Interface Reaction Route to Two Different Kinds of CeO2 Nanotubes
- 14 December 2007
- journal article
- research article
- Published by American Chemical Society (ACS) in Inorganic Chemistry
- Vol. 47 (2), 723-728
- https://doi.org/10.1021/ic701867f
Abstract
CeO2 nanotubes have been synthesized with a simple solid−liquid interface reaction route in the absence of any surfactants. Although the basic reaction principles are similar, two kinds of nanotubes with completely different morphologies and structures can be generated by slightly tuning the postprocessing conditions. The first formation involves employing Ce(OH)CO3 nanorods as both the physical and chemical templates, and the other requires layered Ce(OH)3 as an anisotropic intermediate species. During this process, NaOH and reaction temperature were demonstrated as the key factors responsible for the formation of Ce(OH)3 intermediate and final CeO2 nanotubes with well-defined structures. The structural details were provided by a combination of XRD, SEM, TEM, and HRTEM investigations. Catalytic measurement shows that both nanotubes are very active for CO oxidation, and at 250 °C, the conversion rates of CeO2 nanotubes are 3 times higher than that of the bulk counterpart.This publication has 31 references indexed in Scilit:
- Magnetic properties of template-synthesized cobalt∕polymer composite nanotubesJournal of Applied Physics, 2005
- Nanotubes of Magnesium BorateAngewandte Chemie-International Edition, 2003
- One‐Dimensional Nanostructures: Synthesis, Characterization, and ApplicationsAdvanced Materials, 2003
- Organic Templates for the Generation of Inorganic MaterialsAngewandte Chemie-International Edition, 2003
- Nanotubes of Group 4 Metal DisulfidesAngewandte Chemie-International Edition, 2002
- Taking the InitiativeScience, 2000
- Cage structures and nanotubes of NiCl2Nature, 1998
- Boron Nitride NanotubesScience, 1995
- High-Rate, Gas-Phase Growth of MoS 2 Nested Inorganic Fullerenes and NanotubesScience, 1995
- Polyhedral and cylindrical structures of tungsten disulphideNature, 1992