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

Authors
Krishnan, AbiramLee, Dong-ChanSlagle, IanAhsan, SumaiyatulMitra, SamanthaRead, EthanAlamgir, Faisal M.
Issue Date
19-Mar-2024
Publisher
AMER CHEMICAL SOC
Keywords
X-ray absorption; X-ray emission; spin state; lithium-ion battery; operando
Citation
ACS APPLIED MATERIALS & INTERFACES, v.16, no.13, pp 16096 - 16105
Pages
10
Journal Title
ACS APPLIED MATERIALS & INTERFACES
Volume
16
Number
13
Start Page
16096
End Page
16105
URI
https://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/33036
DOI
10.1021/acsami.3c18424
ISSN
1944-8244
1944-8252
Abstract
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.
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