Sonochemical synthesis, characterization, and electrochemical properties of MnMoO4 nanorods for supercapacitor applications

In this article, we reported the preparation of manganese molybdate (MnMoO4) nanorods by a facile sonochemical method and investigated its electrochemical properties for supercapacitor applications. The microstructure, surface morphology and composition were characterized by using field emission sca...

Full description

Saved in:
Bibliographic Details
Published inMaterials chemistry and physics Vol. 147; no. 3; pp. 836 - 842
Main Authors Veerasubramani, Ganesh Kumar, Krishnamoorthy, Karthikeyan, Sivaprakasam, Radhakrishnan, Kim, Sang Jae
Format Journal Article
LanguageEnglish
Published Elsevier B.V 15.10.2014
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:In this article, we reported the preparation of manganese molybdate (MnMoO4) nanorods by a facile sonochemical method and investigated its electrochemical properties for supercapacitor applications. The microstructure, surface morphology and composition were characterized by using field emission scanning electron microscope (FE-SEM), high resolution-transmission electron microscopy (HR-TEM), X-ray diffraction analysis (XRD), Raman spectroscopy and X-ray photo electron microscopy (XPS). The cyclic voltammetry (CV) curves of sonochemically synthesized α-MnMoO4 nanorods revealed the presence of redox pairs suggesting the pseudocapacitive nature of MnMoO4. A maximum specific capacitance of the α-MnMoO4 nanorods was about 168.32 F g−1 as observed from the galvanostatic charge–discharge (GCD) analysis at a constant current density of 0.5 mA cm−2. Long term cyclic stability study revealed that about 96% of initial capacitance was retained after 2000 cycles. [Display omitted] •MnMoO4 nanorods were synthesized by sonochemical method.•FE-SEM studies show the rod like morphology of MnMoO4.•XRD studies show the presence of monoclinic phase of α-MnMoO4.•Specific capacitance of 168.32 F g−1 was achieved using charge–discharge analysis.
ISSN:0254-0584
1879-3312
DOI:10.1016/j.matchemphys.2014.06.028