Nitrogen-Doped Graphene Nanoribbons as Efficient Metal-Free Electrocatalysts for Oxygen Reduction

被引:147
|
作者
Liu, Mingkai [1 ]
Song, Yanfang [2 ,3 ]
He, Sixin [1 ]
Tjiu, Weng Weei [4 ]
Pan, Jisheng [4 ]
Xia, Yong-Yao [2 ,3 ]
Liu, Tianxi [1 ]
机构
[1] Fudan Univ, Dept Macromol Sci, State Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
[2] Fudan Univ, Inst New Energy, Dept Chem, Shanghai 200433, Peoples R China
[3] Fudan Univ, Inst New Energy, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
[4] ASTAR, Inst Mat Res & Engn, Res Link 3, Singapore 117602, Singapore
基金
中国国家自然科学基金;
关键词
graphene nanoribbon; nitrogen-doped; electrocatalysts; oxygen reduction reaction; CARBON NANOTUBES; ALKALINE-MEDIUM; LITHOGRAPHY; TRANSISTORS; COMPOSITE; MECHANISM; CATALYST; FORM; IRON;
D O I
10.1021/am405900r
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nitrogen-doped graphene nanoribbon (N-GNR) nanomaterials with different nitrogen contents have been facilely prepared via high temperature pyrolysis of graphene nanoribbons (GNR)/polyaniline (PANI) composites. Here, the GNRs with excellent surface integration were prepared by longitudinally unzipping the multiwalled carbon nanotubes. With a high length-to-width ratio, the GNR sheets are prone to form a conductive network by connecting end-to-end to facilitate the transfer of electrons. Different amounts of PANI acting as a N source were deposited on the surface of GNRs via a layer-by-layer approach, resulting in the formation of N-GNR nanomaterials with different N contents after being pyrolyzed. Electrochemical characterizations reveal that the obtained N-8.3-GNR nanomaterial has excellent catalytic activity toward an oxygen reduction reaction (ORR) in an alkaline electrolyte, including large kinetic-limiting current density and long-term stability as well as a desirable four-electron pathway for the formation of water. These superior properties make the N-GNR nanomaterials a promising kind of cathode catalyst for alkaline fuel cell applications.
引用
收藏
页码:4214 / 4222
页数:9
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