Colloid Electrolyte with Changed Li + Solvation Structure for High-Power, Low-Temperature Lithium-Ion Batteries.

Lithium-ion batteries (LIBs) currently suffer from low capacity and fast degradation under fast charging and/or low temperatures. Herein, we design a colloid liquid electrolyte (CLE) where a trace amount of lithium thiocarbonate (LTC) colloids in commercial carbonate electrolyte (1 M LiPF 6 in EC/DMC) not only boosts up σ Li+ but also improves the Li + transfer kinetics at LiNi 0.8 Co 0.15 Al 0.05 O 2 (NCA) cathode/electrolyte interface. The competitive coordination of LTCs with anions and solvents facilitates the dissociation of lithium salts and Li + decoupling, dramatically enhancing the σ Li+ (15 to 4.5 mS cm -1 at 30 and -20 °C, respectively); meanwhile, the desolvation process is accelerated. It demonstrates that LTC colloids induce ∼5 nm ultra-thin Li 2 CO 3 -rich cathode electrolyte interface (CEI), infuse the grain boundary of NCA particles, enhancing interfacial Li + transfer and inhibiting the particle cracks during cycling. Consequently, the Li||CLE||NCA battery delivers a maximum capacity of 135 mAh g -1 at a 10 C rate with 80% retention after 2000 cycles. Moreover, the fast-charging capability under a sub-zero environment is proved (122 mAh g -1 with 90% retention after 400 cycles at 2 C and -10 °C). Our strategy for tailoring the interfacial charge transfer appears generalizable and can practically be extended to the next-generation energy storage systems. This article is protected by copyright. All rights reserved.