ABSTRACT Preparing electrolytes that simultaneously enable high oxidation stability, interfacial compatibility, and intrinsic safety remains a major challenge for high‐voltage lithium metal batteries (LMBs). Herein, we report a phosphorus‐containing multifunctional monomer, ethyl di(2‐(methacryloyloxy)ethyl) phosphate, which enables both LiNO 3 dissolution and in situ polymerization within a liquid electrolyte (LE) to form a flame‐retardant gel polymer electrolyte (GPE). The resulting GPE exhibits excellent ionic conductivity (3.19 × 10 −3 S cm −1 at 25°C), a wide electrochemical stability window (> 4.6 V), and superior flame retardancy. The LiNO 3 in GPE can promote the formation of Li 3 N and LiF in the solid electrolyte interphase (SEI) layer on the Li metal anode, facilitating Li + transport and promoting dense and smooth Li deposition. When applied in Li||LiNi 0.6 Co 0.2 Mn 0.2 O 2 and Li||LiNi 0.8 Co 0.1 Mn 0.1 O 2 cells, the GPE system delivers remarkable cycling stability with capacity retentions of 83.1% after 400 cycles and 91.5% after 200 cycles, respectively. Spectroscopic and structural analyses reveal that the polymer matrix in GPE stabilizes cathode–electrolyte interfaces, mitigates transition‐metal dissolution, and suppresses Li/Ni cation mixing. This work establishes a molecular‐level electrolyte design strategy that integrates LiNO 3 solvation, flame retardancy, and interfacial stabilization, offering a promising pathway toward safe, high‐voltage LMBs.
Ma et al. (Sat,) studied this question.