Ion‐Dipole Chemistry Drives Rapid Evolution of Li Ions Solvation Sheath in Low‐Temperature Li Batteries

Sluggish evolution of lithium ions’ solvation sheath induces large charge‐transfer barriers and high ion diffusion barriers through the passivation layer, resulting in undesirable lithium dendrite formation and capacity loss of lithium batteries, especially at low temperatures. Here, an ion‐dipole strategy by regulating the fluorination degree of solvating agents is proposed to accelerate the evolution of the Li+ solvation sheath. Ethylene carbonate (EC)‐based fluorinated derivatives, fluoroethylene carbonate (FEC) and di‐fluoro ethylene carbonate (DFEC) are used as the solvating agents for a high dielectric constant. As the increase of the fluorination degree from EC to FEC and DFEC, the Li+‐dipole interaction strength gradually decreases from 1.90 to 1.66 and 1.44 eV, respectively. Consequently, the DFEC‐based electrolyte displays six times faster ion desolvation rate than that of a non‐fluorinated EC‐based electrolyte at −20 °C. Furthermore, LiNi0.8Co0.1Mn0.1O2||lithium cells in a DFEC‐based electrolyte retain 91% original capacity after 300 cycles at 25 °C, and 51% room‐temperature capacity at −30 °C. By bridging the gap between the ion‐dipole interactions and the evolution of Li+ solvation sheath, this work provides a new technique toward rational design of electrolyte engineering for low‐temperature lithium batteries. An ion‐dipole strategy by regulating the fluorination degree of solvating agents is proposed to accelerate the evolution of the Li+ solvation sheath, which not only ensures a low Li+ desolvation barrier at the electrode/electrolyte interface during discharging/charging process, but also produces stable interfaces at cathode/anode interfaces and enables stable cycling of high‐voltage lithium metal batteries.