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Ultrafast photoinduced charge separation resulting from self-assembly of a green perylene-based dye into pi-stacked arrays.

作者信息

Fuller Michael J, Sinks Louise E, Rybtchinski Boris, Giaimo Jovan M, Li Xiyou, Wasielewski Michael R

机构信息

Department of Chemistry and Center for Nanofabrication and Molecular Self-Assembly, Northwestern University, Evanston, Illinois 60208-3113, USA.

出版信息

J Phys Chem A. 2005 Feb 17;109(6):970-5. doi: 10.1021/jp044796q.

Abstract

Condensation of 3,4,5-tris(n-dodecyloxy)aniline with the green chromophore 1,7-bis(N-pyrrolidinyl)perylene-3,4;9,10-tetracarboxylic dianhydride yields N,N'-bis(3,4,5-tris(n-dodecyloxy)phenyl)-1,7-bis(N-pyrrolidinyl)perylene-3,4;9,10-bis(dicarboximide), 5PDI-TAP, which absorbs light strongly from 550 to 750 nm. 5PDI-TAP dissolves readily in methylcyclohexane (MCH), resulting in self-assembly into H-aggregates. Small-angle X-ray scattering data obtained on 10(-4) M solutions of 5PDI-TAP in MCH show that the aggregates are pi-stacked monodisperse pentamers. Femtosecond transient absorption spectroscopy on solutions of (5PDI-TAP)5 in MCH shows evidence of charge separation occurring with tau < or = 150 fs between adjacent stacked members of 5PDI-TAP within the pentamer followed by charge recombination with tau = 860 ps. Transmission electron microscopy of 5PDI-TAP films cast from solution show isolated bundles of columnar aggregates. (5PDI-TAP)n is a potentially useful material for organic photovoltaics because efficient photoinduced charge generation is an intrinsic property of the assembly.

摘要

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