1998
DOI: 10.1016/s0022-0728(97)00558-5
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In situ FTIRS study of the electrocatalytic oxidation of carbon monoxide and methanol at platinum–ruthenium bulk alloy electrodes

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Cited by 417 publications
(283 citation statements)
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“…As suggested early by Breiter [59] and confirmed with spectroscopic experiments [60][61][62] after the methanol dehydrogenation to formaldehyde two parallel reactions routes to form CO 2 are possible: via COOH ads or CO ads type of intermediates (reaction 2 and 3).…”
Section: Methanolmentioning
confidence: 58%
“…As suggested early by Breiter [59] and confirmed with spectroscopic experiments [60][61][62] after the methanol dehydrogenation to formaldehyde two parallel reactions routes to form CO 2 are possible: via COOH ads or CO ads type of intermediates (reaction 2 and 3).…”
Section: Methanolmentioning
confidence: 58%
“…3, in which the mass is also based on the total PtRu mass. In the initial stage, all potentiostatic currents decreased rapidly, corresponding to the formation of intermediate species such as CO ads , CH 3 OH ads , and CHO ads during the methanol oxidation reaction [26]. Figure 3 shows that the current density of TiO 2 -PtRu/C (10 %) is higher than that of PtRu/C.…”
Section: Methodsmentioning
confidence: 98%
“…Further these results provide revealing evidence that Ru element in the perovskite structure play a big role in the observed electro-catalytic activity. It is well known fact that during electro-oxidation of alcohols on Pt-Ru catalyst, ruthenium activates water and provides preferential sites for OH group adsorption at low potential (26,27). These OH groups are essential for complete oxidation (to CO 2 ) of the intermediate chemisorbed species.…”
Section: Electro-catalytic Activitymentioning
confidence: 99%