The use of pulse radiolysis to study transient species in conjugated polyme
rs in solutions is discussed, with particular reference to poly(2-methoxy-5
-(2'-ethylhexoxy)-p-phenylenevinylene (MEH-PPV). The excited tripler state
is specifically generated by energy transfer on radiolysis of benzene solut
ions in the presence of suitable sensitisers, and its spectrum is reported.
The presence of vibronic structure suggests a localised tripler state. By
varying the energy of the sensitiser, it is possible to determine the energ
y of the lowest triplet state. Results are also presented for the triplet-t
riplet absorptions and energies of five other common pi -conjugated polymer
s. The MEH-PPV tripler absorption, produced on radiolysis, does not increas
e linearly with either polymer concentration or radiation dose. This is sug
gested to be due to the presence of multiple tripler excitations on the iso
lated polymer chains. Intrachain triplet-triplet annihilation is observed,
and is seen to lead to delayed fluorescence. Spectra are also reported for
the positive and negative charge carriers of MEH-PPV and the other polymers
specifically produced by pulse radiolysis of the polymers in chloroform or
tetrahydrofuran solutions. (C) 2001 Elsevier Science B.V. All rights reser
ved.