Fuel Cell Electrocatalyst Using Polybenzimidazole-Modified Carbon Nanotubes As Support Materials

被引:167
作者
Fujigaya, Tsuyohiko [1 ,2 ]
Nakashima, Naotoshi [1 ,2 ,3 ]
机构
[1] Kyushu Univ, Grad Sch Engn, Dept Appl Chem, Nishi Ku, Fukuoka 8190395, Japan
[2] Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI I2CNER, Nishi Ku, Fukuoka 8190395, Japan
[3] JST CREST, Chiyoda Ku, Tokyo 1020075, Japan
关键词
Carbon nanotubes; Electrocatalyst; Fuel cells; Metal nanoparticle; Polybenzimidazole; ACID-DOPED POLYBENZIMIDAZOLE; POLYMER ELECTROLYTE MEMBRANES; OXYGEN REDUCTION ACTIVITY; METAL NANOPARTICLES; GOLD NANOPARTICLES; PLATINUM NANOPARTICLES; INDIVIDUAL DISSOLUTION; PTRU NANOPARTICLES; CATHODE CATALYST; PROTOGENIC GROUP;
D O I
10.1002/adma.201204461
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Toward the next generation fuel cell systems, the development of a novel electrocatalyst for the polymer electrolyte fuel cell (PEFC) is crucial to overcome the drawbacks of the present electrocatalyst. As a conductive supporting material for the catalyst, carbon nanotubes (CNTs) have emerged as a promising candidate, and many attempts have been carried out to introduce CNT, in place of carbon black. On the other hand, as a polymer electrolyte, polybenzimidazoles (PBIs) have been recognized as a powerful candidate due to the high proton conductivity above 100 degrees C under non-humid conditions. In 2008, we found that these two materials have a strong physical interaction and form a stable hybrid material, in which the PBIs uniformly wrap the surfaces of the CNTs. Furthermore, PBIs serve as effective binding sites for the formation of platinum (Pt) nanoparticles to fabricate a ternary composite (CNT/PBIs/Pt). In this review article, we summarize the fundamental properties of the CNT/PBIs/Pt and discuss their potential as a new electrocatalyst for the PEFC in comparison with the conventional ones. Furthermore, potential applications of CNT/PBIs including use of the materials for oxygen reduction catalysts and reinforcement of PBI films are summarized.
引用
收藏
页码:1666 / 1681
页数:16
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