Integrated plasma synthesis of efficient catalytic nanostructures for fuel cell electrodes

被引:32
作者
Caillard, A.
Charles, C. [1 ]
Boswell, R.
Brault, P.
机构
[1] Australian Natl Univ, Space Plasma Power & Propuls Grp, Res Sch Phys Sci & Engn, Canberra, ACT 0200, Australia
[2] Univ Orleans, Grp Rech Energet Milieux Ionises, UMR 6606, CNRS, F-45067 Orleans 2, France
关键词
D O I
10.1088/0957-4484/18/30/305603
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A single plasma process involving three consecutive steps has been developed for producing high gas flow catalytic nanostructures on the electrodes of proton exchange membrane (PEM) fuel cells (FC). Using a high density helicon radio frequency (13.56 MHz) plasma, nickel is sputtered onto a porous carbon support. Changing the background gas from argon to methane/ hydrogen allowed 2 mu m long, 37 nm diameter carbon nanofibres ( CNFs) to be grown by diffusion through the nickel clusters in a 'tip growth' mechanism at the relatively low temperature of 400 degrees C. The third step involves plasma sputtering of platinum onto the CNFs, resulting in nanoclusters (3-8 nm) being formed on the periphery of the CNFs. Four FC cathodes were synthesized on carbon paper and PTFE/carbon loaded cloth (known as gas diffusion layer, GDL), both with and without CNFs, with the Pt/CNFs nanostructures grown on PTFE/carbon loaded cloth having the best FC performances. Compared with conventional FCs, the efficiency of sputtered platinum in the Pt/CNF based cathode is much higher than in a chemically deposited system over the entire range of operating current. This indicates that combination of different, simple, plasma techniques is an effective method for preparing highly efficient catalyst layers.
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页数:9
相关论文
共 48 条
[1]   A FORMATION MECHANISM FOR CATALYTICALLY GROWN HELIX-SHAPED GRAPHITE NANOTUBES [J].
AMELINCKX, S ;
ZHANG, XB ;
BERNAERTS, D ;
ZHANG, XF ;
IVANOV, V ;
NAGY, JB .
SCIENCE, 1994, 265 (5172) :635-639
[2]   Catalyst gradient for cathode active layer of proton exchange membrane fuel cell [J].
Antoine, O ;
Bultel, Y ;
Ozil, P ;
Durand, R .
ELECTROCHIMICA ACTA, 2000, 45 (27) :4493-4500
[3]  
Baker R.T.K., 1978, CHEM PHYS CARBON, V14, P83
[4]   NUCLEATION AND GROWTH OF CARBON DEPOSITS FROM NICKEL CATALYZED DECOMPOSITION OF ACETYLENE [J].
BAKER, RTK ;
BARBER, MA ;
WAITE, RJ ;
HARRIS, PS ;
FEATES, FS .
JOURNAL OF CATALYSIS, 1972, 26 (01) :51-&
[5]   Carbon nanotubes - the route toward applications [J].
Baughman, RH ;
Zakhidov, AA ;
de Heer, WA .
SCIENCE, 2002, 297 (5582) :787-792
[6]   Platinum, fuel cells, and future US road transport [J].
Borgwardt, RH .
TRANSPORTATION RESEARCH PART D-TRANSPORT AND ENVIRONMENT, 2001, 6 (03) :199-207
[7]   Low temperature synthesis of carbon nanofibres on carbon fibre matrices [J].
Boskovic, BO ;
Golovko, VB ;
Cantoro, M ;
Kleinsorge, B ;
Chuang, ATH ;
Ducati, C ;
Hofmann, S ;
Robertson, J ;
Johnson, BFG .
CARBON, 2005, 43 (13) :2643-2648
[8]   Large-area synthesis of carbon nanofibres at room temperature [J].
Boskovic, BO ;
Stolojan, V ;
Khan, RUA ;
Haq, S ;
Silva, SRP .
NATURE MATERIALS, 2002, 1 (03) :165-168
[9]   Nucleation and growth of carbon nanotubes by microwave plasma chemical vapor deposition [J].
Bower, C ;
Zhou, O ;
Zhu, W ;
Werder, DJ ;
Jin, SH .
APPLIED PHYSICS LETTERS, 2000, 77 (17) :2767-2769
[10]   Plasma-induced alignment of carbon nanotubes [J].
Bower, C ;
Zhu, W ;
Jin, SH ;
Zhou, O .
APPLIED PHYSICS LETTERS, 2000, 77 (06) :830-832