材料科学
阴极
阳极
电化学
氧烷
氧化还原
离子
电池(电)
光电子学
化学工程
纳米技术
电极
物理化学
化学
光谱学
功率(物理)
物理
有机化学
量子力学
工程类
冶金
作者
Jinqiang Gao,Hongyi Chen,Yu Mei,Lianshan Ni,Haoji Wang,Jiangnan Huang,Ningyun Hong,Song Bai,Ye Tian,Wentao Deng,Guoqiang Zou,Hongshuai Hou,Xiaobo Ji
出处
期刊:Nano Energy
[Elsevier]
日期:2023-08-01
卷期号:115: 108747-108747
被引量:20
标识
DOI:10.1016/j.nanoen.2023.108747
摘要
Na4Fe3(PO4)2(P2O7) (NFPP) is an attractive cathode material for sodium-ion batteries (SIBs) due to its low-cost, robust framework, and cross-linked Na+ migrate channels. However, the real implementation of NFPP remains in its infancy, mainly hindered by the inferior intrinsic electronic conductivity. Herein, a doping strategy by incorporating manganese into NFPP lattice (NFMPP) is proposed to lower the band gap and Na+ migrate barriers, thus ultimately rendering robust ligand framework, improved electronic transmission and fast ions diffusion. Greatly, the ultralong-lasting cyclability (88.1% capacity retention for over 10000 cycles at 50 C), impressive rate capability (42.7 mAh g−1 at 200 C), and decent electrochemical performance over a wide operation-temperature range from − 40–60 ℃ are achieved. The structural evolution and charge compensation mechanism during cell operation are systematically explored utilizing in situ X-ray diffraction (XRD) and X-ray absorption near edge structure (XANES) measurements, confirming a minimized volume fluctuation and highly reversible Fe2+/Fe3+ redox reaction. Full cell comprising a NFMPP cathode and pre-sodiated hard carbon anode is also yielded as proof of concept. The superior electrochemical performances, and the insertion/extraction mechanism investigation sheds light to the feasibility of utilizing NFMPP as a cathode material for low-cost and high-performance gride-scale energy storage systems (EESs).
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