High-Performance Fe-N-Doped Graphene Electrocatalysts with pH-Dependent Active Sites for the Oxygen Reduction Reaction

被引:33
作者
Pan, Fuping [1 ,2 ]
Zhao, Qiuping [1 ]
Wang, Jia [1 ]
Zhang, Junyan [1 ]
机构
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Solid Lubricat, Lanzhou 730000, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
active sites; electrocatalysis; Fe-N-doped graphene; fuel cells; oxygen reduction; SUPPORTED PLATINUM NANOPARTICLES; METAL-ORGANIC FRAMEWORKS; NITROGEN; CARBON; CATALYSTS; PYROLYSIS; COMPOSITE; ELECTROREDUCTION; COORDINATION; GRAPHITE;
D O I
10.1002/celc.201500301
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Advanced Fe-N-doped graphene (FeNG) electrocatalysts are developed for the oxygen reduction reaction (ORR) by annealing a mixture of sustainable and low-cost corn starch, urea, and FeCl3. The Fe-N coordinations and Fe/Fe3C nanoparticles can be controllably achieved through space confinement and pyrolysis temperature-induced effects, respectively. Electrochemical tests show that, compared to the commercial Pt/C catalyst, the ORR half-wave potential of FeNG is 99mV more positive in KOH and 34mV more negative in H2SO4, with higher stabilities in both media. More importantly, the ORR mechanisms of FeNG are demonstrated to be diverse in both KOH and H2SO4, owing to the various catalytic centers. The obtained results indicate that the enhanced ORR activity in basic media can mainly be ascribed to quaternary N and Fe/Fe3C sites, whereas the ORR performance in acidic media originates primarily from Fe-N-X complexes. The electrocatalytic origin of these species is governed, primarily, by their unique electronic structures and specific environments in different pH solutions.
引用
收藏
页码:2032 / 2040
页数:9
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