Zhengping Ding , Ran Song , Yu Shen , Huahui Lin , Peng Wei , Xiangqun Zhuge , Ke Qu , Zhenzhong Yang , Yurong Ren
{"title":"2,2,2-Trifluoroethyl nonafluorobutanesulfonate as bifunctional electrolyte additive for high-energy-density 4.5 V LiNi0.8Co0.1Mn0.1O2||Li batteries","authors":"Zhengping Ding , Ran Song , Yu Shen , Huahui Lin , Peng Wei , Xiangqun Zhuge , Ke Qu , Zhenzhong Yang , Yurong Ren","doi":"10.1016/j.electacta.2025.146118","DOIUrl":null,"url":null,"abstract":"<div><div>Combining a high cut-off voltage cathode with a high specific-capacity lithium metal anode offers a promising path toward ultra-high-energy-density batteries (> 400 Wh kg<sup>-1</sup>). However, the practical application of LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub> (NCM811)||Li batteries with a 4.5 V cut-off voltage is challenged by severe interface deterioration. This study introduces a novel bifunctional electrolyte additive called 2,2,2-Trifluoroethyl Nonafluorobutanesulfonate (TNS), designed to form a thin, robust electrolyte interface layer on both cathode and anode surfaces. Detailed analysis reveals that TNS decomposes and modifies the solid-electrolyte-interface layer. Through the synergistic effects of fluoride and sulfonate functional groups, the resulting cathode-electrolyte-interface (CEI) enhances the structural stability of NCM811 while providing a high-efficiency lithium-ion transport channel to accelerate Li<sup>+</sup> insertion and extraction. At a cut-off voltage of 4.5 V, NCM811||Li batteries with 1 % TNS (by weight) exhibit high discharge capacity retention of 74.2 % after 150 cycles at a 1C rate and 60.1 % after 150 cycles at a 2C rate. This study offers valuable insights for designing high-voltage electrolyte additives in ultra-high-energy-density lithium metal batteries.</div></div>","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":"525 ","pages":"Article 146118"},"PeriodicalIF":5.5000,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochimica Acta","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0013468625004803","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
2,2,2-Trifluoroethyl nonafluorobutanesulfonate as bifunctional electrolyte additive for high-energy-density 4.5 V LiNi0.8Co0.1Mn0.1O2||Li batteries
Combining a high cut-off voltage cathode with a high specific-capacity lithium metal anode offers a promising path toward ultra-high-energy-density batteries (> 400 Wh kg-1). However, the practical application of LiNi0.8Co0.1Mn0.1O2 (NCM811)||Li batteries with a 4.5 V cut-off voltage is challenged by severe interface deterioration. This study introduces a novel bifunctional electrolyte additive called 2,2,2-Trifluoroethyl Nonafluorobutanesulfonate (TNS), designed to form a thin, robust electrolyte interface layer on both cathode and anode surfaces. Detailed analysis reveals that TNS decomposes and modifies the solid-electrolyte-interface layer. Through the synergistic effects of fluoride and sulfonate functional groups, the resulting cathode-electrolyte-interface (CEI) enhances the structural stability of NCM811 while providing a high-efficiency lithium-ion transport channel to accelerate Li+ insertion and extraction. At a cut-off voltage of 4.5 V, NCM811||Li batteries with 1 % TNS (by weight) exhibit high discharge capacity retention of 74.2 % after 150 cycles at a 1C rate and 60.1 % after 150 cycles at a 2C rate. This study offers valuable insights for designing high-voltage electrolyte additives in ultra-high-energy-density lithium metal batteries.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.