Dendrite-Free High-Capacity Alkali Metal Batteries by Two-Dimensional Confinement of Desolvated Ions

Alkali metal anodes (Li, Na, and K) hold great promise for energy storage due to their high specific capacities and low reduction potentials. However, the deposition of alkali metals is frequently disrupted by a simultaneous desolvation process, leading to dendrite growth and rapid capacity decay. In this work, we present a general strategy to achieve dendrite-free, high-capacity alkali metal batteries by utilizing the two-dimensional (2D) confinement of desolvated ions. 2D transition metal disulfides (TMDSs) are employed as interlayers with high adsorption energy for alkali metal ions, effectively facilitating the rapid separation of the desolvation process from metal deposition. The desolvated ions, characterized by high diffusivity, are confined within the 2D channels of TMDSs, enabling planar alkali metal deposition without interference from the desolvation process. Furthermore, the TMDS interlayers avoid side reactions between solvents and metals during deposition, resulting in a thin solid electrolyte interphase that promotes fast ion diffusion. This approach enables dendrite-free K metal batteries capable of plating/stripping at 10 mAh cm<sup>-2</sup> and cycling at 36 C for over 3000 cycles. Our strategy provides a novel pathway to advance high-energy metal batteries, significantly enhancing their performance and longevity.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-10-16
DOI
https://doi.org/10.1021/jacs.5c10623
Citations
1
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
0.73
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article

Dendrite-Free High-Capacity Alkali Metal Batteries by Two-Dimensional Confinement of Desolvated Ions

Junhao Wang, Yu Yao, Mingze Ma, Shuhong Jiao et al.
1 citations
Journal of the American Chemical Society
Advanced Battery Materials and Technologies
0.73
article

Dendrite-Free High-Capacity Alkali Metal Batteries by Two-Dimensional Confinement of Desolvated Ions

Junhao Wang, Yu Yao, Mingze Ma, Shuhong Jiao, Weikang Dong, Yue Lin, Ning Lü, Zhiwen Zhuo, Zhiyu Lu, Fangxin Ling, Zixu He, Ruilin Bai, Hanyu Huo, Hai Yang, Shaoming Fang, Zhen Li, Fei Wang, Yu Qiao, Yan Mei Yu, Yu Shao, Junyi Dai
article en
1 citations

Abstract

Alkali metal anodes (Li, Na, and K) hold great promise for energy storage due to their high specific capacities and low reduction potentials. However, the deposition of alkali metals is frequently disrupted by a simultaneous desolvation process, leading to dendrite growth and rapid capacity decay. In this work, we present a general strategy to achieve dendrite-free, high-capacity alkali metal batteries by utilizing the two-dimensional (2D) confinement of desolvated ions. 2D transition metal disulfides (TMDSs) are employed as interlayers with high adsorption energy for alkali metal ions, effectively facilitating the rapid separation of the desolvation process from metal deposition. The desolvated ions, characterized by high diffusivity, are confined within the 2D channels of TMDSs, enabling planar alkali metal deposition without interference from the desolvation process. Furthermore, the TMDS interlayers avoid side reactions between solvents and metals during deposition, resulting in a thin solid electrolyte interphase that promotes fast ion diffusion. This approach enables dendrite-free K metal batteries capable of plating/stripping at 10 mAh cm<sup>-2</sup> and cycling at 36 C for over 3000 cycles. Our strategy provides a novel pathway to advance high-energy metal batteries, significantly enhancing their performance and longevity.

Journal of the American Chemical SocietyVol. 147(43)
Kunming University of Science and Technology (CN), Beijing Institute of Technology (CN), University of Science and Technology of China (CN), Ministry of Education of the People's Republic of China (CN), Jiujiang University (CN), Xiamen University (CN), Zhengzhou University of Light Industry (CN), Jiujiang Vocational University (CN), Faculty (United Kingdom) (GB), Hefei National Center for Physical Sciences at Nanoscale (CN), Division of Materials Science and Engineering (AU), National Synchrotron Radiation Laboratory (CN), Collaborative Innovation Center of Chemistry for Energy Materials (CN), Anhui Normal University (CN)
Openalex Percentile: Top 22%
Advanced Battery Materials and Technologies
0.73
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