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Enabling an Inorganic-Rich Interface via Cationic Surfactant for High-Performance Lithium Metal Batteries

  • Zejun Sun,
  • Jinlin Yang,
  • Hongfei Xu,
  • Chonglai Jiang,
  • Yuxiang Niu,
  • Xu Lian,
  • Yuan Liu,
  • Ruiqi Su,
  • Dayu Liu,
  • Yu Long,
  • Meng Wang,
  • Jingyu Mao,
  • Haotian Yang,
  • Baihua Cui,
  • Yukun Xiao,
  • Ganwen Chen,
  • Qi Zhang,
  • Zhenxiang Xing,
  • Jisheng Pan,
  • Gang Wu,
  • Wei Chen

摘要

An anion-rich electric double layer (EDL) region is favorable for fabricating an inorganic-rich solid–electrolyte interphase (SEI) towards stable lithium metal anode in ester electrolyte. Herein, cetyltrimethylammonium bromide (CTAB), a cationic surfactant, is adopted to draw more anions into EDL by ionic interactions that shield the repelling force on anions during lithium plating. In situ electrochemical surface-enhanced Raman spectroscopy results combined with molecular dynamics simulations validate the enrichment of NO3/FSI anions in the EDL region due to the positively charged CTA+. In-depth analysis of SEI structure by X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectrometry results confirmed the formation of the inorganic-rich SEI, which helps improve the kinetics of Li+ transfer, lower the charge transfer activation energy, and homogenize Li deposition. As a result, the Li||Li symmetric cell in the designed electrolyte displays a prolongated cycling time from 500 to 1300 h compared to that in the blank electrolyte at 0.5 mA cm−2 with a capacity of 1 mAh cm−2. Moreover, Li||LiFePO4 and Li||LiCoO2 with a high cathode mass loading of > 10 mg cm−2 can be stably cycled over 180 cycles.