4.8 Article

Liquid exfoliation of interlayer spacing-tunable 2D vanadium oxide nanosheets: High capacity and rate handling Li-ion battery cathodes

Journal

NANO ENERGY
Volume 39, Issue -, Pages 151-161

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.nanoen.2017.06.044

Keywords

Liquid-phase exfoliation; V2O5 nanosheets; Carbon nanotubes; Li-ion battery; Environmentally friendly; Interlayer spacing

Funding

  1. SFI AMBER
  2. SFI PIYRA
  3. ERC StG 2DNanoCaps
  4. ERC PoC 2DUSD
  5. ERC PoC 2DInk
  6. FP7 MC ITN MoWSeS
  7. Horizon2020 NMP Co-Pilot
  8. ERC SEMANTICS
  9. SFI [11/PI/1087]
  10. CRANN
  11. AMBER
  12. School of Chemistry, Physics of Trinity College Dublin

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With a layered crystal structure and good Li+ storage performance, vanadium pentoxide (V2O5) is potentially a high-energy and cost-effective cathode material for Li-ion batteries (LiBs). Networks of two-dimensional V2O5 nanosheets (2D V2O5 NS), with large interlayer distance, are ideal for enhancing the Li+ diffusion kinetics and thus for building high power LiBs. However, the lack of a simple, scalable and environmentally friendly route to nanosheet production still hinders the development of V2O5 applications. Here we demonstrate, liquid-phase exfoliation (LPE) of commercial V2O5 powder in environmental friendly solvents (water and ethanol) to achieve large quantities of 2D V2O5 NS dispersions. The V2O5 NS are of high-quality whose interlayer spacing can be well manipulated, ranging from 4.4 angstrom to 11.5 angstrom in ethanol and water (forming NS xerogel), respectively. Ultrasonic aerosol printing of V2O5 NS xerogel/single-wall carbon nanotube (SWCNT) blended dispersions resulted in large-area, flexible, and binder-free hybrid electrodes, which showcase a high discharge capacity of 370 mA h g(-1) at 0.05 C, high energy density (555 W h kg(-1)) and power density (2175 W kg(-1)), etc. These properties can be attributed to the synergistic effects between the expanded hydrated NS and the conductive SWCNT matrix; the latter improves the reversible phase transition reactions of the NS, enhances the ion diffusion kinetics, maintains the electrode's mechanical integrity and provides electron transport pathways. The Li+ storage mechanism was investigated, suggesting the capacity was majorly contributed by the non-diffusion controlled process (pseudocapacitive). We believe the LPE/aerosol printing approach is environmentally green, general and scalable, and could be extended to other layered transitional metal oxides or dichalcogenides for fabrication of corresponding flexible, binder-free, conductive composites for energy storage systems.

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