High performance polymer electrolyte fuel cells with ultra-low Pt loading electrodes prepared by dual ion-beam assisted deposition

被引:102
作者
Saha, Madhu Sudan
Gulla, Andrea F.
Allen, Robert J.
Mukerjee, Sanjeev
机构
[1] Northeastern Univ, Dept Chem & Biol Chem, Boston, MA 02115 USA
[2] E TEK Div De Nora N Amer Inc, Somerset, NJ 08873 USA
关键词
low Pt loading; dual IBAD; PEMFC; electrode kinetics; oxygen reduction reaction;
D O I
10.1016/j.electacta.2006.01.006
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Ultra-low pure Pt-based electrodes (0.04-0.12 mg(Pt)/cm(2)) were prepared by dual ion-beam assisted deposition (dual IBAD) method on the surface of a non-catalyzed gas diffusion layer (GDL) substrate. Film thicknesses ranged between 250 and 750 A, these are compared with a control, a conventional Pt/C (1-0 mg(Pt)(MEA)/cm(2), E-TEK). The IBAD electrode constituted a significantly different morphology, where low density Pt deposits (largely amorphous) were formed with varying depths of penetration into the gas diffusion layer, exhibiting a gradual change towards increasing crystalline character (from 250 to 750 A). Mass specific power density of 0.297 g(Pt)/kW is reported with 250 A IBAD deposit (0.04 mg(Pt)/cm(2) for a total MEA loading of 0.08 mg(Pt)/cm(2)) at 0.65 V. This is contrasted with the commercial MEA with a loading of 1 mg(Pt)(MEA)/cm(2) where mass specific power density obtained was 1.18 g(Pt)/kW (at 0.65 V), a value typical of current state of the art commercial electrodes containing Pt/C. The principal shortcoming in this effort is the area specific power density which was in the range of 0.27-0.43 W/cm(2) (for 250-750 angstrom IBAD) at 0.65 V, hence much below the automotive target value of 0.8-0.9 W/cm(2) (at 0.65 V). An attempt to mitigate these losses is reported with the use of patterning. In this context a series of patterns ranging from 45 to 80% Pt coverage were used in conjunction with a hexagonal hole geometry. Up to 30% lowering of mass transport losses were realized. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4680 / 4692
页数:13
相关论文
共 47 条
[1]  
ALLEN RJ, 2000, Patent No. 6077621
[2]   In situ electrochemical deposition of Pt nanoparticles on carbon and inside Nafion [J].
Antoine, O ;
Durand, R .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2001, 4 (05) :A55-A58
[3]   FUEL-CELL TECHNOLOGY AND INNOVATION [J].
APPLEBY, AJ .
JOURNAL OF POWER SOURCES, 1992, 37 (1-2) :223-239
[4]   Characteristics of adsorbed CO and CH3OH oxidation reactions for complex Pt/Ru catalyst systems [J].
Bock, C ;
Blakely, MA ;
MacDougall, B .
ELECTROCHIMICA ACTA, 2005, 50 (12) :2401-2414
[5]  
Cavalca CA, 2001, US Pat, Patent No. 6300000
[6]   Performance of proton exchange membrane fuel cell electrodes prepared by direct deposition of ultrathin platinum on the membrane surface [J].
Cha, SY ;
Lee, WM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1999, 146 (11) :4055-4060
[7]   Performance of a polymer electrolyte membrane fuel cell with thin film catalyst electrodes [J].
Chun, YG ;
Kim, CS ;
Peck, DH ;
Shin, DR .
JOURNAL OF POWER SOURCES, 1998, 71 (1-2) :174-178
[8]   PEMFC anode with very low Pt loadings using pulsed laser deposition [J].
Cunningham, N ;
Irissou, E ;
Lefèvre, M ;
Denis, MC ;
Guay, D ;
Dodelet, JP .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2003, 6 (07) :A125-A128
[9]  
DEBE MK, 1999, Patent No. 97948851
[10]  
DEBE MK, 1999, Patent No. 97948627