Issue 40, 2018, Issue in Progress

Microwave hydrothermal synthesis of α-MnMoO4 nanorods for high electrochemical performance supercapacitors

Abstract

Pristine α-MnMoO4 nanorods were facilely prepared via co-precipitation (Cp) and microwave hydrothermal (MH) methods. X-ray diffraction (XRD) patterns showed pure monoclinic crystalline phase α-MnMoO4 for the heat treated powder at 500 °C. Fourier Transform Infrared (FTIR) spectra showed that the chemical bond structure of α-MnMoO4 corresponds to the strong vibrational modes of Mo–O–Mo, Mo–O and Mo[double bond, length as m-dash]O. Raman spectra showed the structural bonding and crystalline nature of α-MnMoO4. Field Emission Scanning Electron Microscope (FE-SEM) images exposed the nanorod shape of the α-MnMoO4 powder, with diameters of ∼200 nm and lengths of ∼1.6 μm. Electrochemical studies of the Cp- and MH-MnMoO4 nanorods with 2 M NaOH as the electrolyte showed specific capacitances of 143 F g−1 and 551 F g−1, respectively, at a 1 A g−1 constant discharge current density. Cyclic voltammetric (CV) studies of the MH-MnMoO4 nanorods at various scan rates revealed the presence of redox pairs, suggesting a pseudocapacitive nature. The structural stability at different current densities demonstrated the high rate performances and good reversible capacity retention of the calcined MH-MnMoO4 nanorods. A cycling life stability study of MH-MnMoO4 demonstrated a good capacity retention of 89% of the initial specific capacitance at 5 A g−1 after 1000 cycles.

Graphical abstract: Microwave hydrothermal synthesis of α-MnMoO4 nanorods for high electrochemical performance supercapacitors

Article information

Article type
Paper
Submitted
29 Mar 2018
Accepted
07 Jun 2018
First published
20 Jun 2018
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2018,8, 22559-22568

Microwave hydrothermal synthesis of α-MnMoO4 nanorods for high electrochemical performance supercapacitors

S. Jayasubramaniyan, S. Balasundari, P. A. Rayjada, N. Satyanarayana and P. Muralidharan, RSC Adv., 2018, 8, 22559 DOI: 10.1039/C8RA02751J

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