Three-Dimensional Lithium Anode with an In Situ Generated Li2O-Rich Solid Electrolyte Interface for High-Rate and Long-Storage Lithium Battery

The limited rate performance of Li||CFx batteries hinders their wide application, owing to the low conductivity of CFx cathode material and the undesirable solid electrolyte interface (SEI) layer formed on the Li anode surface. Herein, a strategy for constructing a three-dimensional lithium anode (3D-Li anode) with high specific surface area and an in situ formed favorable SEI layer is proposed to enhance the interfacial stability and uniformity of ion transport and realize a Li||CFx battery with remarkable comprehensive performance. A 3D-Li anode (Li@CuO-Cu foam) is successfully constructed by molten Li infusion of a thermal oxidation processed copper foam. The lithiophilicity of the Cu foam framework is optimized by the formed CuO. The Li@CuO-Cu foam||CFx battery exhibits a high discharge specific capacity (1149.6 mAh g−1 at 0.1 C) along with a high discharge plateau voltage (2.65 V). At a high rate of 10 C, the 3D-Li anode-based batteries still demonstrate a discharge specific capacity of 463 mAh g−1, which is about 2.5 times that of the conventional Li||CFx, and exhibit excellent storage performance (620.3 mAh g−1 after storage at 55 °C for 90 days) and a low monthly self-discharge rate (1.28%). This work demonstrates a promising strategy to construct a three-dimensional lithium metal anode and significantly improve the rate and storage performance of Li||CFx batteries.

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Publication Details

Journal
Energies
Published
2024-12-13
DOI
https://doi.org/10.3390/en17246283
Citations
2
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
0.42
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article

Three-Dimensional Lithium Anode with an In Situ Generated Li2O-Rich Solid Electrolyte Interface for High-Rate and Long-Storage Lithium Battery

Zhongzhi Yuan, Yingke Zhou, Xiaohui Tian, Mo Li et al.
2 citations
Energies
Advanced Battery Materials and Technologies
0.42
article

Three-Dimensional Lithium Anode with an In Situ Generated Li2O-Rich Solid Electrolyte Interface for High-Rate and Long-Storage Lithium Battery

Zhongzhi Yuan, Yingke Zhou, Xiaohui Tian, Mo Li, Ping Li, Xiangyu Cheng, Xuan Liu
article en
2 citations

Abstract

The limited rate performance of Li||CFx batteries hinders their wide application, owing to the low conductivity of CFx cathode material and the undesirable solid electrolyte interface (SEI) layer formed on the Li anode surface. Herein, a strategy for constructing a three-dimensional lithium anode (3D-Li anode) with high specific surface area and an in situ formed favorable SEI layer is proposed to enhance the interfacial stability and uniformity of ion transport and realize a Li||CFx battery with remarkable comprehensive performance. A 3D-Li anode (Li@CuO-Cu foam) is successfully constructed by molten Li infusion of a thermal oxidation processed copper foam. The lithiophilicity of the Cu foam framework is optimized by the formed CuO. The Li@CuO-Cu foam||CFx battery exhibits a high discharge specific capacity (1149.6 mAh g−1 at 0.1 C) along with a high discharge plateau voltage (2.65 V). At a high rate of 10 C, the 3D-Li anode-based batteries still demonstrate a discharge specific capacity of 463 mAh g−1, which is about 2.5 times that of the conventional Li||CFx, and exhibit excellent storage performance (620.3 mAh g−1 after storage at 55 °C for 90 days) and a low monthly self-discharge rate (1.28%). This work demonstrates a promising strategy to construct a three-dimensional lithium metal anode and significantly improve the rate and storage performance of Li||CFx batteries.

EnergiesVol. 17(24)
South China Normal University (CN), Wuhan University of Science and Technology (CN)
Affordable and clean energy
Openalex Percentile: Top 36%
Advanced Battery Materials and Technologies
0.42
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Three-Dimensional Lithium Anode with an In Situ Generated Li2O-Rich Solid Electrolyte Interface for High-Rate and Long-Storage Lithium Battery — Zhongzhi Yuan, Yingke Zhou, et al. · Energies (2024) | TGRS Research Map | TGRS