Amorphous Oxyhalide Matters for Achieving Lithium Superionic Conduction

Shumin Zhang, Feipeng Zhao, Lo Yueh Chang, Yu Chun Chuang, Zhen Zhang, Yuanmin Zhu, Xiaoge Hao, Jiamin Fu, Jiatang Chen, Jing Luo, Minsi Li, Yingjie Gao, Yining Huang, Tsun Kong Sham, M. Danny Gu, Yuanpeng Zhang, Graham King, Xueliang Sun

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

The recently surged halide-based solid electrolytes (SEs) are great candidates for high-performance all-solid-state batteries (ASSBs), due to their decent ionic conductivity, wide electrochemical stability window, and good compatibility with high-voltage oxide cathodes. In contrast to the crystalline phases in halide SEs, amorphous components are rarely understood but play an important role in Li-ion conduction. Here, we reveal that the presence of amorphous component is common in halide-based SEs that are prepared via mechanochemical method. The fast Li-ion migration is found to be associated with the local chemistry of the amorphous proportion. Taking Zr-based halide SEs as an example, the amorphization process can be regulated by incorporating O, resulting in the formation of corner-sharing Zr-O/Cl polyhedrons. This structural configuration has been confirmed through X-ray absorption spectroscopy, pair distribution function analyses, and Reverse Monte Carlo modeling. The unique structure significantly reduces the energy barriers for Li-ion transport. As a result, an enhanced ionic conductivity of (1.35 ± 0.07) × 10-3 S cm-1 at 25 °C can be achieved for amorphous Li3ZrCl4O1.5. In addition to the improved ionic conductivity, amorphization of Zr-based halide SEs via incorporation of O leads to good mechanical deformability and promising electrochemical performance. These findings provide deep insights into the rational design of desirable halide SEs for high-performance ASSBs.

Original languageEnglish
Pages (from-to)2977-2985
Number of pages9
JournalJournal of the American Chemical Society
Volume146
Issue number5
DOIs
StatePublished - Feb 7 2024

Funding

This research was supported by the Natural Sciences and Engineering Research Council of Canada (NSERC), the Canada Research Chair Program (CRC), the Canada Foundation for Innovation (CFI), the Ontario Research Foundation (ORF), and the University of Western Ontario (UWO). The synchrotron research was performed at the Canadian Light Source, a national research facility of the University of Saskatchewan, which was supported by the CFI, NSERC, the National Research Council (NRC), the Canadian Institutes of Health Research (CIHR), the Government of Saskatchewan, and the University of Saskatchewan. This work has been partially supported by UT-Battelle, LLC, under Contract No. DE-AC05-00OR22725 with the US Department of Energy. The financial support is partially from Basic Research Foundation of Guangdong Province (Nos. 2022A1515140092 & 2023A1515011166). The TEM work used the resources of the Electron Microscopy Center from Dongguan University of Technolgy and the Cryo-TEM Center, Pico Center from SUSTech Core Research Facilities. Authors thank Sandamini H. Alahakoon from the University of Western Ontario for the assistance of NMR data collection.

FundersFunder number
Basic Research Foundation of Guangdong Province2023A1515011166, 2022A1515140092
U.S. Department of Energy
University of Saskatchewan
Ontario Research Foundation
National Research Council
UT-BattelleDE-AC05-00OR22725
Government of Saskatchewan
Canadian Institutes of Health Research
Natural Sciences and Engineering Research Council of Canada
Canada Foundation for Innovation
Canada Research Chairs
Western University

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