کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5364176 | 1503700 | 2012 | 7 صفحه PDF | دانلود رایگان |

Adding N2 gas during reactive sputtering of a Ti target prevented the target surface from being severely poisoned by oxygen atoms and sustained a high deposition rate for titanium oxynitride films under metal-mode-like sputtering conditions. With progress in the degree of oxidization, films deposited onto a glass substrate varied from TiO1âxNx having a face-centered cubic (fcc) structure to TiO2âxNx having an anatase structure. Titanium oxynitride films deposited on an Al2O3(0Â 0Â 0Â 1) substrate were epitaxial with major orientations toward the (1Â 1Â 1) and (2Â 0Â 0) directions for fcc-TiO1âxNx and (1Â 1Â 2) for anatase-TiO2âxNx. Intermediately oxidized films between TiO1âxNx and TiO2âxNx were amorphous on the glass substrate but crystallized into a Magneli phase, TinO(N)2nâ1, on the Al2O3(0Â 0Â 0Â 1) substrate. Partially substituting oxygen in TiO2 with nitrogen as well as continuously irradiating the growing film surface with a Xe plasma stream preferentially formed anatase rather than rutile. However, the occupation of anion sites with enough oxygen rather than nitrogen was the required condition for anatase crystals to form. The transparent conductive properties of epitaxial TiO2âxNx films on Al2O3(0Â 0Â 0Â 1) were superior to those of microcrystalline films on the glass substrate. Since resistivity and optical transmittance of TiOxNy films vary continuously with changing N2 flow rate, their transparent conductive properties can be controlled more easily than TiOx. Nb5+ ions could be doped as donors in TiO2âxNx anatase crystals.
⺠Reactive sputtering of TiOxNy films was achieved under metal-mode conditions. ⺠Partially substituting O in TiO2 with N formed anatase rather than rutile. ⺠TiO2âxNx on Al2O3(0 0 0 1) was more transparent and conductive than on glass substrate. ⺠Nb5+ ions could be doped as donors in TiO2âxNx anatase crystals.
Journal: Applied Surface Science - Volume 263, 15 December 2012, Pages 307-313