{"title":"Mitigating Oxidation of Li7P2S8I-Based Electrolytes in All-Solid-State Batteries: Cathode Coating versus Electrolyte Interface Engineering","authors":"Zhongkai Wu, Le Yu* and Chuang Yu*, ","doi":"10.1021/acs.iecr.5c0011310.1021/acs.iecr.5c00113","DOIUrl":null,"url":null,"abstract":"<p >Highly electro/chemical compatible solid-state electrolytes are essential for all-solid-state lithium batteries with high power density, and the integration of sulfide and halide electrolytes within a bilayer separator has garnered significant interest due to their enhanced electrochemical stabilities and improved ionic conductivities. Despite these advantages, current sulfide electrolytes do not adequately satisfy the criteria required for high-performance all-solid-state lithium batteries. In this context, we present the synthesis of Li<sub>7</sub>P<sub>2</sub>S<sub>8</sub>I through a combination of ball-milling and heat treatment processes. The resulting Li<sub>7</sub>P<sub>2</sub>S<sub>8</sub>I achieves an ionic conductivity of 1.8 × 10<sup>–3</sup> S cm<sup>–1</sup> and excellent air stability. Subsequently, the Li<sub>2</sub>ZrO<sub>3</sub> coating layer and a bilayer separator comprising Li<sub>7</sub>P<sub>2</sub>S<sub>8</sub>I as the anolyte and Li<sub>3</sub>InCl<sub>6</sub> as the catholyte were constructed to evaluate its compatibility with the LiNi<sub>0.7</sub>Mn<sub>0.1</sub>Co<sub>0.2</sub>O<sub>2</sub> cathode. Electrochemical analysis indicates that while Li<sub>3</sub>InCl<sub>6</sub> is effective in reducing lithium loss from cathode materials, it reacts with Li<sub>7</sub>P<sub>2</sub>S<sub>8</sub>I, leading to the formation of interphases that impede Li-ion transportation, consequently resulting in a more rapid capacity fade after cycling. Meanwhile, the Li-In/Li<sub>7</sub>P<sub>2</sub>S<sub>8</sub>I/Li<sub>2</sub>ZrO<sub>3</sub>@LiNi<sub>0.7</sub>Co<sub>0.1</sub>Mn<sub>0.2</sub>O<sub>2</sub> battery exhibits marginally reduced discharge capacities at identical C rates and superior cycling performances. These findings provide insights into the development of high-performance Li<sub>7</sub>P<sub>2</sub>S<sub>8</sub>I-based all-solid-state batteries.</p>","PeriodicalId":39,"journal":{"name":"Industrial & Engineering Chemistry Research","volume":"64 12","pages":"6269–6278 6269–6278"},"PeriodicalIF":3.9000,"publicationDate":"2025-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Industrial & Engineering Chemistry Research","FirstCategoryId":"5","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.iecr.5c00113","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Highly electro/chemical compatible solid-state electrolytes are essential for all-solid-state lithium batteries with high power density, and the integration of sulfide and halide electrolytes within a bilayer separator has garnered significant interest due to their enhanced electrochemical stabilities and improved ionic conductivities. Despite these advantages, current sulfide electrolytes do not adequately satisfy the criteria required for high-performance all-solid-state lithium batteries. In this context, we present the synthesis of Li7P2S8I through a combination of ball-milling and heat treatment processes. The resulting Li7P2S8I achieves an ionic conductivity of 1.8 × 10–3 S cm–1 and excellent air stability. Subsequently, the Li2ZrO3 coating layer and a bilayer separator comprising Li7P2S8I as the anolyte and Li3InCl6 as the catholyte were constructed to evaluate its compatibility with the LiNi0.7Mn0.1Co0.2O2 cathode. Electrochemical analysis indicates that while Li3InCl6 is effective in reducing lithium loss from cathode materials, it reacts with Li7P2S8I, leading to the formation of interphases that impede Li-ion transportation, consequently resulting in a more rapid capacity fade after cycling. Meanwhile, the Li-In/Li7P2S8I/Li2ZrO3@LiNi0.7Co0.1Mn0.2O2 battery exhibits marginally reduced discharge capacities at identical C rates and superior cycling performances. These findings provide insights into the development of high-performance Li7P2S8I-based all-solid-state batteries.
高电化学/化学兼容性的固态电解质对于高功率密度的全固态锂电池至关重要,硫化物和卤化物电解质在双层分离器中的集成由于其增强的电化学稳定性和改善的离子电导率而引起了极大的兴趣。尽管有这些优点,目前的硫化物电解质还不能充分满足高性能全固态锂电池的要求。在这种情况下,我们提出了通过球磨和热处理工艺相结合的合成Li7P2S8I。Li7P2S8I的离子电导率为1.8 × 10-3 S cm-1,具有优异的空气稳定性。随后,构建了Li2ZrO3涂层和Li7P2S8I为阳极液、Li3InCl6为阴极液的双层分离器,以评估其与LiNi0.7Mn0.1Co0.2O2阴极的相容性。电化学分析表明,虽然Li3InCl6可以有效减少正极材料中的锂损失,但它与Li7P2S8I发生反应,导致形成阻碍锂离子运输的界面相,从而导致循环后容量衰减更快。同时,Li-In/Li7P2S8I/Li2ZrO3@LiNi0.7Co0.1Mn0.2O2电池在相同倍率下的放电容量略有降低,并且具有优异的循环性能。这些发现为高性能基于li7p2s8i的全固态电池的开发提供了见解。
期刊介绍:
ndustrial & Engineering Chemistry, with variations in title and format, has been published since 1909 by the American Chemical Society. Industrial & Engineering Chemistry Research is a weekly publication that reports industrial and academic research in the broad fields of applied chemistry and chemical engineering with special focus on fundamentals, processes, and products.