Control of Interchain Contacts, Solid-State Fluorescence Quantum Yield, and Charge Transport of Cationic Conjugated Polyelectrolytes by Choice of Anion

Autor: Dmitry Korystov, Thuc-Quyen Nguyen, Guillermo C. Bazan, Alexander Mikhailovsky, Renqiang Yang, Andres Garcia
Rok vydání: 2006
Předmět:
Zdroj: Journal of the American Chemical Society. 128:16532-16539
ISSN: 1520-5126
0002-7863
DOI: 10.1021/ja0611341
Popis: Simple procedures are provided for exchanging charge-compensating ions in conjugated polyelectrolytes by progressive dilution of the original species and for determining the degree of ion exchange by using X-ray photoelectron spectroscopy. By using these methods, the bromide ions in poly[(9,9-bis(6'-N,N,N-trimethylammoniumbromide)hexyl)fluorene-co-alt-4,7-(2,1,3-benzothiadiazole)]were exchanged with BF4-, CF3SO3-, PF6-, BPh4-, and B(3,5-(CF3)2C6H3)4- (BArF4-). Absorption, photoluminescence (PL), and PL quantum yields (Phi) were measured in different solvents and in solid films cast from methanol. Examination of the resulting trends, together with the spectral bandshapes in different solvents, suggests that increasing the counteranion (CA) size decreases interchain contacts and aggregation and leads to a substantial increase of Phi in the bulk. Size analysis of polymers containing Br- and BArF4- in water by dynamic light scattering techniques indicates suppression of aggregation by BArF4-. Nanoscale current-voltage measurements of films using conducting atomic force microscopy show that hole mobilities and, more significantly, charge injection barriers are CA dependent. These results show that it is possible to significantly modify the optoelectronic properties of conjugated polyelectrolytes by choosing different counterions. A parent conjugated backbone can thus be fine-tuned for specific applications.
Databáze: OpenAIRE