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Enhancement in optical and structural properties of Zn_(0.85)Mg_(0.15)O nanorods over thin films synthesized by hydrothermal chemical treatment

机译:通过水热化学处理合成的薄膜的Zn_(0.85)Mg_(0.15)Mg_(0.15)o纳米棒的光学和结构性能增强

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We are reporting an enhancement in optical properties by changing the structure of Zn_(0.85)Mg_(0.15)O thin films through formation of crystalline hexagonal nanorods. Zn_(0.85)Mg_(0.15)O thin films were deposited on Si (100) substrate using dielectric sputter followed by annealing in oxygen ambient at temperatures of 700, 800 and 900°C for 10 seconds to reduce oxygen vacancies defects. Deposited thin film annealed at 900 °C (sample A) measured highest peak intensity and it was subjected to controlled the hydrothermal bath conditioning for forming hexagonal nanorods. Four samples were dipped in 2 different solutions with variable molar ratio of zinc nitrate hexahydrate and hexamethylentetramine for 2 and 3 hours, respectively. Samples processed in solution 1 (1:1) ratio for 2 and 3 hours were named B and C and those in solution 2 (2:1) were D and E, respectively. Photoluminescence measurement at 18K demonstrates exciton near-band-edge (NBE) emission peak at 3.61eV from Zn_(0.85)Mg_(0.15)O sample A whereas other samples exhibited slight blue shift along with bimodal peaks. The other peak observed at lower energy 3.43eV corresponds to transitions due to presence of ZnO phase in Zn_(0.85)Mg_(0.15)O. All samples compared to sample A exhibited more than 10 times increment in peak intensities with sample B producing the highest (~ 20 times). Nanorods formation was confirmed using cross-sectional SEM imaging. X-ray diffraction measurements revealed that all Zn_(0.85)Mg_(0.15)O samples had (002) preferred crystal orientation with peak position at 34.7°. All nanorods samples measured lower reflectance compared to sample A, indicating high absorption in nanorods due to high scattering of light at the nanorods surface.
机译:通过形成晶体六边形纳米棒来改变Zn_(0.85)Mg_(0.15)o薄膜的结构,在光学性质中报告了光学性能的提高。使用介电溅射在Si(100)基板上沉积Zn_(0.85)Mg_(0.15)薄膜,然后在700,800和900℃的温度下在氧环境下退火10秒以减少氧空位缺陷。在900℃(样品A)下退火的沉积薄膜测量的最高峰强度,并且对其控制加热浴条件以形成六边形纳米棒。将四个样品浸入2种不同的溶液中,其可变摩尔比分别为硝酸锌六水合物和六甲基四胺,分别为2和3小时。在溶液1(1:1)比例为2和3小时的样品命名为B,C,溶液2(2:1)分别为d和e。在18K时的光致发光测量演示了来自Zn_(0.85)Mg_(0.15)O样品A的3.61EV的Exciton接近带边缘(NBE)发射峰值,而其他样品与双峰峰呈现出轻微的蓝色移位。在较低能量3.43EV下观察到的另一个峰值对应于由于Zn_(0.85)Mg_(0.15)O中存在ZnO相的转变。与样品A相比,所有样品在峰值强度下表现出超过10倍的峰值强度,样品B产生最高(〜20次)。使用横截面SEM成像确认纳米棒形成。 X射线衍射测量显示,所有Zn_(0.85)Mg_(0.15)O样品具有(002)优选的晶体取向,峰位置在34.7°处。与样品A相比,所有纳米棒样品测量较低的反射率,这表明由于纳米棒表面上的光的高散射而在纳米棒中表示高吸收。

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