4.8 Article

Tailoring Rod-Like FeSe2 Coated with Nitrogen-Doped Carbon for High-Performance Sodium Storage

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 28, Issue 30, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201801765

Keywords

anodes; FeSe2; N-C; kinetics behaviors; sodium-ion batteries; ultralong cycling stability

Funding

  1. National Key Research and Development Program of China [2017YFB0102000, 2018YFB0104200]
  2. National Natural Science Foundation of China [51622406, 21673298, 21473258]
  3. National Postdoctoral Program for Innovative Talents [BX00192]
  4. China Postdoctoral Science Foundation [2017M6203552]
  5. Young Elite Scientists Sponsorship Program by CAST [2017QNRC001]
  6. Innovation Mover Program of Central South University [2017CX004, 2018CX005]
  7. Hunan Provincial Science and Technology Plan [2017TP1001]
  8. Provincial Natural Science Foundation of Hunan [2016TP1009]
  9. Hunan Provincial Natural Science Foundation of China [2018JJ3633]
  10. Postgraduate Electronic Design Competition of China [502241802]
  11. Fundamental Research Funds for the Central Universities of Central South University [2018zzts013, 2018zzts369]

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Designing potential anodes for sodium-ion battery with both remarkable durability and high-rate capability has captured enormous attention so far. The engineering of size and morphology is deemed as an effective manner to boost the electrochemical properties. Owing to the anisotropic self-assembly of iron selenide, rod-like FeSe2 coates with nitrogen-doped carbon is prepared through the thermal reaction of Prussian blue with selenium. Notably, the cyano groups are effectively transformed into N-doped carbon with FeNC bonds, which uniformly coats FeSe2, prompting Na+ transportations. Interestingly, the particle size is tailored by heating rates, along with increased carbon content, leading to broadened energy levels for redox reaction. Bestowed by these advantages, the FeSe2/N-C as Na-storage anode delivers impressive electrochemical properties. Even at a rather high rate of 10.0 A g(-1), a considerable capacity of 308 mAh g(-1) is yielded over 10 000 loops. Supported by the detailed analysis of kinetic features, reduced size of particles could bring about the enhanced contributions of pseudocapacitive and quickening rate of ions transferring. The phase evolutions are further investigated by in situ EIS and ex-situ technologies. The work is expected to provide a new strategy to prepare metal-selenide with controllable size and induce the faster kinetic of high-rate materials.

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