Pt-free carbon-based fuel cell catalyst prepared from spherical polyimide for enhanced oxygen diffusion

被引:50
作者
Nabae, Yuta [1 ]
Nagata, Shinsuke [1 ]
Hayakawa, Teruaki [1 ]
Niwa, Hideharu [2 ]
Harada, Yoshihisa [2 ,3 ]
Oshima, Masaharu [3 ]
Isoda, Ayano [4 ]
Matsunaga, Atsushi [4 ]
Tanaka, Kazuhisa [4 ]
Aoki, Tsutomu [4 ]
机构
[1] Tokyo Inst Technol, Dept Organ & Polymer Mat, Meguro Ku, 2-12-1 S8-26 Ookayama, Tokyo 1528552, Japan
[2] Univ Tokyo, Inst Solid State Phys, 5-1-5 Kashiwanoha, Kashiwa, Chiba 2778581, Japan
[3] Univ Tokyo, Synchrotron Radiat Res Org, SPring 8,1-1-1 Koto, Sayo, Hyogo 6795198, Japan
[4] Toshiba Fuel Cell Power Syst Corp, Kawasaki Ku, 4-1 Ukishima Cho, Kawasaki, Kanagawa 2100862, Japan
关键词
REDUCTION REACTION; ACTIVE-SITES; ALLOY CATALYSTS; IRON; PHTHALOCYANINE;
D O I
10.1038/srep23276
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The development of a non-precious metal (NPM) fuel cell catalyst is extremely important to achieve globalization of polymer electrolyte fuel cells due to the cost and scarcity of platinum. Here, we report on a NPM cathode catalyst prepared by the pyrolysis of spherical polyimide nanoparticles that contain small amounts of Fe additive. 60 nm diameter Fe-containing polyimide nanoparticles were successfully synthesized by the precipitation polymerization of pyromellitic acid dianhydride and 1,3,5-tris(4-aminophenyl)benzene with Fe(acac)(3) (acac = acetylacetonate) as an additive. The particles were subsequently carbonized by multistep pyrolysis to obtain the NPM catalyst while retaining the small particle size. The catalyst has good performance and promising durability for fuel cell applications. The fuel cell performance under a 0.2 MPa air atmosphere at 80 degrees C of 1.0 A cm(-2) at 0.46 V is especially remarkable and better than that previously reported.
引用
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页数:7
相关论文
共 29 条
[1]   Direct metalation of a phthalocyanine monolayer on Ag(111) with coadsorbed iron atoms [J].
Bai, Yun ;
Buchner, Florian ;
Wendahl, Matthew T. ;
Kellner, Ina ;
Bayer, Andreas ;
Steinrueck, Hans-Peter ;
Marbach, Hubertus ;
Gottfried, J. Michael .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (15) :6087-6092
[2]   Preparation of carbon alloy catalysts for polymer electrolyte fuel cells from nitrogen-containing rigid-rod polymers [J].
Chokai, Masayuki ;
Taniguchi, Masataka ;
Moriya, Shogo ;
Matsubayashi, Katsuyuki ;
Shinoda, Tsuyoshi ;
Nabae, Yuta ;
Kuroki, Shigeki ;
Hayakawa, Teruaki ;
Kakimoto, Masa-aki ;
Ozaki, Jun-ichi ;
Miyata, Seizo .
JOURNAL OF POWER SOURCES, 2010, 195 (18) :5947-5951
[3]   Active sites of nitrogen-doped carbon materials for oxygen reduction reaction clarified using model catalysts [J].
Guo, Donghui ;
Shibuya, Riku ;
Akiba, Chisato ;
Saji, Shunsuke ;
Kondo, Takahiro ;
Nakamura, Junji .
SCIENCE, 2016, 351 (6271) :361-365
[4]  
Ha SY, 1999, ELECTROCHEM SOLID ST, V2, P461, DOI 10.1149/1.1390871
[5]   Carbon alloy catalysts: Active sites for oxygen reduction reaction [J].
Ikeda, Takashi ;
Boero, Mauro ;
Huang, Sheng-Feng ;
Terakura, Kiyoyuki ;
Oshima, Masaharu ;
Ozaki, Jun-ichi .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (38) :14706-14709
[6]   Possible Oxygen Reduction Reactions for Graphene Edges from First Principles [J].
Ikeda, Takashi ;
Hou, Zhufeng ;
Chai, Guo-Liang ;
Terakura, Kiyoyuki .
JOURNAL OF PHYSICAL CHEMISTRY C, 2014, 118 (31) :17616-17625
[7]  
Jahnke H, 1976, Top Curr Chem, V61, P133
[8]   NEW FUEL CELL CATHODE CATALYST [J].
JASINSKI, R .
NATURE, 1964, 201 (492) :1212-&
[9]   Effect of iron-carbide formation on the number of active sites in Fe-N-C catalysts for the oxygen reduction reaction in acidic media [J].
Kramm, Ulrike I. ;
Herrmann-Geppert, Iris ;
Fiechter, Sebastian ;
Zehl, Gerald ;
Zizak, Ivo ;
Dorbandt, Iris ;
Schmeisser, Dieter ;
Bogdanoff, Peter .
JOURNAL OF MATERIALS CHEMISTRY A, 2014, 2 (08) :2663-2670
[10]   Molecular oxygen reduction in PEM fuel cells:: Evidence for the simultaneous presence of two active sites in Fe-based catalysts [J].
Lefèvre, M ;
Dodelet, JP ;
Bertrand, P .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (34) :8705-8713