Published June 2008 | Version v1
Journal article

CTAB assisted hydrothermal synthesis, controlled conversion and CO oxidation properties of CeO2 nanoplates, nanotubes, and nanorods

  • 1. Department of Chemistry, Shanghai University, Shanghai 200444 (China)
  • 2. Research Center of Nano Science and Technology, Shanghai University, Shanghai 200444 (China)

Description

In this work, CeO2 nanoplates were synthesized by a hydrothermal reaction assisted by hexadecyltrimethylammonium bromide (CTAB) at 100-160 deg. C. The size of nanoplates was around 40 nm. Further experiment showed that the controlled conversion of nanoplates into nanotubes, and nanorods can be realized by changing the reaction time, temperature, and CTAB/Ce3+ ratio value. X-ray diffraction (XRD), transmission electron microscopy (TEM), and Brunauer-Emmett-Teller (BET) nitrogen adsorption-desorption measurements were employed to characterize the samples. The CO oxidation properties of nanorods, nanoplates, and nanotubes were investigated. An enhanced catalytic activity has been found for CO oxidation by using CeO2 nanoplates as compared with CeO2 nanotubes and nanorods, and the crystal surfaces (100) of CeO2 nanoplates were considered to play an important role in determining their catalytic oxidation properties. - Graphical abstract: CeO2 nanoplates were synthesized by hydrothermal reactions assisted by CTAB, and the controlled conversion of nanoplates into nanotubes, and nanorods were realized by changing the CTAB/Ce3+ ratio value, reaction time, and temperature. An excellent catalytic activity is found for CO oxidation using CeO2 nanoplates due to their exposed surface (100)

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jssc.2008.02.011

Additional details

Identifiers

DOI
10.1016/j.jssc.2008.02.011;
PII
S0022-4596(08)00108-4;

Publishing Information

Journal Title
Journal of Solid State Chemistry
Journal Volume
181
Journal Issue
6
Journal Page Range
p. 1298-1306
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.