The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.
XPS on Li-Battery-Related Compounds: Analysis of Inorganic SEI Phases and a Methodology for Charge Correction
Open accessAbstract
Accurate identification of chemical phases associated with the electrode and solid–electrolyte interphase (SEI) is critical for understanding and controlling interfacial degradation mechanisms in lithium-containing battery systems. To study these critical battery materials and interfaces X-ray photoelectron spectroscopy (XPS) is a widely used technique that provides quantitative chemical insights. However, due to the fact that a majority of chemical phases relevant to battery interfaces are poor electronic conductors, phase identification that relies primarily on absolute XPS core-level binding-energies (BEs) can be problematic. Charging during XPS measurements leads to BE shifts that can be difficult to correct. These difficulties are often exacerbated by the coexistence of multiple Li-containing phases in the SEI with overlapping XPS core levels. To facilitate accurate phase identification of battery-relevant phases (and electronically insulating phases in general), we propose a straightforward approach for removing charging effects from XPS data sets. We apply this approach to XPS data sets acquired from six battery-relevant inorganic phases including lithium metal (Li 0 ), lithium oxide (Li 2 O), lithium peroxide (Li 2 O 2 ), lithium hydroxide (LiOH), lithium carbonate (Li 2 CO 3 ), and lithium nitride (Li 3 N). Specifically, we demonstrate that BE separations between core levels present in a particular phase (e.g., BE separation between the O 1s and Li 1s core levels in Li 2 O) provide an additional constraint that can significantly improve reliability of phase identification. For phases like Li 2 O 2 and LiOH where the Li-to-O ratios and BE separations are nearly identical, X-ray excited valence-band spectra can provide additional clues that facilitate accurate phase identification. To accurately identity the phases in this study, we show that in situ growth of Li 2 O on Li 0 provides a means for determining absolute core-level positions, where all charging effects can be accurately removed. Finally, as an exemplary case we apply the charge-correction methodology to XPS data acquired from a symmetric cell based on a Li 2 S–P 2 S 5 solid electrolyte. This analysis demonstrates that accurately accounting for XPS BE shifts as a function of current-bias conditions can provide a direct probe of ionic conductivities associated with battery materials.
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Cited by
Alleviation of Dendrite Formation on Zinc Anodes via Electrolyte Additives
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Metadata
- Authors
- Wood, K. N., & Teeter, G.
- Venue
- ACS Applied Energy Materials
- Publisher
- American Chemical Society (ACS)
- Published
- 2018-08-13
- Volume
- 1
- Issue
- 9
- Pages
- 4493-4504
- ISSN
- 2574-0962 (ISSN-L)
- OpenAlex
- W2885586866
- Cited by
- 676
- References
- 32
- FWCI
- 8.64
- Type
- journal article
- Language
- en
- Open access
- green
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