Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/82697
Title: Formation of hexagonal-molybdenum trioxide (h-MoO3) nanostructures and their pseudocapacitive behavior
Authors: Kumar, Vipin
Wang, Xu
Lee, Pooi See
Keywords: Molybdenum oxide
Electrochemical studies
Issue Date: 2015
Source: Kumar, V., Wang, X., & Lee, P. S. (2015). Formation of hexagonal-molybdenum trioxide (h-MoO3) nanostructures and their pseudocapacitive behavior. Nanoscale, 7(27), 11777-11786.
Series/Report no.: Nanoscale
Abstract: The crystallographic structure and morphology of redox active transition metal oxides have a pronounced effect on their electrochemical properties. In this work, h-MoO3 nanostructures with three distinct morphologies, i.e., pyramidal nanorod, prismatic nanorod and hexagonal nanoplate, were synthesized by a facile solvothermal method. The morphologies of h-MoO3 nanostructures were tailored by a controlled amount of hexamethylenetetramine. An enhanced specific capacitance about 230 F g−1 at an applied current density of 0.25 A g−1 was achieved in h-MoO3 pyramidal nanorods. Electrochemical studies confirmed that the h-MoO3 pyramidal nanorods exhibit superior charge-storage ability. This improved performance can be ascribed to the coexistence of its well exposed crystallographic planes with abundant active sites, i.e., hexagonal window (HW), trigonal cavity (TC) and four-coordinated square window (SW). The mechanism of charge-storage is likely facilitated by the vehicle mechanism of proton transportation due to the availability of the vehicles, i.e., NH4+ and H2O. The promising, distinct and unexploited features of h-MoO3 nanostructures reveal a strong candidate for pseudocapacitive electrode materials.
URI: https://hdl.handle.net/10356/82697
http://hdl.handle.net/10220/40294
ISSN: 2040-3364
DOI: 10.1039/C5NR01505G
Rights: This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:MSE Journal Articles

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