Please use this identifier to cite or link to this item:
http://localhost:8080/xmlui/handle/123456789/4068
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Sabari Arul, N | - |
dc.contributor.author | Mangalaraj, D | - |
dc.contributor.author | Pao Chi, Chen | - |
dc.contributor.author | Ponpandian, N | - |
dc.contributor.author | Meena, P | - |
dc.contributor.author | Yoshitake, Masuda | - |
dc.date.accessioned | 2023-11-06T07:49:14Z | - |
dc.date.available | 2023-11-06T07:49:14Z | - |
dc.date.issued | 2012-09-28 | - |
dc.identifier.uri | https://link.springer.com/article/10.1007/s10971-012-2883-7 | - |
dc.description.abstract | In this paper, CeO2 and cobalt-doped CeO2 nanorods synthesized by surfactant free co-precipitation method. The microstructures of the synthesized products were characterized by XRD, FESEM and TEM. The structural properties of the grown nanorods have been investigated using electron diffraction and X-ray diffraction. High resolution transmission electron microscopy studies show the polycrystalline nature of the Co-doped cerium oxide nanorods with a length of about 300 nm and a diameter of about 10 nm were produced. The X-ray Photoelectron spectrum confirms the presence of cobalt in cerium oxide nanorods. From BET, the specific surface area of the CeO2 (Co-doped) nanostructures (131 m2 g−1) is found to be significantly higher than that of pure CeO2 (52 m2 g−1). The Co-doped cerium nanorods exhibit an excellent photocatalytic performance in rapidly degrading azodyes acid orange 7 (AO7) in aqueous solution under UV illumination. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | Springer Link | en_US |
dc.title | ENHANCED PHOTOCATALYTIC ACTIVITY OF COBALT-DOPED CEO2 NANORODS | en_US |
dc.type | Article | en_US |
Appears in Collections: | 2.Article (11) |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
ENHANCED PHOTOCATALYTIC ACTIVITY OF COBALT-DOPED CEO2 NANORODS.docx | 157.83 kB | Microsoft Word XML | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.