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Electrochemical performance of carbon nanotube-supported cobalt phthalocyanine and its nitrogen-rich derivatives for oxygen reduction
被引:70
|作者:
Xu, Zhanwei
[1
]
Li, Hejun
[1
]
Cao, Gaoxiang
[1
]
Zhang, Qinglin
[1
]
Li, Kezhi
[1
]
Zhao, Xueni
[1
]
机构:
[1] Northwestern Polytech Univ, State Key Lab Solidificat Proc, CC Composites Res Ctr, Xian 710072, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Catalytic activity;
Phthalocyanine;
Nitrogen;
Carbon nanotubes;
Oxygen reduction;
ELECTROCATALYTIC ACTIVITY;
ASCORBIC-ACID;
FUEL-CELL;
ELECTRODES;
METALLOPHTHALOCYANINES;
ELECTROREDUCTION;
NANOPARTICLES;
FABRICATION;
FILMS;
MANGANESE;
D O I:
10.1016/j.molcata.2010.11.018
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:
Multiwalled carbon nanotube (MWCNT)-supported cobalt phthalocyanine (CoPc), cobalt tetrapyridinoporphyrazine (CoTAP), and cobalt tetrapyrazinoporphyrazine (CoPTpz) assemblies are prepared by solid phase synthesis method. The products are characterized by infrared spectroscopy, scanning and transmission electron microscopy and UV-vis spectroscopy. The electrocatalytic activity of the obtained MWCNT-supported CoPc, CoTAP and CoPTpz assemblies is measured by rotating disk electrode techniques and cyclic voltammetry in an oxygen-saturated 0.1 M KOH. The results show that MWCNT-supported CoPc shows a two-step, two-electron process for the reduction of oxygen reduction (ORR), whereas MWCNT-supported CoTAP and CoPTpz electrodes exhibit a one-step, four-electron pathway for ORR, indicating that N atoms in the backbone of the compounds strongly affect the catalytic activity of MWCNT-supported CoPc derivative assemblies. The MWCNT-supported CoTAP and CoPTpz assemblies have higher activity to oxygen reduction than that of MWCNT-supported CoPc attributed to their different catalytic mechanisms to ORR. (C) 2010 Elsevier B.V. All rights reserved.
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页码:89 / 96
页数:8
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