Thermal stabilities of nanoporous metallic electrodes at elevated temperatures

被引:86
作者
Wang, Xiaohong [2 ]
Huang, Hong [1 ,5 ]
Holme, Tim [1 ]
Tian, Xu [3 ]
Prinz, Fritz B. [1 ,4 ]
机构
[1] Stanford Univ, Dept Mech Engn, Rapid Prototyping Lab, Stanford, CA 94305 USA
[2] Tsinghua Univ, Inst Microelect, Beijing 100084, Peoples R China
[3] Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[5] Wright State Univ, Dept Mech & Mat Engn, Dayton, OH 45435 USA
基金
美国国家科学基金会;
关键词
fuel cell; thermal stability; porous thin film; catalyst; alloy;
D O I
10.1016/j.jpowsour.2007.09.066
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
,Currently Pt-based metals are the best catalytic electrodes for fuel cells at operating temperatures below 500 degrees C. Pure platinum electrodes suffer degradation of microstructure over time at elevated temperatures due to Ostwald ripening. In this paper, better thermal stability of Pt-Ni nanoporous thin films relative to pure Pt is reported. Based on ab initio calculations, it was found that both the surface energy of a Pt0.7Ni0.3 cluster and the energy change of the Pt-Ni alloy cluster upon ripening on yttria stabilized zirconia (YSZ) solid electrolyte were lower than pure Pt. This suggested a better thermal stability of Pt0.7Ni0.3 than Pt. In addition, annealing impacts on microstructures and properties of nanoporous Pt and Pt-Ni alloy thin films were examined experimentally. SEM images show dramatic porosity reduction for pure Pt after annealing at temperatures of 400-600 degrees C but insignificant microstructure change for Pt-Ni nanoporous thin films. As a result, in solid oxide fuel cells using nanoporous Pt-Ni cathodic catalysts instead of pure Pt, better stability, lower electrode impedances, and higher power densities were achieved at elevated operating temperatures (350-500 degrees C). (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:75 / 81
页数:7
相关论文
共 27 条
[21]   Materials for fuel-cell technologies [J].
Steele, BCH ;
Heinzel, A .
NATURE, 2001, 414 (6861) :345-352
[22]   Mechanism of catalyst degradation in proton exchange membrane fuel cells [J].
Virkar, Anil V. ;
Zhou, Yingke .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2007, 154 (06) :B540-B547
[23]   Electrodes and performance analysis of a ceria electrolyte SOFC [J].
Wang, S ;
Kato, T ;
Nagata, S ;
Kaneko, T ;
Iwashita, N ;
Honda, T ;
Dokiya, M .
SOLID STATE IONICS, 2002, 152 :477-484
[24]   Microstructural changes of membrane electrode assemblies during PEFC durability testing at high humidity conditions [J].
Xie, J ;
Wood, DL ;
More, KL ;
Atanassov, P ;
Borup, RL .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2005, 152 (05) :A1011-A1020
[25]   Effect of atomic ordering on the catalytic activity of carbon supported PtM (M = Fe, Co, Ni, and Cu) alloys for oxygen reduction in PEMFCs [J].
Xiong, L ;
Manthiram, A .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2005, 152 (04) :A697-A703
[26]   Adsorption and dissociation of O2 on Pt-Co and Pt-Fe alloys [J].
Xu, Y ;
Ruban, AV ;
Mavrikakis, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (14) :4717-4725
[27]   SIZE-DEPENDENT CATALYTIC ACTIVITY OF SUPPORTED METAL-CLUSTERS [J].
XU, Z ;
XIAO, FS ;
PURNELL, SK ;
ALEXEEV, O ;
KAWI, S ;
DEUTSCH, SE ;
GATES, BC .
NATURE, 1994, 372 (6504) :346-348