Sulfonic Acid-Functionalized Graphdiyne for Effective Li–S Battery Separators

Lithium-sulfur (Li-S) batteries enable a promising high-energy-storage system while facing practical challenges regarding lithium dendrites and lithium polysulfides (LiPSs) shuttling. Herein, a fascinating SO<sub>3</sub>H-functionalized graphdiyne (SOGDY) was developed by grafting SO<sub>3</sub>H onto GDY to modify the separator in Li-S batteries. It realizes structure-retained material transformation, that is, SOGDY retains the crystalline all-carbon network and uniform subnanopores from the initial GDY. The abundant SO<sub>3</sub>H and uniform pores create a rapid Li<sup>+</sup> transport relay station, benefit rapid Li<sup>+</sup> transport and even lithium deposition, and prevent lithium dendrite growth. The spatial obstruction and strong polar adsorption sites from SO<sub>3</sub>H effectively inhibit LiPS shuttling. Additionally, SOGDY establishes a fast electron-transfer pathway to facilitate the LiPS conversion. The SOGDY/PP separator exhibited steady cycling at 1 mA cm<sup>-2</sup> over 3500 h in the Li∥Li symmetric battery and achieved outstanding low-temperature and high-rate performance in the Li-S battery with a high initial specific capacity of 804.5 mA h g<sup>-1</sup> and a final capacity of 504.9 mA h g<sup>-1</sup> after 500 cycles at 3 C and -10 °C. This work demonstrates that introducing a stable all-carbon network and uniform functionalized nanopores is an effective strategy to modify the Li-S battery separator.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-08-16
DOI
https://doi.org/10.1021/jacs.4c05107
Citations
88
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
18.36

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article

Sulfonic Acid-Functionalized Graphdiyne for Effective Li–S Battery Separators

Yurui Xue, Wenlong Yang, Lu Qi, Guoxing Li et al.
88 citations
Journal of the American Chemical Society
Advanced Battery Materials and Technologies
18.36
article

Sulfonic Acid-Functionalized Graphdiyne for Effective Li–S Battery Separators

Yurui Xue, Wenlong Yang, Lu Qi, Guoxing Li, Yuliang Li, Taifeng Liu, Yang Kong, Xuming Qiu
article en
88 citations

Abstract

Lithium-sulfur (Li-S) batteries enable a promising high-energy-storage system while facing practical challenges regarding lithium dendrites and lithium polysulfides (LiPSs) shuttling. Herein, a fascinating SO<sub>3</sub>H-functionalized graphdiyne (SOGDY) was developed by grafting SO<sub>3</sub>H onto GDY to modify the separator in Li-S batteries. It realizes structure-retained material transformation, that is, SOGDY retains the crystalline all-carbon network and uniform subnanopores from the initial GDY. The abundant SO<sub>3</sub>H and uniform pores create a rapid Li<sup>+</sup> transport relay station, benefit rapid Li<sup>+</sup> transport and even lithium deposition, and prevent lithium dendrite growth. The spatial obstruction and strong polar adsorption sites from SO<sub>3</sub>H effectively inhibit LiPS shuttling. Additionally, SOGDY establishes a fast electron-transfer pathway to facilitate the LiPS conversion. The SOGDY/PP separator exhibited steady cycling at 1 mA cm<sup>-2</sup> over 3500 h in the Li∥Li symmetric battery and achieved outstanding low-temperature and high-rate performance in the Li-S battery with a high initial specific capacity of 804.5 mA h g<sup>-1</sup> and a final capacity of 504.9 mA h g<sup>-1</sup> after 500 cycles at 3 C and -10 °C. This work demonstrates that introducing a stable all-carbon network and uniform functionalized nanopores is an effective strategy to modify the Li-S battery separator.

Journal of the American Chemical SocietyVol. 146(34)
Shandong University (CN), Chinese Academy of Sciences (CN), Institute of Chemistry (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Taishan Scholar Project of Shandong Province, National Key Research and Development Program of China
Affordable and clean energy
Openalex Percentile: Top 0%
Advanced Battery Materials and Technologies
18.36
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