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Multiscale interfacial stabilization via prelithiation separator engineering for Ah-level anode-free lithium batteries

  • Ahu Shao
  • , Helin Wang
  • , Min Zhang
  • , Jiacheng Liu
  • , Lu Cheng
  • , Yunsong Li
  • , Yuxiang Guo
  • , Zhiqiao Wang
  • , Qiurong Jia
  • , Xin Wang
  • , Xiaoyu Tang
  • , Xiaodong Zhao
  • , Yue Ma
  • Northwestern Polytechnical University Xian
  • Zhengzhou BAK Battery Co. Ltd
  • Shaanxi Raisight Energy Tech Co. Ltd
  • Fujian Blue Ocean & Black Stone Technology Co. Ltd

Research output: Contribution to journalArticlepeer-review

80 Scopus citations

Abstract

Anode-free lithium batteries represent a promising avenue for high-energy-density storage, yet their practical application is hindered by lithium inventory loss from parasitic interfacial reactions, cathode degradation, and limited Li+ reversibility. Herein, we propose a polyolefin separator integrated with a Li2S@C sacrificial layer, achieving multiscale interfacial stabilization in Ah-class anode-free pouch cells. This approach simultaneously replenishes the customized Li+ inventory during the formation cycle and establishes the lithium polysulfide-containing cathode interface with high-voltage tolerance (till 4.5 V). Real-time tracking via in-situ electrochemical impedance spectroscopy and transmission-mode operando X-ray diffraction reveals accelerated Li+ diffusion kinetics and stabilized phase evolution in LiNi0.8Co0.1Mn0.1O2 cathode interfaced with Li2S@C|PE prelithiation separator. Consequently, a 1.22 Ah pouch cell with an Ag-modified Cu foil and LiNi0.8Co0.1Mn0.1O2 cathode is assembled with Li2S@C|PE separator and exhibits gravimetric and volumetric energy densities of 450 Wh kg-1 and 1355 Wh L-1, respectively. This prelithiation protocol demonstrates upscaling potential and generic applicability to secure the interfacial chemistries for anode free/less lithium metal batteries.

Original languageEnglish
Article number4145
JournalNature Communications
Volume16
Issue number1
DOIs
StatePublished - Dec 2025

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