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Post-Synthetic and In Situ Vacancy Repairing of Iron Hexacyanoferrate Toward Highly Stable Cathodes for Sodium-Ion Batteries

Iron hexacyanoferrate (FeHCF) is a promising cathode material for sodium-ion batteries. However, FeHCF always suffers from a poor cycling stability, which is closely related to the abundant vacancy defects in its framework. Herein, post-synthetic and in-situ vacancy repairing strategies are proposed...

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Detalles Bibliográficos
Autores principales: Wan, Min, Zeng, Rui, Meng, Jingtao, Cheng, Zexiao, Chen, Weilun, Peng, Jiayu, Zhang, Wuxing, Huang, Yunhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8642478/
https://www.ncbi.nlm.nih.gov/pubmed/34862572
http://dx.doi.org/10.1007/s40820-021-00742-z
Descripción
Sumario:Iron hexacyanoferrate (FeHCF) is a promising cathode material for sodium-ion batteries. However, FeHCF always suffers from a poor cycling stability, which is closely related to the abundant vacancy defects in its framework. Herein, post-synthetic and in-situ vacancy repairing strategies are proposed for the synthesis of high-quality FeHCF in a highly concentrated Na(4)Fe(CN)(6) solution. Both the post-synthetic and in-situ vacancy repaired FeHCF products (FeHCF-P and FeHCF-I) show the significant decrease in the number of vacancy defects and the reinforced structure, which can suppress the side reactions and activate the capacity from low-spin Fe in FeHCF. In particular, FeHCF-P delivers a reversible discharge capacity of 131 mAh g(−1) at 1 C and remains 109 mAh g(−1) after 500 cycles, with a capacity retention of 83%. FeHCF-I can deliver a high discharge capacity of 158.5 mAh g(−1) at 1 C. Even at 10 C, the FeHCF-I electrode still maintains a discharge specific capacity of 103 mAh g(−1) and retains 75% after 800 cycles. This work provides a new vacancy repairing strategy for the solution synthesis of high-quality FeHCF. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40820-021-00742-z.