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Quantifying metal support interaction in ceria-supported Pt, PtSn and Ru nanoparticles using electrochemical technique
被引:21
|作者:
Dole, Holly A. E.
[1
]
Costa, Ana C. G. S. A.
[1
]
Couillard, Martin
[2
]
Baranova, Elena A.
[1
]
机构:
[1] Univ Ottawa, CCRI, Dept Chem & Biol Engn, 161 Louis Pasteur St, Ottawa, ON K1N 6N5, Canada
[2] Natl Res Council Canada, 1200 Montreal Rd, Ottawa, ON K1A 0R6, Canada
基金:
加拿大自然科学与工程研究理事会;
关键词:
Platinum;
Ruthenium;
Ceria;
Metal-support interaction;
Polarization curves;
Electrochemical promotion;
Ethylene oxidation;
CATALYTIC-ACTIVITY;
OXYGEN MIGRATION;
PROMOTION;
SIZE;
ETHYLENE;
OXIDATION;
CARBON;
PROPANE;
D O I:
10.1016/j.jcat.2015.10.015
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:
Electrochemical promotion and metal-support interaction (MSI) have long been viewed as two separate phenomena; however, more recently it has been shown that, functionally, for ionic and mixed ionic-electronic conducting materials, both are linked by the transfer of ionic species at the interfaces. The purpose of this study was to exhibit a relationship between these two concepts through the use of an electro-chemical technique to evaluate CeO2-supported Pt- and Ru-based nanoparticles. The presence of ceria was found to increase the reaction rate when compared to free-standing Pt and Ru nanoparticles with the metal-support interaction rate enhancement ratios, rho(MSI), up to 14. Polarization measurements established that higher exchange current density, i(0), values correspond to lower open circuit catalytic rates. An apparent self-induced Faradaic efficiency was proposed and determined for each catalyst; lowest value (vertical bar Lambda(MSI)vertical bar approximate to 20) was found for free-standing nanoparticles, while highest value (vertical bar Lambda(MSI)vertical bar = 1053) corresponded to 1 wt% Pt-1/CeO2. (C) 2015 Elsevier Inc. All rights reserved.
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页码:40 / 50
页数:11
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