{"title":"Polysulfide Tandem Conversion for Lithium–Sulfur Batteries","authors":"Zhilong Wang, Jianxiong Gao, Shimeng Zhang, Yu Wu, Yanlan Ren, Yongqi Lu, Xinyu Zhao, Bowen Jin, Mingfei Shao","doi":"10.1002/smll.202409867","DOIUrl":null,"url":null,"abstract":"<p>The electrocatalytic conversion of 16-electron multistep polysulfides is crucial for lithium–sulfur batteries, while it is hard to achieve compatibility between intricate sulfur reduction processes and appropriate catalysts. Herein, a tandem conversion strategy is reported to boost multi-step intermediate reactions of polysulfides transformation by designing an electrocatalyst featuring cobalt and zinc sites (Co/Zn), where the Zn serve as sites for the conversion of long-chain lithium polysulfides (LiPSs), promoting the transformation of S<sub>8</sub> to Li<sub>2</sub>S<sub>4</sub>; the Co sites accelerate the kinetics of the subsequent reduction of Li<sub>2</sub>S<sub>4</sub>. This tandem catalysis method not only enhances the conversion of the initial reactants but also provides additional support for the intermediates, thereby facilitating subsequent reactions to maximize capacity. Consequently, the cell utilizing this precise electrocatalyst delivers a high initial discharge-specific capacity of 1347.5 mAh g<sup>−1</sup> at a rate of 0.1 C, demonstrates outstanding rate performance (796.8 mAh g<sup>−1</sup> at 3 C), and excellent cycle stability with a capacity attenuation rate of 0.086% per cycle at 3.0 C. These results offer insights into the coordinated design of electrocatalysts for sulfur cathodes based on precise catalytic sites and complex multi-step conversion reactions.</p>","PeriodicalId":228,"journal":{"name":"Small","volume":"21 7","pages":""},"PeriodicalIF":12.1000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smll.202409867","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The electrocatalytic conversion of 16-electron multistep polysulfides is crucial for lithium–sulfur batteries, while it is hard to achieve compatibility between intricate sulfur reduction processes and appropriate catalysts. Herein, a tandem conversion strategy is reported to boost multi-step intermediate reactions of polysulfides transformation by designing an electrocatalyst featuring cobalt and zinc sites (Co/Zn), where the Zn serve as sites for the conversion of long-chain lithium polysulfides (LiPSs), promoting the transformation of S8 to Li2S4; the Co sites accelerate the kinetics of the subsequent reduction of Li2S4. This tandem catalysis method not only enhances the conversion of the initial reactants but also provides additional support for the intermediates, thereby facilitating subsequent reactions to maximize capacity. Consequently, the cell utilizing this precise electrocatalyst delivers a high initial discharge-specific capacity of 1347.5 mAh g−1 at a rate of 0.1 C, demonstrates outstanding rate performance (796.8 mAh g−1 at 3 C), and excellent cycle stability with a capacity attenuation rate of 0.086% per cycle at 3.0 C. These results offer insights into the coordinated design of electrocatalysts for sulfur cathodes based on precise catalytic sites and complex multi-step conversion reactions.
16电子多步硫化物的电催化转化对锂硫电池至关重要,但复杂的硫还原过程与合适的催化剂之间很难实现相容性。本文采用串联转化策略,设计了一种具有钴和锌位点(Co/Zn)的电催化剂,其中锌作为长链锂多硫化物(LiPSs)的转化位点,促进了S8向Li2S4的转化,从而促进了多步转化中间反应的发生;Co位点加速了Li2S4的后续还原动力学。这种串联催化方法不仅提高了初始反应物的转化率,而且为中间体提供了额外的支持,从而促进了后续反应的产能最大化。因此,使用这种精密电催化剂的电池在0.1 C的速率下具有1347.5 mAh g−1的高初始放电比容量,在3 C时具有出色的倍率性能(796.8 mAh g−1),并且在3.0 C时具有优异的循环稳定性,每循环容量衰减率为0.086%。这些结果为基于精确催化位点和复杂多步转化反应的硫阴极电催化剂的协调设计提供了新的思路。
期刊介绍:
Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments.
With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology.
Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.