Electrocatalytic Activity of Gold-Platinum Clusters for Low Temperature Fuel Cell Applications

被引:72
作者
Tang, Wei [2 ,3 ]
Jayaraman, Shrisudersan [2 ]
Jaramillo, Thomas F. [2 ]
Stucky, Galen D. [2 ,3 ]
McFarland, Eric W. [1 ,3 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[3] Mitsubishi Chem Ctr Adv Mat, Santa Barbara, CA 93106 USA
关键词
OXYGEN REDUCTION REACTION; SCANNING ELECTROCHEMICAL MICROSCOPY; ALLOY NANOPARTICLE CATALYSTS; DENSITY-FUNCTIONAL THEORY; RUTHENIUM SURFACE-AREAS; METHANOL OXIDATION; CARBON-MONOXIDE; HYDROGEN ELECTROOXIDATION; UNDERPOTENTIAL DEPOSITION; COMBINATORIAL DISCOVERY;
D O I
10.1021/jp8089209
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
The electrocatalytic activity of gold-platinum (Au-Pt) clusters was investigated in acidic and alkaline electrolytes. The clusters were synthesized by electrodeposition on fluorinated tin oxide (FTO) substrates and carbon disks with dimensions from 50 to 200 nm. Methanol electrooxidation (fuel cell anode) and oxygen electroreduction (fuel cell cathode) activities were measured using cyclic voltammetry and chronoamperometry. The results for methanol electrooxidation showed that platinum could be partially substituted by gold to achieve higher resistance to poisoning without affecting the activity in acid electrolyte, while in alkaline environment, a significant overall improvement in performance was observed. On the other hand, for the oxygen electroreduction, kinetic results obtained using a rotating disk electrode (RDE) indicated that Au alloying with Pt does not significantly alter the catalytic activity in acidic electrolyte, while a significant improvement in activity was observed in an alkaline electrolyte, which is attributed to a synergistic effect between the Au and Pt.
引用
收藏
页码:5014 / 5024
页数:11
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