Evaluation of Pt Alloys as Electrocatalysts for Oxalic Acid Oxidation: A Combined Experimental and Computational Study

被引:4
|
作者
Perry, Albert, III [1 ]
Babanova, Sofia [1 ]
Matanovic, Ivana [1 ,2 ]
Neumman, Anica [3 ]
Serov, Alexey [1 ]
Artyushkova, Kateryna [1 ]
Atanassov, Plamen [1 ]
机构
[1] Univ New Mexico, Ctr Microengn Mat CMEM, Dept Chem & Biol Engn, Albuquerque, NM 87131 USA
[2] Los Alamos Natl Lab, Theoret Div, Los Alamos, NM 87545 USA
[3] Oregon State Univ, Sch Chem Biol & Environm Engn, Corvallis, OR 97331 USA
关键词
INITIO MOLECULAR-DYNAMICS; TOTAL-ENERGY CALCULATIONS; ELECTROCHEMICAL OXIDATION; OXYGEN REDUCTION; ADSORPTION BEHAVIOR; PLATINUM-ELECTRODES; ETHYLENE-GLYCOL; CATALYSTS; ELECTROOXIDATION; ALCOHOLS;
D O I
10.1149/2.0861609jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this study we combined experimental approaches and density functional theory to evaluate novel platinum-based materials as electrocatalysts for oxalic acid oxidation. Several Pt alloys, PtSn (1:1), PtSn (19:1), PtRu (1:4), PtRuSn (5:4:1), and PtRhSn (3:1:4), were synthetized using sacrificial support method and tested for oxidation of oxalic acid at pH 4. It was shown that PtSn (1:1) and PtRu (1:4) have higher mass activity relative to Pt. These two materials along with Pt and one of the least active alloys, PtSn (19:1), were further analyzed for the oxidation of oxalic acid at different pHs. The results show that all samples tested followed an identical trend of decreased onset potential with increased pH and increased catalytic activity with decreased pH. Density functional theory was further utilized to gain a fundamental knowledge about the mechanism of oxalic acid oxidation on Pt, PtSn (1:1), and PtRu (1:4). The results of the calculations along with the experimentally observed dependence of generated currents on the oxalic acid concentration indicate that the mechanism of oxalic acid oxidation on Pt proceeds without the participation of surface oxidizing species, while on Pt alloys it involves their participation. (C) The Author(s) 2016. Published by ECS. All rights reserved.
引用
收藏
页码:H787 / H795
页数:9
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