TY - JOUR
T1 - Study of the growth of CeO22 nanoparticles onto titanate nanotubes
AU - Marques, Thalles M.F.
AU - Ferreira, Odair P.
AU - Da Costa, Jose A.P.
AU - Fujisawa, Kazunori
AU - Terrones, Mauricio
AU - Viana, Bartolomeu C.
N1 - Funding Information:
Financial support from the Brazilian funding agencies CNPq (under 303632/2013-5 process number), CAPES (PROCAD 2013 – Grant 183995 ) and FAPEPI is gratefully acknowledged. The authors are indebted to CETENE-Brazil for some TEM images.
Publisher Copyright:
© 2015 Elsevier Ltd.
PY - 2015/8/29
Y1 - 2015/8/29
N2 - We report the study of the growth of CeO2 nanoparticles on the external walls and Ce4+ intercalation within the titanate nanotubes. The materials were fully characterized by multiple techniques, such as: Raman spectroscopy, infrared spectroscopy (FTIR), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM). The ion exchange processes in the titanate nanotubes were carried out using different concentrations of Ce4+ in aqueous solution. Our results indicate that the growth of CeO2 nanoparticles grown mediated by the hydrolysis in the colloidal species of Ce and the attachment onto the titanate nanotubes happened and get it strongly anchored to the titanate nanotube surface by a simple electrostatic interaction between the nanoparticles and titanate nanotubes, which can explain the small size and even distribution of nanoparticles on titanate supports. It was demonstrated that it is possible to control the amount and size of CeO2 nanoparticles onto the nanotube surface, the species of the Ce ions intercalated between the layers of titanate nanotubes, and the materials could be tuned for using in specific catalysis in according with the amount of CeO2 nanoparticles, their oxygen vacancies/defects and the types of Ce species (Ce4+ or Ce3+) present into the nanotubes.
AB - We report the study of the growth of CeO2 nanoparticles on the external walls and Ce4+ intercalation within the titanate nanotubes. The materials were fully characterized by multiple techniques, such as: Raman spectroscopy, infrared spectroscopy (FTIR), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM). The ion exchange processes in the titanate nanotubes were carried out using different concentrations of Ce4+ in aqueous solution. Our results indicate that the growth of CeO2 nanoparticles grown mediated by the hydrolysis in the colloidal species of Ce and the attachment onto the titanate nanotubes happened and get it strongly anchored to the titanate nanotube surface by a simple electrostatic interaction between the nanoparticles and titanate nanotubes, which can explain the small size and even distribution of nanoparticles on titanate supports. It was demonstrated that it is possible to control the amount and size of CeO2 nanoparticles onto the nanotube surface, the species of the Ce ions intercalated between the layers of titanate nanotubes, and the materials could be tuned for using in specific catalysis in according with the amount of CeO2 nanoparticles, their oxygen vacancies/defects and the types of Ce species (Ce4+ or Ce3+) present into the nanotubes.
UR - http://www.scopus.com/inward/record.url?scp=84941344062&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84941344062&partnerID=8YFLogxK
U2 - 10.1016/j.jpcs.2015.08.022
DO - 10.1016/j.jpcs.2015.08.022
M3 - Article
AN - SCOPUS:84941344062
SN - 0022-3697
VL - 87
SP - 213
EP - 220
JO - Journal of Physics and Chemistry of Solids
JF - Journal of Physics and Chemistry of Solids
M1 - 7625
ER -