کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
11008935 | 1840427 | 2018 | 28 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Effect of Eu3+ on the morphology, structural, optical, magnetic, and photocatalytic properties of ZnO nanoparticles
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی مواد
مواد الکترونیکی، نوری و مغناطیسی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
In this study, we attempted to synthesize ZnO nanoparticles with various Eu3+ doping concentrations by a simple coprecipitation method for multifunctional applications. Morphology studies of the synthesized samples revealed the presence of hexagonal-shaped and monodispersed particles. A slight shift in the X-ray diffraction patterns of the Eu3+-doped ZnO samples confirmed the successful incorporation of the dopant ions into the host crystal. A change in the E2 (high)-mode intensity was ample evidence of intrinsic defects associated with the oxygen atoms. Diffuse reflectance spectroscopy studies provided sufficient evidence of tuning of the bandgap of ZnO by Eu3+ doping, with a typical red shift. X-ray photoelectron spectroscopy studies revealed the presence of Eu with a +3 state in the ZnO lattice. All the doped ZnO nanoparticles exhibited typical room-temperature ferromagnetism (RTFM). The Eu3+-doped samples displayed a higher photocatalytic degradation (PCD) of RhB dye under UV light illumination compared with the undoped ZnO nanoparticles. Thus, Eu3+ doping is an effective approach for enhancing the RTFM and PCD properties of ZnO for spintronic and photocatalytic applications.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Superlattices and Microstructures - Volume 123, November 2018, Pages 154-163
Journal: Superlattices and Microstructures - Volume 123, November 2018, Pages 154-163
نویسندگان
B. Poornaprakash, U. Chalapathi, M. Chandra Sekhar, V. Rajendar, S.V. Prabhakar Vattikuti, M. Siva Pratap Reddy, Youngsuk Suh, Si-Hyun Park,