Construction of an inorganic sulfur- and fluorine-rich LiFe0.2Mn0.8PO4 cathode/electrolyte interface using electron-withdrawing anionic groups
摘要
LiTFSI, a lithium salt, has undergone extensive scrutiny in electrolyte research to enhance the performance of lithium-ion batteries, receiving widespread appreciation. In this study, we demonstrate how the use of LiTFSI as a salt-type additive effectively preserves the electrochemical properties of Li‖LiMn0.8Fe0.2PO4 in full cells. Herein, the CF3SO2− group within the TFSI−-anion demonstrates a significant electron absorption capacity which improves the dispersion of negative charges, reduces ion pairing, and enhances solubility. This characteristic enables the creation of a solid electrolyte interphase (SEI) abundant in inorganic nitrogen and sulfur on the electrode surface, thereby boosting the stability of the electrode/electrolyte interface and promoting efficient charge transfer at this boundary. The results illustrate that the addition of 0.5 wt% LiTFSI substantially improves the stability of the electrode/electrolyte interface in Li‖LiMn0.8Fe0.2PO4 batteries. Following 600 cycles, the specific capacity attains 107.1 mAh g−1 with a capacity retention of 86.02%, surpassing the base electrolyte’s retention of 61.24%. These results showcase outstanding electrochemical performance and exceptional cycling stability, confirming the potential of LiTFSI (lithium salts) as an electrolyte additive for upcoming high-energy density lithium batteries.