کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
607882 1454597 2013 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Nitrogen/manganese oxides doped porous carbons derived from sodium butyl naphthalene sulfonate
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی شیمی کلوئیدی و سطحی
پیش نمایش صفحه اول مقاله
Nitrogen/manganese oxides doped porous carbons derived from sodium butyl naphthalene sulfonate
چکیده انگلیسی

High-performance porous carbons have been prepared as supercapacitor electrode materials by co-doped with nitrogen and MnOx via a direct carbonization method, using sodium butyl naphthalene sulfonate (abbr. BNS–Na) as carbon source. It is believed that the in situ formed Na6(SO4)2(CO3) in the product would probably serve as temporary template for producing porous structures. The impacts of nitrogen/MnOx contents as well as the structures upon the capacitive performances were emphatically discussed. It indicates that introducing nitrogen and/or MnOx into the carbon matrix can remarkably improve their capacitive performances based on the cyclic voltammetry and galvanostatic charge–discharge measurements in 6 mol L−1 KOH aqueous solution. The specific capacitances of doped carbons can reach up to ca. 167.0–241.8 F g−1 compared with that of the undoped carbon of ca. 105.6 F g−1. Of these samples, the carbon–Mn-1:30-N-1:15 sample co-doped with nitrogen and MnOx exhibits the highest specific capacitance and energy density up to 241.8 F g−1 and 33.6 Wh kg−1, respectively. In particular, these carbons also exhibit high intrinsic capacitances (i.e., capacitance per surface area) up to ca. 0.66–1.92 F m−2.

Figure optionsDownload high-quality image (72 K)Download as PowerPoint slideHighlights
► A simple carbonization method was developed to prepare porous carbon.
► The doping processes for nitrogen/MnOx are simple and reproducible.
► Doping nitrogen/MnOx into carbons can greatly improve capacitive performances.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Colloid and Interface Science - Volume 398, 15 May 2013, Pages 176–184
نویسندگان
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