Slow sustained releasing LiNO3 from graphite electrode reservoir to regulate solvation structure and stabilize interface

The high de-solvation energy derived from the solvent-rich Li+ solvation sheath and the resultant porous organic-rich electrode/electrolyte interface has hindered the commercialization of low-concentration electrolytes (LCEs). Here, unlike the common method so far reported, we invent an approach of sustained releasing LiNO3 from the graphite (Gr) anode reservoir to optimize the solvation structure and form a stable interface in LCEs. The solubility limit can be overcome by introducing LiNO3 directly in the Gr slurry. Moreover, the stronger binding energy between NO3– and Li+ drives NO3– enter the Li+ solvation sheath, weakening the shielding effect of solvent on Li+, and surprisingly increasing the coordination of PF6- to Li+. Thermodynamically, the corresponding lowest unoccupied molecular orbital energy levels of anions decrease, reducing the de-solvation energy of Li+ and forming a Li3N&LiF-rich solid electrolyte interface (SEI). This inorganic-rich SEI demonstrates advantages of inhibiting the decomposition of solvent and facilitating the transmission of Li+. As a result, the cell with Gr anode containing 1 wt% LiNO3 exhibits superior cycle performance in LCE, almost no degradation within 200 cycles, even higher than that in conventional concentration electrolyte. More importantly, the continuous consumption of NO3– in turn promotes its sustained redissolution from the anode, constituting a virtuous circle of regulating solvation structure, stabilizing interface and improving battery performance. This work blazes a new trail to revive lithium salt additives with low solubility, and expands the design strategy and application prospect of LCEs by building the bridges between regulating the solvation structure and constructing favorable electrode/electrolyte interface.