Space-confinement-induced synthesis of hierarchically nanoporous carbon nanowires for the enhanced electrochemical reduction of oxygen

被引:20
作者
Xu, Jiaoxing [1 ,2 ]
Yu, Qiangmin [1 ,2 ]
Guan, Lunhui [1 ,2 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, Key Lab Design & Assembly Funct Nanostruct, Fuzhou 350002, Peoples R China
[2] Fujian Prov Key Lab Nanomat, Fuzhou 350002, Fujian, Peoples R China
关键词
NITROGEN-DOPED CARBON; HIGH ELECTROCATALYTIC ACTIVITY; METAL-FREE ELECTROCATALYSTS; GRAPHITIC CARBON; NANOTUBES; CATALYST; GROWTH; OXIDE; NANOSHEETS; TEMPLATE;
D O I
10.1039/c4ta07106a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hierarchically nanoporous N-doped carbon nanowires (N-CWs) were prepared by a novel space-confinement-induced assembly strategy, for which nitrogen-enriched pyrimidine and anodic aluminium oxide (AAO) template bearing metal oxides are employed as precursor and nanoscale channels, respectively, and the Fe/Co metal oxide not only blocks the AAO surface from the original surface-templating carbonization, but also introduces nanoporosity with acid etching. Thus-obtained carbon nanowires composed of N-doped graphene-like carbon nanosheets not only contain a high N content (up to similar to 12%), but also possess a hierarchically meso/microporous structure (similar to 1.3 cm(3) g(-1)) with high specific surface area (similar to 455 m(2) g(-1)). This protocol allows for the simultaneous optimization of graphitization, porous structure and surface functionalization. As a result, the prepared N-CWs demonstrate an attractive electrocatalytic capability towards oxygen reduction reaction (ORR). Specifically, in addition to the improved kinetic current density and overpotential, the N-CWs prepared at 700 degrees C show the optimized ORR performance with an electron-transfer number of similar to 4.0, which very close to that of a commercial Pt/C catalyst.
引用
收藏
页码:7093 / 7099
页数:7
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