Preleached Pd-Pt-Ni and binary Pd-Pt electrocatalysts for oxygen reduction reaction in proton exchange membrane fuel cells

被引:51
|
作者
Zhao, Juan
Manthiram, Arumugam [1 ]
机构
[1] Univ Texas Austin, Electrochem Energy Lab, Austin, TX 78712 USA
基金
美国国家科学基金会;
关键词
Fuel cells; Electrocatalysts; Acid-leached catalysts; CO-AU ELECTROCATALYSTS; ALLOY ELECTROCATALYSTS; CATALYSTS; METHANOL; STABILITY; PLATINUM; NANOPARTICLES; ACID; FE; BOROHYDRIDE;
D O I
10.1016/j.apcatb.2010.11.007
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
Ternary preleached Pd-Pt-Ni and binary Pd-Pt catalysts have been synthesized, characterized, and evaluated as oxygen reduction reaction (ORR) electrocatalysts in single cell proton exchange membrane fuel cells (PEMFC), and the data have been compared with those of Pd-Pt-Ni catalyst. All the three catalysts show much improved Pt-mass activity compared to the state-of-the-art Pt catalyst. The preleached catalyst shows surface catalytic activity improvement by a factor of 2 in terms of Pt-mass activity and 3.5 in terms of specific activity compared to commercial Pt. Based on compositional analysis before and after the fuel cell test, the enhanced activity is attributed to an active phase with a Pd-rich core and Pt-rich shell structure. The strain introduced in the outer shell layer by the lattice parameter mismatch between the core and shell could downshift the metal d-band center, reduce the adsorption energy of hydroxyl species, and thus increase the intrinsic activity. The surface morphology and geometric effect induced by compositional and structural changes may also play a role. (c) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:660 / 668
页数:9
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