材料科学
兴奋剂
氟
钠
无机化学
分析化学(期刊)
结晶学
矿物学
冶金
化学
光电子学
色谱法
作者
Haiyang Ding,Yao Jiang,Xinlu Li,Jiafeng He
标识
DOI:10.1021/acsami.5c01638
摘要
Pure-phase iron-based phosphate Na3.4Fe2.4(PO4)1.4P2O7 (NFPP) is anticipated to emerge as a competitive candidate material for sodium-ion batteries (SIBs). Nevertheless, the low electronic conductivity and sluggish sodium ion diffusion kinetics during sodium storage present significant challenges to its electrochemical performance. Consequently, a sodium-rich fluorine-doping strategy has been proposed, and we elucidate the mechanism through which F doping influences the crystal structure and electronic conductivity of NFPP. Both experimental and theoretical calculations demonstrate that F doping expands the diffusion channels for Na+, reduces the band gap and Na+ migration energy barrier, and enhances the intrinsic electronic conductivity of NFPP. Owing to the enhanced charge transport capability, the electrochemical performance of Na3.475Fe2.4(PO4)1.4(P2O7)F0.075 (NFPPF-0.075) significantly surpasses that of the undoped sample. NFPPF-0.075 demonstrates a discharge specific capacity of 113.7 mAh g-1 at 0.1 C; even at a current density of 30 C, the discharge specific capacity is sustained at 84.1 mAh g-1. NFPPF-0.075 also exhibits remarkable cycle stability, achieving a capacity retention of 88.7% over 2000 cycles at 10 C. Furthermore, the NFPPF-0.075||HC full cell demonstrates remarkable rate performance and cycle performance. Therefore, Na3.475Fe2.4(PO4)1.4(P2O7)F0.075 has the potential to serve as a highly promising cathode material for large-scale applications in SIBs.
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