High-frequency (95 GHz) electron paramagnetic resonance study of the photoinduced charge transfer in conjugated polymer-fullerene composites - art. no. 195206

Citation
J. De Ceuster et al., High-frequency (95 GHz) electron paramagnetic resonance study of the photoinduced charge transfer in conjugated polymer-fullerene composites - art. no. 195206, PHYS REV B, 6419(19), 2001, pp. 5206
Citations number
31
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science
Journal title
PHYSICAL REVIEW B
ISSN journal
01631829 → ACNP
Volume
6419
Issue
19
Year of publication
2001
Database
ISI
SICI code
0163-1829(20011115)6419:19<5206:H(GEPR>2.0.ZU;2-R
Abstract
Light-induced electron paramagnetic resonance (LEPR) measurements are repor ted in composites of poly(2-methoxy-5-(3-,7-dimethyloctyloxy)-1,4-phenylene vinylene) (MDMO-PPV) and [6,6]-phenyl-C-61-butyric acid methyl ester (PCBM) , a soluble derivative of C-60. Under illumination of the sample, two param agnetic species are formed due to photoinduced charge transfer between conj ugated polymer and fullerene. One is the positive polaron P+ on the polymer backbone and the other is the radical anion on the methanofullerene. Using high-frequency (95 GHz) LEPR it was possible to separate these two contrib utions to the spectrum on the basis of their g factors, and moreover to res olve the g anisotropy for both radicals. The positive polaron on the conjug ated polymer chain possesses axial symmetry with g values g(parallel to) = 2.0034(1) and g(perpendicular to) = 2.0024(1). EPR on low doped polymer gav e extra proof for the assignment to the positive polaron. The negatively ch arged methanofullerene has a lower, rhombic symmetry with g(x) = 2.0003(1), g(y) = 2.0001(1), and g(z) =1.9982(1). Different spin-lattice relaxation o f both species gives rise to a rapid passage effect for the positive polaro n spectrum.