| کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن | 
|---|---|---|---|---|
| 6605304 | 1424100 | 2017 | 25 صفحه PDF | دانلود رایگان | 
عنوان انگلیسی مقاله ISI
												Facile Synthesis of Mn3O4 Nanoplates-Anchored Graphene Microspheres and Their Applications for Supercapacitors
												
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																																												موضوعات مرتبط
												
													مهندسی و علوم پایه
													مهندسی شیمی
													مهندسی شیمی (عمومی)
												
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												چکیده انگلیسی
												We describe a facile synthesis of Mn3O4 nanoplates (NPs)-anchored graphene microspheres (GSs) and their applications as electrode materials for supercapacitors. The use of GSs as substrate significantly improve the electrochemical performance of Mn3O4, which can be attributed to unique spherical structure of graphene and excellent stability and anti-reunion of Mn3O4 NPs. The success of this synthesis depends on the in situ reduction of Mn cations by carbon from GSs under hydrothermal conditions. The resultant Mn3O4 NPs with an average thickness of 37 nm were uniformly distributed on the surface of GSs. Material characterizations, including XRD, Raman, FTIR and XPS, have been performed to confirm their shape, composition and structure. As a positive material, the as-prepared Mn3O4 NPs/GSs composites exhibited excellent electrochemical property in a three-electrode system. In particular, their specific capacitance reached as high as 317 F gâ1 at a scan rate of 10 mV sâ1, and a remarkable stability (about 100% retention of its initial capacitance) was achieve after 4000 galvanostatic charge-discharge cycles at the current density of 2 A gâ1. Therefore, Mn3O4 NPs/GSs can have been used as an electrode material for supercapacitors.
											ناشر
												Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Electrochimica Acta - Volume 257, 10 December 2017, Pages 155-164
											Journal: Electrochimica Acta - Volume 257, 10 December 2017, Pages 155-164
نویسندگان
												Yangyang Tian, Dongwei Li, Jinglei Liu, Hua Wang, Junfeng Zhang, Yiqun Zheng, Tonghao Liu, Shifeng Hou,