阴极
化学工程
碳纤维
材料科学
纳米技术
化学
磷酸盐
钠
化学稳定性
替代(逻辑)
阳极
无机化学
磷酸铁锂
带隙
光电子学
电子结构
电极
磷酸铁
理论(学习稳定性)
作者
Quan Lu,Tongyin Shen,Chunlin Li,Yujin Wei,Yu Zhou,Mingru Su,Panpan Zhang,Chenteng Sun,Jianchun Wu,Fei Wang,Leyi Zhang,Qianqiu Tian,Yunjian Liu,Renheng Wang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-01-19
卷期号:26 (4): 1375-1384
被引量:10
标识
DOI:10.1021/acs.nanolett.5c05384
摘要
Achieving both long-term stability and superior rate capability in Na 4 Fe 3 (PO 4 ) 2 P 2 O 7 (NFPP) cathodes remains a major challenge for sodium-ion batteries. Herein, we demonstrate a synergistic bond-defect strategy that circumvents this trade-off. The complementary interaction between Zn and F establishes a synergistic bond-defect environment. The strong bonding of Zn 2+ mitigates the charge localization associated with F – doping. Furthermore, the strategy narrows the electronic bandgap to near-metallic values and enhances the degree of graphitization in carbon coatings, resulting in a marked improvement in electronic conductivity. The optimized Na 3.95 Fe 2.95 Zn 0.05 (PO 4 ) 2 P 2 O 6.95 F 0.05 (NFZPPF) exhibits outstanding cycling stability with 76.25% retention after 16,000 cycles at 20 C and remarkable rate performance, delivering 68.6 mAh g –1 at 50 C. Coupled with a hard carbon anode, the full cell retains 88.8% capacity after 200 cycles at 2 C, underscoring its viability for practical sodium-ion storage.
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