Catalysis in Electrochemistry 2011
DOI: 10.1002/9780470929421.ch4
|View full text |Cite
|
Sign up to set email alerts
|

Electrocatalytic Properties of Stepped Surfaces

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
13
0

Year Published

2013
2013
2020
2020

Publication Types

Select...
6
1
1

Relationship

2
6

Authors

Journals

citations
Cited by 16 publications
(13 citation statements)
references
References 99 publications
0
13
0
Order By: Relevance
“…In recent studies this interpretation is questioned due to the anomalous shift with pH of these peaks [48]. For (100) steps, presence of specifically adsorbing anions changes the shape of the voltammetric peak, signaling the possible competitive adsorption of anions on the steps [49]. In this regards, some contribution of anion specific adsorption has been suggested in perchloric acid solutions with the same pH (the peak at 0.27 V shifts to M A N U S C R I P T…”
Section: Adsorption Of the Reaction Product On Stepsmentioning
confidence: 99%
“…In recent studies this interpretation is questioned due to the anomalous shift with pH of these peaks [48]. For (100) steps, presence of specifically adsorbing anions changes the shape of the voltammetric peak, signaling the possible competitive adsorption of anions on the steps [49]. In this regards, some contribution of anion specific adsorption has been suggested in perchloric acid solutions with the same pH (the peak at 0.27 V shifts to M A N U S C R I P T…”
Section: Adsorption Of the Reaction Product On Stepsmentioning
confidence: 99%
“…Figure 3B shows a plot of the maximum reduction current (absolute value) measured at the lowest limit of the potential scan as a function of the step density. For this series of stepped surfaces, the step density is given by [49]:…”
Section: Resultsmentioning
confidence: 99%
“…Since the data were normalized with respect to surface Pt area, this implies that the specific electrocatalytic properties change during the dissolution. Changes like those in the figure may be due to the structure of the catalyst particles (development of steps, edges, and facets [30,31,32]), size effects [33,34,35], or the average distance between the catalyst particles [36] developing differently during the dissolution-redeposition process. (We attempted to take particle size effects explicitly into account in Fig.…”
Section: Resultsmentioning
confidence: 99%