Effects of divalent metal ion (Mg2+, Zn2+ and Be2+) doping on photocatalytic activity of ruthenium oxide-loaded gallium nitride for water splitting

被引:62
作者
Arai, Naoki
Saito, Nobuo
Nishiyama, Hiroshi
Domen, Kazunari
Kobayashi, Hisayoshi
Sato, Kazunori
Inoue, Yasunobu [1 ]
机构
[1] Nagaoka Univ Technol, Dept Chem, Nagaoka, Niigata 94021, Japan
[2] Univ Tokyo, Sch Engn, Dept Chem Syst Engn, Tokyo, Japan
[3] Nagaoka Univ Technol, Dept Environm Engn, Nagaoka, Niigata, Japan
[4] Kyoto Inst Technol, Dept Chem & Mat Technol, Kyoto 606, Japan
基金
日本科学技术振兴机构;
关键词
divalent metal ion doping; photocatalytic activity; water splitting; GaN powder;
D O I
10.1016/j.cattod.2006.08.072
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The effects of divalent metal ion doping on the photocatalytic activity of GaN powder for overall water splitting were studied. The doping of Zn2+, Mg2+ and Be2+ to GaN converted it to be a remarkably active and stable photocatalyst in the presence of RuO2 as a co-catalyst. Both H-2 and O-2 were produced from the initial stage of UV light illumination, and the ratio of H-2 to O-2 attained at the stoichiometric ratio of 2.0 at stationary conditions. Main absorption of undoped GaN was at around 390 nm, and a slight shift to longer wavelength occurred with the divalent metal iondoped GaN. Undoped GaN showed photoluminescence peak due to band gap transition, whereas Zn2+ and Mg2+-doped GaN generated a broad photoluminescence peak having a center at around 450 ran and a tail extending to 600 nm. In RuO2-dispersed Mg2+-doped GaN, with increasing content of Mg in starting materials used for preparation, the activity increased, whereas photoluminescence intensity decreased. The role of divalent metal ion dopants is concluded to produce p-type GaN, which is able to increase the concentration and mobility of holes. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:407 / 413
页数:7
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