Farha Ashraf H, Al Naim Abdullah F, Mazher Javed, Nasr Olfa, Alouane Mohamed Helmi Hadj
Department of Physics, College of Science, King Faisal University, P.O. Box: 400, Al-Ahsa 31982, Saudi Arabia.
Semiconductors Technology Lab, Physics Department, Faculty of Science, Ain Shams University, 11566 Cairo, Egypt.
Materials (Basel). 2020 Feb 15;13(4):879. doi: 10.3390/ma13040879.
A simple single pot sol-gel method is used to prepare ZnNiO nanoparticles at assorted Ni doping levels, 1, 3, 7 and 10 wt.%. Structural and optical properties of nanoparticles are studied by X-ray diffraction (XRD), UV-visible diffuse reflection spectroscopy (DRS), photoluminescence (PL) measurements, scanning electron microscopy (SEM), μ-Raman and X-ray photoelectron-spectroscopy (XPS). A single substitutional solid solution phase is detected in the wurtzite ZnNiO nanoparticles at various doping levels. XRD peak splitting and shifting is ascribed to reduced wurtzite character and presence of crystalline strain in nanoparticles at higher level of Ni doping. The Kubelka-Munk function of DRS data reveals the presence of the Burstein-Moss effect in the optical absorption of ZnNiO nanoparticles. Photoluminescence studies show intense UV-blue emission from ZnNiO nanoparticles. The UV PL also exhibits the Burstein-Moss blue shift in the ZnNiO luminescence. Raman analyses also confirms the wurtzite structure of ZnNiO nanoparticles; however, crystal structural defects and bond stiffness increase with Ni doping. The optical and structural studies presented in this work are pointing towards a multivalent Ni substitution in the nanoparticles.
采用一种简单的单锅溶胶-凝胶法制备了不同镍掺杂水平(1 wt.%、3 wt.%、7 wt.%和10 wt.%)的ZnNiO纳米颗粒。通过X射线衍射(XRD)、紫外-可见漫反射光谱(DRS)、光致发光(PL)测量、扫描电子显微镜(SEM)、μ-拉曼光谱和X射线光电子能谱(XPS)研究了纳米颗粒的结构和光学性质。在不同掺杂水平的纤锌矿型ZnNiO纳米颗粒中检测到单一的替代固溶体相。XRD峰的分裂和位移归因于纤锌矿特性的降低以及在较高镍掺杂水平下纳米颗粒中存在晶体应变。DRS数据的Kubelka-Munk函数揭示了ZnNiO纳米颗粒光吸收中存在Burstein-Moss效应。光致发光研究表明ZnNiO纳米颗粒发出强烈的紫外-蓝光。紫外PL在ZnNiO发光中也表现出Burstein-Moss蓝移。拉曼分析也证实了ZnNiO纳米颗粒的纤锌矿结构;然而,晶体结构缺陷和键刚度随镍掺杂而增加。这项工作中提出的光学和结构研究表明纳米颗粒中存在多价镍替代。