa and use a calibration curve obtained by measuring the emission intensities at 610.4 nm of standard samples, whose atomic ratios of lithium to cobalt are 0, 0.10, 0.30, 0.51, 0.62, 0.80, and 0.99. The lithium distributions of cycled cathodes, which contain LiCoO2 as an active material, obtained by this method are relatively consistent with the Co(III) distributions obtained by X-ray absorption spectroscopy (XAS). XAS is the conventional method to quantitatively display the reaction distribution of a cathode material used in a lithium-ion battery. Additionally, LIES can detect the precipitating decomposition products of the electrolyte, LiF, on the cathode. However, the precision of the lithium ratio using LIBS is not as good as that achieved for the Co(III) ratio obtained using XAS. Therefore, LIBS is suitable to obtain a semi-quantitative lithium distribution in a cathode of a lithium-ion battery through a much simpler procedure than XAS. Furthermore, LIBS has an advantage to detect the decomposition product of the electrolyte using laboratory-scale measurements.
引用
收藏
页码:186 / 191
页数:6
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