Modification of carbon nanotube surfaces with precious metal and transition metal oxide nanoparticles using thin silica layers

被引:13
|
作者
Takenaka, Sakae [1 ,2 ,3 ]
Mikami, Daisuke [1 ]
Tanabe, Eishi [4 ]
Matsune, Hideki [1 ]
Kishida, Masahiro [1 ]
机构
[1] Kyushu Univ, Grad Sch Engn, Dept Chem Engn, Nishi Ku, Fukuoka 8190395, Japan
[2] Japan Sci & Technol Agcy JST, PRESTO, Kawaguchi, Saitama 3320012, Japan
[3] Kyushu Univ, I2CNER, Nishi Ku, Fukuoka 8190395, Japan
[4] Hiroshima Prefectural Technol Res Inst, Higashihiroshima, Hiroshima 7390046, Japan
关键词
Carbon nanotube; Silica layer; Precious metal nanoparticle; Transition metal oxide nanoparticle; OXYGEN REDUCTION REACTION; SELECTIVE HYDROGENATION; PHOSPHORIC-ACID; FUEL-CELLS; METHANOL OXIDATION; CATALYST SUPPORT; PLATINUM; DURABILITY; ELECTROCATALYSTS; PD;
D O I
10.1016/j.apcata.2014.12.025
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
The surfaces of carbon nanotubes (CNTs) were covered with thin silica layers through the application of 3-aminopropyltriethoxysilane (APTES) in order to enhance the deposition of precious metal and transition metal oxide nanoparticles. Pt metal particles smaller than 2nm in diameter could be deposited, using a conventional impregnation method, on CNTs coated with silica layers, whereas Pt particles supported on bare CNT surfaces were approximately 3 nm in diameter. Thus, coating CNTs with thin silica layers enhanced the catalytic activity of the Pt catalysts. In addition, CNTs with thin silica layers could be uniformly covered with transition metal oxide layers (ZrO2, Nb2O5 and Ta2O5) by hydrolysis of the corresponding metal alkoxides. In contrast, metal oxides were very difficult to deposit on bare CNTs. The thin silica layers produced on the CNTs via the use of APTES evidently function as adsorption sites for precursor metals and metal oxides, as well as nucleation sites for metals and metal oxides, allowing the formation of precious metal-CNT and transition metal oxide-CNT composites. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:60 / 67
页数:8
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