材料科学
锂(药物)
氧化还原
离子
光谱学
比例(比率)
纳米技术
分析化学(期刊)
环境化学
冶金
化学
有机化学
医学
物理
量子力学
内分泌学
作者
Abiram Krishnan,Dong‐Chan Lee,Ian Slagle,Sumaiyatul Ahsan,Samantha Mitra,Ethan Read,Faisal M. Alamgir
标识
DOI:10.1021/acsami.3c18424
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]O2 (NMC111), Li[Ni0.8Co0.1Mn0.1]O2 (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.
科研通智能强力驱动
Strongly Powered by AbleSci AI