4.8 Article

Dissecting the Solid Polymer Electrolyte-Electrode Interface in the of Electrochemical Limits

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 14, 期 25, 页码 28716-28728

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c02118

关键词

lithium-ion batteries; solid polymer electrolytes; electrochemical stability window; solid electrolyte interphase; cathode electrolyte interphase; electrochemical impedance spectroscopy; X-ray photoelectron spectroscopy

资金

  1. ERC [771777]
  2. STandUP for Energy
  3. European Research Council (ERC) [771777] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Proper understanding of the formation of solid polymer electrolyte electrode interfacial layer and its impact on cell performance is crucial for practical solid-state lithium-ion batteries. However, probing these solid-solid interfaces is challenging. This study combines electrochemistry and spectroscopic analysis to evaluate the electrochemical stability window of a polyester-based electrolyte and demonstrates the formation of resistive interphase layers at the electrode-electrolyte interface.
Proper understanding of solid polymer electrolyteelectrode interfacial layer formation and its implications on cell performance is a vital step toward realizing practical solid-state lithium-ion batteries. At the same time, probing these solid-solid interfaces is extremely challenging as they are buried within the electrochemical system, thereby efficiently evading exposure to surface-sensitive spectroscopic methods. Still, the probing of interfacial degradation layers is essential to render an accurate picture of the behavior of these materials in the vicinity of their electrochemical stability limits and to complement the incomplete picture gained from electrochemical assessments. In this work, we address this issue in conjunction with presenting a thorough evaluation of the electrochemical stability window of the solid polymer electrolyte poly(epsilon-caprolactone):lithium bis(trifluoromethanesulfonyl)imide (PCL:LiTFSI). According to staircase voltammetry, the electrochemical stability window of the polyester-based electrolyte was found to span from 1.5 to 4 V vs Li+/ Li. Subsequent decomposition of PCL:LiTFSI outside of the stability window led to a buildup of carbonaceous, lithium oxide and salt-derived species at the electrode-electrolyte interface, identified using postmortem spectroscopic analysis. These species formed highly resistive interphase layers, acting as major bottlenecks in the SPE system. Resistance and thickness values of these layers at different potentials were then estimated based on the impedance response between a lithium iron phosphate reference electrode and carbon-coated working electrodes. Importantly, it is only through the combination of electrochemistry and photoelectron spectroscopy that the full extent of the electrochemical performance at the limits of electrochemical stability can be reliably and accurately determined.

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