PEO-based solid polymer electrolytes typically show limited capability for the suppression of Li metal dendrites, which is mainly attributed to their low mechanical strength. To tackle this issue, we improved the mechanical strength of a ternary solid polymer electrolyte (TSPE: PEO-LiTFSI-Pyr 14 TFSI) by integrating Celgard 2500 separator as a high modulus domain. The Celgard-reinforced TSPE (CgTSPE) presents a significantly higher elastic modulus (223 MPa) than TSPE (0.2 MPa) at 60°C, which in result leads to more lithium anode utilization. Specifically, the Columbic efficiency of Li electrodeposition/dissolution during cycling in Li|CgTSPE|Cu cells (≈90%) is distinctly higher than in Li|TSPE|Cu (≈30%). Furthermore, the cycling of Li||Li symmetric cells with CgTSPE displays an improved cycling stability, due to the presence of Celgard, in which high surface area lithium (HSAL), e.g., dendrite formation is suppressed. Operando electrochemical dilatometry (ECD) analysis as well as post mortem surface analysis with SEM reveal the formation of "dead lithium" and cavities under an areal capacity utilization of 5 mAh/cm 2 . It is also suggested by the cycling behavior of the Li||Li cell with high areal capacity utilization that lithium surface treatment is required to completely eliminate the formation of "dead lithium" and of cavities.
Li metal batteries (LMBs) containing cross‐linked polymer electrolytes (PEs) are auspicious candidates for next‐generation batteries. However, the wetting behavior of PEs on uneven Li metal surfaces has been neglected in most studies. Herein, it is shown that microscale defect sites with curved edges play an important role in a wettability‐dependent electrodeposition. The wettability and the viscoelastic properties of PEs are correlated, and the impact of wettability on the nucleation and diffusion near the Li|PE interface is distinguished. It is found that the curvature of the edges is a key factor for the investigation of wetting phenomena. The appearance of microscale defects and phase separation are identified as main causes for erratic nucleation. It is emphasized that the implementation of stable and consistent long‐term cycling performance of LMBs using PEs requires a deeper understanding of the “soft‐solid”–solid contact between PEs and inherently rough Li metal surfaces.
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