Wide visible light-induced dioxygen evolution at an organic photoanode coated with a noble metal oxide catalyst

被引:23
作者
Abe, T [1 ]
Nagai, K
Ogiwara, T
Ogasawara, S
Kaneko, M
Tajiri, A
Norimatsu, T
机构
[1] Hirosaki Univ, Fac Sci & Technol, Dept Mat Sci & Technol, Hirosaki, Aomori 0368561, Japan
[2] Osaka Univ, Inst Laser Engn, Suita, Osaka 5650871, Japan
[3] Ibaraki Univ, Fac Sci, Mito, Ibaraki 3108512, Japan
来源
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 2006年 / 587卷 / 01期
关键词
photoelectrochemistry; molecule-based photoelectrode; water splitting; dioxygen evolution; organic semiconductor;
D O I
10.1016/j.jelechem.2005.11.001
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An organic bilayer composed of 3,4,9,10-peryienetetracarboxyl-bisbenzimidazole (PTCBI, n-type semiconductor) and 29H, 31H-phthalocyanine (H2PC, p-type semiconductor) works as a photoanode capable of O-2 evolution in the water phase especially when the outer surface of H2PC is coated with an IrO2, catalyst. A typical photoelectrode is characterized by the fact that a wide and efficient visible light absorption of < 750 nm by only the PTCBI induces the generation of the photocurrent involving water oxidation at the IrO2/water interface, which is based on the photophysical character of the bilayer. The exciton formed in PTCBI bulk can contribute to carrier generation through its charge separation at the p/n interface, with which the O-2 evolution takes place at the IrO2/water interface coupled with the hole-conducting H2PC layer. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 132
页数:6
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