材料科学
阴极
钠
离子
无机化学
分析化学(期刊)
物理化学
冶金
化学
物理
色谱法
量子力学
作者
Houmou Li,Xinyu Hu,Jiaxin Liang,Xiangyu Wang,Qing Wang,Jiajun Li,Kun Ding,Haimei Liu,Zi‐Feng Ma
标识
DOI:10.1021/acsami.5c03459
摘要
Iron-based pyrophosphates, known for their open 3D channels and low cost, have garnered significant research attention. However, the poor intrinsic conductivity and low theoretical capacity hinder their further development in sodium-ion battery applications. In this study, we designed a sodium ferric pyrophosphate, Na2.67Fe2.67(P2O7)2 (termed NFPO-2.67), with a theoretical specific capacity of 128 mA h g-1 by optimizing the Na/Fe stoichiometric ratio of the substrate material, which expanded the conventional solid solution range in Na4-αFe2+α/2(P2O7)2 from (0 ≤ α ≤ 1) to (0 ≤ α ≤ 4/3). The pure-phase NFPO-2.67 exhibits an operating voltage of ∼3.0 V (vs Na+/Na) and delivers a specific capacity of 124.4 mA h g-1 at 0.1 C (close to its theoretical specific capacity) and an excellent rate performance (93.6 and 70.6 mA h g-1 at 1 and 10 C, respectively), as well as an outstanding cycling stability (70% capacity retention after 5000 cycles at 20 C). The possible mechanisms of their excellent electrochemical performance, including the material structure, energy storage mechanism, and Na+ diffusion kinetics, were further elucidated by using density functional theory (DFT). This work enriches the knowledge on solid solution systems and provides insights for exploring the nonstoichiometric ratios of iron-based pyrophosphate cathode materials in sodium-ion batteries.
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