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Cation-Anion Regulation Engineering in a Flame-Retardant Electrolyte toward Safe Na-Ion Batteries with Appealing Stability

  • Yi Hu Feng
  • , Chengye Lin
  • , Hanwen Qin
  • , Guang Xu Wei
  • , Chao Yang
  • , Yongwei Tang
  • , Xu Zhu
  • , Shuai Sun
  • , Tian Ling Chen
  • , Mengting Liu
  • , Hong Zheng
  • , Xiao Ji
  • , Ya You
  • , Peng Fei Wang
  • Xi'an Jiaotong University
  • Huazhong University of Science and Technology
  • Wuhan University of Technology

科研成果: 期刊稿件文章同行评审

39 引用 (Scopus)

摘要

Great electrochemical stability and intrinsic safety are of critical significance in realizing large-scale applications of Na-ion batteries (NIBs). Unfortunately, the notorious decomposition of the electrolyte and undesirable side reactions on the cathode-electrolyte interphase (CEI) pose major obstacles to the practical implementation of NIBs. Besides, the flammability of traditional carbonate-based electrolytes raises increasing safety concerns about the batteries. Herein, a flame-retardant all-fluorinated electrolyte is proposed to achieve an anion-aggregated inner solvation shell by modulating cation-anion interactions through a low-coordination number cosolvent. The more electrochemically antioxidant fluorinated solvents and anion-dominated interfacial chemistry contribute to the construction of both mechanically and chemically stable F-rich CEI. Such thin, homogeneous interphase effectively inhibits the parasitic reaction, strengthens the interfacial stability, and enables fast Na+ diffusion kinetics on the interface. When employing this electrolyte, the Na0.95Ni0.4Fe0.15Mn0.3Ti0.15O2 (NFMT) cathode delivers remarkable discharge capacity up to 169.7 mAh g-1, with stable cycling at 1C for 500 cycles. Impressively, NFMT//hard carbon pouch cells with such electrolyte also achieve a steady operation for 100 cycles at 0.5C with 86.8% capacity remaining. This study offers a practical reference for developing high-performance and flame-retardant electrolytes.

源语言英语
期刊Journal of the American Chemical Society
DOI
出版状态已接受/待刊 - 2025

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