4.6 Article

Electrospinning synthesis of porous carbon nanofiber supported CoSe2 nanoparticles towards enhanced sodium ion storage

Journal

MATERIALS CHEMISTRY AND PHYSICS
Volume 262, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.matchemphys.2021.124314

Keywords

Sodium ion batteries; CoSe(2 )nanoparticles; Porous carbon nanofibers; PAN/PMMA; Electrochemical performance

Funding

  1. National Natural Science Foundation of China [51905236, 52077175]
  2. China Postdoctoral Science Foundation [2020M673395, 2019M663695]
  3. State Key Laboratory of Electrical Insulation and Power Equipment [EIPE19127]
  4. Natural Science Research Project of Higher Education Institutions in Jiangsu Province [20KJA480005]
  5. Qinglan Engineering Project of Jiangsu Universities

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Porous carbon nanofiber supported CoSe2 nanoparticles were designed and fabricated for sodium-ion batteries, showing excellent sodium-ion storage performances with high reversible capacity and good rate capability.
CoSe2-based anode materials are highly attractive for sodium-ion batteries (SIBs) due to their high theoretical specific capacity, but the weak rate capability and rapid capacity fading hinder their practical application. Herein, porous carbon nanofiber supported CoSe2 nanoparticles (denoted as CS@PCNIFs) are designed and fabricated through electrospinning and subsequent heat treatment with PAN (polyacrylonitrile) as the carbon source and PMMA (polymethyl methacrylate) as the pore-forming agent to design the porous architecture of the carbon nanofibers and control the amount of CoSe2 grains anchored on the fiber surface. Benefiting from the desired structural features including the large specific surface area, appropriate pore volume and robust structure stability, when examined as anode materials for SIBs, the as-prepared CS@PCNIFs demonstrated excellent sodium-ion storage performances. Experimental results show that the CS@PCNIFs with an optimized PAN/PMMA mass ratio of 6:4 can deliver a high reversible capacity of 413.6 mA h g(-1) at 0.2 A g(-1) after 150 cycles and an excellent rate capability of 401.5 mA h g(-1) at 2.0 A g(-1).

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