Semiconducting Diblock Copolymers Synthesized by Means of Controlled Radical Polymerization Techniques

Ulf Stalmach(University of Groningen), Bert de Boer(University of Groningen), Christine Videlot‐Ackermann(University of Groningen), Paul F. van Hutten(University of Groningen), Georges Hadziioannou(University of Groningen)
Journal of the American Chemical Society
May 27, 2000
Cited by 299

Abstract

A donor−acceptor, rod−coil diblock copolymer has been synthesized with the objective of enhancing the photovoltaic efficiency of the PPV−C60 (PPV = poly(p-phenylenevinylene)) system by the incorporation of both components in a molecular architecture that is self-structuring through microphase separation. Diblock copolymers were obtained by using an end-functionalized rigid-rod block of poly(2,5-dioctyloxy-1,4-phenylenevinylene) as a macroinitiator for the nitroxide-mediated controlled radical polymerization of a flexible poly(styrene-stat-chloromethylstyrene) block. The latter block was subsequently functionalized with C60 through atom-transfer radical addition. In a spin-cast film of the final diblock copolymer, the luminescence from PPV is strongly quenched, indicating efficient electron transfer to C60. Under suitable conditions, solution-cast films of these diblock copolymers exhibit micrometer-scale, honeycomb-like patterns of holes.


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