Zhihao Guo , Xiaobao Zhang , Huan Zhao , Yiyang Xiao , Shiang Liang , Ning Wang , Juanyu Yang , Xiaowei Huang
{"title":"In-situ constructing LiOH∙H2O on GaLaZr precursor via spray drying to synthesize Li6.4Ga0.2La3Zr2O12 powder material","authors":"Zhihao Guo , Xiaobao Zhang , Huan Zhao , Yiyang Xiao , Shiang Liang , Ning Wang , Juanyu Yang , Xiaowei Huang","doi":"10.1016/j.nxmate.2025.100580","DOIUrl":null,"url":null,"abstract":"<div><div>Garnet Li<sub>6.4</sub>Ga<sub>0.2</sub>La<sub>3</sub>Zr<sub>2</sub>O<sub>12</sub> (LGLZO) solid-state electrolyte is widely considered as a promising candidate for solid-state lithium batteries. However, the production of LGLZO powder material under real circumstances faces the challenges of production instability, safety hazards and huge energy consumption concerns. Here in this work, a novel method to synthesize cubic LGLZO powder material by in-situ constructing LiOH∙H<sub>2</sub>O on GaLaZr precursor is developed. By virtue of spray drying, a continuous nano LiOH∙H<sub>2</sub>O layer with low crystallinity is successfully coated on the surface of the GaLaZr precursor particles. Revealed by 2D Raman mapping and TEM, the intimate contact and uniform mixing have been realized between LiOH∙H<sub>2</sub>O and GaLaZr precursor. Synthesis temperature of cubic LGLZO without clear secondary phases is lowered as 850 °C. The total ionic conductivity at 303 K of LGLZO is determined to be 1 × 10<sup>−3</sup> S cm<sup>−1</sup> with an activation energy of 0.24 eV while the electronic conductivity is characterized to 1.9 × 10<sup>−8</sup> S cm<sup>−1</sup>. This work enriches the synthesis method of LGLZO powder material and is expected to facilitate its safe and stable scaling-up production for solid-state lithium batteries.</div></div>","PeriodicalId":100958,"journal":{"name":"Next Materials","volume":"8 ","pages":"Article 100580"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Next Materials","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S294982282500098X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
石榴石锂6.4Ga0.2La3Zr2O12(LGLZO)固态电解质被广泛认为是固态锂电池的理想候选材料。然而,在现实条件下生产 LGLZO 粉末材料面临着生产不稳定、安全隐患大、能耗高等问题。本研究开发了一种在 GaLaZr 前驱体上原位构建 LiOH∙H2O 来合成立方 LGLZO 粉末材料的新方法。通过喷雾干燥,成功地在 GaLaZr 前驱体颗粒表面镀上了一层低结晶度的连续纳米 LiOH∙H2O 层。二维拉曼图谱和 TEM 显示,LiOH∙H2O 与 GaLaZr 前驱体之间实现了亲密接触和均匀混合。无明显次生相的立方 LGLZO 的合成温度降低至 850 ℃。经测定,LGLZO 在 303 K 时的总离子电导率为 1 × 10-3 S cm-1,活化能为 0.24 eV;电子电导率为 1.9 × 10-8 S cm-1。这项工作丰富了 LGLZO 粉末材料的合成方法,有望促进其安全稳定地放大生产,用于固态锂电池。
In-situ constructing LiOH∙H2O on GaLaZr precursor via spray drying to synthesize Li6.4Ga0.2La3Zr2O12 powder material
Garnet Li6.4Ga0.2La3Zr2O12 (LGLZO) solid-state electrolyte is widely considered as a promising candidate for solid-state lithium batteries. However, the production of LGLZO powder material under real circumstances faces the challenges of production instability, safety hazards and huge energy consumption concerns. Here in this work, a novel method to synthesize cubic LGLZO powder material by in-situ constructing LiOH∙H2O on GaLaZr precursor is developed. By virtue of spray drying, a continuous nano LiOH∙H2O layer with low crystallinity is successfully coated on the surface of the GaLaZr precursor particles. Revealed by 2D Raman mapping and TEM, the intimate contact and uniform mixing have been realized between LiOH∙H2O and GaLaZr precursor. Synthesis temperature of cubic LGLZO without clear secondary phases is lowered as 850 °C. The total ionic conductivity at 303 K of LGLZO is determined to be 1 × 10−3 S cm−1 with an activation energy of 0.24 eV while the electronic conductivity is characterized to 1.9 × 10−8 S cm−1. This work enriches the synthesis method of LGLZO powder material and is expected to facilitate its safe and stable scaling-up production for solid-state lithium batteries.