4.6 Article

Pomegranate-like mesoporous double carbon-coated Fe2P nanoparticles as advanced anode materials for sodium-ion batteries

Journal

JOURNAL OF MATERIALS SCIENCE
Volume 57, Issue 20, Pages 9389-9402

Publisher

SPRINGER
DOI: 10.1007/s10853-022-07257-x

Keywords

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Funding

  1. National Natural Science Foundation of China [51802128]
  2. Science and Technology Project of Xuzhou [KC21005]
  3. natural science research project of Jiangsu University [21KJA430003]
  4. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX20_2352]
  5. Foundation of State Key Laboratory of High-Efficiency Utilization of Coal and Green Chemical Engineering, China [2020-KF-20]
  6. College Students' Innovation and Entrepreneurship Project [202110320029Z]

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This paper introduces a novel anode material for sodium-ion batteries (SIBs) called pomegranate-like mesoporous double carbon-coated Fe2P nanoparticles (Fe2P@C@NC). The structure of Fe2P@C@NC provides a large specific surface area, pore-volume, excellent electronic conductivity network, and buffering volume expansion. It exhibits excellent performance and speedy electrode reaction kinetics during charge-discharge cycles, delivering a reversible specific capacity of 408 mAh g(-1) with almost no decay after the 100th cycle. It also demonstrates excellent rate capability and durability at high current density. The unique self-confined growth strategy used in synthesizing Fe2P@C@NC has great practical value for next-generation energy storage systems.
Anode materials have limited the development of sodium-ion batteries (SIBs). In this paper, the novel pomegranate-like mesoporous double carbon-coated Fe2P nanoparticles (Fe2P@C@NC), in which Fe2P is confined in the thin carbon shell derived from phytic acid and then wholly embedded into N-doped carbon network, can be applied as anode materials for SIBs. The elaborated structure presents several prominent merits, such as large specific surface area, pore-volume, excellent electronic conductivity network, and buffering volume expansion. All of these endow the structural integrity of Fe2P@C@NC material with excellent performance during charge-discharge cycles and guarantee speedy electrode reaction kinetics. As SIBs anode, Fe2P@C@NC material delivers an excellent reversible specific capacity of 408 mAh g(-1) with almost no decay after the 100th cycles. And it also features excellent rate capability and splendid durability (attenuation rate of 0.05% per cycle with 1000th cycles) at high current density. These results confirm that the unique self-confined growth strategy has a great practical value in synthesizing advanced materials for next-generation energy storage systems. [GRAPHICS] .

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