کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
184548 459578 2015 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Interface polymerization synthesis of conductive polymer/graphite oxide@sulfur composites for high-rate lithium-sulfur batteries
ترجمه فارسی عنوان
سنتز پلیمریزاسیون رابط پلیمر رسانایی / گرافیت اکسید @ سولفور کامپوزیت برای باتری های لیتیوم سولفور با درجه بالا
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
چکیده انگلیسی


• A hybrid nanostructure that incorporate the merits of conductive polymer nanorods and graphite oxide sheets.
• A novel approach based on interface polymerization for synthesizing CP/GO@S ternary composite.
• CP/GO@S ternary composite cathode shows enhanced electrochemical properties compared with CP@S binary composite cathode.
• PEDOT/GO@S composite is the material system that have best electrochemical performance in all CP/GO@S ternary composites.

The novel ternary composites, conductive polymers (CPs)/graphene oxide (GO)@sulfur composites were successfully synthesized via a facile one-pot route and used as cathode materials for Li-S batteries The poly(3,4-ethylenedioxythiophene) (PEDOT)/GO and polyaniline (PANI)/GO composites were prepared by interface polymerization of monomers on the surface of GO sheets. Then sulfur was in-situ deposited on the CPs/GO composites in same solution. The component and structure of the composites were characterized by XPS, TGA, FTIR, SEM, TEM and electrochemical measurements. In this structure, the CPs nanostructures are believed to serve as a conductive matrix and an adsorbing agent, while the highly conductive GO will physically and chemically confine the sulfur and polysulfide within cathode. The PEDOT/GO@S composites with the sulfur content of 66.2 wt% exhibit a reversible discharge capacity of 800.2 mAh g−1 after 200 cycles at 0.5 C, which is much higher than that of PANI/GO@S composites (599.1 mAh g−1) and PANI@S (407.2 mAh g−1). Even at a high rate of 4 C, the PEDOT/GO@S composites still retain a high specific capacity of 632.4 mAh g−1.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Electrochimica Acta - Volume 155, 10 February 2015, Pages 54–60
نویسندگان
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