Chlorine substitution improves interfacial kinetics and safety in lithium-ion batteries, indicating wider application potential.
The carbonate electrolyte such as ethylene carbonate and dimethyl carbonate is prestigious to stabilize the graphite anode and thus enable the unprecedented success of lithium-ion batteries but suffers from high flammability and slow ion-transport kinetics at low temperature. Here, we propose a chlorine atom substitution strategy to address the long-standing challenge of carbonate-based electrolyte. The Cl atom substitution with an electron-withdrawing effect can facilitate the interfacial reaction by weakening the interactions with Li+ and forming LiCl-involved solid electrolyte interphase, as well as terminate the chain reaction of combustion when releasing Cl radicals. At a conventional salt concentration (1 M), the Cl-substituted carbonate electrolyte achieves stable operation of the LiNi0.8Co0.1Mn0.1O2 (NCM811) cathode at a high cut-off voltage (4.6 V) and low-temperature adaption towards graphite (Gr) anode (91.9% capacity retention at −20°C). The Ah-level Gr/NCM811 pouch cell maintains 84.6% capacity retention over 300 cycles and can afford the rigorous nail penetration short-circuit test at a fully charged state. This work provides a promising approach to build cost-efficient electrolytes for safe and energy-dense lithium-ion batteries with wide-temperature application potentials.
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Yang et al. (2025) studied this question.
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