Effects of doping of metal cations on morphology, activity, and visible light response of photocatalysts

被引:188
作者
Kudo, Akihiko
Niishiro, Ryo
Iwase, Akihide
Kato, Hideki
机构
[1] Tokyo Univ Sci, Fac Sci, Dept Appl Chem, Shinjuku Ku, Tokyo 1628601, Japan
[2] Japan Sci & Technol Agcy, CREST, Tokyo, Japan
基金
日本科学技术振兴机构;
关键词
photocatalyst; hydrogen; doping; oxide-; sulfide; nanostructure; visible light response;
D O I
10.1016/j.chemphys.2007.07.024
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
Effects of doping of metal cations into wide band gap semiconductor photocatalysts on morphology, visible light response, and photocatalytic performance were studied. Doping of lanthanide and alkaline earth ions improved activity of a NaTaO3 photocatalyst for water splitting. Lanthanum was the most effective dopant. The NaTaO3:La with a NiO cocatalyst gave 56% of a quantum yield at 270 nm. This remarkable photocatalytic activity was brought by formations of nano-crystal I me particle and surface nano-step structure by the doping. On the other hand, metal cation doping into ZnS, TiO2, and SrTiO3 gave visible light responses for H-2 or O-2 evolution from aqueous solutions containing of sacrificial reagents. The visible light responses were due to the electronic transition from donor levels formed with dopants to conduction bands of the host photocatalysts. Codoping was effective to compensate charge unbalance brought by doping of transition metal cations, resulting in the improvement of visible light response for photocatalytic reactions. Among the transition metal-doped photocatalysts, SrTiO3 doped with Rh (SrTiO3:Rh) was the novel metal oxide photocatalyst that produced H, under visible light irradiation. The SrTiO3:Rh photocatalyst was employed with O-2 evolution photocatalysts such as BiVO4 and WO3 for construction of Z-scheme systems that were active for water splitting into H, and O-2 under visible light irradiation. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:104 / 110
页数:7
相关论文
共 53 条
[1]   Photocatalytic overall water splitting under visible light by TaON and WO3 with an IO3 -/I- shuttle redox mediator [J].
Abe, R ;
Takata, T ;
Sugihara, H ;
Domen, K .
CHEMICAL COMMUNICATIONS, 2005, (30) :3829-3831
[2]  
Anpo M., 1997, CATAL SURV JPN, V1, P169
[3]   Oxide semiconductor materials for solar light energy utilization [J].
Arakawa, H ;
Sayama, K .
RESEARCH ON CHEMICAL INTERMEDIATES, 2000, 26 (02) :145-152
[4]   Visible-light photocatalysis in nitrogen-doped titanium oxides [J].
Asahi, R ;
Morikawa, T ;
Ohwaki, T ;
Aoki, K ;
Taga, Y .
SCIENCE, 2001, 293 (5528) :269-271
[5]  
CAMPET G, 1980, NOUV J CHIM, V4, P501
[6]   Photo- and mechano-catalytic overall water splitting reactions to form hydrogen and oxygen on heterogeneous catalysts [J].
Domen, K ;
Kondo, JN ;
Hara, M ;
Takata, T .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 2000, 73 (06) :1307-1331
[7]   PHOTOCATALYTIC DECOMPOSITION OF WATER INTO H-2 AND O-2 OVER NIO-SRTIO3 POWDER .1. STRUCTURE OF THE CATALYST [J].
DOMEN, K ;
KUDO, A ;
ONISHI, T ;
KOSUGI, N ;
KURODA, H .
JOURNAL OF PHYSICAL CHEMISTRY, 1986, 90 (02) :292-295
[8]  
DOMEN K, 1980, CHEM COMMUN, P543
[9]   SEMICONDUCTING POTASSIUM TANTALATE ELECTRODES - PHOTOASSISTANCE AGENTS FOR EFFICIENT ELECTROLYSIS OF WATER [J].
ELLIS, AB ;
KAISER, SW ;
WRIGHTON, MS .
JOURNAL OF PHYSICAL CHEMISTRY, 1976, 80 (12) :1325-1328
[10]   ELECTROCHEMICAL PHOTOLYSIS OF WATER AT A SEMICONDUCTOR ELECTRODE [J].
FUJISHIMA, A ;
HONDA, K .
NATURE, 1972, 238 (5358) :37-+