The solid electrolyte interphase (SEI) is considered to be the key to the performance of lithium metal batteries (LMBs). The analysis of the SEI and cathode electrolyte interphase (CEI) composition (especially F 1s spectra) by X-ray photoelectron spectroscopy (XPS) has become a consensus among researchers. However, the surface-sensitive XPS characterization is susceptible to LiF artifacts due to several factors, leading to the overexaggerated role of LiF in the analysis of the SEI and CEI. In this paper, we conduct a systematic study on the reasons for the LiF artifacts in the XPS characterization of LMBs. The decomposition of the SEI and CEI components under argon ion sputtering, the reaction between LiCO and LiPF in the electrolyte, influence of different sample pretreatments, the selection of the XPS measurement region, and the measurement time on the resulting spectra are investigated. The results indicate that the high content of LiF in the SEI and CEI may be attributed to the LiF artifacts, and the role of LiF in the SEI may be overexaggerated as a consequence. This work sounds an alarm about the potential misuse of argon ion sputtering and the lack of rigorous XPS characterization in SEI studies. This work also helps to set up standardized XPS characterization to provide a more accurate understanding of the role of SEI components.
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http://dx.doi.org/10.1021/acsami.4c17553 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Department of Physics, Jinan University, Guangzhou, Guangdong 510632, P. R. China.
The solid electrolyte interphase (SEI) is considered to be the key to the performance of lithium metal batteries (LMBs). The analysis of the SEI and cathode electrolyte interphase (CEI) composition (especially F 1s spectra) by X-ray photoelectron spectroscopy (XPS) has become a consensus among researchers. However, the surface-sensitive XPS characterization is susceptible to LiF artifacts due to several factors, leading to the overexaggerated role of LiF in the analysis of the SEI and CEI.
View Article and Find Full Text PDFSci Total Environ
September 2022
Key Laboratory of Environment Optics and Technology, Anhui Institute of Optics and Fine Mechanics, HFIPS, Chinese Academy of Sciences, Hefei, China.
Atmospheric oxidation is a driving force of complex air pollution, and accurate hydroxyl radical (OH) measurement is helpful in investigating the radical-cored photooxidation mechanism in the troposphere. A self-developed laser-induced fluorescence instrument by the Anhui Institute of Optics Fine Mechanics, Chinese Academy of Sciences (AIOFM-LIF), was able to measure OH concentration with high sensitivity and good time resolution, and a detection limit of 1.7 × 10 cm (1σ, 30 s).
View Article and Find Full Text PDFJ Phys Chem B
March 2022
Institute of Chemical Sciences, School of Engineering and Physical Sciences, Heriot-Watt University, Edinburgh EH14 4AS, U.K.
The gas-liquid interface of ionic liquids (ILs) is critically important in many applications, for example, in supported IL phase (SILP) catalysis. Methods to investigate the interfacial structure in these systems will allow their performance to be improved in a rational way. In this study, reactive-atom scattering (RAS), surface tension measurements, and molecular dynamics (MD) simulations were used to study the vacuum interface of mixtures of partially fluorinated and normal alkyl ILs.
View Article and Find Full Text PDFIn this Letter, we present a particle image/tracking velocimetry (PIV/PTV) technique for simultaneous velocity measurement of both fluid and particle phases, adopting newly developed optical phase discrimination methods and novel optical particles. Spherical acrylic (PMMA) particles of diameter ∼(100µ) were used as the particle phase, while fine : phosphors of diameter ∼(1µ) were used as the fluid tracer. Under Nd:YAG 355 nm laser excitation, both the laser-induced fluorescence (LIF) from PMMA and laser-induced phosphorescence (LIP) from : provided sufficiently strong signals for PIV imaging with two non-intensified cameras and were clearly separable for phase discrimination using spectral filters and temporal profiles.
View Article and Find Full Text PDFJ Chem Phys
April 2019
Department of Chemistry and Cherry Emerson Center for Scientific Computation, Emory University, Atlanta, Georgia 30322, USA.
We introduce two new approaches to compute near-degenerate electronic states based on the driven similarity renormalization group (DSRG) framework. The first approach is a unitary multi-state formalism based on the DSRG (MS-DSRG), whereby an effective Hamiltonian is built from a set of state-specific solutions. The second approach employs a dynamic weighting parameter to smoothly interpolate between the multi-state and the state-averaged DSRG schemes.
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