Please use this identifier to cite or link to this item:
DC FieldValueLanguage
dc.contributor.authorPo-Wei Chenzh_TW
dc.contributor.authorShiau-Yuan Huangzh_TW
dc.contributor.authorShuo-Huang Yuanzh_TW
dc.contributor.authorYi-An Chenzh_TW
dc.contributor.authorPo-Wen Hsiaozh_TW
dc.contributor.authorDong-Sing Wuuzh_TW
dc.description.abstractThe complex-oxide materials are multifunctional materials, which have wide applications to the semiconductor and microelectronic fields. The ZnGa2O4 having a wide bandgap of 5.1 eV is one of the promising materials for deep-ultraviolet photodetector (PD) applications. The ZnGa2O4 films are deposited by using conventional radio-frequency magnetron sputtering which is extensively employed in the industry. However, the as-deposited ZnGa2O4 films show the disordered nanocrystalline structure, resulting in the relatively poor performance. Since the Zn atoms can diffuse out of the film structure during the annealing, the ZnGa2O4 material is difficult to get the single-crystalline structure by using the sputtering method. Here, the solid-phase epitaxy method is used for crystallizing the ZnGa2O4 structure via rapid thermal annealing process. The disordered crystal grains as incubated seeds are obtained in the as-deposited ZnGa2O4 film at the substrate temperature of 400 °C. Further annealing under the temperature of 700 °C in 1 min, the ZnGa2O4 film structure approaches the quasi-single-crystalline ZnGa2O4 structure, which is evidenced by checking the transmission electron microscopy. The responsivity of annealed ZnGa2O4 PDs can reach 2.53 A W−1 (at 240 nm and 5 V), which shows a relative enhancement of 256% compared with the as-deposited ZnGa2O4 PDs.zh_TW
dc.titleQuasi-Single-Crystalline ZnGa2O4 Films via Solid Phase Epitaxy for Enhancing Deep-Ultraviolet Photoresponsezh_TW
dc.typejournal articlezh_TW
item.openairetypejournal article-
item.fulltextno fulltext-
Appears in Collections:材料科學與工程學系
Show simple item record

Google ScholarTM


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.