4.7 Article

Highly dispersed FeSe2 nanoparticles in porous carbon nanofibers as advanced anodes for sodium and potassium ion batteries

Journal

JOURNAL OF ALLOYS AND COMPOUNDS
Volume 834, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2020.155265

Keywords

Mesoporous carbon nanofiber; FeSe2; Sodium storage; Potassium ion batteries

Funding

  1. National Natural Science Foundation of China [51672213]
  2. Industrial Innovation Chain of Key Research and Development Project of Shaanxi Province [2018ZDCXL-GY-08-04]
  3. Key Science and Technology Innovation Team Project of Natural Science Foundation of Shaanxi Province [2017KCT-01]
  4. Natural Science Foundation of Shaanxi Province [2018JQ2004]
  5. Foundation of the Education Committee of Shaanxi Province [18JK0798]

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Sodium and potassium ion batteries (SIBs and PIBs) have received a substantial amount of attention in large-scale applications due to the abundance and low price of sodium and potassium metals. However, large-sized Na+ and K+ ions can cause sluggish kinetics, large volume change and unsatisfactory cycling behaviors. Herein, highly dispersed FeSe2 nanoparticles confined in mesoporous carbon nanofibers (FeSe2@C) were prepared via a novel selenization strategy and utilized as an anode material in both SIBs and PIBs for the first time. The mesoporous FeSe2@C nanocomposite possesses unique structural features including a large surface area and the presence of highly dispersed FeSe2 nanoparticles and a 1D mesocarbon nanofiber matrix, which can efficiently enhance electrical conductivity, facilitate electron/ion transportation and alleviate volume variations, thereby enabling fast Na/K storage kinetics, an outstanding structural integrity and a superior Na/K storage performance. For SIBs, FeSe2@C shows a high charge capacity of 483 mAh g(-1) at 0.2 A g(-1) over 100 cycles, which retains a capacity of 359 mAh g(-1) after 200 cycles at 1.0 A g(-1). When employed as anode for PIBs, FeSe2@C displays a high charge capacity of 352 mAh g(-1) at 0.1 A g(-1). Moreover, the electrochemical kinetic analysis confirms that the excellent pseudocapacitive behavior accounts for the superior sodium/potassium storage performance at high current densities. (C) 2020 Elsevier B.V. All rights reserved.

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