Abstract
It is demonstrated by muon spin relaxation and resonance experiments that the switchable spontaneous polarization of the organic ferroelectric compound tris(4-acetylphenyl)amine is governed by the local molecular dynamics of the acetyl group. The implanted muon forms paramagnetic states, which exhibit longitudinal spin relaxation due to the fluctuation of hyperfine fields exerted from unpaired electrons. The first-principle density functional theory calculations indicate that these states are muonated radicals localized at the phenyl group and on the carbon/oxygen of the acetyl group, thereby suggesting that the spin relaxation is dominated by the random torsional motion of an acetyl group around the C–C bond to the phenyl group. The stepwise change in the relative yield of radicals at T0≈350 K and the gradual increase in the spin relaxation rate with temperature (T) indicate that the torsional motion is significantly enhanced by thermal excitation above T0. This occurs concomitantly with the strong enhancement in the atomic displacement parameter of oxygen in the acetyl group (which is non-linear in T), indicating that it is the local molecular motion of the acetyl groups that drives the structural transition.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call