کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1331909 979022 2008 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Controlled synthesis of nanocrystalline CeO2 and Ce1−xMxO2−δ (M=Zr, Y, Ti, Pr and Fe) solid solutions by the hydrothermal method: Structure and oxygen storage capacity
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Controlled synthesis of nanocrystalline CeO2 and Ce1−xMxO2−δ (M=Zr, Y, Ti, Pr and Fe) solid solutions by the hydrothermal method: Structure and oxygen storage capacity
چکیده انگلیسی

CeO2 and Ce1−xMxO2−δ (M=Zr, Ti, Pr, Y and Fe) nanocrystallites of 5–10 nm sizes have been synthesized by hydrothermal method using diethylenetriamine (DETA) and melamine as complexing agents. Compounds have been characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and energy dispersive X-ray analysis (EDX) and their structures have been refined by the Rietveld method. All the compounds crystallize in cubic fluorite structure. Even up to 50% Zr and Y, 40% Ti, 25% Pr and 15% Fe is substituted for Ce4+ in CeO2 by this method. Sizes of crystallites can be tuned by changing the complexing agent and reaction temperature. Nanocrystalline CeO2 and Ce1−xZrxO2 prepared here have higher or at least competitive oxygen storage capacity (OSC) than those reported in literature. Ce1−xFexO2−δ shows higher OSC and higher percentage of CO oxidation at lower temperature than Ce1−xZrxO2.

CeO2 and Ce1−xMxO2−δ (M=Zr, Ti, Pr, Y and Fe) nanocrystallites of 5–10 nm sizes have been synthesized by hydrothermal method using diethylenetriamine (DETA) and melamine as complexing agents. Ce1−xFexO2−δ shows higher OSC and higher percentage of CO oxidation at lower temperature than Ce1−xZrxO2. CO conversion with lattice oxygen from (a) CeO2 (5 nm), (b) Ce0.75Zr0.25O2, (c) Ce0.50Zr0.50O2 and (d) Ce0.85Fe0.15O1.85.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Solid State Chemistry - Volume 181, Issue 12, December 2008, Pages 3248–3256
نویسندگان
, ,