1956
DOI: 10.1021/ja01599a007
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Heats of Adsorption of Oxygen on Nickel, Platinum and Silver1

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Cited by 46 publications
(6 citation statements)
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“…Starting from the dissociative chemisorption of oxygen on Au catalysts, research activities reported on the necessity of a thermal activation in order to chemisorb O 2 on Au. 255 Using a static O 2 adsorption measurements in a pressure range of 4-8 mbar, Fukushima et al 256 reported that the amount of O 2 adsorbed on different Au based supports (silica, magnesia and alumina) increases concomitantly with the increase of temperature (from 170 1C to 450 1C). By increasing the temperature, the adsorption becomes reversible at 340 1C where the isobar reaches a maximum.…”
Section: Chemisorption Methodsmentioning
confidence: 99%
“…Starting from the dissociative chemisorption of oxygen on Au catalysts, research activities reported on the necessity of a thermal activation in order to chemisorb O 2 on Au. 255 Using a static O 2 adsorption measurements in a pressure range of 4-8 mbar, Fukushima et al 256 reported that the amount of O 2 adsorbed on different Au based supports (silica, magnesia and alumina) increases concomitantly with the increase of temperature (from 170 1C to 450 1C). By increasing the temperature, the adsorption becomes reversible at 340 1C where the isobar reaches a maximum.…”
Section: Chemisorption Methodsmentioning
confidence: 99%
“…Oxygen, however, readily adsorbs on Pt with a low activation energy, about 3 kcal/mole (40,41). The initial heat of adsorption for molecular oxygen is about 10-17 kcal/mole (38,42,43), and molecules readily dissociate into oxygen atoms, with a dissociative heat of adsorption of about 53-70 kcal/mole (44)(45)(46).…”
Section: Possible Rate-determining Steps--thermodynamicmentioning
confidence: 99%
“…Ag has the capability of adsorbing oxygen-containing species, such as carbon dioxide, 20 phosphates, 21 and silicate, 22 and the oxygen-containing species adsorptions have been found to be much stronger on Ag than on Pt. 23 It is thus speculated that the nine oxygen atomscontaining quaternary phosphonium functional group in the TPQPOH ionomer may be more strongly attracted to the Ag surface than Pt, leading to the tighter and more efficient catalyst-ionomer interface. To verify this assumption, a small model phosphonium molecule, benzyl tris(2,4,6-trimethoxyphenyl) quaternary phosphonium chloride (BTQPCl, Scheme S1, ESI †), was synthesized and added into the supporting electrolyte to investigate its adsorption on both Ag and Pt bulk metal surfaces in ORR RDE tests (Fig.…”
mentioning
confidence: 99%