Mg Doping Induced Effects on Structural, Optical, and Electrical Properties as Well as Cytotoxicity of CeO sub(2) Nanostructures
Here, Mg sub(x)Ce sub(1-x)O sub(2) (where x = 0, 0.01, 0.02, 0.03, 0.04, and 0.05) nanostructures have been successfully synthesized by using a simple, easy, and cost-effective soft chemical method. X-ray diffraction (XRD) patterns substantiate the single-phase formation of a CeO sub(2) cubic fluori...
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Published in | Metallurgical and materials transactions. B, Process metallurgy and materials processing science Vol. 47; no. 2; pp. 1363 - 1368 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
01.04.2016
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Subjects | |
Online Access | Get full text |
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Summary: | Here, Mg sub(x)Ce sub(1-x)O sub(2) (where x = 0, 0.01, 0.02, 0.03, 0.04, and 0.05) nanostructures have been successfully synthesized by using a simple, easy, and cost-effective soft chemical method. X-ray diffraction (XRD) patterns substantiate the single-phase formation of a CeO sub(2) cubic fluorite structure for all samples. Infrared spectroscopy results depict the presence of peaks only related to Ce-O bonding, which confirms the XRD results. It has been observed via ultraviolet (UV)-visible spectroscopy that Mg doping has tuned the optical band gap of CeO sub(2) significantly. The electrical conductivity of CeO sub(2) nanostructures has been found to increase with Mg doping, which is attributed to enhancement in carrier concentration due to the different valance states of dopant and host ions. Selective cytotoxic behavior of Mg sub(x)Ce sub(1-x)O sub(2) nanostructures has been determined for neuroblastoma (SH-SY5Y) cancerous and HEK-293 healthy cells. Both doped and undoped CeO sub(2) nanostructures have been found to be toxic for cancer cells and safe toward healthy cells. This selective toxic behavior of the synthesized nanostructures has been assigned to the different levels of reactive oxygen species (ROS) generation in different types of cells. This makes the synthesized nanostructures a potential option for cancer therapy in the near future. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-2 |
ISSN: | 1073-5615 1543-1916 |
DOI: | 10.1007/s11663-015-0560-2 |