Lyotropic polymer liquid crystal coating; Enabling lamellar ion-conduction pathways for superior C-Rate performance in NCM523 cathodes

Marium, M.*; 青木 健太郎*; He, Y.*; 山本 勝宏*; Suwansoontorn, A.*; 生田 聖也*; 原 光生*; 永野 修作*; 長尾 祐樹*; 西川 慶*; 宮崎 司*; 青木 裕之  ; 小林 成*; 簾 智仁*; 一杉 太郎*; 是津 信行*

Marium, M.*; Aoki, Kentaro*; He, Y.*; Yamamoto, Katsuhiro*; Suwansoontorn, A.*; Ikuta, Seiya*; Hara, Mitsuo*; Nagano, Shusaku*; Nagao, Yuki*; Nishikawa, Kei*; Miyazaki, Tsukasa*; Aoki, Hiroyuki; Kobayashi, Shigeru*; Sudare, Tomohito*; Hitosugi, Taro*; Zettsu, Nobuyuki*

High C-rate capability and energy-density stability are crucial for advanced lithium-ion batteries (LIBs). However, these two characteristics typically conflict in conventional systems. Herein, a lyotropic polymer liquid crystal (LPLC)-based coating was applied to the surface of LiNiCoMnO (NCM523) cathode to construct a highly ion-conductive artificial cathode electrolyte interface (CEI) layer, aiming to supersede traditional CEIs for LIBs. The coating material, composed of an amphiphilic lithium-substituted alkyl-sulfonated polyimide (ASPI-Li) and an appropriate amount of organic liquid electrolyte, forms nanoscale ion conduction channels that act as an artificial CEI layer, providing enhanced local Li-ion activity at the NCM523 surface. The ion-conduction channels, regulated by the layered structure within the ASPI-Li coating layer, significantly accelerated ion-diffusion kinetics at the electrode/electrolyte interface, thereby delivering superior C-rate capability at ambient temperatures compared with conventional LIB systems. This work, guided by molecular design, provides insights into the development of next-generation artificial CEI layers for efficient and sustainable energy-storage systems.