Co(II)-porphyrin-decorated carbon nanotubes as catalysts for oxygen reduction reactions: an approach for fuel cell improvement

被引:133
作者
Sonkar, Piyush Kumar [1 ]
Prakash, Kamal [2 ]
Yadav, Mamta [1 ]
Ganesan, Vellaichamy [1 ]
Sankar, Muniappan [2 ]
Gupta, Rupali [1 ]
Yadav, Dharmendra Kumar [1 ]
机构
[1] Banaras Hindu Univ, Inst Sci, Dept Chem, Varanasi 221005, Uttar Pradesh, India
[2] Indian Inst Technol, Dept Chem, Roorkee 247667, Uttarakhand, India
关键词
ELECTROCATALYTIC ACTIVITY; COBALT PORPHYRINS; GRAPHENE OXIDE; METAL-FREE; SYNERGISTIC CATALYST; PERFORMANCE; COMPOSITE; ELECTRODES; PLATINUM; SPECTRA;
D O I
10.1039/c6ta10482g
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
The development of high-performance and cost-effective catalysts for the oxygen reduction reaction (ORR) is essential for the advancement of fuel cells. In thiswork, three different functionalized cobalt porphyrins, mesotetraphenylporphyrinatocobalt(II) (CoTPP), meso-tetrakis(4'-hydroxyphenyl) porphyrinatocobalt(II) (CoTHPP) and meso-tetrakis(4'-carboxy-phenyl) porphyrinatocobalt(II) (CoTCPP), are prepared. These porphyrins are immobilized non-covalently on multiwalled carbon nanotubes (MWCNTs) and used for the ORR in 0.1 M HClO4, 0.1 M phosphate buffer solution (pH 7.0) and 0.1 M KOH media. The composite materials are characterized by using spectroscopic and electrochemical techniques and their oxygen reduction efficiencies are compared in different media. Kinetic interpretations and hydrodynamic voltammetry (in three media) studies demonstrated that the MWCNT-CoTPP, MWCNT-CoTHPP and MWCNT-CoTCPP composite materials exhibit significant efficiency with decreased overpotential, considerable methanol tolerance and long term operational stability (up to 3000 cycles) for the ORR similar to commercially available platinum carbon (Pt-C) catalysts. These results reveal that the new MWCNT-cobalt porphyrin composite materials can be a potential alternative to the expensive Pt-C catalysts or other commercial cathode materials in fuel cells.
引用
收藏
页码:6263 / 6276
页数:14
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