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Formation of a Ground‐State Charge‐Transfer Complex in Polyfluorene//[6,6]‐Phenyl‐C61 Butyric Acid Methyl Ester (PCBM) Blend Films and Its Role in the Function of Polymer/PCBM Solar Cells
Author(s) -
BensonSmith J. J.,
Goris L.,
Vandewal K.,
Haenen K.,
Manca J. V.,
Vanderzande D.,
Bradley D. D. C.,
Nelson J.
Publication year - 2007
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.200600484
Subject(s) - polyfluorene , materials science , polymer , polymer solar cell , photocurrent , photoluminescence , organic solar cell , ground state , chemical engineering , photochemistry , polymer blend , polymer chemistry , optoelectronics , composite material , conjugated system , copolymer , chemistry , physics , quantum mechanics , engineering
Evidence is presented for the formation of a weak ground‐state charge‐transfer complex in the blend films of poly[9,9‐dioctylfluorene‐ co ‐ N ‐(4‐methoxyphenyl)diphenylamine] polymer (TFMO) and [6,6]‐phenyl‐C 61 butyric acid methyl ester (PCBM), using photothermal deflection spectroscopy (PDS) and photoluminescence (PL) spectroscopy. Comparison of this polymer blend with other polyfluorene polymer/PCBM blends shows that the appearance of this ground‐state charge‐transfer complex is correlated to the ionization potential of the polymer, but not to the optical gap of the polymer or the surface morphology of the blend film. Moreover, the polymer/PCBM blend films in which this charge‐transfer complex is observed also exhibit efficient photocurrent generation in photovoltaic devices, suggesting that the charge‐transfer complex may be involved in charge separation. Possible mechanisms for this charge‐transfer state formation are discussed as well as the significance of this finding to the understanding and optimization of polymer blend solar cells.