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Rational determination of exchange current density for hydrogen electrode reactions at carbon-supported Pt catalysts
被引:41
|作者:
Sun, Yubao
[1
]
Lu, Juntao
[1
]
Zhuang, Lin
[1
]
机构:
[1] Wuhan Univ, Coll Chem & Mol Sci, Hubei Key Lab Electrochem Power Sources, Wuhan 430072, Peoples R China
基金:
美国国家科学基金会;
关键词:
Hydrogen electrode reactions;
Exchange current density;
Platinum;
Rotating disk electrode;
Fuel cells;
OXIDATION REACTION;
REACTION-KINETICS;
OXYGEN REDUCTION;
PLATINUM;
NANOPARTICLES;
ELECTROCATALYST;
PERFORMANCE;
SURFACES;
POISONS;
ACID;
D O I:
10.1016/j.electacta.2009.09.047
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
The rotating disk electrode (RDE) is a useful technique for precise determination of exchange current density (j(0)) in electrochemistry. For the study of powder catalysts, a common practice is to apply the powder onto an inert disk substrate (such as glassy carbon). However, this approach in its usual version will lead to wrong results for the exchange current density of hydrogen electrode reactions at carbon-supported Pt nanoparticles (Pt/C) because of the poor utilization of the loaded Pt nanoparticles. Our new approach is to dilute the Pt/C powder with a large amount of pristine carbon support to make the catalyst layer. In this way, all the catalyst particles in the catalyst layer have nearly the same and much enhanced mass transport so that rational exchange current density can be obtained. Using the new approach. the current density for hydrogen electrode reactions at Pt/C in 0.1 M perchloric acid at 25 degrees C is found to be 27.2 +/- 3.5 mA/cm(2) with an apparent activation energy 43 kJ/mol. These results are in agreement with the j(0) estimation based on real fuel cell experiments. (C) 2009 Elsevier Ltd. All rights reserved.
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页码:844 / 850
页数:7
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