1994
DOI: 10.1016/0039-6028(94)91209-2
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A reactive oxygen adlayer on Cu(110) at 100 K

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Cited by 33 publications
(21 citation statements)
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“…The oxygen species involved in these reactions could be atomic or molecular; in principle, we do not have direct evidence of their nature. However, the spectroscopic features of CO−O 2 interactions, as for the CO stretching region frequencies, are very similar to those reported by Hollins and Pritchard on oxidized Cu(110), and much experimental evidence, coming from different surface science techniques, indicates that on the Cu(110) surface, oxygen chemisorption is dissociative also at T < 300 K. Therefore, also in our case, atomic oxygen, adsorbed on copper particles, can be presumed. Moreover, it was found, on Cu(110), by HREELS, LEED, and TPD 40 that the exposure to oxygen at 100 K produces a very reactive oxygen species that oxidizes CO to CO 2 , desorbing below 200 K; moreover, on the same surface, a (2 × 1) phase was also detected that can oxidize CO only at temperatures higher than 430 K. The more reactive oxygen species, O - like, was associated with isolated oxygen atoms; the less reactive one, O 2- like, was associated with reconstructed Cu−O−Cu planes.…”
Section: Resultssupporting
confidence: 89%
“…The oxygen species involved in these reactions could be atomic or molecular; in principle, we do not have direct evidence of their nature. However, the spectroscopic features of CO−O 2 interactions, as for the CO stretching region frequencies, are very similar to those reported by Hollins and Pritchard on oxidized Cu(110), and much experimental evidence, coming from different surface science techniques, indicates that on the Cu(110) surface, oxygen chemisorption is dissociative also at T < 300 K. Therefore, also in our case, atomic oxygen, adsorbed on copper particles, can be presumed. Moreover, it was found, on Cu(110), by HREELS, LEED, and TPD 40 that the exposure to oxygen at 100 K produces a very reactive oxygen species that oxidizes CO to CO 2 , desorbing below 200 K; moreover, on the same surface, a (2 × 1) phase was also detected that can oxidize CO only at temperatures higher than 430 K. The more reactive oxygen species, O - like, was associated with isolated oxygen atoms; the less reactive one, O 2- like, was associated with reconstructed Cu−O−Cu planes.…”
Section: Resultssupporting
confidence: 89%
“…23,34 -36 Recently, Sasaki et al, by the use of EELS, LEED, and TPD, have reported that the oxygen-as-exposed surface at 100 K is much more reactive for CO oxidation, compared to the Cu͑110͒͑2ϫ1͒-O surface. 40 The postannealing treatment of oxygen-as-exposed surface at 100 K greatly influences the CO oxidation reaction, and once the Cu͑110͒͑2ϫ1͒-O surface is formed, CO oxidation is almost completely suppressed. We consider that such mobile disordered oxygen atoms also play an important role in the CO oxidation on Cu͑110͒.…”
Section: B Reaction Mechanism Of Co Oxidation On Pt(111)mentioning
confidence: 99%
“…CO oxidation was reported to carry out on copper films at 473-623 K with a small activation energy barrier. 1 Up to now, experimental and theoretical studies had been performed for diverse copper surfaces and clusters such as Cu(100), [8][9][10] Cu(110), 8,[10][11][12][13][14][15][16][17][18] Cu(111), 8,10,14,19 Cu(311), 11,12 pyramidal Cu 55 cluster, 21 and copper nanocluster. 22,23 By synthesizing highly dispersed Au-Cu alloy nanoparticles, Mou's group demonstrated that the gold-copper bimetallic catalysts had superior performance to monometallic gold and copper catalysts, exhibiting the synergy between gold and copper.…”
Section: Introductionmentioning
confidence: 99%