Nitrogen‐Superdoped 3D Graphene Networks for High‐Performance Supercapacitors

An N‐superdoped 3D graphene network structure with an N‐doping level up to 15.8 at% for high‐performance supercapacitor is designed and synthesized, in which the graphene foam with high conductivity acts as skeleton and nested with N‐superdoped reduced graphene oxide arogels. This material shows a h...

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Veröffentlicht in:Advanced materials (Weinheim) 2017-09, Vol.29 (36), p.n/a
Hauptverfasser: Zhang, Weili, Xu, Chuan, Ma, Chaoqun, Li, Guoxian, Wang, Yuzuo, Zhang, Kaiyu, Li, Feng, Liu, Chang, Cheng, Hui‐Ming, Du, Youwei, Tang, Nujiang, Ren, Wencai
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Sprache:eng
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Zusammenfassung:An N‐superdoped 3D graphene network structure with an N‐doping level up to 15.8 at% for high‐performance supercapacitor is designed and synthesized, in which the graphene foam with high conductivity acts as skeleton and nested with N‐superdoped reduced graphene oxide arogels. This material shows a highly conductive interconnected 3D porous structure (3.33 S cm−1), large surface area (583 m2 g−1), low internal resistance (0.4 Ω), good wettability, and a great number of active sites. Because of the multiple synergistic effects of these features, the supercapacitors based on this material show a remarkably excellent electrochemical behavior with a high specific capacitance (of up to 380, 332, and 245 F g−1 in alkaline, acidic, and neutral electrolytes measured in three‐electrode configuration, respectively, 297 F g−1 in alkaline electrolytes measured in two‐electrode configuration), good rate capability, excellent cycling stability (93.5% retention after 4600 cycles), and low internal resistance (0.4 Ω), resulting in high power density with proper high energy density. A N‐superdoped 3D graphene network structure is synthesized to achieve a highly conductive interconnected 3D porous structure and high N‐doping level simultaneously. The supercapacitors based on this material show a remarkably high capacity, good rate capability, and excellent cycling stability.
ISSN:0935-9648
1521-4095
DOI:10.1002/adma.201701677