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朝着具有最佳结构-导电特性的方钠石型 LiPSCl 固态电解质的简易合成。

Facile Synthesis toward the Optimal Structure-Conductivity Characteristics of the Argyrodite LiPSCl Solid-State Electrolyte.

机构信息

Department of Radiation Science and Technology , Delft University of Technology , Mekelweg 15 , 2629 JB Delft , The Netherlands.

Institute for Molecules and Materials , Radboud University Nijmegen , Heyendaalseweg 135 , 6525 AJ Nijmegen , The Netherlands.

出版信息

ACS Appl Mater Interfaces. 2018 Oct 3;10(39):33296-33306. doi: 10.1021/acsami.8b07476. Epub 2018 Sep 20.

DOI:10.1021/acsami.8b07476
PMID:30199216
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6172600/
Abstract

The high Li-ion conductivity of the argyrodite LiPSCl makes it a promising solid electrolyte candidate for all-solid-state Li-ion batteries. For future application, it is essential to identify facile synthesis procedures and to relate the synthesis conditions to the solid electrolyte material performance. Here, a simple optimized synthesis route is investigated that avoids intensive ball milling by direct annealing of the mixed precursors at 550 °C for 10 h, resulting in argyrodite LiPSCl with a high Li-ion conductivity of up to 4.96 × 10 S cm at 26.2 °C. Both the temperature-dependent alternating current impedance conductivities and solid-state NMR spin-lattice relaxation rates demonstrate that the LiPSCl prepared under these conditions results in a higher conductivity and Li-ion mobility compared to materials prepared by the traditional mechanical milling route. The origin of the improved conductivity appears to be a combination of the optimal local Cl structure and its homogeneous distribution in the material. All-solid-state cells consisting of an 80LiS-20LiI cathode, the optimized LiPSCl electrolyte, and an In anode showed a relatively good electrochemical performance with an initial discharge capacity of 662.6 mAh g when a current density of 0.13 mA cm was used, corresponding to a C-rate of approximately C/20. On direct comparison with a solid-state battery using a solid electrolyte prepared by the mechanical milling route, the battery made with the new material exhibits a higher initial discharge capacity and Coulombic efficiency at a higher current density with better cycling stability. Nevertheless, the cycling stability is limited by the electrolyte stability, which is a major concern for these types of solid-state batteries.

摘要

硫代磷酸亚砜氯(LiPSCl)具有较高的锂离子电导率,使其成为全固态锂离子电池有前途的固体电解质候选材料。为了未来的应用,必须确定简便的合成工艺,并将合成条件与固体电解质材料性能联系起来。在此,研究了一种简单的优化合成路线,该路线通过直接在 550°C 下将混合前体退火 10 小时来避免剧烈的球磨,从而得到具有高达 4.96×10 S cm 的锂离子电导率的硫代磷酸亚砜氯,在 26.2°C 时。交流阻抗电导率和固态 NMR 自旋晶格弛豫率的温度依赖性均表明,与传统机械球磨路线制备的材料相比,在这些条件下制备的 LiPSCl 具有更高的电导率和锂离子迁移率。电导率提高的原因似乎是优化的局部 Cl 结构及其在材料中的均匀分布的组合。由 80LiS-20LiI 阴极、优化的 LiPSCl 电解质和 In 阳极组成的全固态电池在使用 0.13 mA cm 的电流密度时具有相对较好的电化学性能,初始放电容量为 662.6 mAh g,相应的 C 率约为 C/20。与使用机械球磨路线制备的固体电解质的固态电池直接进行比较,使用新材料制成的电池在较高的电流密度下具有更高的初始放电容量和库仑效率以及更好的循环稳定性。然而,循环稳定性受到电解质稳定性的限制,这是此类固态电池的主要关注点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7198/6172600/cc4f2862db81/am-2018-07476f_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7198/6172600/e3fc04a3c668/am-2018-07476f_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7198/6172600/9c8f23c5b459/am-2018-07476f_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7198/6172600/add42bfd655b/am-2018-07476f_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7198/6172600/060d410dcabf/am-2018-07476f_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7198/6172600/28a4f8394701/am-2018-07476f_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7198/6172600/cc4f2862db81/am-2018-07476f_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7198/6172600/e3fc04a3c668/am-2018-07476f_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7198/6172600/9c8f23c5b459/am-2018-07476f_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7198/6172600/add42bfd655b/am-2018-07476f_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7198/6172600/060d410dcabf/am-2018-07476f_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7198/6172600/28a4f8394701/am-2018-07476f_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7198/6172600/cc4f2862db81/am-2018-07476f_0002.jpg

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