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Freestanding 1T‐Mn x Mo 1– x S 2– y Se y and MoFe 2 S 4– z Se z Ultrathin Nanosheet‐Structured Electrodes for Highly Efficient Flexible Solid‐State Asymmetric Supercapacitors
Author(s) -
Pan Uday Narayan,
Sharma Vikas,
Kshetri Tolendra,
Singh Thangjam Ibomcha,
Paudel Dasu Ram,
Kim Nam Hoon,
Lee Joong Hee
Publication year - 2020
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.202001691
Subject(s) - nanosheet , fabrication , materials science , supercapacitor , doping , transition metal , nanotechnology , electrochemistry , nonmetal , electrode , intercalation (chemistry) , metal , phase (matter) , optoelectronics , inorganic chemistry , chemistry , metallurgy , medicine , biochemistry , alternative medicine , organic chemistry , pathology , catalysis
Fabrication of hierarchical nanosheet arrays of 1T phase of transition‐metal dichalcogenides is indeed a critical task, but it holds immense potential for energy storage. A single‐step strategy is employed for the fabrication of stable 1T‐Mn x Mo 1– x S 2– y Se y and MoFe 2 S 4– z Se z hierarchical nanosheet arrays on carbon cloth as positive and negative electrodes, respectively. The flexible asymmetric supercapacitor constructed with these two electrodes exhibits an excellent electrochemical performance (energy density of ≈69 Wh kg −1  at a power density of 0.985 kW kg −1 ) with ultralong cyclic stability of ≈83.5% capacity retention, after 10 000 consecutive cycles. Co‐doping of the metal and nonmetal boosts the charge storage ability of the transition‐metal chalcogenides following enrichment in the metallic 1T phase, improvement in the surface area, and expansion in the interlayer spacing in tandem, which is the key focus of the present study. This study explicitly demonstrates the exponential enhancement of specific capacity of MoS 2 following intercalation and doping of Mn and Se, and Fe 2 S 3 following doping of Mo and Se could be an ideal direction for the fabrication of novel energy‐storage materials with high‐energy storage ability.

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