Enhancing ethanol oxidation rate at PtRu electro-catalysts using metal-oxide additives

被引:35
|
作者
Zignani, S. C. [1 ]
Baglio, V. [1 ]
Sebastian, D. [1 ]
Siracusano, S. [1 ]
Arico, A. S. [1 ]
机构
[1] Ist Tecnol Avanzate Energia Nicola Giordano, CNR ITAE, Via Salita S Lucia Contesse 5, I-98126 Messina, Italy
关键词
Direct ethanol fuel cells; metal-oxide promoters; PtRu/C catalyst; ethanol electro-oxidation; FUEL-CELL; ANODE CATALYSTS; METHANOL OXIDATION; RECENT PROGRESS; ELECTROOXIDATION; ELECTROCATALYSTS; RU; NANOPARTICLES; PERFORMANCE; PTSN/C;
D O I
10.1016/j.electacta.2016.01.085
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Metal oxides are investigated, as additives of a PtRu/C catalyst, for enhancing the electro-oxidation of ethanol in acidic solution. High surface area TiO2 and SnO2 additives are synthesized and physicochemically characterized. These oxides are added to PtRu/C during the catalytic ink preparation to obtain tri-metallic composite electrodes. These composite electro-catalysts are investigated for the ethanol electro-oxidation in half-cell configuration in comparison with additive-free PtRu/C and Pt/C catalysts. The PtRu-based composite catalyst containing SnO2 promoter shows a lower onset potential and larger current density for ethanol oxidation than the additive-free catalyst and that containing TiO2 promoter. The composite catalysts (PtRu/C + metal oxide) are also used in a direct ethanol fuel cell under practical operating conditions and assessed against the benchmark PtRu catalyst. An increase in performance is recorded with the composite tri-metallic electrodes. The analysis of electro-catalytic activity towards ethanol oxidation reaction and ethanolic residues coverage indicates an enhanced capability to activate ethanol chemisorption or a larger electroactive surface area, together with a faster intrinsic activity at lower overpotential, as the reasons for the improved performance with the use of metal oxide additives. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:183 / 191
页数:9
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