کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1487841 1510715 2014 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Facile synthesis of stoichiometric zinc ferrite nanocrystal clusters with superparamagnetism and high magnetization
ترجمه فارسی عنوان
سنتز ناپیوسته خوشه های نانو کریستال فریت روی ستونی با ابررسانای پارامغناطیس و مغناطش بالا
موضوعات مرتبط
مهندسی و علوم پایه مهندسی مواد سرامیک و کامپوزیت
چکیده انگلیسی


• Stoichiometric ZnFe2O4 MNCs was synthesized via a one-step solvothermal method without any additives.
• Nitrates (Fe(NO3)3 and Zn(NO3)2) were used as reactants.
• The ZnFe2O4 MNCs show superparamagnetism and high saturation magnetization.

Stoichiometric ZnFe2O4 magnetic nanocrystal clusters (MNCs) with an average diameter of 127 nm have been successfully synthesized by using a one-step solvothermal method without any additives, where nitrates (Fe(NO3)3 and Zn(NO3)2) were used as reactants. Different characterization techniques were used, such as XRD, ICP-AES, TEM, HRTEM, XPS, and SQUID. The results demonstrate that the stoichiometric ZnFe2O4 is superparamagnetic, and the saturation magnetization (35.9 ± 0.1 emu/g at 300 K, 78.0 ± 0.1 emu/g at 5 K) is higher than that reported in some references. However, when FeCl3 and ZnCl2 were used as reactants that replaced the nitrates at the same experimental conditions, ZnFe2O4 · 40Fe3O4 was synthesized. The NO3− decreased the Fe2+ concentration through oxidation and reduction reactions in the polyol method for the formation of ZnFe2O4. A possible mechanism for the stoichiometric ZnFe2O4 formation was proposed and discussed, based on the time-resolved experiments.

Stoichiometric ZnFe2O4 was successfully synthesized with nitrates as reactants. The stoichiometric ZnFe2O4 is superparamagnetic, and the saturation magnetization is higher than that reported in references.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Materials Research Bulletin - Volume 60, December 2014, Pages 270–278
نویسندگان
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