Control of shell thickness in silica-coating of Agl nanoparticles

被引:8
作者
Kobayashi, Y. [1 ,2 ]
Misawa, K. [1 ]
Takeda, M. [3 ]
Ohuchi, N. [3 ]
Kasuya, A. [4 ]
Konno, M. [1 ]
机构
[1] Tohoku Univ, Dept Chem Engn, Grad Sch Engn, Aoba Ku, Sendai, Miyagi 9808579, Japan
[2] Ibaraki Univ, Fac Engn, Dept Biomol Funct Engn, Ibaraki 3168511, Japan
[3] Tohoku Univ, Grad Sch Med, Div Surg Oncol, Aoba Ku, Sendai, Miyagi 9808574, Japan
[4] Tohoku Univ, Ctr Interdisciplinary Res, Aoba Ku, Sendai, Miyagi 9808574, Japan
来源
ADVANCED MATERIALS AND PROCESSING IV | 2007年 / 29-30卷
关键词
Agl; nanoparticle; core-shell; silica-coating; sol-gel; Stober method;
D O I
10.4028/www.scientific.net/AMR.29-30.191
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Silica-coating of Agl nanoparticles with a Stober method was carried out to find out reaction conditions for control of the shell thickness. The Agl nanoparticles were prepared from AgClO4 and KI with the use of 3-mercaptopropyltrimethoxysilane (MPS) as a silane coupling agent and dimethylamine (DMA) catalyst for alkoxide hydrolysis. The silica-coating was performed at 4.5 x 10(-6)-4.5x10(-5) M MPS, 11-20 M water, 0.002-0.1 M DMA and 0.005-0.04 M tetraethylorthosilicate at Agl concentrations of 0.1-1 mM. Consequently, Agl-silica core-shell particles could be prepared with the use of 4.5 x 10(-5) M MPS, 20 M water, 0.01 M DMA and 1 mM Agl. Silica shell thickness could be varied from 15 to 28 nm with an increase in the TEOS concentration from 0.005 to 0.04 M.
引用
收藏
页码:191 / +
页数:2
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