2008
DOI: 10.1016/j.jpowsour.2008.04.083
|View full text |Cite
|
Sign up to set email alerts
|

Electro-deposition on carbon black and carbon nanotubes of Pt nanostructured catalysts for methanol oxidation

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

1
57
0

Year Published

2014
2014
2021
2021

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 102 publications
(58 citation statements)
references
References 47 publications
1
57
0
Order By: Relevance
“…3 [2], where t on is the pulse length and t off is the time between two pulses and t tot is the total deposition time. The scheme for pulse electrodeposition is shown in Fig.…”
Section: Resultsmentioning
confidence: 99%
See 3 more Smart Citations
“…3 [2], where t on is the pulse length and t off is the time between two pulses and t tot is the total deposition time. The scheme for pulse electrodeposition is shown in Fig.…”
Section: Resultsmentioning
confidence: 99%
“…For the application of such coatings, the supports used were usually metallic and nonmetallic materials which are characterized by very high degree of adhesion for the coating of the metallic deposits [1]. Recently, significant interest has been raised in utilizing electrodeposition for the formation of an array of metal nanoparticles on the surface of different carbon supports [2,3]. The reason for this particular interest is to obtain M/C materials with maximum electrochemically active surface area, which requires formation of the electrodeposits not only on the surface but also in the pores of the carbon support.…”
Section: Introductionmentioning
confidence: 99%
See 2 more Smart Citations
“…Secondly, ED mostly happens on the outer surface of the carbon support, due to its hydrophobicity, thereby improving contact with the proton exchange membrane when the PEMFC is assembled [13]. This also allows lowering Pt content in the fuel cell electrode (<0.1 mg cm −2 ) [14], due to its high utilization and avoiding Pt losses in the depth of the catalyst layer as normally happens with conventional electrode preparation methods, such as pasting and spraying [14]. At the same time, the hydrophobicity of the carbon support also often leads to poor contact with the electro-plating solution, and the resulting loading of Pt NPs on the support is often low with poor spatial distribution [15].…”
Section: Introductionmentioning
confidence: 99%