材料科学
无定形固体
溶解
电化学
同步加速器
化学能
钴
阴极
纳米技术
衍射
锂电池
镍
锂(药物)
锂钴氧化物
锰
电池(电)
千分尺
氧化物
过渡金属
化学工程
磷酸铁锂
化学过程
图像分辨率
X射线晶体学
金属
电铸
固溶体
分析化学(期刊)
化学
同步辐射
纳米颗粒
电极
化学成像
场电子发射
极化(电化学)
化学还原
相(物质)
高分辨率
作者
Chayene G. Anchieta,Barthélémy Lelotte,Hari Vignesh Ramasamy,Alexander Forster,Ali Coşkun,Mario El Kazzi,Darío Ferreira Sánchez
出处
期刊:Small methods
[Wiley]
日期:2025-12-19
卷期号:10 (3): e01793-e01793
标识
DOI:10.1002/smtd.202501793
摘要
ABSTRACT Understanding the dynamics of complex heterogeneous battery materials under realistic operation conditions with micrometer spatial and relevant temporal resolutions remains challenging. This work presents a synchrotron‐based operando chemical imaging methodology using microfocus X‐ray diffraction (µ‐XRD) scanning imaging. The approach is applied to an all‐solid‐state battery (ASSB) with high‐energy lithium‐rich nickel manganese cobalt layered oxide (Li‐rich NCM) as active cathode material, Li 3 YCl 6 as catholyte, amorphous Li 3 PS 4 separator layer, and metallic lithium as anode. Operando XRD mapping unveils the nature and location of phase transformations along one complete cycle. The ASSB is integrated in the multipurpose custom‐designed electrochemical cell, which allows optimal exit solid angle for XRD analysis, permitting the resolution of the local chemistry in time and space across a relatively large field of view. We observed the following phenomena: (i) heterogeneous lithiation and delithiation processes within tens of individual Li‐rich NCM particles, indicating intraparticle differential lithium diffusion, (ii) the reversible formation of YCl 2 (H 2 O) 6 Cl, attributed to water residues, and (iii) the irreversible dissolution of Li 2 S and formation of LiOH parasitic phases. (iii) This study opens new perspectives for broader applications in energy technologies, such as Na‐ion, Zinc–Air, Li‐air, Li‐ion, and Li‐S.
科研通智能强力驱动
Strongly Powered by AbleSci AI