Atomic layer deposition of a high-density aminopropylsiloxane network on silica through sequential reactions of γ-aminopropyltrialkoxysilanes and water

被引:52
作者
Ek, S
Iiskola, EI
Niinistö, L
Vaittinen, J
Pakkanen, TT
Keränen, J
Auroux, A
机构
[1] Aalto Univ, Inorgan & Analyt Chem Lab, FIN-02015 Espoo, Finland
[2] Univ Joensuu, Dept Chem, FIN-80101 Joensuu, Finland
[3] Inst Rech Catalyse, CNRS, UPR 5401, F-69626 Villeurbanne, France
关键词
D O I
10.1021/la035472g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel gas-phase procedure for the control of amino group density on porous silica through consecutive reactions of aminopropylalkoxysilanes and water vapor was developed. First heat-treated silica was saturated with trifunctional gamma-aminopropyltrimethoxysilane (APTMS) or gamma-aminopropyltriethoxysilane (APTS) in an atomic layer deposition reactor. During this step, precursor molecules were bound onto the surface both mono- and bidentately forming siloxane bridges with the silanol groups of silica. Then surface densities of 1.8 APTMS or 2.0 APTS molecules/nm(2) were achieved. Next the aminosilylated surface was treated with water vapor in order to hydroxylate the free alkoxy groups of chemisorbed arninosilane molecules. At the same time, the silanol groups on the silica surface, which had remained unreacted during the first step, were revealed below the hydrolyzed alkoxy groups. These silanol groups of silica and hydrolyzed alkoxy groups were able to react further with the next feed of aminosilane molecules. The above-mentioned aminosilane/water vapor cycles, that is, two consecutive steps, could be repeated several times, and the amino group content on silica could be controlled through the number of aminosilane/water cycles. After four cycles, the surface was observed to be saturated and maximum amino group density was achieved. Then, by performing four or five cycles, surface densities of up to 3.0 APTS or APTMS molecules/nm(2) were obtained. With this procedure, a high-density arninopropylsiloxane network is grown through horizontal polymerization of aminosilane molecules on the surface. With bifunctional gamma-aminopropyldiethoxymethylsilane (APDMS), the repetition of aminosilane/water cycles did not increase the amino group content because of a lack of free and reactive ethoxy groups on the aminosilylated silica surface due to the bidentate bonding of APDMS molecules on silica.
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收藏
页码:10601 / 10609
页数:9
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