| کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن | 
|---|---|---|---|---|
| 6614020 | 459623 | 2014 | 9 صفحه PDF | دانلود رایگان | 
عنوان انگلیسی مقاله ISI
												Influence of pyrolyzing atmosphere on the catalytic activity and structure of Co-based catalysts for oxygen reduction reaction
												
											ترجمه فارسی عنوان
													تأثیر جو فتوسنتز بر فعالیت کاتالیزوری و ساختار کاتالیزورهای همگرا برای واکنش اکسیژن کاهش 
													
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																																												کلمات کلیدی
												واکنش کاهش اکسیژن، کاتالیزور غیر فلزات گرانبها، نیتروژن دوپینگ، کاتالیزور مبتنی بر همکاری، فضای پیلوری
																																							
												موضوعات مرتبط
												
													مهندسی و علوم پایه
													مهندسی شیمی
													مهندسی شیمی (عمومی)
												
											چکیده انگلیسی
												In this study, impact of pyrolyzing atmosphere on the catalytic activity and structure of non-precious metal Co-based catalysts for oxygen reduction reaction in acid and alkaline medium are investigated. These non-precious metal Co-based catalysts are prepared from pyrolyzing carbon-supported cobalt diethylenetriamine chelate (CoDETA/C) in Ar, N2 and CO2 atmosphere, respectively. X-ray diffraction indicates that metallic Co nanoparticles with different size are present on each catalyst. X-ray photoelectron spectroscopy shows that the Nat.% is CoDETA/C-Ar (1.54) > CoDETA/C-N2 (1.39) > CoDETA/C-CO2 (0.42), pyridinic-N and amino-N in CoDETA/C-N2 is the highest among these three catalysts, while pyrrolic-N, graphitic-N and oxidized-N in CoDETA/C-Ar is higher than that in the other two catalysts. Electrochemical activity demonstrated by cyclic voltammograms and rotating ring disk electrode in O2-saturated acid and alkaline electrolyte shows that pyrolyzing atmosphere has an important effect on the catalytic activity and a maximum catalytic activity is obtained in N2 atmosphere, followed by in Ar then CO2 atmosphere, in terms of onset and half-wave potentials, ORR peak potential and current, limiting current, number of electrons transferred and H2O selectivity. The increase in catalytic activity may mainly attribute to the enhanced contents of pyridinic-N and amino-N.
											ناشر
												Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Electrochimica Acta - Volume 115, 1 January 2014, Pages 1-9
											Journal: Electrochimica Acta - Volume 115, 1 January 2014, Pages 1-9
نویسندگان
												Hui-Juan Zhang, Haoliang Li, Xiangtai Li, Bin Zhao, Zi-Feng Ma, Junhe Yang, 
											