Study of Pt Dissolution During Formic Acid Oxidation On Thin Films Deposited Via Surface Limited Redox Replacements

2013 ◽  
Vol 225 ◽  
pp. 323-329 ◽  
Author(s):  
Erwan Bertin ◽  
Sébastien Garbarino ◽  
Daniel Guay ◽  
José Solla-Gullón ◽  
Francisco J. Vidal-Iglesias ◽  
...  

ACS Catalysis ◽  
2013 ◽  
Vol 3 (8) ◽  
pp. 1709-1718 ◽  
Author(s):  
M. Fayette ◽  
J. Nutariya ◽  
N. Vasiljevic ◽  
N. Dimitrov

2011 ◽  
Vol 158 (8) ◽  
pp. B1019 ◽  
Author(s):  
Sun-Mi Hwang ◽  
John E. Bonevich ◽  
Jae Jeong Kim ◽  
Thomas P. Moffat

Surfaces ◽  
2019 ◽  
Vol 2 (2) ◽  
pp. 372-386 ◽  
Author(s):  
Yongan Tang ◽  
Shouzhong Zou

Cubic, octahedral, and rhombic dodecahedral gold nanocrystals enclosed by {100}, {111}, and {110} facets, respectively, were prepared by a seed-mediated growth method at the room temperature. Palladium thin films were coated on these Au nanocrystals by a redox replacement approach to explore their catalytic activities. It is revealed that formic acid and carbon monoxide oxidation in 0.1 M HClO4 on Au nanocrystals coated with one monolayer (ML) of Pd are facet-dependent and resemble those obtained from corresponding Pd single crystals and Pd films deposited on bulk Au single crystals, suggesting epitaxial growth of Pd overlayers on the Au nanocrystal surfaces. As the Pd film thickness increased, formic acid oxidation current density decreased and the CO oxidation potential moved to more negative. The catalytic activity remained largely unchanged after 3–5 MLs of Pd deposition. The specific adsorption of (bi)sulfate was shown to hinder the formic acid oxidation and the effect decreased with the increasing Pd film thickness. These observations were explained in the framework of the d-band theory. This study highlights the feasibility of engineering high-performance catalysts through deposition of catalytically active metal thin films on facet-controlled inert nanocrystals.


2013 ◽  
Vol 78 (8) ◽  
pp. 1189-1202 ◽  
Author(s):  
Jelena Lovic ◽  
Dusan Tripkovic ◽  
Ksenija Popovic ◽  
Vladislava Jovanovic ◽  
Amalija Tripkovic

Formic acid oxidation was studied on two Pt-Bi catalysts, Pt2Bi and polycrystalline Pt modified by irreversible adsorbed Bi (Pt/Biirr) in order to establish the difference between the effects of Biirr and Bi in alloyed state. The results were compared to pure Pt. It was found that both bimetallic catalysts were more active than Pt with the onset potentials shifted to more negative values and the currents at 0.0 V vs. SCE (under steady state conditions) improved up to two order of magnitude. The origin of Pt2Bi high activity and stability is increased selectivity toward formic acid dehydrogenation caused by the ensemble and electronic effect and suppression of Bi leaching from the surface during formic acid oxidation. However, although Pt/Biirr also shows remarkable initial activity compared to pure Pt, dissolution of Bi is not suppressed and the poisoning of the electrode surface induced by dehydration path is observed. Comparison of the initial quasi-steady state and potentiodynamic results obtained for these two Pt-Bi catalysts revealed that the electronic effect, existing only in the alloy, contributes earlier start of the reaction, while the maximum current density is determined by the ensemble effect.


2019 ◽  
Vol 6 (3) ◽  
pp. 104-107
Author(s):  
Marina Vladimirovna Lebedeva ◽  
Alexey Petrovich Antropov ◽  
Alexander Victorovich Ragutkin ◽  
Nicolay Andreevich Yashtulov

In paper electrode materials with palladium nanoparticles on polymer matrix substrates for energy sources have been formed. Nanocomposites were investigated by atomic force and scanning electron microscopy. The catalytic activity of formed electrodes in the formic acid oxidation reaction was evaluated by voltammetry method.


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