Robust and Adhesive Laminar Solid Electrolyte with Homogenous and Fast Li‐Ion Conduction for High‐Performance All‐Solid‐State Lithium Metal Battery

Abstract

Abstract Constructing composite solid electrolytes (CSEs) integrating the merits of inorganic and organic components is a promising approach to developing high‐performance all‐solid‐state lithium metal batteries (ASSLMBs). CSEs are now capable of achieving homogeneous and fast Li‐ion flux, but how to escape the trade‐off between mechanical modulus and adhesion is still a challenge. Herein, a strategy to address this issue is proposed, that is, intercalating highly conductive, homogeneous, and viscous‐fluid ionic conductors into robust coordination laminar framework to construct laminar solid electrolyte with homogeneous and fast Li‐ion conduction (LSE‐HFC). A 9 µm‐thick LSH‐HFC, in which poly(ethylene oxide)/succinonitrile is adsorbed by coordination laminar framework with metal–organic framework nanosheets as building blocks, is used here as an example to determine the validity. The Li‐ion transfer mechanism is verified and works across the entire LSE‐HFC, which facilitates homogeneous Li‐ion flux and low migration energy barriers, endowing LSE‐HFC with high ionic conductivity of 5.62 × 10−4 S cm−1 and Li‐ion transference number of 0.78 at 25 °C. Combining the outstanding mechanical strength against punctures and the enhanced adhesion force with electrodes, LSE‐HFC harvests uniform Li plating/stripping behavior. These enable the realization of high‐energy‐density ASSLMBs with excellent cycling stability when being assembled as LiFePO4/Li and LiNi0.6Mn0.2Co0.2O2/Li cells.

Keywords

• adhesion
• all‐solid‐state lithium metal batteries
• homogeneous and fast Li‐ion flux
• mechanical modulus
• thin laminar solid electrolytes