{"title":"Endowing Metal Oxychloride Solid Electrolytes with Improved Li Compatibility","authors":"Lv Hu, Jingming Yao, Changshun Li, Kejun Yan, Jinfeng Zhu, Jinzhu Wang, Hui Li, Fang Chen, Huaican Chen, Wen Yin, Jie Ma, Jun Jiang, Zhuoying Zhu*, Jianyu Huang* and Cheng Ma*, ","doi":"10.1021/jacs.5c13676","DOIUrl":null,"url":null,"abstract":"<p >Typically, the Li incompatibility of inorganic solid electrolytes (ISEs) arises from the presence of non-Li metal cations, which will be reduced into electronic conductors to promote further reactions. Making such ISEs compatible with Li can significantly expand the candidate pool for ISEs in Li metal batteries, but, to this end, the Li/ISE interphase, which inevitably contains electronic conductors, must become electron-blocking. Here, we propose a nonmetal cation incorporation strategy to achieve such a seemingly paradoxical goal. By populating the ISE with nonmetal cations that would yield electron-blocking reduction products, we can make the electron-blocking species in the Li/ISE interphase predominate over the electronic conductors, thereby blocking electron percolation. This strategy significantly improves the Li compatibility in Zr-based oxychloride ISEs, which possess numerous advantages but have always been Li-incompatible; the 0.8Li<sub>2</sub>SO<sub>4</sub>–ZrCl<sub>4</sub> ISE we design enables stable cycling of Li symmetric cells (5000 h), Li–LiNi<sub>0.92</sub>Co<sub>0.06</sub>Mn<sub>0.02</sub>O<sub>2</sub> cells (80% capacity retention for 170 cycles), and Li<sub>13</sub>Si<sub>4</sub>–LiNi<sub>0.92</sub>Co<sub>0.06</sub>Mn<sub>0.02</sub>O<sub>2</sub> cells (80% capacity retention for 1312 cycles) at 25 °C. Our strategy opens new avenues for the development of Li-compatible ISEs.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"148 26","pages":"27072–27088"},"PeriodicalIF":16.6000,"publicationDate":"2026-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/jacs.5c13676","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/6/23 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Typically, the Li incompatibility of inorganic solid electrolytes (ISEs) arises from the presence of non-Li metal cations, which will be reduced into electronic conductors to promote further reactions. Making such ISEs compatible with Li can significantly expand the candidate pool for ISEs in Li metal batteries, but, to this end, the Li/ISE interphase, which inevitably contains electronic conductors, must become electron-blocking. Here, we propose a nonmetal cation incorporation strategy to achieve such a seemingly paradoxical goal. By populating the ISE with nonmetal cations that would yield electron-blocking reduction products, we can make the electron-blocking species in the Li/ISE interphase predominate over the electronic conductors, thereby blocking electron percolation. This strategy significantly improves the Li compatibility in Zr-based oxychloride ISEs, which possess numerous advantages but have always been Li-incompatible; the 0.8Li2SO4–ZrCl4 ISE we design enables stable cycling of Li symmetric cells (5000 h), Li–LiNi0.92Co0.06Mn0.02O2 cells (80% capacity retention for 170 cycles), and Li13Si4–LiNi0.92Co0.06Mn0.02O2 cells (80% capacity retention for 1312 cycles) at 25 °C. Our strategy opens new avenues for the development of Li-compatible ISEs.
期刊介绍:
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