Physicochemical and Redox Characteristics of Fe Ion-doped CeO2 Nanoparticles

We report the structural, thermal, optical, and redox properties of Fe‐doped cerium oxide (CeO2) nanoparticles, obtained using the polyol‐co‐precipitation process. X‐ray diffraction data reveal the formation of single‐phase structurally isomorphous CeO2. The presence of Fe3+ may act as electron acce...

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Published in:Journal of the Chinese Chemical Society (Taipei) Vol. 62; no. 10; pp. 925 - 932
Main Authors: Ansari, Anees A., Labis, J., Alam, Manawwer, Ramay, Shahid M., Ahmad, Naushad, Mahmood, Asif
Format: Journal Article
Language:English
Published: Weinheim WILEY-VCH Verlag 01-10-2015
WILEY‐VCH Verlag
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Summary:We report the structural, thermal, optical, and redox properties of Fe‐doped cerium oxide (CeO2) nanoparticles, obtained using the polyol‐co‐precipitation process. X‐ray diffraction data reveal the formation of single‐phase structurally isomorphous CeO2. The presence of Fe3+ may act as electron acceptor and/or hole donor, facilitating longer lived charge carrier separation in Fe‐doped CeO2 nanoparticles as confirmed by optical band gap energy. The increased content of localized defect states in the ceria gap and corresponding shift of the optical absorption edge towards visible range in Fe‐doped samples can significantly improve the optical activity of nanocrystalline ceria. The better‐quality redox performances of the Fe‐doped CeO2 nanoparticles, compared with undoped CeO2 nanoparticles, were ascribed mainly to a decrease in band gap energy and an increase in specific surface area of the material. As observed from TPR studies all Fe ‐doped CeO2 nanoparticles, particularly the 10 mol % Fe doped CeO2 nanoproduct, exhibit excellent reduction performance. We report the structural, thermal, optical, and redox properties of Fe ‐doped cerium oxide (CeO2) nanoparticles, obtained using the polyolco‐precipitation process.
Bibliography:istex:77415E21E0B523A3DDC516C1044606596DE461EE
ArticleID:JCCS201500195
ark:/67375/WNG-P0S5KMQR-4
ISSN:0009-4536
2192-6549
DOI:10.1002/jccs.201500195