Issue 46, 2021

Rational synthesis of CoFeP@nickel–manganese sulfide core–shell nanoarrays for hybrid supercapacitors

Abstract

Transition metal phosphide electrodes, particularly those with unique morphologies and micro-/nanostructures, have demonstrated desirable capabilities for hybrid supercapacitor applications by virtue of their superior electrical conductivity and high electrochemical activity. Here, three-dimensional hierarchical CoFeP@nickel–manganese sulfide nanoarrays were in situ constructed on a flexible carbon cloth via a hydrothermal method, a phosphorization process, followed by an electrodeposition approach. In this smart nanoarchitecture, CoFeP nanorods grown on carbon cloth act as the conductive core for rapid electron transfer, while the nickel–manganese sulfide nanosheets decorated on the surface of CoFeP serve as the shell for efficient ion diffusion, forming a stable core–shell heterostructure with enhanced electrical conductivity. Benefiting from the synergy of the two components and the generation of a heterointerface with a modified electronic structure, The CoFeP@nickel–manganese sulfide electrodes deliver a high capacity of 260.7 mA h g−1 at 1 A g−1, excellent rate capability, and good cycling stability. More importantly, an aqueous hybrid supercapacitor based on CoFeP@nickel–manganese sulfide as a positive electrode and a lotus pollen-derived hierarchical porous carbon as a negative electrode is constructed to display a maximum energy density of 60.1 W h kg−1 at 371.8 W kg−1 and a good cycling stability of 85.7% capacitance retention after 10 000 cycles.

Graphical abstract: Rational synthesis of CoFeP@nickel–manganese sulfide core–shell nanoarrays for hybrid supercapacitors

Supplementary files

Article information

Article type
Paper
Submitted
20 Sep 2021
Accepted
31 Oct 2021
First published
01 Nov 2021

Dalton Trans., 2021,50, 17181-17193

Rational synthesis of CoFeP@nickel–manganese sulfide core–shell nanoarrays for hybrid supercapacitors

Y. Wang, Y. Zhang, C. Du, J. Chen, Z. Tian, M. Xie and L. Wan, Dalton Trans., 2021, 50, 17181 DOI: 10.1039/D1DT03196A

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