2009
DOI: 10.1016/j.electacta.2009.05.061
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In situ ATR-FTIR study of bulk CO oxidation on a polycrystalline Pt electrode

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Cited by 25 publications
(96 citation statements)
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“…Also noted is that the abnormal "rise and drop" of the CO B band at the initial stage of the main CO oxidation in Fig. 2 was attributed to the diffusion of CO L from terrace sites to step edge sites to form CO B thereon in the absence of Cl − [28]. The absence of such a conversion of CO L to CO B in the presence of Cl − can be related to the specific adsorption of Cl − which blocks the CO L diffusion to these sites.…”
Section: Resultsmentioning
confidence: 94%
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“…Also noted is that the abnormal "rise and drop" of the CO B band at the initial stage of the main CO oxidation in Fig. 2 was attributed to the diffusion of CO L from terrace sites to step edge sites to form CO B thereon in the absence of Cl − [28]. The absence of such a conversion of CO L to CO B in the presence of Cl − can be related to the specific adsorption of Cl − which blocks the CO L diffusion to these sites.…”
Section: Resultsmentioning
confidence: 94%
“…On the other hand, Samjeské et al [27] depicted a model in which CO oxidation initiated at steps and proceeded with the diffusion of terrace CO to steps based on the assumption made by Lebedeva et al [6] that CO diffused fast on Pt. Coincidently, Hanawa et al observed a transient rise of the CO B band intensity before its main oxidation, which was ascribed to the diffusion of CO L from terraces to step edges with the subsequent formation of CO B there [28]. Recently, CO diffusion on stepped Pt(1 1 1) was studied by STM and the results showed that steps provided fast diffusion channels for CO [29].…”
Section: Resultsmentioning
confidence: 96%
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“…However, this is not a favored process on Pt and only happens at potentials more positive than 0.4 V vs RHE in acid [42,43] and alkaline [44,45]. In order for the reactions to proceed, the anode potential has to be higher than this which decreases the total cell voltage.…”
Section: Pt-based Catalysismentioning
confidence: 99%
“…[1][2][3][4] For PEFC anode and cathode catalysts, the activity and its degradation have been analyzed by multilateral techniques such as X-ray photoelectron spectroscopy combined with an electrochemical cell (EC-XPS), 2,[5][6][7][8] in situ Fourier-transform infrared spectroscopy (FTIR), [9][10][11][12][13][14][15][16][17][18][19][20][21][22] electrochemical quartz crystal microbalance (EQCM), [23][24][25][26] in situ scanning tunneling microscopy (STM), [27][28][29][30][31] in addition to conventional electrochemical measurements such as rotating disk electrode (RDE), [32][33][34] channel flow electrode (CFE), 21,35,36 and channel flow double electrode (CFDE) methods. [37][38][39][40][41][42] Based on these results, new practical catalysts have been synthesized.…”
Section: Introductionmentioning
confidence: 99%