Author
Listed:
- Guo-Xing Li
(The Pennsylvania State University)
- Rong Kou
(Southern Methodist University)
- Au Nguyen
(The Pennsylvania State University)
- Ke Wang
(The Pennsylvania State University)
- Yu-Sheng Li
(The Pennsylvania State University)
- Jongcheol Lee
(The Pennsylvania State University)
- Seong H. Kim
(The Pennsylvania State University)
- Donghai Wang
(The Pennsylvania State University
Southern Methodist University)
Abstract
Stabilizing lithium (Li) metal anodes has long been hindered by the challenge of forming a stable solid–electrolyte interphase, stemming from the inherently high reactivity of Li metal with liquid electrolytes. Here we developed a progressive dual-passivation polymer coating strategy to stabilize Li-metal anodes, achieving exceptional cycle life of Li-metal batteries in carbonate electrolyte. Unlike current approaches, the synthesized copolymer coating passivates the Li-metal anode while also tailoring the Li-ion solvation structure by facilitating selective anion decoordination in a binary salt carbonate electrolyte. This process leads to the formation of an integrated solid–electrolyte interphase, featuring a chemical passivation outer layer predominant in LiF generated by the polymer coating and an anion-derived Li2O-prevalent inner layer from the electrolyte decomposition. Consequently, this coating strategy remarkably enhances the stability of Li-metal anodes, enabling double-layer Li||NMC811 pouch cells to maintain 80% of their initial capacity up to 611 cycles under a low electrolyte/capacity (E/C) ratio of 2.0 g Ah−1.
Suggested Citation
Guo-Xing Li & Rong Kou & Au Nguyen & Ke Wang & Yu-Sheng Li & Jongcheol Lee & Seong H. Kim & Donghai Wang, 2025.
"Long-cycling lithium-metal batteries via an integrated solid–electrolyte interphase promoted by a progressive dual-passivation coating,"
Nature Energy, Nature, vol. 10(8), pages 941-950, August.
Handle:
RePEc:nat:natene:v:10:y:2025:i:8:d:10.1038_s41560-025-01803-y
DOI: 10.1038/s41560-025-01803-y
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