1997
DOI: 10.1016/s0927-7757(96)03927-1
|View full text |Cite
|
Sign up to set email alerts
|

Determination of the acid-base properties for 3-amino, 3-chloro and 3-mercaptopropyltrimethoxysilane coatings on silica surfaces by XPS

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

4
58
0

Year Published

2002
2002
2015
2015

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 72 publications
(62 citation statements)
references
References 7 publications
4
58
0
Order By: Relevance
“…This additional state correlates to various possible interactions of the amine group with adsorbed water, the surface, and inter-and intramolecular silanol groups [9,19,26]. Consequently, the higher binding energy state can be attributed to multilayer formation, as amine groups then interact with the silanol groups of the next layer [19].…”
Section: Surface Analysismentioning
confidence: 98%
“…This additional state correlates to various possible interactions of the amine group with adsorbed water, the surface, and inter-and intramolecular silanol groups [9,19,26]. Consequently, the higher binding energy state can be attributed to multilayer formation, as amine groups then interact with the silanol groups of the next layer [19].…”
Section: Surface Analysismentioning
confidence: 98%
“…One way to circumvent this issue is to derivatize the substrate with a layer of molecules designed to enhance metal nucleation by interacting strongly with both the substrate and the incoming metal atoms (i.e., a molecular adhesive), thereby suppressing surface diffusion and promoting the growth of continuous metal fi lms at low thickness. [34][35][36][37] Thiol functionalized silanes have previously been investigated for this purpose, since thiols have a strong affi nity for Au and Ag, whilst organosilanes couple with native hydroxyl groups on a variety of substrate materials [34][35][36] to form strong siloxane bonds. Hatton et al [ 37 ] have previously reported the viability of this approach for Au fi lms on glass using a thiol functionalized molecular adhesive layer and have demonstrated application in organic light-emitting diodes.…”
Section: Introductionmentioning
confidence: 99%
“…3(b)), which was fitted for two components at 399.7 and 401.9 eV and assigned to non-protonated and protonated imidazole groups, respectively. The protonation could be due to the interaction with the surface silanol groups, 3,9 as they have pK a values in the range of 3.67 to 4.82, and 6.37 to 7.01 10 and alkylimidazole has a pK a value around 7.5.…”
Section: Resultsmentioning
confidence: 99%