کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
182913 459528 2016 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Hierarchical iron nickel oxide architectures derived from metal-organic frameworks as efficient electrocatalysts for oxygen evolution reaction
ترجمه فارسی عنوان
معماری اکسید نیکل آهن سلسله مراتبی به دست آمده از چارچوب فلزات آلی به عنوان الکتروکاتالیست های کارآمد برای واکنش تکامل اکسیژن
کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
چکیده انگلیسی


• Hierarchical iron nickel oxide architectureswere prepared using MOFs as sacrificial template.
• Iron nickel oxide were explored as a novel electrocatalyst for catalyzing OERin alkaline media.
• Electrocatalytic activity toward OER of iron nickel oxides is dependent on the Fe/Ni ratio.
• Spinel structured NiFe2O4 plays a dominating role in OER activity of iron nickel oxides.

In this study, a series of iron nickel oxide (Fe-Ni-Ox) architectures with different Fe/Ni ratios are synthesized by using corresponding Fe-Ni-based metal-organic frameworks (MOFs) as self-templates for the first time. The characterization on microstructures suggest that Fe/Ni ratio significantly affects the morphology and phase composition of Fe-Ni-Ox architectures. The Fe-rich samples exhibit spindle-like structures while the Ni-rich samples consist of irregular nanoparticle aggregates, and the higher Ni ratio is favorable for the formation of Fe-Ni-spinel strucutre in product. Serving as nonprecious electrocatalysts, the Fe-Ni-Ox architectures exhibit the remarkable electrocatalytic activity toward oxygen evolution reaction (OER) in alkaline medium, which is found to be closely dependent on composition of Fe-Ni-Ox catalysts. The active phase of spinel-structured NiFe2O4 plays a dominating role in enhancing the electrocatalytic OER activity of the Fe-Ni-Ox architectures. Based on the X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy analysis, the possible OER mechanism of the Fe-Ni-Ox architectures is unraveled as well.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Electrochimica Acta - Volume 208, 1 August 2016, Pages 17–24
نویسندگان
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