Adlayer structure of and electrochemical O2 reduction on cobalt porphine-modiried and cobalt octaethylporphyrin-modifled Au(111) in HClO4

被引:87
作者
Yoshimoto, S
Inukai, J
Tada, A
Abe, T
Morimoto, T
Osuka, A
Furuta, H
Itaya, K
机构
[1] Tohoku Univ, Grad Sch Engn, Dept Appl Chem, Sendai, Miyagi 9808579, Japan
[2] Tohoku Univ, New Ind Creat Hatchery Ctr, Sendai, Miyagi 9808579, Japan
[3] CREST JST, Kawaguchi, Saitama 3320012, Japan
[4] Kyoto Univ, Grad Sch Sci, Dept Chem, Kyoto 6068502, Japan
[5] Kyushu Univ, Grad Sch Engn, Dept Chem & Biochem, Fukuoka 8128581, Japan
关键词
D O I
10.1021/jp0366421
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
Adlayers of cobalt(II) porphine (COP) and [2,3,7,8,12,13,17,18-octaethyl-21H,23-H-porphine]cobalt(II) (CoOEP) were formed on Au(111) by immersing the substrate in a benzene solution containing either CoP or CoOEP molecules and investigated in 0.1 M HClO4 by using in situ scanning tunneling microscopy. Highly ordered arrays of COP were observed on the Au(111)-(1x1) surface under controlled potential conditions. The adlayer of CoOEP molecules was also highly ordered, whereas the Au(111) substrate was found to become reconstructed upon adsorption of CoOEP. Both COP and CoOEP molecules were closely packed on Au(111). On the adlayers of COP and CoOEP, the electrochemical reduction Of O-2 was examined in 0.1 M HClO4 saturated with O-2. The adlayers of both COP and CoOEP on Au(111) enhanced the reduction Of O-2.
引用
收藏
页码:1948 / 1954
页数:7
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