dc.contributor.author | Tuncolu, I. G. | |
dc.contributor.author | Açıksarı, C. | |
dc.contributor.author | Suvacı, Ender | |
dc.contributor.author | Özel, Emel | |
dc.contributor.author | Rembeza, S. I. | |
dc.contributor.author | Rembeza, E. S. | |
dc.contributor.author | Svistova, T. V. | |
dc.date.accessioned | 2019-10-22T16:58:51Z | |
dc.date.available | 2019-10-22T16:58:51Z | |
dc.date.issued | 2015 | |
dc.identifier.issn | 0955-2219 | |
dc.identifier.issn | 1873-619X | |
dc.identifier.uri | https://dx.doi.org/10.1016/j.jeurceramsoc.2015.07.003 | |
dc.identifier.uri | https://hdl.handle.net/11421/21647 | |
dc.description | WOS: 000360511400014 | en_US |
dc.description.abstract | The preparation of (SnO2)(x)(ZnO)(1-x) powder as a ceramic target material via hydrothermal synthesis within a broad range of x values (x = 0-1) was investigated. The phase development and particle characteristics of the Zn2SnO4 powders were evaluated. The phase formations of the (SnO2)(x)(ZnO)(1-x) system in the range from x = 0.0 to 1.00 were mapped, and the ZnO, SnO2 and Zn2SnO4 phases were found to depend on the changing x value. The effects of the processing parameters, including the treatment temperature (180-220 degrees C), time (0-24h) and initial concentrations of precursors (Sn:Zn = 0.125:0.3,0.2:0.48, 0.25:0.6, 0.35:0.84, 0.5:1.20), on the formation mechanism of Zn2SnO4 were discussed in detail. Almost single phase Zn2SnO4 occurs only when x = 0.29 (Zn/Sn= 2.4:1) for the (SnO2)(x)(ZnO)(1-x) composite system at 220 degrees C for 24h. The results reveal that the target prepared from synthesized Zn2SnO4 powder can be successfully used to develop thin film transistor channels | en_US |
dc.description.sponsorship | Scientific and Technological Research Council of Turkey (TUBITAK) [111M670]; Anadolu University [1303F056, 1305F086]; State Program of Ministry Science and Education of Russian Federation [280, 3.574.2014/K] | en_US |
dc.description.sponsorship | This study was sponsored by a bilateral research project between Turkey & Russia under the contact number 111M670 by the Scientific and Technological Research Council of Turkey (TUBITAK). The work was also supported by Anadolu University under the contract numbers 1303F056 and 1305F086. The work was also supported by the State Program of Ministry Science and Education of Russian Federation project N 280 and program N 3.574.2014/K. We would like to thank to Pinar KAYA and Tayfun OZMEN for their helps. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Elsevier Sci LTD | en_US |
dc.relation.isversionof | 10.1016/j.jeurceramsoc.2015.07.003 | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Chemical Preparation | en_US |
dc.subject | Hydrothermal Synthesis | en_US |
dc.subject | Zinc Stannate (Zn2Sno4) | en_US |
dc.title | Synthesis of Zn2SnO4 powders via hydrothermal method for ceramic targets | en_US |
dc.type | article | en_US |
dc.relation.journal | Journal of the European Ceramic Society | en_US |
dc.contributor.department | Anadolu Üniversitesi, Mühendislik Fakültesi, Malzeme Bilimi ve Mühendisliği Bölümü | en_US |
dc.identifier.volume | 35 | en_US |
dc.identifier.issue | 14 | en_US |
dc.identifier.startpage | 3885 | en_US |
dc.identifier.endpage | 3892 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.contributor.institutionauthor | Suvacı, Ender | |