Skip to main content

Research Repository

Advanced Search

Nano-channel-based physical and chemical synergic regulation for dendrite-free lithium plating

Guo, Qiang; Deng, Wei; Xia, Shengjie; Zhang, Zibo; Zhao, Fei; Hu, Binjie; Zhang, Sasa; Zhou, Xufeng; Chen, George Zheng; Liu, Zhaoping

Nano-channel-based physical and chemical synergic regulation for dendrite-free lithium plating Thumbnail


Authors

Qiang Guo

Wei Deng

Shengjie Xia

Zibo Zhang

Fei Zhao

Binjie Hu

Sasa Zhang

Xufeng Zhou

Zhaoping Liu



Abstract

Uncontrollable dendrite growth resulting from the non-uniform lithium ion (Li+) flux and volume expansion in lithium metal (Li) negative electrode leads to rapid performance degradation and serious safety problems of lithium metal batteries. Although N-containing functional groups in carbon materials are reported to be effective to homogenize the Li+ flux, the effective interaction distance between lithium ions and N-containing groups should be relatively small (down to nanometer scale) according to the Debye length law. Thus, it is necessary to carefully design the microstructure of N-containing carbon materials to make the most of their roles in regulating the Li+ flux. In this work, porous carbon nitride microspheres (PCNMs) with abundant nanopores have been synthesized and utilized to fabricate a uniform lithiophilic coating layer having hybrid pores of both the nano- and micrometer scales on the Cu/Li foil. Physically, the three-dimensional (3D) porous framework is favorable for absorbing volume changes and guiding Li growth. Chemically, this coating layer can render a suitable interaction distance to effectively homogenize the Li+ flux and contribute to establishing a robust and stable solid electrolyte interphase (SEI) layer with Li-F, Li-N, and Li-O-rich contents based on the Debye length law. Such a physical-chemical synergic regulation strategy using PCNMs can lead to dendrite-free Li plating, resulting in a low nucleation overpotential and stable Li plating/stripping cycling performance in both the Li‖Cu and the Li‖Li symmetric cells. Meanwhile, a full cell using the PCNM coated Li foil negative electrode and a LiFePO4 positive electrode has delivered a high capacity retention of ∼ 80% after more than 200 cycles at 1 C and achieved a remarkable rate capability. The pouch cell fabricated by pairing the PCNM coated Li foil negative electrode with a NCM 811 positive electrode has retained ∼ 73% of the initial capacity after 150 cycles at 0.2 C.

Journal Article Type Article
Acceptance Date Jun 4, 2021
Online Publication Date Jul 9, 2021
Publication Date 2021-10
Deposit Date Jun 18, 2021
Publicly Available Date Jul 15, 2021
Journal Nano Research
Print ISSN 1998-0124
Electronic ISSN 1998-0000
Peer Reviewed Peer Reviewed
Volume 14
Issue 10
Pages 3585-3597
DOI https://doi.org/10.1007/s12274-021-3643-1
Public URL https://nottingham-repository.worktribe.com/output/5690592
Publisher URL https://link.springer.com/article/10.1007/s12274-021-3643-1

Files





You might also like



Downloadable Citations