Author
Listed:
- Huasen Shen
(Jianghan University
Jianghan University)
- Zhaohuai Li
(Jianghan University
Jianghan University)
- Jiantao Li
(Argonne National Laboratory)
- Qiu He
(Sichuan University)
- Mengjun Li
(Jianghan University)
- Yunan Tian
(Jianghan University)
- Guoning Wu
(Jianghan University)
- Yan Zhao
(Sichuan University)
- Xuanxuan Zhang
(Inc.)
- Jingjing Xiao
(Inc.)
- Khalil Amine
(Argonne National Laboratory)
- Yuyu Li
(Jianghan University
Jianghan University)
- Ming Xie
(Jianghan University)
- Jun Lu
(Zhejiang University)
Abstract
The growth of lithium (Li) dendrites and the accumulation of dead Li (i.e., Li metal regions which are electronically disconnected from the current collector) significantly undermine the safety and performance of Li metal batteries. This study employs kilogram–scale atomic layer deposition technology to construct zinc oxide with a preferential (002) crystal orientation, which homogeneously forms on commercial carbon nanotube papers. Our approach emphasizes the importance of achieving a moderate Li adsorption energy and low Li migration energy barriers to suppress Li dendrite growth. In this work, we introduce the concept of “catalytic” effect for dead Li reconversion, as validated through time–of–flight secondary ion mass spectrometry, leading to a Li plating/stripping efficiency of 99.89%. The Ah–level Li metal pouch cells with high–nickel positive electrodes achieve a specific energy of 380 Wh kg−1 (based on the mass of the whole pouch cell) and demonstrate stable cycling under demanding conditions. Analysis of the cycled pouch cells confirms the structural integrity and provides insights into the mechanism of the dead Li “catalytic” conversion.
Suggested Citation
Huasen Shen & Zhaohuai Li & Jiantao Li & Qiu He & Mengjun Li & Yunan Tian & Guoning Wu & Yan Zhao & Xuanxuan Zhang & Jingjing Xiao & Khalil Amine & Yuyu Li & Ming Xie & Jun Lu, 2025.
"Industrializable interlayer with catalytic conversion of dead lithium for Ah–level Nickel–rich lithium metal batteries,"
Nature Communications, Nature, vol. 16(1), pages 1-13, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-60609-4
DOI: 10.1038/s41467-025-60609-4
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