4.8 Article

Quantifying the apparent electron transfer number of electrolyte decomposition reactions in anode-free batteries

期刊

JOULE
卷 6, 期 9, 页码 2122-2137

出版社

CELL PRESS
DOI: 10.1016/j.joule.2022.07.003

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资金

  1. National Key R&D Program of China
  2. National Natural Science Foundation of China
  3. China Postdoctoral Science Foundation
  4. Tsinghua University Initiative Scientific Research Program
  5. Beijing Institute of Technology Research Fund Program for Young Scholars
  6. [2021YFB2500300]
  7. [2021YFB2400300]
  8. [22108149]
  9. [2021M691755]
  10. [2021M700404]

向作者/读者索取更多资源

Solid electrolyte interphase (SEI) is crucial for the stability of non-aqueous batteries. However, the quantitative understanding of electrolyte decomposition mechanism is limited. In this study, the apparent electron transfer number (ETN) is obtained as a quantitative descriptor in lithium metal batteries, providing insights into the decomposition mechanism of electrolyte components.
Solid electrolyte interphase (SEI) is pivotal in dictating the stability of anodes in non-aqueous batteries. However, electrolyte decom-position mechanism as an indispensable piece of the puzzle to construct a stable SEI is with few quantitative understandings. Here-in, as a quantitative descriptor, the apparent electron transfer num-ber (ETN) is acquired by a facile yet precise methodology in working lithium metal batteries with lithium bis(fluorosulfonyl)imide (LiFSI)-dimethyl carbonate (DMC)-based localized high-concentration electrolyte. Through accurate measurements of the electrolyte evolution and concurrently accumulated inactive Li by electrolyte quantitative nuclear magnetic resonance (ely-qNMR) and titration-qNMR, respectively, the decomposition rates of different electro-lyte components and ETNs that define the fate of electrolyte can all be acquired in a one-stopfashion. The recognition of ETNs (1.0 for DMC and 5.1 for LiFSI) provides pioneering insights into the electrolyte decomposition mechanism and affords new visions for electrolyte design to promote the continuous rise of non -aqueous rechargeable batteries.

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