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Catalyst-Mediated Interfacial Prelithiation for Energy/Power-Dense and Ultralong-Life Lithium Batteries

  • Ahu Shao
  • , Chunwei Li
  • , Jiacheng Liu
  • , Zhiqiao Wang
  • , Qiurong Jia
  • , Xin Wang
  • , Zhaohui Wang
  • , Jiangan Wang
  • , Fei Xu
  • , Yue Ma
  • Northwestern Polytechnical University Xian
  • Ltd.
  • Ltd.
  • Hunan University

科研成果: 期刊稿件文章同行评审

摘要

The irreversible cation depletion and interfacial degradation fundamentally limit the practical energy output and cycling endurance of lithium-free anode batteries. Here, we propose a catalyst-mediated interfacial prelithiation strategy that offsets irreversible lithium loss, precisely optimizes Li+ kinetics and interfacial stability for energy/power-dense cell prototypes. The sulfurized polyacrylonitrile (SPAN) catalyst, featuring electron-withdrawing sulfur sites, facilitates C-C bond cleavage through S-Li interactions. The Li2C2O4@SPAN composite delivers a delithiation voltage of 3.90 V and a highly efficient Li utilization of 99.5%. When paired with the LiNi0.8Co0.1Mn0.1O2 cathode, the prelithiation layer achieves Li+ replenishment areal capacities up to 1.1 mAh cm−2. Furthermore, the bilayer configuration spatially isolates prelithiation agents from the cathode's redox center, alleviating the gas-induced structural collapse and stress accumulation. Meanwhile, the SPAN-derived ROSO3Li species form a robust cathode interphase with LiF domains, accelerating Li+ transport and stabilizing the 4.5 V charging process. Under the lean-electrolyte condition (1.7 g Ah−1) in 1.28 Ah pouch cells, the Cu||NCM811-LS prototype achieves gravimetric/volumetric energy densities of 460 Wh kg−1/1083 Wh L−1 and a peak power output of 858 W kg−1. In addition, a 2.8 Ah Gr||NCM811 cell incorporating this prelithiation reservoir maintains a capacity retention of 88.2% over 1000 cycles. As a “drop-in” solution requiring no changes to cell assembly, this interfacial prelithiation paradigm aligns with scalable industrial manufacturing, affording a readily adoptable path toward energy/power-dense lithium batteries.

源语言英语
期刊Advanced Functional Materials
DOI
出版状态已接受/待刊 - 2026

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