Enhanced Photoanodic Output at an Organic p/n Bilayer in the Water Phase by Means of the Formation of Whiskered Phthalocyanine

被引:14
作者
Abe, Toshiyuki [1 ]
Tanno, Yoshinori [1 ]
Ebina, Toshihiro [1 ]
Miyakushi, Shouichi [1 ]
Nagai, Keiji [2 ]
机构
[1] Hirosaki Univ, Grad Sch Sci & Technol, Dept Frontier Mat Chem, Hirosaki, Aomori 0368561, Japan
[2] Tokyo Inst Technol, Chem Resources Lab, Midori Ku, Yokohama, Kanagawa 2268503, Japan
关键词
organic p/n bilayer; perylene derivative; phthalocyanine; whisker; visible-light-responsive photoelectrode; photoelectrochemishy; Langmuir adsorption equilibrium; MOLECULAR-HYDROGEN EVOLUTION; INDUCED DIOXYGEN EVOLUTION; PHOTOVOLTAIC CELLS; SOLAR-CELLS; PHOTOELECTRODE; WORKING; SYSTEM; FILM; NANOPARTICLES; TRANSISTORS;
D O I
10.1021/am302209b
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The photoelectrode characteristics of an organic p/n bilayer in the water phase were studied with respect to film; 3,4,9,10-perylenetetracarboxylic-bisbenzimidazole (PTCBI, an n-type semiconductor) was used in combination with 29H,31H-phthalocyanine (H2Pc, a p-type semiconductor). When H2Pc was vapor-deposited on top of the PTCBI layer on a heated substrate (cf. degree of pressure, ca. 5.0 x 10(-4) Pa; temperature at the substrate, 120 degrees C), a transmission electron microscopic image showed an enhanced contact area of the p/n interface in comparison with that prepared at r.t., due to the formation of a whisker H2Pc. The PTCBI/H2Pc bilayer can work as a photoanode along with photophysical events in its interior. The rate-limiting charge transfer at the H2Pc/water interface was kinetically analyzed assuming the Langmuir adsorption equilibrium at that interface. Kinetic analysis demonstrated that the increased contact area can successfully lead to efficient photoinduced carrier generation; particularly, when a thick whisker of H2Pc was formed, the magnitude of the oxidation kinetics at the H2Pc/water interface was approximately 2.5 times higher than that without thermal treatment.
引用
收藏
页码:1248 / 1253
页数:6
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