Liang Jianwen, Li Xiaona, Kim Jung Tae, Hao Xiaoge, Duan Hui, Li Ruying, Sun Xueliang
Department of Mechanical and Materials Engineering, University of Western Ontario, 1151 Richmond St, London, Ontario, N6A 3K7, Canada.
Angew Chem Int Ed Engl. 2023 Mar 20;62(13):e202217081. doi: 10.1002/anie.202217081. Epub 2023 Feb 16.
Insertion-type compounds based on oxides and sulfides have been widely identified and well-studied as cathode materials in lithium-ion batteries. However, halides have rarely been used due to their high solubility in organic liquid electrolytes. Here, we reveal the insertion electrochemistry of VX (X=Cl, Br, I) by introducing a compatible halide solid-state electrolyte with a wide electrochemical stability window. X-ray absorption near-edge structure analyses reveal a two-step lithiation process and the structural transition of typical VCl . Fast Li insertion/extraction in the layered VX active materials and favorable interface guaranteed by the compatible electrode-electrolyte design enables high rate capability and stable operation of all-solid-state Li-VX batteries. The findings from this study will contribute to developing intercalation insertion electrochemistry of halide materials and exploring novel electrode materials in viable energy storage systems.
基于氧化物和硫化物的嵌入型化合物作为锂离子电池的阴极材料已被广泛识别和深入研究。然而,由于卤化物在有机液体电解质中的高溶解度,它们很少被使用。在这里,我们通过引入具有宽电化学稳定窗口的兼容卤化物固态电解质,揭示了VX(X = Cl、Br、I)的嵌入电化学。X射线吸收近边结构分析揭示了典型VCl的两步锂化过程和结构转变。层状VX活性材料中快速的锂嵌入/脱出以及由兼容的电极-电解质设计保证的良好界面,使得全固态锂-VX电池具有高倍率性能和稳定运行。这项研究的结果将有助于发展卤化物材料的嵌入电化学,并在可行的储能系统中探索新型电极材料。