1988
DOI: 10.1016/0039-6028(88)90382-2
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Ag electrode reaction in NaOH solution studied by in-situ Raman spectroscopy

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Cited by 85 publications
(54 citation statements)
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“…This is caused either by higher oxygen loading, resulting in less charge donation from silver to  * molecular orbital of adsorbed The bands at 870-875 cm -1 could be associated to the bending vibration of Ag-OH hydroxyl groups [42,78] generated in the presence of ppm amounts of H 2 O in the gas flow, while the low frequency bands at 470-475 cm -1 fail in the region of the Ag-O stretching vibration that can be attributed to atomic oxygen species. [39,46] On the other hand, the bands at 338, 603-604 and 790-802 cm -1 observed on Ag(100) at 200ºC and on Ag(111) at 250ºC are associated to subsurface oxo-species and to surface oxygen species (labeled O) stabilized by the presence of subsurface oxygen, [39,[45][46]48] and indicate that oxygen diffusion into the bulk takes place on Ag(100) at a much lower temperature than on Ag(111) facet.…”
Section: Oxygen Activation On Ag(100) and Ag(111) Catalystsmentioning
confidence: 99%
“…This is caused either by higher oxygen loading, resulting in less charge donation from silver to  * molecular orbital of adsorbed The bands at 870-875 cm -1 could be associated to the bending vibration of Ag-OH hydroxyl groups [42,78] generated in the presence of ppm amounts of H 2 O in the gas flow, while the low frequency bands at 470-475 cm -1 fail in the region of the Ag-O stretching vibration that can be attributed to atomic oxygen species. [39,46] On the other hand, the bands at 338, 603-604 and 790-802 cm -1 observed on Ag(100) at 200ºC and on Ag(111) at 250ºC are associated to subsurface oxo-species and to surface oxygen species (labeled O) stabilized by the presence of subsurface oxygen, [39,[45][46]48] and indicate that oxygen diffusion into the bulk takes place on Ag(100) at a much lower temperature than on Ag(111) facet.…”
Section: Oxygen Activation On Ag(100) and Ag(111) Catalystsmentioning
confidence: 99%
“…Thus, it was concluded that the Raman intensity for libration might increase with increasing alkali metal and OH ¹ concentrations. [27][28][29] In this cyclic voltammogram, the current responses were found to increase gradually over successive ORCs, which is attributable to the increased roughness of the Ag electrode surface caused by repeated potential cycling. Figure 4 represents the variation of the in situ Raman spectra of the Ag electrode in an aqueous solution with 0.5 mol dm ¹3 NaOH.…”
Section: ¹1mentioning
confidence: 98%
“…According to a previous report, the Raman intensity for bending Electrochemistry, 82(5), 396-400 (2014) vibration of HOH adsorbed on an electrode surface is dependent on electrode potential. 21 It is interesting to see that the intensity of the Raman lines starts to increase at about ¹0.8 V, which correspond to the potential zero charge, 21,28 and becomes higher at more negative values of the electrode potential. This dependence of the intensity of the libration Raman band on the potential is almost the same in both directions of the potential sweep.…”
Section: ¹1mentioning
confidence: 99%
“…Strujni pik A 1 odgovara adsorpciji OH -jona [12][13][14][15]. Strujni pikovi A 4 i A 5 odgovaraju formiranju oksida srebra, najpre Ag 2 O tipa I, zatim Ag 2 O tipa II [16].…”
Section: Btaunclassified