TY - JOUR
T1 - Construction of dual metal ferrite-based core-shell nanostructures as low-cost multimetal electrode for boosting energy density of flexible asymmetric supercapattery
AU - Bandgar, Shubhangi B.
AU - Vadiyar, Madagonda M.
AU - Jambhale, Chitra L.
AU - Ye, Zhibin
AU - Kim, Jin Hyeok
AU - Kolekar, Sanjay S.
N1 - Publisher Copyright:
© 2021
PY - 2021/4
Y1 - 2021/4
N2 - We report the synthesis and fabrication of economically cheaper and binder-free hierarchical core-shell nanostructures of copper ferrite nanorods and nickel ferrite nanosheets (CuFe2O4–NR@NiFe2O4–NS) via a two-step wet chemical technique. The unique core-shell (nanorods@nanosheets) nanostructures offer multiple redox couples (Cu2+, Fe3+, and Ni2+), smaller ion diffusion path, and faster electron movement. When evaluated as an individual electrode in aqueous potassium hydroxide solution, the as-synthesized CuFe2O4–NR@NiFe2O4–NS electrode demonstrate superior electrochemical behaviour with concurrent specific capacity of 1366 C g−1 at current rate 1 A g−1, and 94% capacity retention over 10,000 cycles. A flexible asymmetric supercapattery device is assembled comprising positive electrode of CuFe2O4–NR@NiFe2O4–NS and negative electrode of reduced graphene oxide (rGO) with PVA-KOH semisolid electrolyte. The ASC cell manifest enhanced specific energy of 72 Wh kg−1, specific power of 0.287 kW kg−1 and outstanding cycle life (~97% of retention over 10,000 cycles at 10 A g−1). The superior specific capacity, capacity retention, and excellent cyclic life endow such multimetal ferrite-based core-shell architecture with tremendous potential for use as electrode materials for fabricating next generation energy storage devices.
AB - We report the synthesis and fabrication of economically cheaper and binder-free hierarchical core-shell nanostructures of copper ferrite nanorods and nickel ferrite nanosheets (CuFe2O4–NR@NiFe2O4–NS) via a two-step wet chemical technique. The unique core-shell (nanorods@nanosheets) nanostructures offer multiple redox couples (Cu2+, Fe3+, and Ni2+), smaller ion diffusion path, and faster electron movement. When evaluated as an individual electrode in aqueous potassium hydroxide solution, the as-synthesized CuFe2O4–NR@NiFe2O4–NS electrode demonstrate superior electrochemical behaviour with concurrent specific capacity of 1366 C g−1 at current rate 1 A g−1, and 94% capacity retention over 10,000 cycles. A flexible asymmetric supercapattery device is assembled comprising positive electrode of CuFe2O4–NR@NiFe2O4–NS and negative electrode of reduced graphene oxide (rGO) with PVA-KOH semisolid electrolyte. The ASC cell manifest enhanced specific energy of 72 Wh kg−1, specific power of 0.287 kW kg−1 and outstanding cycle life (~97% of retention over 10,000 cycles at 10 A g−1). The superior specific capacity, capacity retention, and excellent cyclic life endow such multimetal ferrite-based core-shell architecture with tremendous potential for use as electrode materials for fabricating next generation energy storage devices.
KW - asymmetric supercapacitor
KW - core-shell
KW - multimetal ferrites
KW - nanorods
KW - nanosheets
UR - http://www.scopus.com/inward/record.url?scp=85100492584&partnerID=8YFLogxK
U2 - 10.1016/j.est.2021.102379
DO - 10.1016/j.est.2021.102379
M3 - Article
AN - SCOPUS:85100492584
SN - 2352-152X
VL - 36
JO - Journal of Energy Storage
JF - Journal of Energy Storage
M1 - 102379
ER -