Monitoring Redox Processes in Lithium-Ion Batteries by Laboratory-Scale Operando X-ray Emission Spectroscopy

被引:0
|
作者
Krishnan, Abiram [1 ]
Lee, Dong-Chan [1 ,2 ]
Slagle, Ian [1 ]
Ahsan, Sumaiyatul [1 ]
Mitra, Samantha [1 ,3 ]
Read, Ethan [1 ]
Alamgir, Faisal M. [1 ]
机构
[1] Georgia Inst Technol, Sch Mat Sci & Engn, Atlanta, GA 30332 USA
[2] Hongik Univ, Dept Chem Engn, 94 Wausan Ro, Seoul 04066, South Korea
[3] Georgia Inst Technol, Sch Mech Engn, Atlanta, GA 30332 USA
基金
美国国家科学基金会;
关键词
X-ray absorption; X-ray emission; spin state; lithium-ion battery; operando; METAL TRANSITION; SENSITIVE PROBE; PROTONATION; MECHANISM; LICOO2; OXYGEN;
D O I
10.1021/acsami.3c18424
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Tracking changes in the chemical state of transition metals in alkali-ion batteries is crucial to understanding the redox chemistry during operation. X-ray absorption spectroscopy (XAS) is often used to follow the chemistry through observed changes in the chemical state and local atomic structure as a function of the state-of-charge (SoC) in batteries. In this study, we utilize an operando X-ray emission spectroscopy (XES) method to observe changes in the chemical state of active elements in batteries during operation. Operando XES and XAS were compared by using a laboratory-scale setup for four different battery systems: LiCoO2 (LCO), Li[Ni1/3Co1/3Mn1/3]O-2 (NMC111), Li[Ni0.8Co0.1Mn0.1]O-2 (NMC811), and LiFePO4 (LFP) under a constant current charging the battery in 10 h (C/10 charge rate). We show that XES, despite narrower chemical shifts in comparison to XAS, allows us to fingerprint the battery SOC in real time. We further demonstrate that XES can be used to track the change in net spin of the probed atoms by analyzing changes in the emission peak shape. As a test case, the connection between net spin and the local chemical and structural environment was investigated by using XES and XAS in the case of electrochemically delithiated LCO in the range of 2-10% lithium removal.
引用
收藏
页码:16096 / 16105
页数:10
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