Organic semi-conducting architectures for supramolecular electronics

被引:43
|
作者
Leclère, P
Surin, M
Jonkheijm, P
Henze, O
Schenning, APHJ
Biscarini, F
Grimsdale, AC
Feast, WJ
Meijer, EW
Müllen, K
Brédas, JL
Lazzaroni, R
机构
[1] Univ Mons, Serv Chim Mat Nouveaux, B-7000 Mons, Belgium
[2] Eindhoven Univ Technol, Lab Macromol & Organ Chem, NL-5600 MB Eindhoven, Netherlands
[3] Univ Durham, IRC Polymer Sci & Technol, Durham DH1 3LE, England
[4] CNR, ISMN, I-40129 Bologna, Italy
[5] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
[6] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
关键词
scanning probe microscopy;
D O I
10.1016/j.eurpolymj.2004.01.040
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The properties of organic electronic materials in the solid-state are determined not only by those of individual molecules but also by those of ensembles of molecules. The ability to control the architectures of these ensembles is thus essential for optimizing the properties of conjugated materials for use in electronic devices (light emitting diodes, field effect transistors, solar cells,...) and is primordial for potential technological applications in nanoelectronics. Here, we report on the observation by atomic force microscopy (AFM) of 1D and 2D nanoscale architectures obtained in the solid-state from solutions of molecularly-dissolved conjugated block copolymers or oligomers, and demonstrate that the conjugated molecules can organize onto a surface over lengthscales from nanometers to several microns, forming semiconducting fibrils or bi-dimensional organizations (monolayers) by pi-stacking processes (by changing the sample preparation conditions). (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:885 / 892
页数:8
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