{"title":"揭示锂硫电池固液界面上 Li2S 晶体的自动催化生长过程","authors":"Zhen Wu, Mingliang Liu, Wenfeng He, Tong Guo, Wei Tong, Erjun Kan, Xiaoping Ouyang, Fen Qiao, Junfeng Wang, Xueliang Sun, Xin Wang, Junwu Zhu, Ali Coskun, Yongsheng Fu","doi":"10.1038/s41467-024-53797-y","DOIUrl":null,"url":null,"abstract":"<p>Electrocatalysts are extensively employed to suppress the shuttling effect in lithium-sulfur (Li-S) batteries. However, it remains challenging to probe the sulfur redox reactions and mechanism at the electrocatalyst/LiPS interface after the active sites are covered by the solid discharge products Li<sub>2</sub>S/Li<sub>2</sub>S<sub>2</sub>. Here, we demonstrate the intrinsic autocatalytic activity of the Li<sub>2</sub>S (100) plane towards lithium polysulfides on single-atom nickel (SANi) electrocatalysts. Guided by theoretical models and experimental data, it is concluded that LiPS dissociates into Li<sub>2</sub>S<sub>2</sub> and short-chain LiPS on the Li<sub>2</sub>S (100) plane. Subsequently, Li<sub>2</sub>S<sub>2</sub> undergoes further lithiation to Li<sub>2</sub>S on the Li<sub>2</sub>S (100) surface, generating a new Li<sub>2</sub>S (100) layer, thus enabling the autocatalytic formation of a new Li<sub>2</sub>S (100) surface. Benefiting from the autocatalytic growth of Li<sub>2</sub>S, the concentration of LiPS in the electrolyte remains at a lower level, enabling Li-S batteries under high loading and low electrolyte conditions to exhibit superior electrochemical performance.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"66 1","pages":""},"PeriodicalIF":14.7000,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unveiling the autocatalytic growth of Li2S crystals at the solid-liquid interface in lithium-sulfur batteries\",\"authors\":\"Zhen Wu, Mingliang Liu, Wenfeng He, Tong Guo, Wei Tong, Erjun Kan, Xiaoping Ouyang, Fen Qiao, Junfeng Wang, Xueliang Sun, Xin Wang, Junwu Zhu, Ali Coskun, Yongsheng Fu\",\"doi\":\"10.1038/s41467-024-53797-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Electrocatalysts are extensively employed to suppress the shuttling effect in lithium-sulfur (Li-S) batteries. However, it remains challenging to probe the sulfur redox reactions and mechanism at the electrocatalyst/LiPS interface after the active sites are covered by the solid discharge products Li<sub>2</sub>S/Li<sub>2</sub>S<sub>2</sub>. Here, we demonstrate the intrinsic autocatalytic activity of the Li<sub>2</sub>S (100) plane towards lithium polysulfides on single-atom nickel (SANi) electrocatalysts. Guided by theoretical models and experimental data, it is concluded that LiPS dissociates into Li<sub>2</sub>S<sub>2</sub> and short-chain LiPS on the Li<sub>2</sub>S (100) plane. Subsequently, Li<sub>2</sub>S<sub>2</sub> undergoes further lithiation to Li<sub>2</sub>S on the Li<sub>2</sub>S (100) surface, generating a new Li<sub>2</sub>S (100) layer, thus enabling the autocatalytic formation of a new Li<sub>2</sub>S (100) surface. Benefiting from the autocatalytic growth of Li<sub>2</sub>S, the concentration of LiPS in the electrolyte remains at a lower level, enabling Li-S batteries under high loading and low electrolyte conditions to exhibit superior electrochemical performance.</p>\",\"PeriodicalId\":19066,\"journal\":{\"name\":\"Nature Communications\",\"volume\":\"66 1\",\"pages\":\"\"},\"PeriodicalIF\":14.7000,\"publicationDate\":\"2024-11-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Communications\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1038/s41467-024-53797-y\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-024-53797-y","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Unveiling the autocatalytic growth of Li2S crystals at the solid-liquid interface in lithium-sulfur batteries
Electrocatalysts are extensively employed to suppress the shuttling effect in lithium-sulfur (Li-S) batteries. However, it remains challenging to probe the sulfur redox reactions and mechanism at the electrocatalyst/LiPS interface after the active sites are covered by the solid discharge products Li2S/Li2S2. Here, we demonstrate the intrinsic autocatalytic activity of the Li2S (100) plane towards lithium polysulfides on single-atom nickel (SANi) electrocatalysts. Guided by theoretical models and experimental data, it is concluded that LiPS dissociates into Li2S2 and short-chain LiPS on the Li2S (100) plane. Subsequently, Li2S2 undergoes further lithiation to Li2S on the Li2S (100) surface, generating a new Li2S (100) layer, thus enabling the autocatalytic formation of a new Li2S (100) surface. Benefiting from the autocatalytic growth of Li2S, the concentration of LiPS in the electrolyte remains at a lower level, enabling Li-S batteries under high loading and low electrolyte conditions to exhibit superior electrochemical performance.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.