材料科学
兴奋剂
化学工程
纳米颗粒
纳米技术
煅烧
电池(电)
氟化物
无机化学
催化作用
光电子学
化学
有机化学
功率(物理)
物理
量子力学
工程类
作者
Min Liu,Biaobing Chen,Tianjing Wu,Hui Li,Xiaolin Liu,Gang Wang,Manfang Chen,Zhenhua Yang,Yiming Bai,Xianyou Wang
标识
DOI:10.1016/j.cej.2022.138774
摘要
Conversion-type iron fluoride promises a high energy density and redox potential, which is considered an extremely promising candidate for next-generation high-specific-energy and low-cost Li-ion battery. Unfortunately, its commercialization is plagued by the poor rate capability and fast capacity degradation resulting from its inferior electronic conductivity and large volumetric expansion. Herein, a three-dimensional sandwich architecture of rGO-encapsulated Ni/Co dual‐doped FeF3·0.33H2O nanoparticles (NC-FF) is fabricated by co-precipitation and subsequent calcination. The results show that the flower-like Ni/Co dual‐doped FeF3·0.33H2O nanoparticles are firmly encapsulated within highly conductive rGO sheets through MOC bonding interaction, which constructs a robust electronic/ionic network and a buffer layer against the severe volume variation. The Ni-doping can facilitate to the capacity improvement by expanding the cell volume, and the Co-doping can promote the rate capability and cycling stability enhancement by accelerating Li+ migration. Benefiting from the synergies of Ni/Co dual-doping and encapsulation of rGO, the NC-FF exhibits a high-rate capability of 200.1 mAh g−1 at 5.0 C and good cycle stability of 177.8 mAh g−1 after 400cycles. Moreover, the NC-FF|Graphite symmetric-cell still shows a high reversible capacity of 396.2 mAh g−1 at 1.0C and good cycle stability of 247.5 mAh g−1 after 100cycles.
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