Charge-Driven Selective Adsorption of Sodium Dodecyl Sulfate on Graphene Oxide Visualized by Atomic Force Microscopy

被引:24
|
作者
Glover, A. Jaeton [1 ]
Adamson, Douglas H. [2 ]
Schniepp, Hannes C. [1 ]
机构
[1] Coll William & Mary, Dept Appl Sci, Williamsburg, VA 23185 USA
[2] Univ Connecticut, Inst Mat Sci Polymer Program, Storrs, CT 06269 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2012年 / 116卷 / 37期
基金
美国国家科学基金会;
关键词
CARBON NANOTUBES; FUNCTIONALIZED GRAPHENE; ELECTRONIC-STRUCTURE; ORIENTATIONAL ORDER; AGGREGATION NUMBER; ANIONIC SURFACTANT; GRAPHITE OXIDE; MICELLES; ORGANIZATION; REDUCTION;
D O I
10.1021/jp305717v
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Using liquid-cell atomic force microscopy, we investigated molecular adsorption of sodium dodecyl sulfate (SDS) from aqueous solution onto single-layer graphenes that were oxidized to different degrees. SDS did not adsorb onto graphene oxide (GO) featuring an atomic carbon:oxygen (C:O) ratio of 2.0. Reduced GO (C:O ratio: 10.7), in contrast, was covered with micellar SDS aggregates, featuring a height of approximate to 2 nm and lateral feature sizes of approximate to 5 nm. This selective adsorption depending on the degree of oxidation can be explained by electrostatic repulsion between the negatively charged SDS head groups and the negatively charged hydroxyl groups on oxidized graphene. Our results suggest it will be possible to translate this adsorption selectivity into separation techniques that fractionate GO into subsets featuring different degrees of oxidation. Such fractionation techniques are likely to enable the preparation of GO with more well-defined electronic properties and make GO interesting as a band gap material.
引用
收藏
页码:20080 / 20085
页数:6
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