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Solid-Solution Anion-Enhanced Electrochemical Performances of Metal Sulfides/Selenides for Sodium-Ion Capacitors: The Case of FeS2- xSe x.

Yaqiong LongJing YangXin GaoXuena XuWeiliu FanJian YangShifeng HouYitai Qian
Published in: ACS applied materials & interfaces (2018)
Transition-metal sulfides/selenides are explored as advanced electrode materials for nonaqueous sodium-ion capacitors, using FeS2- xSe x as an example. A solid solution of S/Se in FeS2- xSe x allows it to combine the high capacity of FeS2 and the good diffusion kinetics of FeSe2 together, thereby exhibiting excellent cycle stability (∼220 mA h g-1 after 6000 cycles at 2 A g-1) and superior rate capability (∼210 mA h g-1 at 40 A g-1) within 0.8-3.0 V. These results are much better than those of FeS2 and FeSe2, confirming the advantages of S/Se solid solution, as supported by EIS spectra, DFT calculations, and electronic conductivity. As FeS2- xSe x is paired with the activated carbon (AC) as Na-ion capacitors, this device is also better than sodium-ion batteries of FeS2- xSe x//Na3V2(PO4)3 and sodium-ion capacitors of metal oxides//AC, particularly at high rates. These results open a new door for the applications of sulfides/selenides in another device of electrochemical energy storage.
Keyphrases
  • ionic liquid
  • gold nanoparticles
  • transition metal
  • ion batteries
  • molecular dynamics
  • molecular dynamics simulations
  • molecular docking
  • monte carlo