Resource type
Date created
2018-04-01
Authors/Contributors
Abstract
The thickness of alcohol based monolayers on silicon oxide surfaces were investigated using angle-resolved X-ray photoelectron spectroscopy (ARXPS). Advantages of using alcohols as building blocks for the formation of monolayers include their widespread availability, ease of handling, and stability against side reactions. Recent progress in microwave assisted reactions demonstrated the ease of forming uniform monolayers with alcohol based reagents. The studies shown herein provide a detailed investigation of the thickness of monolayers prepared from a series of aliphatic alcohols of different chain lengths. Monolayers of 1-butanol, 1-hexanol, 1-octanol, 1-decanol, and 1-dodecanol were each successfully formed through microwave assisted reactions and characterized by ARXPS techniques. The thickness of these monolayers consistently increased by ∼1.0 Å for every additional methylene (CH2) within the hydrocarbon chain of the reagents. Tilt angles of the molecules covalently attached to silicon oxide surfaces were estimated to be ∼35° for each type of reagent. These results were consistent with the observations reported for thiol based or silane based monolayers on either gold or silicon oxide surfaces, respectively. The results of this study also suggest that the alcohol based monolayers are uniform at a molecular level.
Document
Identifier
DOI: 10.1016/j.apsusc.2017.12.022
Published as
"Determining the Thickness of Aliphatic Alcohol Monolayers Covalently Attached to Silicon Oxide Surfaces Using Angle-Resolved X-ray Photoelectron Spectroscopy," Lee, A.W.H.; Kim, D.; Gates, B.D., Applied Surface Science, 2017, 436 (1), 907-911. https://doi.org/10.1016/j.apsusc.2017.12.022
Publication details
Publication title
Applied Surface Science
Document title
Determining the Thickness of Aliphatic Alcohol Monolayers Covalently Attached to Silicon Oxide Surfaces Using Angle-Resolved X-ray Photoelectron Spectroscopy
Date
2017
Volume
436
Issue
1
First page
907
Last page
911
Publisher DOI
10.1016/j.apsusc.2017.12.022
Copyright statement
Copyright is held by the author(s).
Scholarly level
Peer reviewed?
Yes
Funder
Language
English
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