Preparation of platinized strontium titanate covered with hollow silica and its activity for overall water splitting in a novel phase-boundary photocatalytic system

被引:40
作者
Ikeda, Shigeru
Hirao, Ko
Ishino, Satoru
Matsumura, Michio
Ohtani, Bunsho
机构
[1] Osaka Univ, Res Ctr Solar Energy Chem, Osaka 5608531, Japan
[2] Japan Sci & Technol Agcy, PRESTO, Convers & Control Adv Chem, Kawaguchi, Japan
[3] Hokkaido Univ, Catalysis Res Ctr, Sapporo, Hokkaido 0010021, Japan
关键词
photocatalytic water splitting; platinum loaded photocatalysts; gas-water interface; silica coating; amphiphilicity; core-shell structure; void space; backward reaction; photostability;
D O I
10.1016/j.cattod.2006.05.037
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Platinum-loaded strontium titanate (Pt-SrTiO3) (core) -silica (shell) powder was prepared by double-layer winding of a carbon and a silica layer on Pt-SrTiO3 followed by heat treatment to remove the carbon layer. Scanning electron microscope (SEM) observation and analyses of the BET surface area suggested that the powder has a void space between Pt-SrTiO3 (core) and silica (shell). When the surface of the powder was partially modified with a fluoroalkylsilylation agent, thus-obtained material assembled at a gas-water interface and acted as a photocatalyst for overall water splitting to produce hydrogen (H-2) and oxygen (O-2). Probably due to the suppression of a backward reaction, production of water from H-2 and O-2, on the platinum, the overall efficiency of this system was higher than that of the conventional suspension system. Moreover, while the Pt-SrTiO3 powders directly covered with fluoroalkylethylsilyl groups showed low photostability, i.e., prolonged irradiation precipitated some of the surface-modified particles in water owing to photocatalytic decomposition of surface fluoroalkylethylsilyl groups, this material could retain its location at the phase boundary. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:343 / 349
页数:7
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