Pt and PtRu catalyst bilayers increase efficiencies for ethanol oxidation in proton exchange membrane electrolysis and fuel cells

被引:39
作者
Altarawneh, Rakan M. [1 ]
Pickup, Peter G. [1 ]
机构
[1] Mem Univ, Dept Chem, St John, NF A1B 3X7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Ethanol oxidation; Electrolysis; Direct ethanol fuel cell; Efficiency; Product distribution; Stoichiometry; Catalyst bilayer; CARBON-DIOXIDE; ACETALDEHYDE; ELECTROOXIDATION; PERFORMANCE; PLATINUM; ENERGY;
D O I
10.1016/j.jpowsour.2017.09.014
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
Polarization curves, product distributions, and reaction stoichiometries have been measured for the oxidation of ethanol at anodes consisting of Pt and PtRu bilayers and a homogeneous mixture of the two catalysts. These anode structures all show synergies between the two catalysts that can be attributed to the oxidation of acetaldehyde produced at the PtRu catalyst by the Pt catalyst. The use of a PtRu layer over a Pt layer produces the strongest effect, with higher currents than a Pt on PtRu bilayer, mixed layer, or either catalyst alone, except for Pt at high potentials. Reaction stoichiometries (average number of electrons transferred per ethanol molecule) were closer to the values for Pt alone for both of the bilayer configurations but much lower for PtRu and mixed anodes. Although Pt alone would provide the highest overall fuel cell efficiency at low power densities, the PtRu on Pt bilayer would provide higher power densities without a significant loss of efficiency. The origin of the synergy between the Pt and PtRu catalysts was elucidated by separation of the total current into the individual components for generation of carbon dioxide and the acetaldehyde and acetic acid byproducts. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:27 / 32
页数:6
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