ArticleThe journal of physical chemistry. C, Nanomaterials and interfaces2022
Characterization of Electrochemical Processes in Metal-Organic Batteries by X-ray Raman Spectroscopy.
Article in The journal of physical chemistry. C, Nanomaterials and interfaces, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 11 citations in OpenAlex.
- Article
- Revitalizing Li-S batteries: the power of electrolyte additives.RSC advances · 2025Review
- LJournal of synchrotron radiation · 2024Article
- Organic Cathodes, a Path toward Future Sustainable Batteries: Mirage or Realistic Future?Chemistry of materials : a publication of the American Chemical Society · 2024Review
- TEXS: in-vacuum tender X-ray emission spectrometer with 11 Johansson crystal analyzers.Journal of synchrotron radiation · 2020Article
- Resonant inelastic X-ray scattering using a miniature dispersive Rowland refocusing spectrometer.Journal of synchrotron radiation · 2020Article
Corrections and comments
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Authors and funding
12 authors at 5 institutions in 3 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
X-ray Raman spectroscopy (XRS) is an emerging spectroscopic technique that utilizes inelastic scattering of hard X-rays to study X-ray absorption edges of low Z elements in bulk material. It was used to identify and quantify the amount of carbonyl bonds in a cathode sample, in order to track the redox reaction inside metal-organic batteries during the charge/discharge cycle. XRS was used to record the oxygen K-edge absorption spectra of organic polymer cathodes from different multivalent metal-organic batteries. The amount of carbonyl bond in each sample was determined by modeling the oxygen K-edge XRS spectra with the linear combination of two reference compounds that mimicked the fully charged and the fully discharged phases of the battery. To interpret experimental XRS spectra, theoretical calculations of oxygen K-edge absorption spectra based on density functional theory were performed. Overall, a good agreement between the amount of carbonyl bond present during different stages of battery cycle, calculated from linear combination of standards, and the amount obtained from electrochemical characterization based on measured capacity was achieved. The electrochemical mechanism in all studied batteries was confirmed to be a reduction of double carbonyl bond and the intermediate anion was identified with the help of theoretical calculations. X-ray Raman spectroscopy of the oxygen K-edge was shown to be a viable characterization technique for accurate tracking of the redox reaction inside metal-organic batteries.
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Registered trials
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