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dc.contributor.authorTitipun Thongtemen_US
dc.contributor.authorAnukorn Phuruangraten_US
dc.contributor.authorSomchai Thongtemen_US
dc.date.accessioned2018-09-10T03:44:34Z-
dc.date.available2018-09-10T03:44:34Z-
dc.date.issued2008-03-01en_US
dc.identifier.issn02728842en_US
dc.identifier.other2-s2.0-38149045650en_US
dc.identifier.other10.1016/j.ceramint.2006.11.001en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=38149045650&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/60538-
dc.description.abstractLiNi0.5Co0.5VO4nano-crystals were solvothermally prepared using a mixture of LiOH·H2O, Ni(NO3)2·6H2O, Co(NO3)2·6H2O and NH4VO3in isopropanol at 150-200 °C followed by 300-600 °C calcination to form powders. TGA curves of the solvothermal products show weight losses due to evaporation and decomposition processes. The purified products seem to form at 500 °C and above. The products analyzed by XRD, selected area electron diffraction (SAED), energy dispersive X-ray (EDX) and atomic absorption spectrophotometer (AAS) correspond to LiNi0.5Co0.5VO4. V-O stretching vibrations of VO4tetrahedrons analyzed using FTIR and Raman spectrometer are in the range of 620-900 cm-1. A solvothermal reaction at 150 °C for 10 h followed by calcination at 600 °C for 6 h yields crystals with lattice parameter of 0.8252 ± 0.0008 nm. Transmission electron microscope (TEM) images clearly show that the solvothermal temperatures play a more important role in the size formation than the reaction times. © 2006 Elsevier Ltd and Techna Group S.r.l.en_US
dc.subjectMaterials Scienceen_US
dc.titleFormation of LiNi0.5Co0.5VO4 nano-crystals by solvothermal reactionen_US
dc.typeJournalen_US
article.title.sourcetitleCeramics Internationalen_US
article.volume34en_US
article.stream.affiliationsChiang Mai Universityen_US
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