{"title":"Implanting Non‐Lithiated Metal into Fluoride/Nitride Hybrid Matrix Enabling Tailored Lithium/Garnet Interface Chemistry for Durable Solid‐State Lithium Batteries","authors":"Xiaohui Kan, Xiaotong Chang, Kaiyue Liu, Mengyang Jia, Zhijie Bi, Xiangxin Guo","doi":"10.1002/adfm.202512506","DOIUrl":null,"url":null,"abstract":"Garnet‐type Li<jats:sub>7</jats:sub>La<jats:sub>3</jats:sub>Zr<jats:sub>2</jats:sub>O<jats:sub>12</jats:sub> has been regarded as a promising electrolyte for solid‐state lithium batteries due to its high ionic conductivity and wide potential window. Unfortunately, the critical dendrite infiltration endows garnet with great limitations toward practical applications. Herein, a hybrid interlayer consisting of Ni nanocrystals encircled by fluoride/nitride matrix with mixed ionic‐electronic conductivity is in situ established to tailor Li/garnet interface chemistry via synergetic conversion reactions between NiF<jats:sub>2</jats:sub>/LiNO<jats:sub>3</jats:sub> and Li. Specifically, the inner non‐lithiated metallic Ni nanocrystal exhibits no obsession of alloy hardening during high‐temperature aging or long‐term cycling, reliably retaining its basic role of uniformizing interfacial electric‐field distribution. In addition, the outer fluoride/nitride bulk with balanced ionic conductivity and interface energy toward Li inhibits the electron tunneling and dendrite invasion from the Li anode. Consequently, a dendrite‐free Li plating/stripping can be achieved even at a critical current density of as high as 1.5 mA cm<jats:sup>−2</jats:sup>. Besides, the resultant solid‐state LiNi<jats:sub>0.6</jats:sub>Co<jats:sub>0.2</jats:sub>Mn<jats:sub>0.2</jats:sub>O<jats:sub>2</jats:sub>/Li cell based on such interface engineering displays an initial discharge capacity of 159 mAh g<jats:sup>−1</jats:sup>, followed by a high capacity retention of 77.4% after 300 cycles. This study provides a novel strategy for the construction of mixed‐conductivity interlayers by implanting non‐lithiated metal particles into inorganic‐rich fast ion conductors to reinforce the Li/garnet interface.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"690 1","pages":""},"PeriodicalIF":18.5000,"publicationDate":"2025-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202512506","RegionNum":1,"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
Garnet‐type Li7La3Zr2O12 has been regarded as a promising electrolyte for solid‐state lithium batteries due to its high ionic conductivity and wide potential window. Unfortunately, the critical dendrite infiltration endows garnet with great limitations toward practical applications. Herein, a hybrid interlayer consisting of Ni nanocrystals encircled by fluoride/nitride matrix with mixed ionic‐electronic conductivity is in situ established to tailor Li/garnet interface chemistry via synergetic conversion reactions between NiF2/LiNO3 and Li. Specifically, the inner non‐lithiated metallic Ni nanocrystal exhibits no obsession of alloy hardening during high‐temperature aging or long‐term cycling, reliably retaining its basic role of uniformizing interfacial electric‐field distribution. In addition, the outer fluoride/nitride bulk with balanced ionic conductivity and interface energy toward Li inhibits the electron tunneling and dendrite invasion from the Li anode. Consequently, a dendrite‐free Li plating/stripping can be achieved even at a critical current density of as high as 1.5 mA cm−2. Besides, the resultant solid‐state LiNi0.6Co0.2Mn0.2O2/Li cell based on such interface engineering displays an initial discharge capacity of 159 mAh g−1, followed by a high capacity retention of 77.4% after 300 cycles. This study provides a novel strategy for the construction of mixed‐conductivity interlayers by implanting non‐lithiated metal particles into inorganic‐rich fast ion conductors to reinforce the Li/garnet interface.
石榴石型Li7La3Zr2O12因其高离子电导率和宽电位窗而被认为是一种很有前途的固态锂电池电解质。不幸的是,临界枝晶渗透使石榴石在实际应用中受到很大的限制。本文在原位建立了一种由氟化/氮化混合离子电子电导率的Ni纳米晶体组成的杂化夹层,通过NiF2/LiNO3与Li之间的协同转化反应来调整Li/石榴石界面的化学性质。具体而言,在高温时效或长期循环过程中,内部非锂化金属镍纳米晶没有表现出合金硬化的困扰,可靠地保持了其均匀界面电场分布的基本作用。此外,具有平衡离子电导率和界面能的外氟/氮体抑制了来自锂阳极的电子隧穿和枝晶入侵。因此,即使在高达1.5 mA cm−2的临界电流密度下,也可以实现无枝晶的锂电镀/剥离。此外,基于该界面工程的固态LiNi0.6Co0.2Mn0.2O2/Li电池的初始放电容量为159 mAh g−1,循环300次后容量保持率高达77.4%。该研究提供了一种构建混合导电性中间层的新策略,通过在富无机快离子导体中植入非锂化金属颗粒来增强Li/石榴石界面。
期刊介绍:
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