Customizing Pore Structure and Lithiophilic Sites Dual‐Gradient Free‐Standing 3D Lithium‐Based Anode to Enable Excellent Lithium Metal Batteries

Developing 3D hosts is one of the most promising strategies for putting forward the practical application of lithium(Li)-based anodes. However, the concentration polarization and uniform electric field of the traditional 3D hosts result in undesirable "top growth" of Li, reduced space utilization, and obnoxious dendrites. Herein, a novel dual-gradient 3D host (GDPL-3DH) simultaneously possessing gradient-distributed pore structure and lithiophilic sites is constructed by an electrospinning route. Under the synergistic effect of the gradient-distributed pore and lithiophilic sites, the GDPL-3DH exhibits the gradient-increased electrical conductivity from top to bottom. Also, Li is preferentially and uniformly deposited at the bottom of the GDPL-3DH with a typical "bottom-top" mode confirmed by the optical and SEM images, without Li dendrites. Consequently, an ultra-long lifespan of 5250 h of a symmetrical cell at 2 mA cm<sup>-2</sup> with a fixed capacity of 2 mAh cm<sup>-2</sup> is achieved. Also, the full cells based on the LiFePO<sub>4</sub>, S/C, and LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub> cathodes all exhibit excellent performances. Specifically, the LiFePO<sub>4</sub>-based cell maintains a high capacity of 136.8 mAh g<sup>-1</sup> after 700 cycles at 1 C (1 C = 170 mA g<sup>-1</sup>) with 94.7% capacity retention. The novel dual-gradient strategy broadens the perspective of regulating the mechanism of lithium deposition.

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Publication Details

Journal
Small
Published
2024-08-09
DOI
https://doi.org/10.1002/smll.202405227
Citations
8
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
1.67

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article

Customizing Pore Structure and Lithiophilic Sites Dual‐Gradient Free‐Standing 3D Lithium‐Based Anode to Enable Excellent Lithium Metal Batteries

Yuanfu Deng, Jiafeng He, Xiangxiang Fu, Rui Zhang et al.
8 citations
Small
Advancements in Battery Materials
1.67
article

Customizing Pore Structure and Lithiophilic Sites Dual‐Gradient Free‐Standing 3D Lithium‐Based Anode to Enable Excellent Lithium Metal Batteries

Yuanfu Deng, Jiafeng He, Xiangxiang Fu, Rui Zhang, Guohua Chen, Wanting Li, Yangming Hu
article en
8 citations

Abstract

Developing 3D hosts is one of the most promising strategies for putting forward the practical application of lithium(Li)-based anodes. However, the concentration polarization and uniform electric field of the traditional 3D hosts result in undesirable "top growth" of Li, reduced space utilization, and obnoxious dendrites. Herein, a novel dual-gradient 3D host (GDPL-3DH) simultaneously possessing gradient-distributed pore structure and lithiophilic sites is constructed by an electrospinning route. Under the synergistic effect of the gradient-distributed pore and lithiophilic sites, the GDPL-3DH exhibits the gradient-increased electrical conductivity from top to bottom. Also, Li is preferentially and uniformly deposited at the bottom of the GDPL-3DH with a typical "bottom-top" mode confirmed by the optical and SEM images, without Li dendrites. Consequently, an ultra-long lifespan of 5250 h of a symmetrical cell at 2 mA cm<sup>-2</sup> with a fixed capacity of 2 mAh cm<sup>-2</sup> is achieved. Also, the full cells based on the LiFePO<sub>4</sub>, S/C, and LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub> cathodes all exhibit excellent performances. Specifically, the LiFePO<sub>4</sub>-based cell maintains a high capacity of 136.8 mAh g<sup>-1</sup> after 700 cycles at 1 C (1 C = 170 mA g<sup>-1</sup>) with 94.7% capacity retention. The novel dual-gradient strategy broadens the perspective of regulating the mechanism of lithium deposition.

SmallVol. 20(47)
Beijing Institute of Technology (CN), City University of Hong Kong (HK), Cell Technology (China) (HK), South China University of Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 16%
Advancements in Battery Materials
1.67
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