期刊
JOURNAL OF POWER SOURCES
卷 251, 期 -, 页码 30-37出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.jpowsour.2013.11.027
关键词
Electrooxidation; Electrocatalysis; Fuel cell; Kinetic isotope effect; Formic acid
资金
- Ministry of Science, Poland
- Alexander von Humboldt-Stiftung
Kinetics and mechanism of formic acid (FA) oxidation on platinum and upd-lead ad-atoms modified platinum electrodes have been studied using unlabelled and deuterated compounds. Poisoning of the electrode surface by CO-like species was prevented by suppression of dissociative chemisorption of FA due to a fast competitive underpotential deposition of lead ad-atoms on the Pt surface from an acidic solution containing Pb2+ cations. Modification of the Pt electrode with upd lead induced a catalytic effect in the direct electrooxidation of physisorbed FA to CO2. With increasing degree of HID substitution, the rate of this reaction decreased in the order: HCOOH > DCOOH >= HCOOD > DCOOD. HCOOH was oxidized 8.5-times faster on a Pt/Pb electrode than DCOOD. This primary kinetic isotope effect proves that the C-H- and O-H-bonds are simultaneously cleaved in the rate determining step. A secondary kinetic isotope effect was found in the dissociative chemisorption of FA in the hydrogen adsorption-desorption range on a bare Pt electrode after HID exchange in the C-H bond, wherein the influence of deuterium substitution in the O-H group was negligibly small. Thus the C-H bond cleavage is accompanied by the C-OH and not the O-H bond split in the FA decomposition, producing CO-like species on the Pt surface sites. (C) 2013 Elsevier B.V. All rights reserved.
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