Hostname: page-component-586b7cd67f-r5fsc Total loading time: 0 Render date: 2024-11-23T09:13:10.833Z Has data issue: false hasContentIssue false

Ce0.97Cu0.03O2 Nanocatalysts Synthesized via Microwave-assisted Hydrothermal Method: Characterization and CO-PROX Catalytic Efficiency

Published online by Cambridge University Press:  09 May 2013

Vinícius D. Araújo*
Affiliation:
Instituto de Física de São Carlos, Universidade de São Paulo, Rio Claro, São Paulo, Brasil.
Waldir Avansi
Affiliation:
INCTMN, LIEC, IQ, Universidade Estadual Paulista, Araraquara, São Paulo, Brasil.
Artur J.S. Mascarenhas
Affiliation:
Instituto de Química, Universidade Federal da Bahia, Salvador, Bahia, Brasil.
Heloysa M.C. Andrade
Affiliation:
Instituto de Química, Universidade Federal da Bahia, Salvador, Bahia, Brasil.
Elson Longo
Affiliation:
INCTMN, LIEC, IQ, Universidade Estadual Paulista, Araraquara, São Paulo, Brasil.
Maria I.B. Bernardi
Affiliation:
Instituto de Física de São Carlos, Universidade de São Paulo, Rio Claro, São Paulo, Brasil.
*
*correspondent author: [email protected] Phone: (55 16) 3373-9828 Fax: (55 16) 3373-9824
Get access

Abstract

In the work presented here, Ce0.97Cu0.03O2 nanoparticles were synthesized by a microwave-assisted hydrothermal method under different synthesis temperatures. The obtained nanoparticles were tested as catalysts in preferential oxidation of CO to obtain CO-free H2 (PROX reaction). The samples were characterized by X-ray diffraction, transmission electron microscopy (TEM), electron paramagnetic resonance spectroscopy (EPR) and temperature-programmed reduction (TPR). X-ray diffraction measurements detected the presence of pure cubic CeO2 for all synthesized samples. TEM images of the Ce0.97Cu0.03O2 nanoparticles revealed that samples synthesized at 80°C are composed mainly of nanospheres with an average size of 20 nm. The formation of some nanorods with an average diameter of 8 nm and 40 nm in length, and the size reduction of the nanoparticles from 20 to approximately 15 nm is observed with increasing synthesis temperature. EPR spectra indicated that copper is found well dispersed in sample synthesized at 160°C, located predominant in surface sites of ceria. For samples synthesized at 80 and 120°C, the species are less dispersed than in the other one, resulting in the formation of Cu2+−Cu2+ dimmers at the surface of ceria. TPR profiles presented two reduction peaks, one below 400°C attributed to the reduction of different copper species and a second peak around 800°C attributed to the reduction of Ce4+→ Ce3+ species located in the volume of the nanoparticles. The peak related to the reduction of copper species shifts to lower temperatures with increasing synthesis temperature, i.e., the sample synthesized at 160°C is more easily reduced than the ones synthesized at 120 and 80°C. The nanoparticles showed active as catalysts for the CO-PROX reaction. The microwave-assisted method revealed efficient for the synthesis of Ce0.97Cu0.03O2 nanoparticles with copper species selective for the CO-PROX reaction, which reaches CO conversions up to 92% for the sample synthesized at 160°C.

Type
Articles
Copyright
Copyright © Materials Research Society 2013 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Araújo, V. D., Bellido, J. D. A., Bernardi, M. I. B., Assaf, J. M., and Assaf, E. M., “CuO–CeO2 catalysts synthesized in one-step: Characterization and PROX performance,” Int. J. Hydrog. Energy, vol. 37, pp. 54985507, 2012.CrossRefGoogle Scholar
Li, Y., Dong, X., Gao, J., Hei, D., Zhou, X., and Zhang, H., “A highly sensitive [gamma]-radiation dosimeter based on the CeO2 nanowires,” Phys. E: Low-dimensional Syst. Nanostruct., vol. 41, pp. 15501553, 2009.CrossRefGoogle Scholar
Gao, F., Lu, Q., and Komarneni, S., “Fast Synthesis of Cerium Oxide Nanoparticles and Nanorods,” J. Nanosci. Nanotechnol., vol. 6, pp. 38123819, 2006.CrossRefGoogle ScholarPubMed
Larson, A. C. and Dreele, R. B. V., “General Structure Analysis System (GSAS),” in Los Alamos National Laboratory Report LAUR 86-748, ed, 1994.Google Scholar
Wang, X., Rodriguez, J. A., Hanson, J. C., Gamarra, D., Martínez-Arias, A., and Fernández-García, M., “In Situ Studies of the Active Sites for the Water Gas Shift Reaction over Cu−CeO2 Catalysts: Complex Interaction between Metallic Copper and Oxygen Vacancies of Ceria,” J. Phys. Chem. B, vol. 110, pp. 428434, 2005.CrossRefGoogle Scholar
Ratnasamy, P., Srinivas, D., Satyanarayana, C. V. V., Manikandan, P., Senthil Kumaran, R. S., Sachin, M., and Shetti, V. N., “Influence of the support on the preferential oxidation of CO in hydrogen-rich steam reformates over the CuO-CeO2-ZrO2 system,” J. Catal., vol. 221, pp. 455465, 2004.CrossRefGoogle Scholar
Avgouropoulos, G., Ioannides, T., and Matralis, H., “Influence of the preparation method on the performance of CuO-CeO2 catalysts for the selective oxidation of CO,” Appl. Catal. B: Environ., vol. 56, pp. 8793, 2005.CrossRefGoogle Scholar
Caputo, T., Lisi, L., Pirone, R., and Russo, G., “On the role of redox properties of CuO/CeO2 catalysts in the preferential oxidation of CO in H2-rich gases,” Appl. Catal. A-Gen., vol. 348, pp. 4253, Sep 2008.CrossRefGoogle Scholar
Gamarra, D., Munuera, G., Hungría, A. B., Fernández-García, M., Conesa, J. C., Midgley, P. A., Wang, X. Q., Hanson, J. C., Rodríguez, J. A., and Martínez-Arias, A, “Structure−Activity Relationship in Nanostructured Copper−Ceria-Based Preferential CO Oxidation Catalysts,” J. Phys. Chem. C, vol. 111, pp. 1102611038, 2007.CrossRefGoogle Scholar
Gamarra, D., Belver, C., Fernández-García, M., and Martínez-Arias, A., “Selective CO Oxidation in Excess H2 over Copper−Ceria Catalysts: Identification of Active Entities/Species,” J. Amer. Chem. Soc., vol. 129, pp. 1206412065, 2007.CrossRefGoogle ScholarPubMed