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A multi-technique approach to understanding delithiation damage in LiCoO(2) thin films

We report on the delithiation of LiCoO(2) thin films using oxalic acid (C(2)H(2)O(4)) with the goal of understanding the structural degradation of an insertion oxide associated with Li chemical extraction. Using a multi-technique approach that includes synchrotron radiation X-ray diffraction, scanni...

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Detalles Bibliográficos
Autores principales: Salagre, E., Quílez, S., de Benito, R., Jaafar, M., van der Meulen, H. P., Vasco, E., Cid, R., Fuller, E. J., Talin, A. A., Segovia, P., Michel, E. G., Polop, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187655/
https://www.ncbi.nlm.nih.gov/pubmed/34103560
http://dx.doi.org/10.1038/s41598-021-91051-3
Descripción
Sumario:We report on the delithiation of LiCoO(2) thin films using oxalic acid (C(2)H(2)O(4)) with the goal of understanding the structural degradation of an insertion oxide associated with Li chemical extraction. Using a multi-technique approach that includes synchrotron radiation X-ray diffraction, scanning electron microscopy, micro Raman spectroscopy, photoelectron spectroscopy and conductive atomic force microscopy we reveal the balance between selective Li extraction and structural damage. We identify three different delithiation regimes, related to surface processes, bulk delithiation and damage generation. We find that only a fraction of the grains is affected by the delithiation process, which may create local inhomogeneities. However, the bulk delithiation regime is effective to delithiate the LCO film. All experimental evidence collected indicates that the delithiation process in this regime mimics the behavior of LCO upon electrochemical delithiation. We discard the formation of Co oxalate during the chemical extraction process. In conclusion, the chemical route to Li extraction provides additional opportunities to investigate delithiation while avoiding the complications associated with electrolyte breakdown and simplifying in-situ measurements.