Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/95591
Title: Shape-controlled synthesis of MnO2 nanostructures with enhanced electrocatalytic activity for oxygen reduction
Authors: Xiao, Wei
Wang, Deli
Lou, David Xiong Wen
Keywords: DRNTU::Science::Medicine::Biomedical engineering
Issue Date: 2010
Source: Xiao, W., Wang, D., & Lou, D. X. W. (2010). Shape-Controlled Synthesis of MnO2 Nanostructures with Enhanced Electrocatalytic Activity for Oxygen Reduction. The Journal of Physical Chemistry C, 114(3), 1694-1700.
Series/Report no.: The journal of physical chemistry C
Abstract: In this work, three types of MnO2 nanostructures, viz., microsphere/nanosheet core−corona hierarchical architectures, one-dimensional (1D) nanorods, and nanotubes, have been synthesized employing a simple hydrothermal process. The formation mechanisms have been rationalized. The materials have been thoroughly characterized by X-ray diffraction, Brunauer−Emmett−Teller spectrometry, field-emission scanning electron miscroscopy, energy dispersive spectroscopy, and transmission electron microscopy. The microsphere/nanosheet core−corona hierarchical structures are found to be the layered birnessite-type MnO2, while 1D nanorods and nanotubes are of the α-MnO2 phase. These MnO2 nanostructures are used as a model system for studying the shape/phase-dependent electrocatalytic properties for the oxygen reduction reaction, which have be investigated by cyclic and linear sweep voltammetry. It is found that α-MnO2 nanorods/tubes possess largely enhanced electrocatalytic activity compared to birnessite-type MnO2 core−corona spheres despite the latter having a much higher specific surface area. The vast difference in electrocatalytic activity is discussed in terms of crystal structure, oxygen adsorption mode, and exposed crystal facets.
URI: https://hdl.handle.net/10356/95591
http://hdl.handle.net/10220/8311
DOI: 10.1021/jp909386d
Rights: © 2009 American Chemical Society.
Fulltext Permission: none
Fulltext Availability: No Fulltext
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