Hierarchical self-assembly of all-organic photovoltaic devices

被引:62
作者
Huang, CH
McClenaghan, ND
Kuhn, A
Bravic, G
Bassani, DM [1 ]
机构
[1] Univ Bordeaux 1, CNRS, UMR 5802, LCOO,Ctr Rech Chim Mol, F-33405 Talence, France
[2] Univ Bordeaux 1, ENSCPB, LACReM, F-33607 Pessac, France
[3] Univ Bordeaux 1, CNRS, Inst Chim Mat Condensee Bordeaux, F-33608 Pessac, France
关键词
oligomer; fullerene; electron donor; hydrogen-bonding; photovoltaic; self-assembly;
D O I
10.1016/j.tet.2005.09.150
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Photovoltaic devices built by a hierarchical self-assembly process using hydrogen-bonding terminated self-assembled monolayers (SAMs) on gold and the combination of a hydrogen-bonding barbituric acid appended fullerene and a complementary melamine terminated pi-conjugated thiophene-based oligomer are presented. The incorporation of these electron donor (oligomer) and electron acceptor (methanofullerene) assemblies into simple photovoltaic (PV) devices as thin films leads to a 2.5 fold-enhancement in photocurrent compared to analogous systems comprising non-hydrogen-bonding C-60-oligomer systems, which is ascribed to higher molecular-level ordering. The modification of the gold electrode surface with self-assembled monolayers hearing hydrogen-bonding molecular recognition endgroups was seen to further enhance the PV response of the corresponding functional supramolecular device. This superposition of two types of self-assembly facilitates the generation of binary supramolecular fullerene-containing architectures. Importantly, all functional materials are accessible in a direct fashion. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2050 / 2059
页数:10
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