Oxygen-Induced Structural Disruption for Improved Li+ Transport and Electrochemical Stability of Li3PS4

被引:13
作者
Deck, Michael J. [1 ]
Chien, Po-Hsiu [2 ]
Poudel, Tej P. [1 ]
Jin, Yongkang [1 ]
Liu, Haoyu [1 ]
Hu, Yan-Yan [1 ,2 ]
机构
[1] Florida State Univ, Dept Chem & Biochem, 95 Chieftan Way, Tallahassee, FL 32306 USA
[2] Natl High Magnet Field Lab, Ctr Interdisciplinary Magnet Resonance, 1800 East Paul Dirac Dr, Tallahassee, FL 32310 USA
基金
美国国家科学基金会;
关键词
energy storage; ionic conductivity; solid electrolytes; solid-state NMR; IONIC-CONDUCTIVITY; LITHIUM-ION; SOLID ELECTROLYTES; CRYSTAL-STRUCTURE; OXYSULFIDE; METAL; BATTERIES; DIFFUSION; REDOX; GLASS;
D O I
10.1002/aenm.202302785
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The performance of all-solid-state batteries (ASSBs) relies on the Li+ transport and stability characteristics of solid electrolytes (SEs). Li3PS4 is notable for its stability against lithium metal, yet its ionic conductivity remains a limiting factor. This study leverages local structural disorder via O substitution to achieve an ionic conductivity of 1.38 mS cm(-1) with an activation energy of 0.34 eV for Li3PS4-xOx (x = 0.31). Optimal O substitution transforms Li+ transport from 2D to 3D pathways with increased ion mobility. Li3PS3.69O0.31 exhibits improvements in the critical current density and stability against Li metal and retains its electrochemical stability window compared with Li3PS4. The practical implementation of Li3PS3.69O0.31 in ASSBs half-cells, particularly when coupled with TiS2 as the cathode active material, demonstrates substantially enhanced capacity and rate performance. This work elucidates the utility of introducing local structural disorder to ameliorate SE properties and highlights the benefits of strategically combining the inherent strengths of sulfides and oxides via creating oxysulfide SEs.
引用
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页数:11
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