2015
DOI: 10.1039/c4ta06793b
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Mechanism analysis of the capacitance contributions and ultralong cycling-stability of the isomorphous MnO2@MnO2 core/shell nanostructures for supercapacitors

Abstract: The isomorphous MnO2@MnO2 core/shell nanostructures synthesized through a facile hydrothermal process showed remarkable electrochemical performance, i.e., a high specific capacitance with excellent cycling stability.

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Cited by 151 publications
(81 citation statements)
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“…Such enhanced energy storage of the hierarchical electrode material was attributed to the following aspects: The large surface area provided by the MnO 2 NSAs on MnO 2 HNPAs increased the surface wettability of the electrode with the electrolyte solution, very few MnO 2 NSAs on MnO 2 HNPAs were dissolved during cycling, and inner MnO 2 NSAs underwent further activation. This enhancement in energy storage properties on cycling has been observed previously in binder-free electrode materials [43,[58][59][60][61]. After cycling tests, the XPS spectrum of the corresponding sample clearly showed the presence of Mn and O without any impurities (inset of Fig.…”
Section: Resultssupporting
confidence: 52%
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“…Such enhanced energy storage of the hierarchical electrode material was attributed to the following aspects: The large surface area provided by the MnO 2 NSAs on MnO 2 HNPAs increased the surface wettability of the electrode with the electrolyte solution, very few MnO 2 NSAs on MnO 2 HNPAs were dissolved during cycling, and inner MnO 2 NSAs underwent further activation. This enhancement in energy storage properties on cycling has been observed previously in binder-free electrode materials [43,[58][59][60][61]. After cycling tests, the XPS spectrum of the corresponding sample clearly showed the presence of Mn and O without any impurities (inset of Fig.…”
Section: Resultssupporting
confidence: 52%
“…Thereby, the material can more easily participate in reversible redox reactions with the electrolyte solution, facilitating fast electrochemical kinetics during charging and discharging [39]. Many 3D and core-shell-like morphologies of MnO [43]. However, these methods are based on template/surfactant-assisted chemical synthesis, which entails complicated growth steps.…”
Section: Introductionmentioning
confidence: 98%
“…For example, the A@B structure: NiCo2O4@MnO2 [9,19,20], ZnCo2O4@MnO2 [21], CuCo2O4@MnO2 [22],Co3O4@MnO2 [10,23,24], NiCo2S4@MnO2, [25,26], ZnO2@MnO2 [17], Fe2O3@MnO2 [27], MnO2@MnO2 [28], TiO2@MnO2 [29,30], CuO@MnO2 [31],Co3O4@Au@MnO2 [32], Co3O4@Pt@MnO2 [33], WO3-x@Au@MnO2 [34], MnO2/Mn/MnO2 [35]; the A/B structure: NiCo2O4/MnO2 [36,37], Ni(OH)2/MnO2 [8,13], NiCo2S4/MnO2 [38],…”
Section: Introductionmentioning
confidence: 99%
“…Metal oxide electrodes have been paid more and more attention because the rapid reversible redox reaction can penetrate into the electrode while the energy can be stored in the three-dimensional space to improve the energy density [8][9][10]. At present, the promising metal oxide electrode materials are mainly MnOx (x =1, 2, 3/2, 4/3) [11][12][13][14][15], NiO [16], Co3O4 [17], V2O5 [18] and RuO2 [19].…”
mentioning
confidence: 99%