Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/91733
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dc.titleSurface Ni2+ diffusion in sol-gel-derived tetragonal and monoclinic ZrO2 matrices
dc.contributor.authorZeng, H.C.
dc.contributor.authorLin, J.
dc.contributor.authorTeo, W.K.
dc.contributor.authorLoh, F.C.
dc.contributor.authorTan, K.L.
dc.date.accessioned2014-10-09T08:21:37Z
dc.date.available2014-10-09T08:21:37Z
dc.date.issued1995-02-01
dc.identifier.citationZeng, H.C.,Lin, J.,Teo, W.K.,Loh, F.C.,Tan, K.L. (1995-02-01). Surface Ni2+ diffusion in sol-gel-derived tetragonal and monoclinic ZrO2 matrices. Journal of Non-Crystalline Solids 181 (1-2) : 49-57. ScholarBank@NUS Repository.
dc.identifier.issn00223093
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/91733
dc.description.abstractTetragonal and monoclinic ZrO2 gel matrices have been synthesized from the zirconium n-propoxide-acetylacetone-water-isopropanol system. Surface Ni2+ ion diffusion in these sol-gel-derived tetragonal and monoclinic zirconia matrices have been studied with Fourier transform infrared spectroscopy, differential thermal analysis and X-ray photoelectron spectroscopy (XPS). It is found that the Ni2+ metal ion diffuses into the ZrO2 continuously over the temperature range of 400-600°C for both tetragonal and monoclinic ZrO2 matrices, and later forms a thermodynamically stable Ni2+/ZrO2 solid solution at the elevated calcination temperatures. Higher Ni2+ surface contents in tetragonal ZrO2 are measured by XPS, indicating a larger specific surface area for tetragonal gel matrix. In addition to the +2 oxidation state, +3 for Ni is also detected in Ni/ZrO2 systems. The atomic ratio of Ni2+/Ni3+ varies and peaks at 700°C in the tetragonal ZrO2. However, in the monoclinic case, the ratio remains constant throughout the course of experiments. Diffusion thermodynamic quantities are investigated and the diffusion activation energy determined for Ni2+ ion in ZrO2 matrices is 0.40 eV. The oxidation states of surface metals (Ni and Zr) and crystallinity of the system during the phase transformation are also addressed. © 1995.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentPHYSICS
dc.contributor.departmentCHEMICAL ENGINEERING
dc.description.sourcetitleJournal of Non-Crystalline Solids
dc.description.volume181
dc.description.issue1-2
dc.description.page49-57
dc.description.codenJNCSB
dc.identifier.isiutNOT_IN_WOS
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