Influence of different additives on the morphology, defect state and luminescence of ZnO nanoparticles

发光 纳米颗粒 材料科学 化学工程 三乙氧基硅烷 硅烷 拉曼光谱 Zeta电位 表面改性 溴化铵 纳米技术 硅烷 肺表面活性物质 物理 光电子学 光学 工程类 冶金
作者
I. Perhaţia,Laura Mureşan,Alexandra Belcovici,Adriana Popa,Gheorghe Borodi,Amalia Mesaroș,Lucian Barbu‐Tudoran
出处
期刊:Colloids and Surfaces A: Physicochemical and Engineering Aspects [Elsevier BV]
卷期号:684: 133102-133102 被引量:5
标识
DOI:10.1016/j.colsurfa.2023.133102
摘要

Zinc oxide (ZnO) is an important multifunctional material with applications in various environmental, drug delivery, sensing, and optoelectronics domains. Binding of different molecules on ZnO enhances the properties and characteristics of nanoparticles through surface modification. In this study, varieties of ZnO nanoparticles (ZnO-NP) are prepared using different additives via simple, low-cost precipitation technique at room temperature. The surface state of ZnO-NP was controlled by three surfactants and two silanes, namely: cetyltrimethyl-ammonium bromide, tween 20, heptaethylene glycol monododecyl ether, 3-aminopropyl triethoxysilane, and tetraethoxysilane. The modified ZnO samples were characterized by various analytical techniques, X-ray diffraction, Raman, FT-IR spectroscopy, surface area analysis and electron paramagnetic resonance. The surface area of the samples significantly increases when silanes are used during the synthesis. Scanning electron microscopy shows the formation of either rounded nanoparticles or layered structures. Depending on the type of additives the zeta potential of colloids increase from 25.92 mV up to 40.36 mV. In this study we show that the chemical nature of additives and the stability of colloids play an important role in the generation of luminescent radiative processes. The green luminescence of ZnO colloids is either enhanced or quenched due to the interaction of additives with the particles surface through covalent, electrostatic, and hydrogen bonds. The ZnO surface becomes more or less permissive toward the movement of surface defects, with formation of oxygen vacancies (VO+ and VO++) responsible for the luminescent response.

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