Electronic Interactions of n-Doped Perylene Diimide Groups Appended to Polynorbornene Chains: Implications for Electron Transport in Organic Electronics

被引:6
作者
Nguyen, Minh T. [1 ]
Biberdorf, Joshua D. [1 ]
Holliday, Bradley J.
Jones, Richard A. [1 ]
机构
[1] Univ Texas Austin, Dept Chem, 105 E 24th St Stop A5300, Austin, TX 78712 USA
基金
美国国家科学基金会;
关键词
brush polymers; organic semiconductors; perylene diimide; radical anions; redox conductivity; NON-FULLERENE ACCEPTOR; POLYMER SOLAR-CELLS; CHARGE-TRANSPORT; PHOTOVOLTAIC PERFORMANCE; PHYSICAL-PROPERTIES; SMALL-MOLECULE; PI-PI; CONDUCTIVITY; EFFICIENCY; MORPHOLOGY;
D O I
10.1002/marc.201700420
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A polymer consisting of a polynorbornene backbone with perylene diimide (PDI) pendant groups on each monomeric unit is synthesized via ring opening metathesis polymerization. The PDI pendant groups along the polymer backbone, studied by UV-vis absorption, fluorescence emission, and electron paramagnetic resonance spectroscopy in addition to electrochemical methods, show evidence of molecular aggregation and corresponding electronic coupling with neighboring groups, which forms pathways for efficient electron transport from one group to another in a specific reduced form. When n-doped, the title polymer shows redox conductivity of 5.4 x 10(-3) S cm(-1), comparable with crystalline PDI materials, and is therefore a promising material for use in organic electronics.
引用
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页数:7
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