EPR study of polarons in a conducting polymer with nondegenerate ground states: Alkali metal complexes of poly (p-phenylene) and phenylene oligomers

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Abstract
EPR measurements are used to characterize electronic states relevant for carrier transport in alkali metaldoped poly(p‐phenylene), PPP, fully deuterated poly(p‐phenylene), DPPP, and phenylene oligomers. Observed spin concentrations per carbon are at least one decade higher than the Curie spin concentration for Na‐doped polyacetylene. The number of these spins, which likely corresponds to polarons (mobile radical anions), is much less than the amount of alkali metaldopant, suggesting that much of the charge on the polymer chains is in bipolarons (spinless dianions). Relevant to the interaction between spins on the polymer chain and the metal cations, the observed g values are close to the free electron value and do not substantially vary with the donor dopant, temperature, or the molecular weight of the phenylene chain. Although the spin‐orbit effect on g values is small, room temperature linewidth tends to increase with increasing atomic number of dopant—suggesting some interaction, albeit a smaller magnitude effect than for alkali‐metal graphite complexes. The EPRlinewidths are exchange narrowed and proton hyperfine broadening is significant. The latter explains the generally broader linewidths for doped PPP than for doped DPPP. The measured susceptibilities have a temperature dependence which suggests equilibrium between separated polaron defects and singlet and triplet spin states formed intermolecularly via polaron pairing. The interaction is antiferromagnetic and the binding energy between polarons is about 2.2 to 3.3 meV. An upper limit estimate of the Fermi‐surface density of states for K‐doped PPP (0.7 states/eV phenyl) is derived from an upper limit estimate of Pauli susceptibility.