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Mn3O4 nanoflakes/rGO composites with moderate pore size and (O=)C-O-Mn bond for enhanced supercapacitor performance.

Authors :
Huang, Zechuan
Li, Shaomin
Li, Zhao
Li, Jianying
Zhang, Gen
Cao, Liujun
Liu, Hao
Source :
Journal of Alloys & Compounds. Jul2020, Vol. 830, pN.PAG-N.PAG. 1p.
Publication Year :
2020

Abstract

Moderate pore size and (O=)C-O-Mn bonds are designed in Mn 3 O 4 nanoflakes/reduced graphene oxide composites to enhance the specific capacitance and cycling performance of electrodes for supercapacitors. Manganese oxide nanoflakes grow on the surface of graphene oxides via chemical precipitation. After annealing, (O=)C-O-Mn bonds are formed between Mn 3 O 4 and graphene to enhance structural stability of electrode materials. Moreover, the pore size in Mn 3 O 4 enlarges with the increased annealing temperature driven by phase transition and lattice reforming. The moderate pore size of 5–10 nm in Mn 3 O 4 contributes to electrolyte ion diffusion and improves the capacitive-controlled energy storage. In three-electrode system, Mn 3 O 4 nanoflakes/reduced graphene oxide composites with optimal pore size of 5–10 nm and (O=)C-O-Mn bond deliver high specific capacitance (351 F g−1 at 0.5 A g−1) and good cycling performance (80.1% of maximum capacitance after 10,000 cycles). To probe practical applications, Mn 3 O 4 nanoflakes/reduced graphene oxide composites and active carbon are employed as positive electrode and negative electrode, respectively, to assemble asymmetrical supercapacitors. This asymmetrical supercapacitor demonstrates high energy density (36.76 Wh kg−1) and good cycling performance (93.5% after 5000 cycles). • The moderate pore size in Mn 3 O 4 is optimized by controlling annealing temperature. • (O=)C-O-Mn bonds are formed and characterized by FTIR and XPS spectra. • The composites display excellent specific capacitance and cycling life. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09258388
Volume :
830
Database :
Academic Search Index
Journal :
Journal of Alloys & Compounds
Publication Type :
Academic Journal
Accession number :
142668957
Full Text :
https://doi.org/10.1016/j.jallcom.2020.154637